'en:retardation'
(id=15059006 ; fe=en:retardation ; type=1 ; niveau=200 ;
luminosité=25 ;
somme entrante=121603 creation date=2020-10-11 touchdate=2025-09-30 21:35:15.000) ≈ 6122 relations sortantes
- en:retardation --
r_associated #0: 65 / 1 ->
arriérations mentales
n1=en:retardation | n2=arriérations mentales | rel=r_associated | relid=0 | w=65
- en:retardation --
r_associated #0: 65 / 1 ->
déficience mentale
n1=en:retardation | n2=déficience mentale | rel=r_associated | relid=0 | w=65
- en:retardation --
r_associated #0: 58 / 0.892 ->
débilité
n1=en:retardation | n2=débilité | rel=r_associated | relid=0 | w=58
- en:retardation --
r_associated #0: 57 / 0.877 ->
médecine
n1=en:retardation | n2=médecine | rel=r_associated | relid=0 | w=57
- en:retardation --
r_associated #0: 57 / 0.877 ->
retard mental
n1=en:retardation | n2=retard mental | rel=r_associated | relid=0 | w=57
- en:retardation --
r_associated #0: 56 / 0.862 ->
en:mental retardation
n1=en:retardation | n2=en:mental retardation | rel=r_associated | relid=0 | w=56
- en:retardation --
r_associated #0: 56 / 0.862 ->
Retard mental
n1=en:retardation | n2=Retard mental | rel=r_associated | relid=0 | w=56
- en:retardation --
r_associated #0: 55 / 0.846 ->
en:intellectual disability
n1=en:retardation | n2=en:intellectual disability | rel=r_associated | relid=0 | w=55
- en:retardation --
r_associated #0: 55 / 0.846 ->
retard
n1=en:retardation | n2=retard | rel=r_associated | relid=0 | w=55
- en:retardation --
r_associated #0: 54 / 0.831 ->
idiotie
n1=en:retardation | n2=idiotie | rel=r_associated | relid=0 | w=54
- en:retardation --
r_associated #0: 54 / 0.831 ->
sous-développement
n1=en:retardation | n2=sous-développement | rel=r_associated | relid=0 | w=54
- en:retardation --
r_associated #0: 52 / 0.8 ->
débilité
(Nom)
n1=en:retardation | n2=débilité (Nom) | rel=r_associated | relid=0 | w=52
- en:retardation --
r_associated #0: 52 / 0.8 ->
en:mental handicap
n1=en:retardation | n2=en:mental handicap | rel=r_associated | relid=0 | w=52
- en:retardation --
r_associated #0: 51 / 0.785 ->
oligophrénie
n1=en:retardation | n2=oligophrénie | rel=r_associated | relid=0 | w=51
- en:retardation --
r_associated #0: 49 / 0.754 ->
arriération mentale
n1=en:retardation | n2=arriération mentale | rel=r_associated | relid=0 | w=49
- en:retardation --
r_associated #0: 48 / 0.738 ->
en:learning disability
n1=en:retardation | n2=en:learning disability | rel=r_associated | relid=0 | w=48
- en:retardation --
r_associated #0: 47 / 0.723 ->
sottise
n1=en:retardation | n2=sottise | rel=r_associated | relid=0 | w=47
- en:retardation --
r_associated #0: 45 / 0.692 ->
arriération
n1=en:retardation | n2=arriération | rel=r_associated | relid=0 | w=45
- en:retardation --
r_associated #0: 42 / 0.646 ->
action
n1=en:retardation | n2=action | rel=r_associated | relid=0 | w=42
- en:retardation --
r_associated #0: 40 / 0.615 ->
arriéré
(retard mental)
n1=en:retardation | n2=arriéré (retard mental) | rel=r_associated | relid=0 | w=40
- en:retardation --
r_associated #0: 40 / 0.615 ->
débilité mentale
n1=en:retardation | n2=débilité mentale | rel=r_associated | relid=0 | w=40
- en:retardation --
r_associated #0: 40 / 0.615 ->
déficience
n1=en:retardation | n2=déficience | rel=r_associated | relid=0 | w=40
- en:retardation --
r_associated #0: 40 / 0.615 ->
déficience intellectuelle
n1=en:retardation | n2=déficience intellectuelle | rel=r_associated | relid=0 | w=40
- en:retardation --
r_associated #0: 40 / 0.615 ->
déficit intellectuel
n1=en:retardation | n2=déficit intellectuel | rel=r_associated | relid=0 | w=40
- en:retardation --
r_associated #0: 40 / 0.615 ->
en:mental deficiency
n1=en:retardation | n2=en:mental deficiency | rel=r_associated | relid=0 | w=40
- en:retardation --
r_associated #0: 40 / 0.615 ->
en:mental deterioration
n1=en:retardation | n2=en:mental deterioration | rel=r_associated | relid=0 | w=40
- en:retardation --
r_associated #0: 40 / 0.615 ->
en:psychomotor retardation
n1=en:retardation | n2=en:psychomotor retardation | rel=r_associated | relid=0 | w=40
- en:retardation --
r_associated #0: 40 / 0.615 ->
handicap intellectuel
n1=en:retardation | n2=handicap intellectuel | rel=r_associated | relid=0 | w=40
- en:retardation --
r_associated #0: 40 / 0.615 ->
handicapé mental
n1=en:retardation | n2=handicapé mental | rel=r_associated | relid=0 | w=40
- en:retardation --
r_associated #0: 40 / 0.615 ->
imbécillité
n1=en:retardation | n2=imbécillité | rel=r_associated | relid=0 | w=40
- en:retardation --
r_associated #0: 40 / 0.615 ->
mental
n1=en:retardation | n2=mental | rel=r_associated | relid=0 | w=40
- en:retardation --
r_associated #0: 40 / 0.615 ->
processus pathologique
n1=en:retardation | n2=processus pathologique | rel=r_associated | relid=0 | w=40
- en:retardation --
r_associated #0: 40 / 0.615 ->
psychiatrie
n1=en:retardation | n2=psychiatrie | rel=r_associated | relid=0 | w=40
- en:retardation --
r_associated #0: 40 / 0.615 ->
quotient intellectuel
n1=en:retardation | n2=quotient intellectuel | rel=r_associated | relid=0 | w=40
- en:retardation --
r_associated #0: 40 / 0.615 ->
retards mentaux
n1=en:retardation | n2=retards mentaux | rel=r_associated | relid=0 | w=40
- en:retardation --
r_associated #0: 37 / 0.569 ->
cognition
n1=en:retardation | n2=cognition | rel=r_associated | relid=0 | w=37
- en:retardation --
r_associated #0: 37 / 0.569 ->
retardement
n1=en:retardation | n2=retardement | rel=r_associated | relid=0 | w=37
- en:retardation --
r_associated #0: 35 / 0.538 ->
retard mental, retard de croissance, surdité, microgénitalisme lié au sexe
n1=en:retardation | n2=retard mental, retard de croissance, surdité, microgénitalisme lié au sexe | rel=r_associated | relid=0 | w=35
- en:retardation --
r_associated #0: 32 / 0.492 ->
aliénation
n1=en:retardation | n2=aliénation | rel=r_associated | relid=0 | w=32
- en:retardation --
r_associated #0: 30 / 0.462 ->
arriération mentale profonde
n1=en:retardation | n2=arriération mentale profonde | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
auditifs
n1=en:retardation | n2=auditifs | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
crétinisme
n1=en:retardation | n2=crétinisme | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
développement mental tardif
n1=en:retardation | n2=développement mental tardif | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
dysphasie et aphasie
n1=en:retardation | n2=dysphasie et aphasie | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:'ballooned' neurons with autofluorescent fine granular material
n1=en:retardation | n2=en:'ballooned' neurons with autofluorescent fine granular material | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:'double contour' convolutional calcification on ct scan
n1=en:retardation | n2=en:'double contour' convolutional calcification on ct scan | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:'dragonfly-like' pattern
n1=en:retardation | n2=en:'dragonfly-like' pattern | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:'dragonfly' pattern on imaging
n1=en:retardation | n2=en:'dragonfly' pattern on imaging | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:'eye of the tiger' sign on mri
n1=en:retardation | n2=en:'eye of the tiger' sign on mri | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:'globoid multinucleated cells' in brain tissue
n1=en:retardation | n2=en:'globoid multinucleated cells' in brain tissue | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:'spheroid' inclusions in axons
n1=en:retardation | n2=en:'spheroid' inclusions in axons | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:1p36 deletion syndrome
n1=en:retardation | n2=en:1p36 deletion syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:3-4 hz slow sharp waves seen on eeg
n1=en:retardation | n2=en:3-4 hz slow sharp waves seen on eeg | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:3-6 hz polyspike eeg
n1=en:retardation | n2=en:3-6 hz polyspike eeg | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:3-methylglutaconic aciduria with deafness, encephalopathy, and leigh-like syndrome
n1=en:retardation | n2=en:3-methylglutaconic aciduria with deafness, encephalopathy, and leigh-like syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:6-pyruvoyl-tetrahydropterin synthase deficiency
n1=en:retardation | n2=en:6-pyruvoyl-tetrahydropterin synthase deficiency | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:a subset of patients develop frontotemporal dementia
n1=en:retardation | n2=en:a subset of patients develop frontotemporal dementia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:a subset of patients have neurologic abnormalities
n1=en:retardation | n2=en:a subset of patients have neurologic abnormalities | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:abducens nerve palsy (cn vi)
n1=en:retardation | n2=en:abducens nerve palsy (cn vi) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:abnormal 'cap' on the dorsal pons extending into the fourth ventricle
n1=en:retardation | n2=en:abnormal 'cap' on the dorsal pons extending into the fourth ventricle | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:abnormal 'hobby horse' ataxic gait
n1=en:retardation | n2=en:abnormal 'hobby horse' ataxic gait | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:abnormal behavior
n1=en:retardation | n2=en:abnormal behavior | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:abnormal brain myelination
n1=en:retardation | n2=en:abnormal brain myelination | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:abnormal cell orientation
n1=en:retardation | n2=en:abnormal cell orientation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:abnormal coordination
n1=en:retardation | n2=en:abnormal coordination | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:abnormal cortical eeg discharges triggered by intermittent light
n1=en:retardation | n2=en:abnormal cortical eeg discharges triggered by intermittent light | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:abnormal cortical gyration
n1=en:retardation | n2=en:abnormal cortical gyration | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:abnormal cortical lamination
n1=en:retardation | n2=en:abnormal cortical lamination | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:abnormal cortical layering
n1=en:retardation | n2=en:abnormal cortical layering | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:abnormal corticospinal tract decussation
n1=en:retardation | n2=en:abnormal corticospinal tract decussation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:abnormal eeg (abnormal slowing of background activity)
n1=en:retardation | n2=en:abnormal eeg (abnormal slowing of background activity) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:abnormal eeg (poor alpha rhythms)
n1=en:retardation | n2=en:abnormal eeg (poor alpha rhythms) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:abnormal eeg activity during sleep
n1=en:retardation | n2=en:abnormal eeg activity during sleep | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:abnormal eeg with epileptiform changes
n1=en:retardation | n2=en:abnormal eeg with epileptiform changes | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:abnormal fetal duplication
n1=en:retardation | n2=en:abnormal fetal duplication | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:abnormal gait (67%)
n1=en:retardation | n2=en:abnormal gait (67%) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:abnormal gait due to muscle weakness
n1=en:retardation | n2=en:abnormal gait due to muscle weakness | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:abnormal gray and white matter differentiation in frontal, occipital, and cerebellar regions on ct scan
n1=en:retardation | n2=en:abnormal gray and white matter differentiation in frontal, occipital, and cerebellar regions on ct scan | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:abnormal gyral pattern
n1=en:retardation | n2=en:abnormal gyral pattern | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:abnormal gyri
n1=en:retardation | n2=en:abnormal gyri | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:abnormal gyri (in 1 of 2 patients)
n1=en:retardation | n2=en:abnormal gyri (in 1 of 2 patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:abnormal hippocampus
n1=en:retardation | n2=en:abnormal hippocampus | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:abnormal hypothalamo-pituitary axis
n1=en:retardation | n2=en:abnormal hypothalamo-pituitary axis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:abnormal interictal eeg (in some patients)
n1=en:retardation | n2=en:abnormal interictal eeg (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:abnormal involuntary movement
n1=en:retardation | n2=en:abnormal involuntary movement | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:abnormal lipid peak on brain mrs
n1=en:retardation | n2=en:abnormal lipid peak on brain mrs | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:abnormal lower motor neuron morphology
n1=en:retardation | n2=en:abnormal lower motor neuron morphology | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:abnormal movement
n1=en:retardation | n2=en:abnormal movement | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:abnormal myelination
n1=en:retardation | n2=en:abnormal myelination | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:abnormal ocular motility
n1=en:retardation | n2=en:abnormal ocular motility | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:abnormal pap smear
n1=en:retardation | n2=en:abnormal pap smear | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:abnormal posture
n1=en:retardation | n2=en:abnormal posture | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:abnormal primitive reflexes
n1=en:retardation | n2=en:abnormal primitive reflexes | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:abnormal purkinje cells
n1=en:retardation | n2=en:abnormal purkinje cells | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:abnormal rapid eye movement sleep
n1=en:retardation | n2=en:abnormal rapid eye movement sleep | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:abnormal results investigation nos
n1=en:retardation | n2=en:abnormal results investigation nos | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:abnormal septum pellucidum
n1=en:retardation | n2=en:abnormal septum pellucidum | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:abnormal signals in the thalami seen on mri
n1=en:retardation | n2=en:abnormal signals in the thalami seen on mri | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:abnormal sleep pattern
n1=en:retardation | n2=en:abnormal sleep pattern | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:abnormal sleep-wake cycles
n1=en:retardation | n2=en:abnormal sleep-wake cycles | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:abnormal spike waves
n1=en:retardation | n2=en:abnormal spike waves | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:abnormal sulci
n1=en:retardation | n2=en:abnormal sulci | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:abnormal t2-weighted signals in the occipital white and gray matter
n1=en:retardation | n2=en:abnormal t2-weighted signals in the occipital white and gray matter | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:abnormal urine test result
n1=en:retardation | n2=en:abnormal urine test result | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:abnormal visual evoked potential
n1=en:retardation | n2=en:abnormal visual evoked potential | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:abnormal visual evoked potential (vep)
n1=en:retardation | n2=en:abnormal visual evoked potential (vep) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:abnormal visual sensitivity of the brain in reaction to intermittent photic stimulation
n1=en:retardation | n2=en:abnormal visual sensitivity of the brain in reaction to intermittent photic stimulation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:abnormal white matter signals, in the basal ganglia or cerebellum seen on brain mri
n1=en:retardation | n2=en:abnormal white matter signals, in the basal ganglia or cerebellum seen on brain mri | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:abnormalities, drug-induced
n1=en:retardation | n2=en:abnormalities, drug-induced | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:abnormality of brainstem morphology
n1=en:retardation | n2=en:abnormality of brainstem morphology | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:abnormality of ocular smooth pursuit
n1=en:retardation | n2=en:abnormality of ocular smooth pursuit | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:abnormality of the cerebellum
n1=en:retardation | n2=en:abnormality of the cerebellum | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:abnormality of the corpus callosum
n1=en:retardation | n2=en:abnormality of the corpus callosum | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:abnormality of the posterior cranial fossa
n1=en:retardation | n2=en:abnormality of the posterior cranial fossa | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:abnormality, severe teratoid
n1=en:retardation | n2=en:abnormality, severe teratoid | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:abnormally marked pontobulbar sulcus
n1=en:retardation | n2=en:abnormally marked pontobulbar sulcus | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:absence of anterior pituitary
n1=en:retardation | n2=en:absence of anterior pituitary | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:absence of balloon cells (in type iia)
n1=en:retardation | n2=en:absence of balloon cells (in type iia) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:absence of cerebral aneurysms
n1=en:retardation | n2=en:absence of cerebral aneurysms | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:absence of language development
n1=en:retardation | n2=en:absence of language development | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:absence of lower motor neuron involvement
n1=en:retardation | n2=en:absence of lower motor neuron involvement | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:absence of myelin in the posterior column of the spinal cord (1 patient)
n1=en:retardation | n2=en:absence of myelin in the posterior column of the spinal cord (1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:absence of neurologic manifestations
n1=en:retardation | n2=en:absence of neurologic manifestations | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:absence of neuropathologic findings in the brainstem and anterior horn cells
n1=en:retardation | n2=en:absence of neuropathologic findings in the brainstem and anterior horn cells | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:absence of olfactory bulbs
n1=en:retardation | n2=en:absence of olfactory bulbs | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:absence of primitive reflexes
n1=en:retardation | n2=en:absence of primitive reflexes | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:absence of septum pellucidum
n1=en:retardation | n2=en:absence of septum pellucidum | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:absence of spontaneous movements
n1=en:retardation | n2=en:absence of spontaneous movements | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:absence of the basal ganglia
n1=en:retardation | n2=en:absence of the basal ganglia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:absence of the cerebellar vermis
n1=en:retardation | n2=en:absence of the cerebellar vermis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:absence of the inferior olives
n1=en:retardation | n2=en:absence of the inferior olives | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:absence of the olfactory bulbs and tracts
n1=en:retardation | n2=en:absence of the olfactory bulbs and tracts | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:absence of transverse pontine fibers
n1=en:retardation | n2=en:absence of transverse pontine fibers | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:absence of vestibular schwannomas at age greater than 18 years
n1=en:retardation | n2=en:absence of vestibular schwannomas at age greater than 18 years | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:absence or atrophy of the putamen
n1=en:retardation | n2=en:absence or atrophy of the putamen | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:absence or hypoplasia of the anterior limb of the internal capsule
n1=en:retardation | n2=en:absence or hypoplasia of the anterior limb of the internal capsule | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:absence seizures (in some)
n1=en:retardation | n2=en:absence seizures (in some) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:absence seizures (stage 2 and 3)
n1=en:retardation | n2=en:absence seizures (stage 2 and 3) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:absence seizures may occur
n1=en:retardation | n2=en:absence seizures may occur | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:absent cisterna magna
n1=en:retardation | n2=en:absent cisterna magna | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:absent corpus callosum (variable)
n1=en:retardation | n2=en:absent corpus callosum (variable) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:absent cortical responses of somatosensory evoked potentials
n1=en:retardation | n2=en:absent cortical responses of somatosensory evoked potentials | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:absent development
n1=en:retardation | n2=en:absent development | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:absent myelination of the brain (severe connatal form)
n1=en:retardation | n2=en:absent myelination of the brain (severe connatal form) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:absent olfactory bulbs
n1=en:retardation | n2=en:absent olfactory bulbs | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:absent olfactory tract or bulbs
n1=en:retardation | n2=en:absent olfactory tract or bulbs | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:absent olfactory tracts and bulbs
n1=en:retardation | n2=en:absent olfactory tracts and bulbs | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:absent optic nerves, chiasm, and tracts
n1=en:retardation | n2=en:absent optic nerves, chiasm, and tracts | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:absent or delayed psychomotor development, severe
n1=en:retardation | n2=en:absent or delayed psychomotor development, severe | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:absent or delayed speech development
n1=en:retardation | n2=en:absent or delayed speech development | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:absent or immature dentate nuclei
n1=en:retardation | n2=en:absent or immature dentate nuclei | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:absent or limited speech development
n1=en:retardation | n2=en:absent or limited speech development | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:absent or poor expressive speech
n1=en:retardation | n2=en:absent or poor expressive speech | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:absent pituitary
n1=en:retardation | n2=en:absent pituitary | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:absent posterior pituitary bright spot
n1=en:retardation | n2=en:absent posterior pituitary bright spot | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:absent primitive reflexes
n1=en:retardation | n2=en:absent primitive reflexes | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:absent rem sleep
n1=en:retardation | n2=en:absent rem sleep | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:absent speech
n1=en:retardation | n2=en:absent speech | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:absent superior division of oculomotor nerve and corresponding alpha motor neurons
n1=en:retardation | n2=en:absent superior division of oculomotor nerve and corresponding alpha motor neurons | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:academic disorders, developmental
n1=en:retardation | n2=en:academic disorders, developmental | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:accumulation of autofluorescent material in neurons
n1=en:retardation | n2=en:accumulation of autofluorescent material in neurons | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:accumulation of pas-positive diastase-resistant neuronal inclusion bodies in the cerebral cortex (collins bodies)
n1=en:retardation | n2=en:accumulation of pas-positive diastase-resistant neuronal inclusion bodies in the cerebral cortex (collins bodies) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:acephalostomia
n1=en:retardation | n2=en:acephalostomia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:acne
n1=en:retardation | n2=en:acne | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:acoustic trauma
n1=en:retardation | n2=en:acoustic trauma | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:acquired deformity of limb
n1=en:retardation | n2=en:acquired deformity of limb | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:acquired deformity of spine
n1=en:retardation | n2=en:acquired deformity of spine | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:acranias
n1=en:retardation | n2=en:acranias | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:acromelic frontonasal dysostosis
n1=en:retardation | n2=en:acromelic frontonasal dysostosis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:actin depolymerizing factor/cofilin-immunoreactive eosinophilic rod-like cytoplasmic inclusions in neocortical and thalamic neurons
n1=en:retardation | n2=en:actin depolymerizing factor/cofilin-immunoreactive eosinophilic rod-like cytoplasmic inclusions in neocortical and thalamic neurons | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:actin- and actin depolymerizing factor/cofilin-immunoreactive eosinophilic spherical structures in the striatum
n1=en:retardation | n2=en:actin- and actin depolymerizing factor/cofilin-immunoreactive eosinophilic spherical structures in the striatum | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:action and postural tremor
n1=en:retardation | n2=en:action and postural tremor | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:action dystonia
n1=en:retardation | n2=en:action dystonia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:action myoclonus
n1=en:retardation | n2=en:action myoclonus | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:action myoclonus (triggered by voluntary movements)
n1=en:retardation | n2=en:action myoclonus (triggered by voluntary movements) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:actual effective cognition
n1=en:retardation | n2=en:actual effective cognition | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:acute alcohol abuse
n1=en:retardation | n2=en:acute alcohol abuse | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:acute bronchitis and bronchiolitis
n1=en:retardation | n2=en:acute bronchitis and bronchiolitis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:acute cerebrovascular accidents
n1=en:retardation | n2=en:acute cerebrovascular accidents | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:acute damage meniscus knee
n1=en:retardation | n2=en:acute damage meniscus knee | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:acute encephalopathy
n1=en:retardation | n2=en:acute encephalopathy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:acute episodes of neuropathic symptoms
n1=en:retardation | n2=en:acute episodes of neuropathic symptoms | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:acute episodes of neuropathic symptoms (hcp)
n1=en:retardation | n2=en:acute episodes of neuropathic symptoms (hcp) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:acute laryngitis and/or tracheitis
n1=en:retardation | n2=en:acute laryngitis and/or tracheitis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:acute lymphadenitis
n1=en:retardation | n2=en:acute lymphadenitis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:acute miliary tuberculosis
n1=en:retardation | n2=en:acute miliary tuberculosis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:acute myocardial infarction
n1=en:retardation | n2=en:acute myocardial infarction | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:acute nasopharyngitis
n1=en:retardation | n2=en:acute nasopharyngitis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:acute necrotizing encephalopathy
n1=en:retardation | n2=en:acute necrotizing encephalopathy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:acute neurologic decompensation (in later-onset cases)
n1=en:retardation | n2=en:acute neurologic decompensation (in later-onset cases) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:acute neurologic deficits due to cerebrovascular disease
n1=en:retardation | n2=en:acute neurologic deficits due to cerebrovascular disease | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:acute otitis media/myringitis
n1=en:retardation | n2=en:acute otitis media/myringitis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:acute poliomyelitis
n1=en:retardation | n2=en:acute poliomyelitis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:acute stress/transient/situational disturbance
n1=en:retardation | n2=en:acute stress/transient/situational disturbance | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:acute tonsillitis
n1=en:retardation | n2=en:acute tonsillitis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:addiction
n1=en:retardation | n2=en:addiction | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:additional sex chromosome
n1=en:retardation | n2=en:additional sex chromosome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:adenylosuccinate lyase deficiency (disorder)
n1=en:retardation | n2=en:adenylosuccinate lyase deficiency (disorder) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:adipose tissue in subarachnoid space
n1=en:retardation | n2=en:adipose tissue in subarachnoid space | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:adjustment disorder
n1=en:retardation | n2=en:adjustment disorder | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:adjustment disorders (incl subtypes)
n1=en:retardation | n2=en:adjustment disorders (incl subtypes) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:adjustment stress reaction syndrome
n1=en:retardation | n2=en:adjustment stress reaction syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:adult attention deficit hyperactivity disorder
n1=en:retardation | n2=en:adult attention deficit hyperactivity disorder | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:adverse effect medical agent proper dose
n1=en:retardation | n2=en:adverse effect medical agent proper dose | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:adverse effect of physical agent
n1=en:retardation | n2=en:adverse effect of physical agent | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:afebrile seizure
n1=en:retardation | n2=en:afebrile seizure | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:affected arteries have electron-dense granular material close to vascular smooth muscle cell membranes
n1=en:retardation | n2=en:affected arteries have electron-dense granular material close to vascular smooth muscle cell membranes | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:affected arteries show loss of smooth muscle cells
n1=en:retardation | n2=en:affected arteries show loss of smooth muscle cells | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:affected children are unable to sit without support
n1=en:retardation | n2=en:affected children are unable to sit without support | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:affective psychosis
n1=en:retardation | n2=en:affective psychosis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:agenesis
n1=en:retardation | n2=en:agenesis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:agenesis of corpus callosum, partial or complete (rare)
n1=en:retardation | n2=en:agenesis of corpus callosum, partial or complete (rare) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:agenesis of pineal gland
n1=en:retardation | n2=en:agenesis of pineal gland | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:agenesis of the anterior commissure
n1=en:retardation | n2=en:agenesis of the anterior commissure | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:agenesis of the corpus callosum (1 patient)
n1=en:retardation | n2=en:agenesis of the corpus callosum (1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:agenesis of the corpus callosum (in 1 of 2 patients)
n1=en:retardation | n2=en:agenesis of the corpus callosum (in 1 of 2 patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:agenesis of the corpus callosum (in 2 patients)
n1=en:retardation | n2=en:agenesis of the corpus callosum (in 2 patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:agenesis of the corpus callosum (less common)
n1=en:retardation | n2=en:agenesis of the corpus callosum (less common) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:agenesis of the corpus callosum (patient a)
n1=en:retardation | n2=en:agenesis of the corpus callosum (patient a) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:agenesis of the corpus callosum (rare)
n1=en:retardation | n2=en:agenesis of the corpus callosum (rare) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:agenesis of the corpus callosum (variable)
n1=en:retardation | n2=en:agenesis of the corpus callosum (variable) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:agenesis of the occipital lobes (1 patient)
n1=en:retardation | n2=en:agenesis of the occipital lobes (1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:agenesis of the rostrum of corpus callosum
n1=en:retardation | n2=en:agenesis of the rostrum of corpus callosum | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:agenesis or hypogenesis of the cerebellar vermis
n1=en:retardation | n2=en:agenesis or hypogenesis of the cerebellar vermis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:agenesis or hypoplasia of the corpus callosum
n1=en:retardation | n2=en:agenesis or hypoplasia of the corpus callosum | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:agenesis or severe hypoplasia of cerebellar vermis
n1=en:retardation | n2=en:agenesis or severe hypoplasia of cerebellar vermis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:aggregation of snca-immunopositive inclusions
n1=en:retardation | n2=en:aggregation of snca-immunopositive inclusions | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:aggression
n1=en:retardation | n2=en:aggression | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:agitation
n1=en:retardation | n2=en:agitation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:agnosia
n1=en:retardation | n2=en:agnosia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:agraphia
n1=en:retardation | n2=en:agraphia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:agyria (1 patient)
n1=en:retardation | n2=en:agyria (1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:agyria (posterior-to-anterior gradient)
n1=en:retardation | n2=en:agyria (posterior-to-anterior gradient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:agyria (wws)
n1=en:retardation | n2=en:agyria (wws) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:aicardi syndrome
n1=en:retardation | n2=en:aicardi syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:aicardi-goutieres syndrome 7
n1=en:retardation | n2=en:aicardi-goutieres syndrome 7 | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:akathisia
n1=en:retardation | n2=en:akathisia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:akinesia
n1=en:retardation | n2=en:akinesia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:akinetic mutism (in some patients)
n1=en:retardation | n2=en:akinetic mutism (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:albinism
n1=en:retardation | n2=en:albinism | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:albright's hereditary osteodystrophy
n1=en:retardation | n2=en:albright's hereditary osteodystrophy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:alcohol dependence
n1=en:retardation | n2=en:alcohol dependence | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:alcohol-related disorders
n1=en:retardation | n2=en:alcohol-related disorders | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:alcohol-related intrauterine disorder
n1=en:retardation | n2=en:alcohol-related intrauterine disorder | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:all other perinatal morbidity
n1=en:retardation | n2=en:all other perinatal morbidity | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:allgrove syndrome
n1=en:retardation | n2=en:allgrove syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:alobar holoprosencephaly (rare)
n1=en:retardation | n2=en:alobar holoprosencephaly (rare) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:alobar hpe shows absence of interhemispheric cleavage and single ventricle
n1=en:retardation | n2=en:alobar hpe shows absence of interhemispheric cleavage and single ventricle | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:alpha thalassemia x-linked mental retardation syndrome
n1=en:retardation | n2=en:alpha thalassemia x-linked mental retardation syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:alpha-b-crystallin expression in oligodendrocytes
n1=en:retardation | n2=en:alpha-b-crystallin expression in oligodendrocytes | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:alpha-synuclein immunoreactive neuronal and glial inclusions
n1=en:retardation | n2=en:alpha-synuclein immunoreactive neuronal and glial inclusions | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:alpha-synuclein-containing inclusions
n1=en:retardation | n2=en:alpha-synuclein-containing inclusions | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:alpha-synuclein-immunoreactive lewy neurites
n1=en:retardation | n2=en:alpha-synuclein-immunoreactive lewy neurites | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:alpha-synuclein-immunreactive lewy bodies
n1=en:retardation | n2=en:alpha-synuclein-immunreactive lewy bodies | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:altered breathing patterns
n1=en:retardation | n2=en:altered breathing patterns | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:altered mental status
n1=en:retardation | n2=en:altered mental status | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:alternating hemiplegia of childhood 1
n1=en:retardation | n2=en:alternating hemiplegia of childhood 1 | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:alzheimer disease, early onset
n1=en:retardation | n2=en:alzheimer disease, early onset | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:alzheimer's disease
n1=en:retardation | n2=en:alzheimer's disease | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:amastia
n1=en:retardation | n2=en:amastia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:amaurosis congenita of leber, type 1
n1=en:retardation | n2=en:amaurosis congenita of leber, type 1 | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:amaurotic familial idiocy
n1=en:retardation | n2=en:amaurotic familial idiocy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ambulation difficulty
n1=en:retardation | n2=en:ambulation difficulty | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:amegakaryocytic thrombocytopenia with congenital malformation
n1=en:retardation | n2=en:amegakaryocytic thrombocytopenia with congenital malformation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:amnesia
n1=en:retardation | n2=en:amnesia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:amniotic band syndrome
n1=en:retardation | n2=en:amniotic band syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:amyloid deposition in the leptomeningeal vessels, brainstem, spinal cord
n1=en:retardation | n2=en:amyloid deposition in the leptomeningeal vessels, brainstem, spinal cord | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:amyloid plaques may be present
n1=en:retardation | n2=en:amyloid plaques may be present | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:amyloid-like plaques are not immunoreactive to app (104760)
n1=en:retardation | n2=en:amyloid-like plaques are not immunoreactive to app (104760) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:amyloid-like plaques, immunoreactive to prp, predominantly in the cerebellum
n1=en:retardation | n2=en:amyloid-like plaques, immunoreactive to prp, predominantly in the cerebellum | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:amyotrophic lateral sclerosis
n1=en:retardation | n2=en:amyotrophic lateral sclerosis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:amyotrophy, distal, severe
n1=en:retardation | n2=en:amyotrophy, distal, severe | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:anal fissure/perianal abscess
n1=en:retardation | n2=en:anal fissure/perianal abscess | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:anarthria speech disorder
n1=en:retardation | n2=en:anarthria speech disorder | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:anauxetic dysplasia
n1=en:retardation | n2=en:anauxetic dysplasia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:anencephalus and similar anomalies
n1=en:retardation | n2=en:anencephalus and similar anomalies | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:anencephaly
n1=en:retardation | n2=en:anencephaly | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:anencephaly (1 patient)
n1=en:retardation | n2=en:anencephaly (1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:angelman syndrome
n1=en:retardation | n2=en:angelman syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:angiitis, cerebral
n1=en:retardation | n2=en:angiitis, cerebral | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:angina
n1=en:retardation | n2=en:angina | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:angiographically 'silent'
n1=en:retardation | n2=en:angiographically 'silent' | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:angulation of the frontal horns
n1=en:retardation | n2=en:angulation of the frontal horns | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:anisocoria
n1=en:retardation | n2=en:anisocoria | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ankle clonus
n1=en:retardation | n2=en:ankle clonus | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ankle clonus (in some patients)
n1=en:retardation | n2=en:ankle clonus (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ankle clonus (in some)
n1=en:retardation | n2=en:ankle clonus (in some) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ankle or knee clonus
n1=en:retardation | n2=en:ankle or knee clonus | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ankle reflex absent
n1=en:retardation | n2=en:ankle reflex absent | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ankyloglossia
n1=en:retardation | n2=en:ankyloglossia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:anomalies of the folding of the right sylvian area
n1=en:retardation | n2=en:anomalies of the folding of the right sylvian area | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:anomalies of the temporal area
n1=en:retardation | n2=en:anomalies of the temporal area | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:anomaly congenital special senses
n1=en:retardation | n2=en:anomaly congenital special senses | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:anomia
n1=en:retardation | n2=en:anomia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:anosmia
n1=en:retardation | n2=en:anosmia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:anosmia (1 patient)
n1=en:retardation | n2=en:anosmia (1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:anosmia (in contiguous gene syndrome patients)
n1=en:retardation | n2=en:anosmia (in contiguous gene syndrome patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:anosmia (in some patients)
n1=en:retardation | n2=en:anosmia (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:antenatal intracerebral hemorrhage
n1=en:retardation | n2=en:antenatal intracerebral hemorrhage | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:anterior basal encephalocele
n1=en:retardation | n2=en:anterior basal encephalocele | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:anterior commissure not evident
n1=en:retardation | n2=en:anterior commissure not evident | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:anterior horn atrophy
n1=en:retardation | n2=en:anterior horn atrophy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:anterior horn cell impairment
n1=en:retardation | n2=en:anterior horn cell impairment | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:anterior pachygyria and posterior agyria
n1=en:retardation | n2=en:anterior pachygyria and posterior agyria | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:anterior pituitary adenoma
n1=en:retardation | n2=en:anterior pituitary adenoma | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:anterior pituitary hypoplasia
n1=en:retardation | n2=en:anterior pituitary hypoplasia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:anterior sacral meningocele
n1=en:retardation | n2=en:anterior sacral meningocele | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:anterior temporal lobe subcortical cysts
n1=en:retardation | n2=en:anterior temporal lobe subcortical cysts | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:antisocial behavior
n1=en:retardation | n2=en:antisocial behavior | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:anxiety
n1=en:retardation | n2=en:anxiety | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:anxiety adverse event
n1=en:retardation | n2=en:anxiety adverse event | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:anxiety disorder
n1=en:retardation | n2=en:anxiety disorder | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:anxiety disorder/anxiety state
n1=en:retardation | n2=en:anxiety disorder/anxiety state | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:anxiety disorders and symptoms
n1=en:retardation | n2=en:anxiety disorders and symptoms | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:apathy
n1=en:retardation | n2=en:apathy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:aphasia
n1=en:retardation | n2=en:aphasia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:aplasia of corpus callosum
n1=en:retardation | n2=en:aplasia of corpus callosum | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:aplasia of olfactory bulbs, bilateral
n1=en:retardation | n2=en:aplasia of olfactory bulbs, bilateral | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:aplasia of the corpus callosum (wws) encephalocele (1 patient, meb)
n1=en:retardation | n2=en:aplasia of the corpus callosum (wws) encephalocele (1 patient, meb) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:aplasia of the inferior half of the cerebellar vermis
n1=en:retardation | n2=en:aplasia of the inferior half of the cerebellar vermis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:aplasia of the vermis
n1=en:retardation | n2=en:aplasia of the vermis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:aplasia, nos
n1=en:retardation | n2=en:aplasia, nos | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:aplasia/hypoplasia of the cerebellar vermis
n1=en:retardation | n2=en:aplasia/hypoplasia of the cerebellar vermis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:aplasia/hypoplasia of the cerebellum
n1=en:retardation | n2=en:aplasia/hypoplasia of the cerebellum | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:aplasia/hypoplasia of the corpus callosum
n1=en:retardation | n2=en:aplasia/hypoplasia of the corpus callosum | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:apoptotic neurons
n1=en:retardation | n2=en:apoptotic neurons | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:appendicitis
n1=en:retardation | n2=en:appendicitis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:appendicular hypertonia
n1=en:retardation | n2=en:appendicular hypertonia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:approximately 30% of patients show normal early development
n1=en:retardation | n2=en:approximately 30% of patients show normal early development | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:apraxia (in some patients)
n1=en:retardation | n2=en:apraxia (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:apraxia, verbal
n1=en:retardation | n2=en:apraxia, verbal | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:apraxias
n1=en:retardation | n2=en:apraxias | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:aqueductal stenosis
n1=en:retardation | n2=en:aqueductal stenosis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:arachnoid cyst
n1=en:retardation | n2=en:arachnoid cyst | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:arachnoid cyst (in some patients)
n1=en:retardation | n2=en:arachnoid cyst (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:arachnoid cysts (1 patient)
n1=en:retardation | n2=en:arachnoid cysts (1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:arachnoid cysts (in one family)
n1=en:retardation | n2=en:arachnoid cysts (in one family) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:arachnoid cysts of the cerebellopontine angle (reported in 1 family)
n1=en:retardation | n2=en:arachnoid cysts of the cerebellopontine angle (reported in 1 family) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:arachnoid hemangiomata
n1=en:retardation | n2=en:arachnoid hemangiomata | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:arachnoidal cysts
n1=en:retardation | n2=en:arachnoidal cysts | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:areflexia
n1=en:retardation | n2=en:areflexia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:areflexia (30%)
n1=en:retardation | n2=en:areflexia (30%) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:areflexia of lower limbs
n1=en:retardation | n2=en:areflexia of lower limbs | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:areflexia of upper limbs
n1=en:retardation | n2=en:areflexia of upper limbs | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:argininemia
n1=en:retardation | n2=en:argininemia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:argininosuccinic aciduria
n1=en:retardation | n2=en:argininosuccinic aciduria | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:argyrophilic hyperphosphorylated tau-positive inclusions (pick bodies)
n1=en:retardation | n2=en:argyrophilic hyperphosphorylated tau-positive inclusions (pick bodies) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:arhinencephaly
n1=en:retardation | n2=en:arhinencephaly | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:arhinencephaly (1 patient)
n1=en:retardation | n2=en:arhinencephaly (1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:arithmetic disorder
n1=en:retardation | n2=en:arithmetic disorder | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:arm flexion
n1=en:retardation | n2=en:arm flexion | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:arm pain
n1=en:retardation | n2=en:arm pain | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:arnold-chiari i malformation
n1=en:retardation | n2=en:arnold-chiari i malformation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:arnold-chiari malformation
n1=en:retardation | n2=en:arnold-chiari malformation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:arrest of psychomotor development after seizure onset
n1=en:retardation | n2=en:arrest of psychomotor development after seizure onset | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:arrested hydrocephalus (rare)
n1=en:retardation | n2=en:arrested hydrocephalus (rare) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:arrhythmia
n1=en:retardation | n2=en:arrhythmia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:arthrogryposis, mental retardation, and seizures
n1=en:retardation | n2=en:arthrogryposis, mental retardation, and seizures | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:articulation difficulties
n1=en:retardation | n2=en:articulation difficulties | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:articulation, unintelligible
n1=en:retardation | n2=en:articulation, unintelligible | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:articulatory defect
n1=en:retardation | n2=en:articulatory defect | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:aspartylglycosaminuria
n1=en:retardation | n2=en:aspartylglycosaminuria | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:asperger syndrome
n1=en:retardation | n2=en:asperger syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:asperger syndrome (rare)
n1=en:retardation | n2=en:asperger syndrome (rare) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:associated with paresthesias and dysesthesias
n1=en:retardation | n2=en:associated with paresthesias and dysesthesias | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:associated with syringomyelia (186700)
n1=en:retardation | n2=en:associated with syringomyelia (186700) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:association between poor metabolizers (pm) and parkinson disease
n1=en:retardation | n2=en:association between poor metabolizers (pm) and parkinson disease | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:asthma
n1=en:retardation | n2=en:asthma | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:astrocyte
n1=en:retardation | n2=en:astrocyte | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:astrocytes show reactive changes
n1=en:retardation | n2=en:astrocytes show reactive changes | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:astrocytic gliosis
n1=en:retardation | n2=en:astrocytic gliosis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:astrocytosis
n1=en:retardation | n2=en:astrocytosis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:astrogliosis (in some patients)
n1=en:retardation | n2=en:astrogliosis (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:asymmetric brain development
n1=en:retardation | n2=en:asymmetric brain development | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:asymmetry at onset (74%)
n1=en:retardation | n2=en:asymmetry at onset (74%) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:asymmetry of symptoms
n1=en:retardation | n2=en:asymmetry of symptoms | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ataxia
n1=en:retardation | n2=en:ataxia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ataxia (1 patient)
n1=en:retardation | n2=en:ataxia (1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ataxia (cvs+)
n1=en:retardation | n2=en:ataxia (cvs+) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ataxia (deletion patients)
n1=en:retardation | n2=en:ataxia (deletion patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ataxia (early-onset form)
n1=en:retardation | n2=en:ataxia (early-onset form) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ataxia (if untreated)
n1=en:retardation | n2=en:ataxia (if untreated) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ataxia (in some patients)
n1=en:retardation | n2=en:ataxia (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ataxia (less common)
n1=en:retardation | n2=en:ataxia (less common) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ataxia (type i and type ii, infantile and juvenile)
n1=en:retardation | n2=en:ataxia (type i and type ii, infantile and juvenile) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ataxia (uncommon)
n1=en:retardation | n2=en:ataxia (uncommon) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ataxia in those who survive
n1=en:retardation | n2=en:ataxia in those who survive | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ataxia may develop in middle age (less common)
n1=en:retardation | n2=en:ataxia may develop in middle age (less common) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ataxia with febrile episodes (rare)
n1=en:retardation | n2=en:ataxia with febrile episodes (rare) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ataxia with jerky arm movements
n1=en:retardation | n2=en:ataxia with jerky arm movements | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ataxia worsens in the dark
n1=en:retardation | n2=en:ataxia worsens in the dark | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ataxia, (1 family)
n1=en:retardation | n2=en:ataxia, (1 family) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ataxia, cerebellar (in some patients)
n1=en:retardation | n2=en:ataxia, cerebellar (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ataxia, cerebellar (upper and lower limbs affected)
n1=en:retardation | n2=en:ataxia, cerebellar (upper and lower limbs affected) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ataxia, cerebellar, limb and gait
n1=en:retardation | n2=en:ataxia, cerebellar, limb and gait | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ataxia, episodic (episodes last from hours to days)
n1=en:retardation | n2=en:ataxia, episodic (episodes last from hours to days) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ataxia, episodic, occurring after febrile illness or stress
n1=en:retardation | n2=en:ataxia, episodic, occurring after febrile illness or stress | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ataxia, fatal x-linked, with deafness and loss of vision
n1=en:retardation | n2=en:ataxia, fatal x-linked, with deafness and loss of vision | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ataxia, gait and appendicular
n1=en:retardation | n2=en:ataxia, gait and appendicular | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ataxia, mild
n1=en:retardation | n2=en:ataxia, mild | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ataxia, spastic, childhood-onset, autosomal recessive, with optic atrophy and mental retardation
n1=en:retardation | n2=en:ataxia, spastic, childhood-onset, autosomal recessive, with optic atrophy and mental retardation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ataxias, appendicular
n1=en:retardation | n2=en:ataxias, appendicular | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ataxias, sensory
n1=en:retardation | n2=en:ataxias, sensory | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ataxias, truncal
n1=en:retardation | n2=en:ataxias, truncal | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ataxic gait
n1=en:retardation | n2=en:ataxic gait | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ataxic gait (in some patients)
n1=en:retardation | n2=en:ataxic gait (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ataxic gait (juvenile form)
n1=en:retardation | n2=en:ataxic gait (juvenile form) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ataxic movements
n1=en:retardation | n2=en:ataxic movements | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:atelencephaly
n1=en:retardation | n2=en:atelencephaly | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:atherosclerosis excluding heart/brain
n1=en:retardation | n2=en:atherosclerosis excluding heart/brain | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:athetoid and dystonic hand movements (in some patients)
n1=en:retardation | n2=en:athetoid and dystonic hand movements (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:athetosis
n1=en:retardation | n2=en:athetosis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:athetosis (in some patients)
n1=en:retardation | n2=en:athetosis (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:athetosis (later)
n1=en:retardation | n2=en:athetosis (later) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:athetosis, mild (in one patient)
n1=en:retardation | n2=en:athetosis, mild (in one patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:atlantoaxial instability
n1=en:retardation | n2=en:atlantoaxial instability | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:atopic conjunctivitis
n1=en:retardation | n2=en:atopic conjunctivitis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:atopic dermatitis/eczema
n1=en:retardation | n2=en:atopic dermatitis/eczema | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:atresia
n1=en:retardation | n2=en:atresia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:atretic occipital cephalocele
n1=en:retardation | n2=en:atretic occipital cephalocele | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:atrial fibrillation and flutter
n1=en:retardation | n2=en:atrial fibrillation and flutter | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:atrial septal defect
n1=en:retardation | n2=en:atrial septal defect | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:atrophic pons (in some)
n1=en:retardation | n2=en:atrophic pons (in some) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:atrophy and weakness of limb musculature
n1=en:retardation | n2=en:atrophy and weakness of limb musculature | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:atrophy and weakness of the tongue, jaw, and throat muscles
n1=en:retardation | n2=en:atrophy and weakness of the tongue, jaw, and throat muscles | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:atrophy may be more severe in the left hemisphere
n1=en:retardation | n2=en:atrophy may be more severe in the left hemisphere | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:atrophy of cerebellum, brainstem, cervical spinal cord
n1=en:retardation | n2=en:atrophy of cerebellum, brainstem, cervical spinal cord | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:atrophy of corpus callosum
n1=en:retardation | n2=en:atrophy of corpus callosum | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:atrophy of hippocampal dentate gyrus
n1=en:retardation | n2=en:atrophy of hippocampal dentate gyrus | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:atrophy of pyramids
n1=en:retardation | n2=en:atrophy of pyramids | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:atrophy of the cerebellar vermis seen on mri
n1=en:retardation | n2=en:atrophy of the cerebellar vermis seen on mri | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:atrophy of the dentate nucleus
n1=en:retardation | n2=en:atrophy of the dentate nucleus | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:atrophy of the frontal and parietal cortex
n1=en:retardation | n2=en:atrophy of the frontal and parietal cortex | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:atrophy of the granular cell layer of the cerebellum
n1=en:retardation | n2=en:atrophy of the granular cell layer of the cerebellum | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:atrophy of the motor cortex in older patients seen on mri
n1=en:retardation | n2=en:atrophy of the motor cortex in older patients seen on mri | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:atrophy of the pituitary (1 patient)
n1=en:retardation | n2=en:atrophy of the pituitary (1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:atrophy of the pons (in some patients)
n1=en:retardation | n2=en:atrophy of the pons (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:atrophy of the posterior columns and spinocerebellar tracts
n1=en:retardation | n2=en:atrophy of the posterior columns and spinocerebellar tracts | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:atrophy of the spinal cord
n1=en:retardation | n2=en:atrophy of the spinal cord | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:atrophy of the spinal cord and cerebellar tracts
n1=en:retardation | n2=en:atrophy of the spinal cord and cerebellar tracts | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:atrophy, thin hemisphere
n1=en:retardation | n2=en:atrophy, thin hemisphere | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:atrophy/degeneration involving the spinal cord
n1=en:retardation | n2=en:atrophy/degeneration involving the spinal cord | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:attacks characterized by lethargy, incoordination, loss of motor skills
n1=en:retardation | n2=en:attacks characterized by lethargy, incoordination, loss of motor skills | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:attacks of disabling daytime drowsiness and low alertness
n1=en:retardation | n2=en:attacks of disabling daytime drowsiness and low alertness | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:attention deficit conduct and disruptive behavior disorders
n1=en:retardation | n2=en:attention deficit conduct and disruptive behavior disorders | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:attention deficit disorder
n1=en:retardation | n2=en:attention deficit disorder | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:attention deficit hyperactivity disorder
n1=en:retardation | n2=en:attention deficit hyperactivity disorder | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:attenuated gyri
n1=en:retardation | n2=en:attenuated gyri | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:atypical absence seizure
n1=en:retardation | n2=en:atypical absence seizure | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:atypical absence, atonic/tonic, or tonic-clonic seizures
n1=en:retardation | n2=en:atypical absence, atonic/tonic, or tonic-clonic seizures | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:auditory auras
n1=en:retardation | n2=en:auditory auras | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:auditory, olfactory, and visual auras
n1=en:retardation | n2=en:auditory, olfactory, and visual auras | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:aura
n1=en:retardation | n2=en:aura | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:aura (in some instances)
n1=en:retardation | n2=en:aura (in some instances) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:aura may occur
n1=en:retardation | n2=en:aura may occur | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:autism
n1=en:retardation | n2=en:autism | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:autism (rare)
n1=en:retardation | n2=en:autism (rare) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:autism or autistic features
n1=en:retardation | n2=en:autism or autistic features | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:autofluorescent lipopigment in neurons
n1=en:retardation | n2=en:autofluorescent lipopigment in neurons | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:autofluorescent pigment in microglia and macrophages
n1=en:retardation | n2=en:autofluorescent pigment in microglia and macrophages | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:automatism
n1=en:retardation | n2=en:automatism | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:autonomic abnormalities
n1=en:retardation | n2=en:autonomic abnormalities | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:autonomic disturbances
n1=en:retardation | n2=en:autonomic disturbances | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:autonomic dysfunction (in patients with hsan2d)
n1=en:retardation | n2=en:autonomic dysfunction (in patients with hsan2d) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:autonomic dysfunction may occur
n1=en:retardation | n2=en:autonomic dysfunction may occur | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:autonomic dysregulation
n1=en:retardation | n2=en:autonomic dysregulation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:autonomic features may occur
n1=en:retardation | n2=en:autonomic features may occur | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:autonomic features may occur (diaphoresis, tachycardia, hyperthermia, hypertension)
n1=en:retardation | n2=en:autonomic features may occur (diaphoresis, tachycardia, hyperthermia, hypertension) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:autonomic instability (22%)
n1=en:retardation | n2=en:autonomic instability (22%) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:autonomic involvement
n1=en:retardation | n2=en:autonomic involvement | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:autonomic involvement affecting limbs during episodes
n1=en:retardation | n2=en:autonomic involvement affecting limbs during episodes | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:autonomic involvement may occur
n1=en:retardation | n2=en:autonomic involvement may occur | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:autonomic manifestations
n1=en:retardation | n2=en:autonomic manifestations | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:autonomic nervous system disorders
n1=en:retardation | n2=en:autonomic nervous system disorders | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:autonomic signs
n1=en:retardation | n2=en:autonomic signs | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:autonomic symptoms
n1=en:retardation | n2=en:autonomic symptoms | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:average intellect
n1=en:retardation | n2=en:average intellect | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:axenfeld-rieger anomaly with partially absent eye muscles, distinctive face, hydrocephaly, and skeletal abnormalities
n1=en:retardation | n2=en:axenfeld-rieger anomaly with partially absent eye muscles, distinctive face, hydrocephaly, and skeletal abnormalities | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:axial dystonia
n1=en:retardation | n2=en:axial dystonia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:axial hypotonia (1 patient)
n1=en:retardation | n2=en:axial hypotonia (1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:axial hypotonia (rare)
n1=en:retardation | n2=en:axial hypotonia (rare) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:axial imbalance (34%)
n1=en:retardation | n2=en:axial imbalance (34%) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:axial muscle stiffness, symmetric
n1=en:retardation | n2=en:axial muscle stiffness, symmetric | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:axial rigidity
n1=en:retardation | n2=en:axial rigidity | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:axis i diagnosis
n1=en:retardation | n2=en:axis i diagnosis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:axis ii diagnosis
n1=en:retardation | n2=en:axis ii diagnosis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:axis iii diagnosis
n1=en:retardation | n2=en:axis iii diagnosis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:axis iv diagnosis
n1=en:retardation | n2=en:axis iv diagnosis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:axis v diagnosis
n1=en:retardation | n2=en:axis v diagnosis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:axonal 'spheroid' inclusions
n1=en:retardation | n2=en:axonal 'spheroid' inclusions | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:axonal 'spheroid' inclusions in the cns
n1=en:retardation | n2=en:axonal 'spheroid' inclusions in the cns | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:axonal dystrophy
n1=en:retardation | n2=en:axonal dystrophy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:axonal dystrophy (in some patients)
n1=en:retardation | n2=en:axonal dystrophy (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:axonal loss
n1=en:retardation | n2=en:axonal loss | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:axonal loss and gliosis in the corticospinal tracts
n1=en:retardation | n2=en:axonal loss and gliosis in the corticospinal tracts | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:axonal spheroids
n1=en:retardation | n2=en:axonal spheroids | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:axonal spheroids in the dorsal column
n1=en:retardation | n2=en:axonal spheroids in the dorsal column | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:axonal swelling of spinal nerve roots and cranial nerves
n1=en:retardation | n2=en:axonal swelling of spinal nerve roots and cranial nerves | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:axonal swelling or thickening
n1=en:retardation | n2=en:axonal swelling or thickening | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:axonal swelling or thickening in the cns
n1=en:retardation | n2=en:axonal swelling or thickening in the cns | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:axonal swellings or spheroids
n1=en:retardation | n2=en:axonal swellings or spheroids | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:babinski sign
n1=en:retardation | n2=en:babinski sign | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:back pain
n1=en:retardation | n2=en:back pain | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:background slowing
n1=en:retardation | n2=en:background slowing | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:balanitis
n1=en:retardation | n2=en:balanitis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:baller-gerold syndrome
n1=en:retardation | n2=en:baller-gerold syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:balloon cells (in type iib)
n1=en:retardation | n2=en:balloon cells (in type iib) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ballooned neurons
n1=en:retardation | n2=en:ballooned neurons | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:band heterotopia (1 patient)
n1=en:retardation | n2=en:band heterotopia (1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:bardet-biedl syndrome
n1=en:retardation | n2=en:bardet-biedl syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:bardet-biedl syndrome 1 (disorder)
n1=en:retardation | n2=en:bardet-biedl syndrome 1 (disorder) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:bardet-biedl syndrome 13
n1=en:retardation | n2=en:bardet-biedl syndrome 13 | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:bardet-biedl syndrome 14 (disorder)
n1=en:retardation | n2=en:bardet-biedl syndrome 14 (disorder) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:bardet-biedl syndrome 16
n1=en:retardation | n2=en:bardet-biedl syndrome 16 | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:bardet-biedl syndrome 2 (disorder)
n1=en:retardation | n2=en:bardet-biedl syndrome 2 (disorder) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:bardet-biedl syndrome 6
n1=en:retardation | n2=en:bardet-biedl syndrome 6 | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:bardet-biedl syndrome 7
n1=en:retardation | n2=en:bardet-biedl syndrome 7 | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:bardet-biedl syndrome 8
n1=en:retardation | n2=en:bardet-biedl syndrome 8 | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:bardet-biedl syndrome 9
n1=en:retardation | n2=en:bardet-biedl syndrome 9 | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:bartter syndrome, antenatal type 1
n1=en:retardation | n2=en:bartter syndrome, antenatal type 1 | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:bartter syndrome, antenatal, type 2
n1=en:retardation | n2=en:bartter syndrome, antenatal, type 2 | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:bartter syndrome, type 4a
n1=en:retardation | n2=en:bartter syndrome, type 4a | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:bartter syndrome, type 4b
n1=en:retardation | n2=en:bartter syndrome, type 4b | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:basal ganglia atrophy
n1=en:retardation | n2=en:basal ganglia atrophy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:basal ganglia atrophy, progressive
n1=en:retardation | n2=en:basal ganglia atrophy, progressive | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:basal ganglia calcification
n1=en:retardation | n2=en:basal ganglia calcification | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:basal ganglia calcifications (in some patients)
n1=en:retardation | n2=en:basal ganglia calcifications (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:basal ganglia calcifications (rare)
n1=en:retardation | n2=en:basal ganglia calcifications (rare) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:basal ganglia cysts
n1=en:retardation | n2=en:basal ganglia cysts | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:basal ganglia dysfunction
n1=en:retardation | n2=en:basal ganglia dysfunction | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:basal ganglia gliosis
n1=en:retardation | n2=en:basal ganglia gliosis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:basal ganglia lesions may be present before onset of clinical symptoms
n1=en:retardation | n2=en:basal ganglia lesions may be present before onset of clinical symptoms | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:basal ganglia lesions seen on mri
n1=en:retardation | n2=en:basal ganglia lesions seen on mri | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:basal ganglia lucencies
n1=en:retardation | n2=en:basal ganglia lucencies | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:basal ganglion degeneration
n1=en:retardation | n2=en:basal ganglion degeneration | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:bathing disability
n1=en:retardation | n2=en:bathing disability | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:beaulieu-boycott-innes syndrome
n1=en:retardation | n2=en:beaulieu-boycott-innes syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:begins in limbs, later generalized (childhood onset)
n1=en:retardation | n2=en:begins in limbs, later generalized (childhood onset) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:behavior disorders
n1=en:retardation | n2=en:behavior disorders | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:behavioral and emotional disorder with onset in childhood
n1=en:retardation | n2=en:behavioral and emotional disorder with onset in childhood | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:behavioral disability
n1=en:retardation | n2=en:behavioral disability | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:behavioral syndrome associated with physiological disturbance and physical factors
n1=en:retardation | n2=en:behavioral syndrome associated with physiological disturbance and physical factors | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:behavioral variant of frontotemporal dementia
n1=en:retardation | n2=en:behavioral variant of frontotemporal dementia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:behaviors, adaptive
n1=en:retardation | n2=en:behaviors, adaptive | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:behr syndrome
n1=en:retardation | n2=en:behr syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:benign digestive system neoplasm
n1=en:retardation | n2=en:benign digestive system neoplasm | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:benign female breast neoplasm
n1=en:retardation | n2=en:benign female breast neoplasm | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:benign neoplasm of male genital organ
n1=en:retardation | n2=en:benign neoplasm of male genital organ | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:benign nervous system neoplasm
n1=en:retardation | n2=en:benign nervous system neoplasm | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:benign obstetric neoplasm
n1=en:retardation | n2=en:benign obstetric neoplasm | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:benign prostatic hyperplasia
n1=en:retardation | n2=en:benign prostatic hyperplasia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:benign respiratory neoplasm
n1=en:retardation | n2=en:benign respiratory neoplasm | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:benign thyroid gland neoplasm
n1=en:retardation | n2=en:benign thyroid gland neoplasm | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:benign urinary system neoplasm
n1=en:retardation | n2=en:benign urinary system neoplasm | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:benign/unspecified neoplasms
n1=en:retardation | n2=en:benign/unspecified neoplasms | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:beta-amyloid-positive senile plaques
n1=en:retardation | n2=en:beta-amyloid-positive senile plaques | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:beta-mannosidosis
n1=en:retardation | n2=en:beta-mannosidosis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:between 2 and 7% of children will develop afebrile seizure disorders later in life
n1=en:retardation | n2=en:between 2 and 7% of children will develop afebrile seizure disorders later in life | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:biemond syndrome ii
n1=en:retardation | n2=en:biemond syndrome ii | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:bilateral calcification of basal ganglia and cerebellum
n1=en:retardation | n2=en:bilateral calcification of basal ganglia and cerebellum | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:bilateral convulsive seizures
n1=en:retardation | n2=en:bilateral convulsive seizures | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:bilateral perisylvian cortical malformations on mri
n1=en:retardation | n2=en:bilateral perisylvian cortical malformations on mri | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:bilateral schizencephaly
n1=en:retardation | n2=en:bilateral schizencephaly | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:bilateral signals in the basal ganglia
n1=en:retardation | n2=en:bilateral signals in the basal ganglia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:bilateral striatal lucencies on imaging
n1=en:retardation | n2=en:bilateral striatal lucencies on imaging | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:bilateral striatal necrosis
n1=en:retardation | n2=en:bilateral striatal necrosis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:bilateral thalamic lesions on mri
n1=en:retardation | n2=en:bilateral thalamic lesions on mri | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:bilateral, symmetric intracerebral calcifications, especially in the basal ganglia and periventricular areas
n1=en:retardation | n2=en:bilateral, symmetric intracerebral calcifications, especially in the basal ganglia and periventricular areas | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:biliary atresia
n1=en:retardation | n2=en:biliary atresia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:biopsy in both types shows neuronal cytomegaly (large, bizarre, maloriented neurons) in the laminar cortex
n1=en:retardation | n2=en:biopsy in both types shows neuronal cytomegaly (large, bizarre, maloriented neurons) in the laminar cortex | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:biopsy shows foamy lipid-laden macrophages
n1=en:retardation | n2=en:biopsy shows foamy lipid-laden macrophages | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:biopsy shows white matter hypomyelination, demyelination, gliosis
n1=en:retardation | n2=en:biopsy shows white matter hypomyelination, demyelination, gliosis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:bipolar and related disorders
n1=en:retardation | n2=en:bipolar and related disorders | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:bipolar disorder
n1=en:retardation | n2=en:bipolar disorder | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:blake's pouch (rare)
n1=en:retardation | n2=en:blake's pouch (rare) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:blepharitis/stye/chalazion
n1=en:retardation | n2=en:blepharitis/stye/chalazion | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:blepharophimosis syndrome ohdo type
n1=en:retardation | n2=en:blepharophimosis syndrome ohdo type | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:blepharophimosis with facial and genital anomalies and mental retardation
n1=en:retardation | n2=en:blepharophimosis with facial and genital anomalies and mental retardation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:blindness
n1=en:retardation | n2=en:blindness | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:blindness all degrees/types
n1=en:retardation | n2=en:blindness all degrees/types | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:blocked lacrimal duct of infant
n1=en:retardation | n2=en:blocked lacrimal duct of infant | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:blood-brain barrier
n1=en:retardation | n2=en:blood-brain barrier | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:blurring of the gray-white junction (in type iib)
n1=en:retardation | n2=en:blurring of the gray-white junction (in type iib) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:blurry cortical-white matter junction due to spillover of abnormal neurons (in type iib)
n1=en:retardation | n2=en:blurry cortical-white matter junction due to spillover of abnormal neurons (in type iib) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:board and poorly defined gyri
n1=en:retardation | n2=en:board and poorly defined gyri | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:body mass index 30+ - obesity
n1=en:retardation | n2=en:body mass index 30+ - obesity | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:boil/abscess nose
n1=en:retardation | n2=en:boil/abscess nose | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:borderline intelligence
n1=en:retardation | n2=en:borderline intelligence | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:borderline mental retardation (i.q. 70-85)
n1=en:retardation | n2=en:borderline mental retardation (i.q. 70-85) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:bowen-conradi syndrome
n1=en:retardation | n2=en:bowen-conradi syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:brachydactyly, type a1, with short stature, scoliosis, microcephaly, ptosis, hearing loss, and mental retardation
n1=en:retardation | n2=en:brachydactyly, type a1, with short stature, scoliosis, microcephaly, ptosis, hearing loss, and mental retardation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:bradykinesia
n1=en:retardation | n2=en:bradykinesia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:bradykinesia (in severe cases)
n1=en:retardation | n2=en:bradykinesia (in severe cases) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:brain
n1=en:retardation | n2=en:brain | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:brain abscess
n1=en:retardation | n2=en:brain abscess | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:brain and spinal cord structure
n1=en:retardation | n2=en:brain and spinal cord structure | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:brain atrophy (1 family)
n1=en:retardation | n2=en:brain atrophy (1 family) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:brain atrophy (1 patient)
n1=en:retardation | n2=en:brain atrophy (1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:brain atrophy (in some patients)
n1=en:retardation | n2=en:brain atrophy (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:brain atrophy seen on mri
n1=en:retardation | n2=en:brain atrophy seen on mri | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:brain atrophy, particularly of the frontal and temporal lobes
n1=en:retardation | n2=en:brain atrophy, particularly of the frontal and temporal lobes | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:brain calcification (if left untreated)
n1=en:retardation | n2=en:brain calcification (if left untreated) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:brain cell
n1=en:retardation | n2=en:brain cell | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:brain cerebrospinal fluid pathway
n1=en:retardation | n2=en:brain cerebrospinal fluid pathway | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:brain circuit
n1=en:retardation | n2=en:brain circuit | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:brain commissure
n1=en:retardation | n2=en:brain commissure | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:brain edema
n1=en:retardation | n2=en:brain edema | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:brain edema following head injury (less common)
n1=en:retardation | n2=en:brain edema following head injury (less common) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:brain imaging shows calcification of the dentate nucleus
n1=en:retardation | n2=en:brain imaging shows calcification of the dentate nucleus | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:brain imaging shows cortical atrophy
n1=en:retardation | n2=en:brain imaging shows cortical atrophy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:brain imaging shows decreased white matter density
n1=en:retardation | n2=en:brain imaging shows decreased white matter density | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:brain imaging shows diffuse white matter abnormalities
n1=en:retardation | n2=en:brain imaging shows diffuse white matter abnormalities | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:brain imaging shows functional defects in the cortical and subcortical motor-related areas of the frontal lobe
n1=en:retardation | n2=en:brain imaging shows functional defects in the cortical and subcortical motor-related areas of the frontal lobe | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:brain imaging shows generalized atrophy
n1=en:retardation | n2=en:brain imaging shows generalized atrophy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:brain imaging shows hypomyelination
n1=en:retardation | n2=en:brain imaging shows hypomyelination | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:brain imaging shows lesions in the thalami, brainstem, and cerebellum
n1=en:retardation | n2=en:brain imaging shows lesions in the thalami, brainstem, and cerebellum | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:brain imaging shows white-matter hypodensities and demyelination
n1=en:retardation | n2=en:brain imaging shows white-matter hypodensities and demyelination | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:brain injury
n1=en:retardation | n2=en:brain injury | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:brain iron accumulation (in some patients)
n1=en:retardation | n2=en:brain iron accumulation (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:brain iron accumulation in the basal ganglia (in some patients)
n1=en:retardation | n2=en:brain iron accumulation in the basal ganglia (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:brain morphology
n1=en:retardation | n2=en:brain morphology | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:brain mri shows abnormal cortical thickening in the anteromesial frontal areas (1 family)
n1=en:retardation | n2=en:brain mri shows abnormal cortical thickening in the anteromesial frontal areas (1 family) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:brain mri shows abnormal gyral pattern in frontal lobes
n1=en:retardation | n2=en:brain mri shows abnormal gyral pattern in frontal lobes | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:brain mri shows arrest in myelination
n1=en:retardation | n2=en:brain mri shows arrest in myelination | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:brain mri shows cerebellar atrophy
n1=en:retardation | n2=en:brain mri shows cerebellar atrophy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:brain mri shows cerebellar atrophy (1 patient)
n1=en:retardation | n2=en:brain mri shows cerebellar atrophy (1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:brain mri shows cerebellar hypoplasia
n1=en:retardation | n2=en:brain mri shows cerebellar hypoplasia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:brain mri shows cortical atrophy
n1=en:retardation | n2=en:brain mri shows cortical atrophy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:brain mri shows diffusion abnormalities
n1=en:retardation | n2=en:brain mri shows diffusion abnormalities | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:brain mri shows flattening of the ventral pons
n1=en:retardation | n2=en:brain mri shows flattening of the ventral pons | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:brain mri shows hyperintensities in the basal ganglia
n1=en:retardation | n2=en:brain mri shows hyperintensities in the basal ganglia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:brain mri shows hypoplasia of the corpus callosum
n1=en:retardation | n2=en:brain mri shows hypoplasia of the corpus callosum | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:brain mri shows hypoplastic pituitary
n1=en:retardation | n2=en:brain mri shows hypoplastic pituitary | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:brain mri shows lesions consistent with epileptic episodes
n1=en:retardation | n2=en:brain mri shows lesions consistent with epileptic episodes | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:brain mri shows lesions in the basal ganglia
n1=en:retardation | n2=en:brain mri shows lesions in the basal ganglia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:brain mri shows molar tooth sign
n1=en:retardation | n2=en:brain mri shows molar tooth sign | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:brain mri shows proportionate pontocerebellar hypoplasia
n1=en:retardation | n2=en:brain mri shows proportionate pontocerebellar hypoplasia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:brain mri shows signal abnormalities in the basal ganglia
n1=en:retardation | n2=en:brain mri shows signal abnormalities in the basal ganglia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:brain mri shows t2-weighted hyperintensities (17%)
n1=en:retardation | n2=en:brain mri shows t2-weighted hyperintensities (17%) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:brain mrs shows decreased creatine content
n1=en:retardation | n2=en:brain mrs shows decreased creatine content | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:brain mrs shows reduced choline and inositol peaks in the parieto-occipital white matter
n1=en:retardation | n2=en:brain mrs shows reduced choline and inositol peaks in the parieto-occipital white matter | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:brain part
n1=en:retardation | n2=en:brain part | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:brain pathway
n1=en:retardation | n2=en:brain pathway | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:brain prp-immunoreactive amyloid plaques (in 10% if patients with sporadic cjd and in variant cjd)
n1=en:retardation | n2=en:brain prp-immunoreactive amyloid plaques (in 10% if patients with sporadic cjd and in variant cjd) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:brain region
n1=en:retardation | n2=en:brain region | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:brain regulatory center
n1=en:retardation | n2=en:brain regulatory center | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:brain small vessel disease with hemorrhage
n1=en:retardation | n2=en:brain small vessel disease with hemorrhage | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:brain stem
n1=en:retardation | n2=en:brain stem | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:brain stem atrophy
n1=en:retardation | n2=en:brain stem atrophy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:brain stem atrophy, progressive
n1=en:retardation | n2=en:brain stem atrophy, progressive | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:brain stem disorder
n1=en:retardation | n2=en:brain stem disorder | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:brain subcortex
n1=en:retardation | n2=en:brain subcortex | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:brain tissue shows abnormal spherical aggregates of iron and ferritin in the basal ganglia, forebrain, and cerebellum
n1=en:retardation | n2=en:brain tissue shows abnormal spherical aggregates of iron and ferritin in the basal ganglia, forebrain, and cerebellum | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:brain tissue shows cavitation of the basal ganglia
n1=en:retardation | n2=en:brain tissue shows cavitation of the basal ganglia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:brain vascular anomalies (rare)
n1=en:retardation | n2=en:brain vascular anomalies (rare) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:brain ventricle
n1=en:retardation | n2=en:brain ventricle | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:brain white matter hyperintensities on mri
n1=en:retardation | n2=en:brain white matter hyperintensities on mri | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:brainstem atrophy
n1=en:retardation | n2=en:brainstem atrophy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:brainstem concavity
n1=en:retardation | n2=en:brainstem concavity | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:brainstem damage
n1=en:retardation | n2=en:brainstem damage | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:brainstem dysplasia
n1=en:retardation | n2=en:brainstem dysplasia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:brainstem hypoplasia (1 patient)
n1=en:retardation | n2=en:brainstem hypoplasia (1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:brainstem hypoplasia (in some patients)
n1=en:retardation | n2=en:brainstem hypoplasia (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:brainstem lesions, hyperintense on t2-weighted imaging
n1=en:retardation | n2=en:brainstem lesions, hyperintense on t2-weighted imaging | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:brainstem may show neuronal loss
n1=en:retardation | n2=en:brainstem may show neuronal loss | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:brainstem white matter lesions
n1=en:retardation | n2=en:brainstem white matter lesions | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:branchial cleft remnant
n1=en:retardation | n2=en:branchial cleft remnant | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:breast disorder in pregnancy/puerperium other
n1=en:retardation | n2=en:breast disorder in pregnancy/puerperium other | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:breathing difficulty due to vocal cord paralysis
n1=en:retardation | n2=en:breathing difficulty due to vocal cord paralysis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:brief involuntary movements of upper extremities
n1=en:retardation | n2=en:brief involuntary movements of upper extremities | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:brisk knee reflexes (early-on)
n1=en:retardation | n2=en:brisk knee reflexes (early-on) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:brisk lower limb reflexes (in some patients)
n1=en:retardation | n2=en:brisk lower limb reflexes (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:brisk reflexes
n1=en:retardation | n2=en:brisk reflexes | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:brisk reflexes (1 patient)
n1=en:retardation | n2=en:brisk reflexes (1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:brisk tendon reflex
n1=en:retardation | n2=en:brisk tendon reflex | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:broad gait
n1=en:retardation | n2=en:broad gait | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:broad-based gait
n1=en:retardation | n2=en:broad-based gait | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:broad-based gait (1 patient)
n1=en:retardation | n2=en:broad-based gait (1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:broca's aphasia
n1=en:retardation | n2=en:broca's aphasia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:bruxism
n1=en:retardation | n2=en:bruxism | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:buccolingofacial dyspraxia
n1=en:retardation | n2=en:buccolingofacial dyspraxia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:bulbar and upper limb symptoms more severe than lower limb symptoms
n1=en:retardation | n2=en:bulbar and upper limb symptoms more severe than lower limb symptoms | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:bulbar dysfunction
n1=en:retardation | n2=en:bulbar dysfunction | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:bulbar dysfunction (e.g. dysarthria and dysphagia)
n1=en:retardation | n2=en:bulbar dysfunction (e.g. dysarthria and dysphagia) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:bulbar dysfunction (in some patients)
n1=en:retardation | n2=en:bulbar dysfunction (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:bulbar dysfunction (juvenile-onset, less common)
n1=en:retardation | n2=en:bulbar dysfunction (juvenile-onset, less common) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:bulbar involvement
n1=en:retardation | n2=en:bulbar involvement | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:bulbar paresis
n1=en:retardation | n2=en:bulbar paresis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:bulbar signs
n1=en:retardation | n2=en:bulbar signs | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:bulbar spasticity
n1=en:retardation | n2=en:bulbar spasticity | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:bulbar symptoms may occur (less common)
n1=en:retardation | n2=en:bulbar symptoms may occur (less common) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:bulbar weakness
n1=en:retardation | n2=en:bulbar weakness | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:bulbus cordis anomalies and anomalies of cardiac septal closure
n1=en:retardation | n2=en:bulbus cordis anomalies and anomalies of cardiac septal closure | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:bulging of the caudate nuclei
n1=en:retardation | n2=en:bulging of the caudate nuclei | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:burning or tingling of plantar surface of foot (in some patients)
n1=en:retardation | n2=en:burning or tingling of plantar surface of foot (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:burning pain in the limbs
n1=en:retardation | n2=en:burning pain in the limbs | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:burst suppression pattern on neonatal eeg
n1=en:retardation | n2=en:burst suppression pattern on neonatal eeg | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:burst suppression pattern seen on eeg
n1=en:retardation | n2=en:burst suppression pattern seen on eeg | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:by 10-15 years after onset, postural dystonia spreads to all limbs
n1=en:retardation | n2=en:by 10-15 years after onset, postural dystonia spreads to all limbs | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:c3hex, decreased ability to smell
n1=en:retardation | n2=en:c3hex, decreased ability to smell | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:calcification in the pons and cerebellum
n1=en:retardation | n2=en:calcification in the pons and cerebellum | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:calcification may occur in other brain regions, including cerebellum, thalamus, white matter
n1=en:retardation | n2=en:calcification may occur in other brain regions, including cerebellum, thalamus, white matter | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:calcification of the amygdala and the amygdala-hippocampal transition area
n1=en:retardation | n2=en:calcification of the amygdala and the amygdala-hippocampal transition area | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:calcification of the falx
n1=en:retardation | n2=en:calcification of the falx | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:calcifications in white matter, basal ganglia, brainstem, cerebellum, and spinal cord
n1=en:retardation | n2=en:calcifications in white matter, basal ganglia, brainstem, cerebellum, and spinal cord | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:calcifications may be seen in the thalamus, hippocampus, subcortical white matter, and cortex
n1=en:retardation | n2=en:calcifications may be seen in the thalamus, hippocampus, subcortical white matter, and cortex | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:calcifications of cerebral ventricles
n1=en:retardation | n2=en:calcifications of cerebral ventricles | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:calicification of the falx cerebri
n1=en:retardation | n2=en:calicification of the falx cerebri | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:camptodactyly syndrome, guadalajara type i
n1=en:retardation | n2=en:camptodactyly syndrome, guadalajara type i | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:candidal meningitis (in some patients)
n1=en:retardation | n2=en:candidal meningitis (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:carbamoyl-phosphate synthetase i deficiency
n1=en:retardation | n2=en:carbamoyl-phosphate synthetase i deficiency | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:carcinomatosis (unknown primary site)
n1=en:retardation | n2=en:carcinomatosis (unknown primary site) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cardiac and circulatory congenital anomalies
n1=en:retardation | n2=en:cardiac and circulatory congenital anomalies | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cardiovascular abnormalities
n1=en:retardation | n2=en:cardiovascular abnormalities | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cardiovascular neoplasm
n1=en:retardation | n2=en:cardiovascular neoplasm | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:caroli disease
n1=en:retardation | n2=en:caroli disease | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:carpal tunnel syndrome
n1=en:retardation | n2=en:carpal tunnel syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cataplexy
n1=en:retardation | n2=en:cataplexy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cataplexy often triggered by strong emotions
n1=en:retardation | n2=en:cataplexy often triggered by strong emotions | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cataplexy, paroxysmal weakness or paralysis
n1=en:retardation | n2=en:cataplexy, paroxysmal weakness or paralysis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cataract
n1=en:retardation | n2=en:cataract | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:catatonia
n1=en:retardation | n2=en:catatonia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:catatonic behavior
n1=en:retardation | n2=en:catatonic behavior | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cauda equina syndrome
n1=en:retardation | n2=en:cauda equina syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:caudal dysplasia
n1=en:retardation | n2=en:caudal dysplasia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:caudate atrophy
n1=en:retardation | n2=en:caudate atrophy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:caudate nuclei atrophy
n1=en:retardation | n2=en:caudate nuclei atrophy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cavitating leukoencephalopathy
n1=en:retardation | n2=en:cavitating leukoencephalopathy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cavitating white matter degeneration
n1=en:retardation | n2=en:cavitating white matter degeneration | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cavum septum pellucidum atrophy
n1=en:retardation | n2=en:cavum septum pellucidum atrophy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cavum vergae
n1=en:retardation | n2=en:cavum vergae | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ccerebellar ataxia
n1=en:retardation | n2=en:ccerebellar ataxia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cdgiw
n1=en:retardation | n2=en:cdgiw | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cebocephaly
n1=en:retardation | n2=en:cebocephaly | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cell loss and gliosis in the basal ganglia
n1=en:retardation | n2=en:cell loss and gliosis in the basal ganglia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:celosomy
n1=en:retardation | n2=en:celosomy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:central canal malformation
n1=en:retardation | n2=en:central canal malformation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:central facial nerve paralysis (rare)
n1=en:retardation | n2=en:central facial nerve paralysis (rare) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:central facial palsy (in some patients)
n1=en:retardation | n2=en:central facial palsy (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:central hypotonia
n1=en:retardation | n2=en:central hypotonia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:central nervous system
n1=en:retardation | n2=en:central nervous system | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:central nervous system degeneration
n1=en:retardation | n2=en:central nervous system degeneration | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:central nervous system demyelination
n1=en:retardation | n2=en:central nervous system demyelination | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:central nervous system depression (disorder)
n1=en:retardation | n2=en:central nervous system depression (disorder) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:central nervous system involvement (in some patients)
n1=en:retardation | n2=en:central nervous system involvement (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:central nervous system involvement in approximately 50% of patients
n1=en:retardation | n2=en:central nervous system involvement in approximately 50% of patients | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:central nervous system malformations (40%)
n1=en:retardation | n2=en:central nervous system malformations (40%) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:central nervous system neoplasm
n1=en:retardation | n2=en:central nervous system neoplasm | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:central nervous system part
n1=en:retardation | n2=en:central nervous system part | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:central nervous system space
n1=en:retardation | n2=en:central nervous system space | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:central neural pathway/tract
n1=en:retardation | n2=en:central neural pathway/tract | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar and brainstem atrophy, mild (1 patient)
n1=en:retardation | n2=en:cerebellar and brainstem atrophy, mild (1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar ataxia
n1=en:retardation | n2=en:cerebellar ataxia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar ataxia (1 patient)
n1=en:retardation | n2=en:cerebellar ataxia (1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar ataxia (in 1 of 3 families)
n1=en:retardation | n2=en:cerebellar ataxia (in 1 of 3 families) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar ataxia (may be permanent in 50% of patients)
n1=en:retardation | n2=en:cerebellar ataxia (may be permanent in 50% of patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar ataxia (rare)
n1=en:retardation | n2=en:cerebellar ataxia (rare) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar ataxia (seen in hhs variant)
n1=en:retardation | n2=en:cerebellar ataxia (seen in hhs variant) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar ataxia during episodes
n1=en:retardation | n2=en:cerebellar ataxia during episodes | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar ataxia, adult-onset (in 1 family)
n1=en:retardation | n2=en:cerebellar ataxia, adult-onset (in 1 family) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar ataxia, gait and stance
n1=en:retardation | n2=en:cerebellar ataxia, gait and stance | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar ataxia, limb and trunk
n1=en:retardation | n2=en:cerebellar ataxia, limb and trunk | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar ataxia, mental retardation, and dysequilibrium syndrome 4
n1=en:retardation | n2=en:cerebellar ataxia, mental retardation, and dysequilibrium syndrome 4 | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar ataxia, mild, late-onset
n1=en:retardation | n2=en:cerebellar ataxia, mild, late-onset | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar ataxia, severe
n1=en:retardation | n2=en:cerebellar ataxia, severe | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar ataxia, slowly progressive
n1=en:retardation | n2=en:cerebellar ataxia, slowly progressive | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar atrophy
n1=en:retardation | n2=en:cerebellar atrophy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar atrophy (1 patient)
n1=en:retardation | n2=en:cerebellar atrophy (1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar atrophy (96% of patients)
n1=en:retardation | n2=en:cerebellar atrophy (96% of patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar atrophy (especially in the superior cerebellar vermis)
n1=en:retardation | n2=en:cerebellar atrophy (especially in the superior cerebellar vermis) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar atrophy (especially of the vermis)
n1=en:retardation | n2=en:cerebellar atrophy (especially of the vermis) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar atrophy (in 1 family)
n1=en:retardation | n2=en:cerebellar atrophy (in 1 family) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar atrophy (in adulthood)
n1=en:retardation | n2=en:cerebellar atrophy (in adulthood) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar atrophy (in some patients)
n1=en:retardation | n2=en:cerebellar atrophy (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar atrophy (juvenile form)
n1=en:retardation | n2=en:cerebellar atrophy (juvenile form) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar atrophy (reported in 1 patient)
n1=en:retardation | n2=en:cerebellar atrophy (reported in 1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar atrophy in most cases
n1=en:retardation | n2=en:cerebellar atrophy in most cases | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar atrophy in older patients
n1=en:retardation | n2=en:cerebellar atrophy in older patients | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar atrophy seen on mri
n1=en:retardation | n2=en:cerebellar atrophy seen on mri | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar atrophy with signal hyperintensity in the cerebellar cortex seen on t2-weighted mri
n1=en:retardation | n2=en:cerebellar atrophy with signal hyperintensity in the cerebellar cortex seen on t2-weighted mri | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar atrophy, diffuse, severe
n1=en:retardation | n2=en:cerebellar atrophy, diffuse, severe | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar atrophy, mild
n1=en:retardation | n2=en:cerebellar atrophy, mild | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar atrophy, mild (1 patient)
n1=en:retardation | n2=en:cerebellar atrophy, mild (1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar atrophy, mild (in 1 of 3 families)
n1=en:retardation | n2=en:cerebellar atrophy, mild (in 1 of 3 families) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar atrophy, particularly of the hemispheres
n1=en:retardation | n2=en:cerebellar atrophy, particularly of the hemispheres | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar atrophy, progressive
n1=en:retardation | n2=en:cerebellar atrophy, progressive | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar atrophy, progressive (1 patient)
n1=en:retardation | n2=en:cerebellar atrophy, progressive (1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar atrophy, progressive (cerebellar vermal atrophy before cerebral atrophy)
n1=en:retardation | n2=en:cerebellar atrophy, progressive (cerebellar vermal atrophy before cerebral atrophy) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar atrophy, progressive (in some patients)
n1=en:retardation | n2=en:cerebellar atrophy, progressive (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar atrophy, severe
n1=en:retardation | n2=en:cerebellar atrophy, severe | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar calcifications
n1=en:retardation | n2=en:cerebellar calcifications | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar cell paucity, more marked in vermis than hemispheres
n1=en:retardation | n2=en:cerebellar cell paucity, more marked in vermis than hemispheres | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar cortex shows normal layers
n1=en:retardation | n2=en:cerebellar cortex shows normal layers | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar cortical degeneration
n1=en:retardation | n2=en:cerebellar cortical degeneration | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar cyst
n1=en:retardation | n2=en:cerebellar cyst | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar cyst (rare)
n1=en:retardation | n2=en:cerebellar cyst (rare) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar cysts (meb)
n1=en:retardation | n2=en:cerebellar cysts (meb) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar degeneration
n1=en:retardation | n2=en:cerebellar degeneration | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar diseases
n1=en:retardation | n2=en:cerebellar diseases | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar dysarthria
n1=en:retardation | n2=en:cerebellar dysarthria | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar dysfunction, progressive
n1=en:retardation | n2=en:cerebellar dysfunction, progressive | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar dysplasia
n1=en:retardation | n2=en:cerebellar dysplasia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar enlargement
n1=en:retardation | n2=en:cerebellar enlargement | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar gangliocytoma manifesting as seizure and tremor
n1=en:retardation | n2=en:cerebellar gangliocytoma manifesting as seizure and tremor | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar hemangioblastoma
n1=en:retardation | n2=en:cerebellar hemangioblastoma | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar hemorrhage (rare)
n1=en:retardation | n2=en:cerebellar hemorrhage (rare) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar herniation (rare)
n1=en:retardation | n2=en:cerebellar herniation (rare) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar heterotopias
n1=en:retardation | n2=en:cerebellar heterotopias | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar hypoplasia (1 patient)
n1=en:retardation | n2=en:cerebellar hypoplasia (1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar hypoplasia (in 1 of 2 patients)
n1=en:retardation | n2=en:cerebellar hypoplasia (in 1 of 2 patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar hypoplasia (in 1 of 2 sibs)
n1=en:retardation | n2=en:cerebellar hypoplasia (in 1 of 2 sibs) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar hypoplasia (in most patients)
n1=en:retardation | n2=en:cerebellar hypoplasia (in most patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar hypoplasia (in some patients)
n1=en:retardation | n2=en:cerebellar hypoplasia (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar hypoplasia (in some)
n1=en:retardation | n2=en:cerebellar hypoplasia (in some) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar hypoplasia (male)
n1=en:retardation | n2=en:cerebellar hypoplasia (male) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar hypoplasia (reported in 1 family)
n1=en:retardation | n2=en:cerebellar hypoplasia (reported in 1 family) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar hypoplasia (seen in hhs variant)
n1=en:retardation | n2=en:cerebellar hypoplasia (seen in hhs variant) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar hypoplasia (seen in recessive form)
n1=en:retardation | n2=en:cerebellar hypoplasia (seen in recessive form) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar hypoplasia (variable)
n1=en:retardation | n2=en:cerebellar hypoplasia (variable) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar hypoplasia due to enlarged foramen magnum
n1=en:retardation | n2=en:cerebellar hypoplasia due to enlarged foramen magnum | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar hypoplasia or agenesis
n1=en:retardation | n2=en:cerebellar hypoplasia or agenesis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar hypoplasia predominantly affecting the vermis
n1=en:retardation | n2=en:cerebellar hypoplasia predominantly affecting the vermis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar hypoplasia, mild (in some patients)
n1=en:retardation | n2=en:cerebellar hypoplasia, mild (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar hypoplasia, mild asymmetric (rare)
n1=en:retardation | n2=en:cerebellar hypoplasia, mild asymmetric (rare) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar hypoplasia, particularly of the hemispheres
n1=en:retardation | n2=en:cerebellar hypoplasia, particularly of the hemispheres | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar hypoplasia, severe (wws)
n1=en:retardation | n2=en:cerebellar hypoplasia, severe (wws) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar hypoplasia/atrophy (27%)
n1=en:retardation | n2=en:cerebellar hypoplasia/atrophy (27%) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar lesion nos
n1=en:retardation | n2=en:cerebellar lesion nos | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar medulloblastoma (rare)
n1=en:retardation | n2=en:cerebellar medulloblastoma (rare) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar neuronal loss
n1=en:retardation | n2=en:cerebellar neuronal loss | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar origin most likely
n1=en:retardation | n2=en:cerebellar origin most likely | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar signs
n1=en:retardation | n2=en:cerebellar signs | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar signs (in some patients)
n1=en:retardation | n2=en:cerebellar signs (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar signs (less common)
n1=en:retardation | n2=en:cerebellar signs (less common) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar signs (may be permanent in 50% of patients)
n1=en:retardation | n2=en:cerebellar signs (may be permanent in 50% of patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar signs (more common in variant cjd)
n1=en:retardation | n2=en:cerebellar signs (more common in variant cjd) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar signs during episodes
n1=en:retardation | n2=en:cerebellar signs during episodes | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar signs may develop
n1=en:retardation | n2=en:cerebellar signs may develop | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar signs, mild (in 1 of 3 families)
n1=en:retardation | n2=en:cerebellar signs, mild (in 1 of 3 families) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar stroke
n1=en:retardation | n2=en:cerebellar stroke | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar tonsil herniation
n1=en:retardation | n2=en:cerebellar tonsil herniation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar tonsillar herniation
n1=en:retardation | n2=en:cerebellar tonsillar herniation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar vermis aplasia or hypoplasia
n1=en:retardation | n2=en:cerebellar vermis aplasia or hypoplasia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar vermis atrophy
n1=en:retardation | n2=en:cerebellar vermis atrophy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar vermis hypoplasia
n1=en:retardation | n2=en:cerebellar vermis hypoplasia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar vermis hypoplasia (in 1 patient)
n1=en:retardation | n2=en:cerebellar vermis hypoplasia (in 1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar vermis hypoplasia (in some patients)
n1=en:retardation | n2=en:cerebellar vermis hypoplasia (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellar white matter lesions on mri
n1=en:retardation | n2=en:cerebellar white matter lesions on mri | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebellum
n1=en:retardation | n2=en:cerebellum | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebral and cerebellar atrophy
n1=en:retardation | n2=en:cerebral and cerebellar atrophy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebral arterial hemorrhage
n1=en:retardation | n2=en:cerebral arterial hemorrhage | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebral arterial thrombosis
n1=en:retardation | n2=en:cerebral arterial thrombosis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebral atrophy
n1=en:retardation | n2=en:cerebral atrophy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebral atrophy (1 patient)
n1=en:retardation | n2=en:cerebral atrophy (1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebral atrophy (in 1 family)
n1=en:retardation | n2=en:cerebral atrophy (in 1 family) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebral atrophy (in severe cases)
n1=en:retardation | n2=en:cerebral atrophy (in severe cases) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebral atrophy (in some patients)
n1=en:retardation | n2=en:cerebral atrophy (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebral atrophy (rare)
n1=en:retardation | n2=en:cerebral atrophy (rare) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebral atrophy (reported in 1 patient)
n1=en:retardation | n2=en:cerebral atrophy (reported in 1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebral atrophy diffuse
n1=en:retardation | n2=en:cerebral atrophy diffuse | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebral atrophy, diffuse, severe
n1=en:retardation | n2=en:cerebral atrophy, diffuse, severe | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebral atrophy, frontotemporal, progressive
n1=en:retardation | n2=en:cerebral atrophy, frontotemporal, progressive | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebral atrophy, generalized mild
n1=en:retardation | n2=en:cerebral atrophy, generalized mild | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebral atrophy, mild
n1=en:retardation | n2=en:cerebral atrophy, mild | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebral atrophy, mild, diffuse
n1=en:retardation | n2=en:cerebral atrophy, mild, diffuse | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebral atrophy, progressive
n1=en:retardation | n2=en:cerebral atrophy, progressive | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebral atrophy, progressive, from anterior to posterior
n1=en:retardation | n2=en:cerebral atrophy, progressive, from anterior to posterior | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebral atrophy, severe
n1=en:retardation | n2=en:cerebral atrophy, severe | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebral calcification
n1=en:retardation | n2=en:cerebral calcification | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebral cavernous malformation
n1=en:retardation | n2=en:cerebral cavernous malformation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebral cortex myoclonus
n1=en:retardation | n2=en:cerebral cortex myoclonus | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebral cortex with spongiform changes
n1=en:retardation | n2=en:cerebral cortex with spongiform changes | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebral cortical and cerebellar atrophy (patient a)
n1=en:retardation | n2=en:cerebral cortical and cerebellar atrophy (patient a) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebral cortical atrophy, diffuse
n1=en:retardation | n2=en:cerebral cortical atrophy, diffuse | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebral cortical atrophy, especially frontal lobes
n1=en:retardation | n2=en:cerebral cortical atrophy, especially frontal lobes | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebral cortical neurodegeneration
n1=en:retardation | n2=en:cerebral cortical neurodegeneration | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebral cyst
n1=en:retardation | n2=en:cerebral cyst | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebral degeneration
n1=en:retardation | n2=en:cerebral degeneration | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebral demyelination and inflammation
n1=en:retardation | n2=en:cerebral demyelination and inflammation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebral dysmyelination
n1=en:retardation | n2=en:cerebral dysmyelination | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebral edema
n1=en:retardation | n2=en:cerebral edema | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebral hemorrhage
n1=en:retardation | n2=en:cerebral hemorrhage | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebral hypomyelination
n1=en:retardation | n2=en:cerebral hypomyelination | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebral hypoplasia
n1=en:retardation | n2=en:cerebral hypoplasia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebral infarction
n1=en:retardation | n2=en:cerebral infarction | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebral infarction dandy-walker malformation
n1=en:retardation | n2=en:cerebral infarction dandy-walker malformation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebral malformations
n1=en:retardation | n2=en:cerebral malformations | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebral oligogyria
n1=en:retardation | n2=en:cerebral oligogyria | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebral palsy
n1=en:retardation | n2=en:cerebral palsy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebral palsy, spastic quadriplegic, 1
n1=en:retardation | n2=en:cerebral palsy, spastic quadriplegic, 1 | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebral spongiosis
n1=en:retardation | n2=en:cerebral spongiosis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebral thrombosis
n1=en:retardation | n2=en:cerebral thrombosis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebral thrombosis (e.g. 612283.0014 protein c deficiency)
n1=en:retardation | n2=en:cerebral thrombosis (e.g. 612283.0014 protein c deficiency) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebral vasculitis or vasculopathy (rare)
n1=en:retardation | n2=en:cerebral vasculitis or vasculopathy (rare) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebral white matter atrophy, progressive
n1=en:retardation | n2=en:cerebral white matter atrophy, progressive | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebral white matter lesion
n1=en:retardation | n2=en:cerebral white matter lesion | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebral white matter lesions (1 patient)
n1=en:retardation | n2=en:cerebral white matter lesions (1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebrofaciothoracic dysplasia
n1=en:retardation | n2=en:cerebrofaciothoracic dysplasia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebrooculonasal syndrome
n1=en:retardation | n2=en:cerebrooculonasal syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebrospinal fluid
n1=en:retardation | n2=en:cerebrospinal fluid | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebrospinal fluid glucose decreased
n1=en:retardation | n2=en:cerebrospinal fluid glucose decreased | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebrospinal fluid may show decreased levels of homovanillic acid (hva)
n1=en:retardation | n2=en:cerebrospinal fluid may show decreased levels of homovanillic acid (hva) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebrotendinous xanthomatosis
n1=en:retardation | n2=en:cerebrotendinous xanthomatosis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebrovascular accident
n1=en:retardation | n2=en:cerebrovascular accident | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebrovascular accident (in some patients)
n1=en:retardation | n2=en:cerebrovascular accident (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebrovascular disorder
n1=en:retardation | n2=en:cerebrovascular disorder | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebrovascular ischemia
n1=en:retardation | n2=en:cerebrovascular ischemia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebrovascular ischemic attacks, transient (proceed secondary neurologic findings)
n1=en:retardation | n2=en:cerebrovascular ischemic attacks, transient (proceed secondary neurologic findings) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cerebrum
n1=en:retardation | n2=en:cerebrum | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ceroid lipofuscinosis, neuronal, 1
n1=en:retardation | n2=en:ceroid lipofuscinosis, neuronal, 1 | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ceroid lipofuscinosis, neuronal, 5
n1=en:retardation | n2=en:ceroid lipofuscinosis, neuronal, 5 | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ceroid lipofuscinosis, neuronal, 9 (disorder)
n1=en:retardation | n2=en:ceroid lipofuscinosis, neuronal, 9 (disorder) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:certain congenital musculoskeletal deformities
n1=en:retardation | n2=en:certain congenital musculoskeletal deformities | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cervical cord compression
n1=en:retardation | n2=en:cervical cord compression | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cervical disorder
n1=en:retardation | n2=en:cervical disorder | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cervical myelopathy
n1=en:retardation | n2=en:cervical myelopathy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:changes in physical activity
n1=en:retardation | n2=en:changes in physical activity | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:characteristic arm position with wrist and elbow flexion
n1=en:retardation | n2=en:characteristic arm position with wrist and elbow flexion | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:characteristic electroencephalogram (eeg) discharges
n1=en:retardation | n2=en:characteristic electroencephalogram (eeg) discharges | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:characteristic findings on mri
n1=en:retardation | n2=en:characteristic findings on mri | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:characteristic periodic eeg complexes (only in sporadic and familial cjd, not in variant cjd)
n1=en:retardation | n2=en:characteristic periodic eeg complexes (only in sporadic and familial cjd, not in variant cjd) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:charge syndrome
n1=en:retardation | n2=en:charge syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cheilognathopalatoschisis
n1=en:retardation | n2=en:cheilognathopalatoschisis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cheilognathoschisis
n1=en:retardation | n2=en:cheilognathoschisis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:chiari i malformation of the cerebellum (in some patients)
n1=en:retardation | n2=en:chiari i malformation of the cerebellum (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:chiari i malformation on mri
n1=en:retardation | n2=en:chiari i malformation on mri | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:chiari i malformation on mri (some)
n1=en:retardation | n2=en:chiari i malformation on mri (some) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:chiari malformation (uncommon)
n1=en:retardation | n2=en:chiari malformation (uncommon) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:chiari malformation type ii
n1=en:retardation | n2=en:chiari malformation type ii | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:chiari type i
n1=en:retardation | n2=en:chiari type i | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:chiari type i malformation (in some patients)
n1=en:retardation | n2=en:chiari type i malformation (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:chicken pox
n1=en:retardation | n2=en:chicken pox | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:childhood emotional disorder
n1=en:retardation | n2=en:childhood emotional disorder | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:childhood or adolescent disorder of social functioning
n1=en:retardation | n2=en:childhood or adolescent disorder of social functioning | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:childhood polyphagia
n1=en:retardation | n2=en:childhood polyphagia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cholecystitis with cholelithiasis
n1=en:retardation | n2=en:cholecystitis with cholelithiasis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:chorea
n1=en:retardation | n2=en:chorea | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:chorea (in some patients)
n1=en:retardation | n2=en:chorea (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:chorea of all limbs
n1=en:retardation | n2=en:chorea of all limbs | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:chorea of hands
n1=en:retardation | n2=en:chorea of hands | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:chorea-ballism
n1=en:retardation | n2=en:chorea-ballism | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:chorea, mild (in some)
n1=en:retardation | n2=en:chorea, mild (in some) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:chorea, prominent (in some patients)
n1=en:retardation | n2=en:chorea, prominent (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:choreic movements (10 to 22% of patients)
n1=en:retardation | n2=en:choreic movements (10 to 22% of patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:choreic movements, episodic
n1=en:retardation | n2=en:choreic movements, episodic | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:choreoathetoid movements
n1=en:retardation | n2=en:choreoathetoid movements | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:choreoathetosis
n1=en:retardation | n2=en:choreoathetosis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:choreoathetosis (2 patients)
n1=en:retardation | n2=en:choreoathetosis (2 patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:choreoathetosis (described in 1 patient)
n1=en:retardation | n2=en:choreoathetosis (described in 1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:choreoathetosis (in 79%), more frequent at disease onset
n1=en:retardation | n2=en:choreoathetosis (in 79%), more frequent at disease onset | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:choreoathetosis (in a subset of patients)
n1=en:retardation | n2=en:choreoathetosis (in a subset of patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:choreoathetosis (in some patients)
n1=en:retardation | n2=en:choreoathetosis (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:choreoathetosis of the face, trunk, extremities
n1=en:retardation | n2=en:choreoathetosis of the face, trunk, extremities | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:choreodystonia of the upper limbs
n1=en:retardation | n2=en:choreodystonia of the upper limbs | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:choristoma
n1=en:retardation | n2=en:choristoma | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:choroid plexus calcification
n1=en:retardation | n2=en:choroid plexus calcification | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:choroid plexus cyst
n1=en:retardation | n2=en:choroid plexus cyst | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:choroid plexus papilloma (in some patients)
n1=en:retardation | n2=en:choroid plexus papilloma (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:choroideremia, deafness, and mental retardation
n1=en:retardation | n2=en:choroideremia, deafness, and mental retardation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:chromosome 10q26 deletion syndrome
n1=en:retardation | n2=en:chromosome 10q26 deletion syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:chromosome 13q14 deletion syndrome
n1=en:retardation | n2=en:chromosome 13q14 deletion syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:chromosome 15q24 deletion syndrome
n1=en:retardation | n2=en:chromosome 15q24 deletion syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:chromosome 15q26-qter deletion syndrome
n1=en:retardation | n2=en:chromosome 15q26-qter deletion syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:chromosome 16p12.2-p11.2 deletion syndrome, 7.1- to 8.7-mb
n1=en:retardation | n2=en:chromosome 16p12.2-p11.2 deletion syndrome, 7.1- to 8.7-mb | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:chromosome 17q12 duplication syndrome
n1=en:retardation | n2=en:chromosome 17q12 duplication syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:chromosome 19q13.11 deletion syndrome
n1=en:retardation | n2=en:chromosome 19q13.11 deletion syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:chromosome 1p32-p31 deletion syndrome
n1=en:retardation | n2=en:chromosome 1p32-p31 deletion syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:chromosome 22q11.2 microduplication syndrome
n1=en:retardation | n2=en:chromosome 22q11.2 microduplication syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:chromosome 2p16.1-p15 deletion syndrome
n1=en:retardation | n2=en:chromosome 2p16.1-p15 deletion syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:chromosome 2q32-q33 deletion syndrome
n1=en:retardation | n2=en:chromosome 2q32-q33 deletion syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:chromosome 2q37 deletion syndrome
n1=en:retardation | n2=en:chromosome 2q37 deletion syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:chromosome 5p13 duplication syndrome
n1=en:retardation | n2=en:chromosome 5p13 duplication syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:chromosome 6pter-p24 deletion syndrome
n1=en:retardation | n2=en:chromosome 6pter-p24 deletion syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:chromosome 9p deletion syndrome
n1=en:retardation | n2=en:chromosome 9p deletion syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:chromosome disorder
n1=en:retardation | n2=en:chromosome disorder | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:chronic bronchitis/bronchiectasis
n1=en:retardation | n2=en:chronic bronchitis/bronchiectasis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:chronic cystic disease breast
n1=en:retardation | n2=en:chronic cystic disease breast | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:chronic encephalopathy
n1=en:retardation | n2=en:chronic encephalopathy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:chronic enteritis/ulcerative colitis
n1=en:retardation | n2=en:chronic enteritis/ulcerative colitis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:chronic headaches
n1=en:retardation | n2=en:chronic headaches | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:chronic internal knee derangement
n1=en:retardation | n2=en:chronic internal knee derangement | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:chronic lymphocytic meningitis
n1=en:retardation | n2=en:chronic lymphocytic meningitis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:chronic mental disorder
n1=en:retardation | n2=en:chronic mental disorder | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:chronic otitis other infection ear
n1=en:retardation | n2=en:chronic otitis other infection ear | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:chronic pain
n1=en:retardation | n2=en:chronic pain | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:chronic physical disability
n1=en:retardation | n2=en:chronic physical disability | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:chronic skin ulcer
n1=en:retardation | n2=en:chronic skin ulcer | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:chronic subtype, headaches occur without remission for 1 year
n1=en:retardation | n2=en:chronic subtype, headaches occur without remission for 1 year | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:chronic-progressive course with episodes of rapid deterioration following fever or head trauma
n1=en:retardation | n2=en:chronic-progressive course with episodes of rapid deterioration following fever or head trauma | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:chronic/non specific lymphadenitis
n1=en:retardation | n2=en:chronic/non specific lymphadenitis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cirrhosis/other liver disease
n1=en:retardation | n2=en:cirrhosis/other liver disease | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:citrullinemia
n1=en:retardation | n2=en:citrullinemia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ck syndrome
n1=en:retardation | n2=en:ck syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:classical lissencephaly
n1=en:retardation | n2=en:classical lissencephaly | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:classical phenylketonuria
n1=en:retardation | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cleft jaw
n1=en:retardation | n2=en:cleft jaw | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cleft lip
n1=en:retardation | n2=en:cleft lip | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cleft maxilla
n1=en:retardation | n2=en:cleft maxilla | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cleft palate
n1=en:retardation | n2=en:cleft palate | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cleft palate with cleft lip
n1=en:retardation | n2=en:cleft palate with cleft lip | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cleft palate, cardiac defect, genital anomalies, and ectrodactyly
n1=en:retardation | n2=en:cleft palate, cardiac defect, genital anomalies, and ectrodactyly | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:clinical anxiety
n1=en:retardation | n2=en:clinical anxiety | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:clonic convulsion
n1=en:retardation | n2=en:clonic convulsion | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:clonus
n1=en:retardation | n2=en:clonus | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:clonus may occur
n1=en:retardation | n2=en:clonus may occur | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:closed-lip schizencephaly
n1=en:retardation | n2=en:closed-lip schizencephaly | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:clubfoot
n1=en:retardation | n2=en:clubfoot | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:clumsiness
n1=en:retardation | n2=en:clumsiness | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:clumsiness (82%)
n1=en:retardation | n2=en:clumsiness (82%) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:clumsiness (mild)
n1=en:retardation | n2=en:clumsiness (mild) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:clumsiness in childhood
n1=en:retardation | n2=en:clumsiness in childhood | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:clumsiness, unsteadiness
n1=en:retardation | n2=en:clumsiness, unsteadiness | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:clumsy gait
n1=en:retardation | n2=en:clumsy gait | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cluster headache
n1=en:retardation | n2=en:cluster headache | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cns component
n1=en:retardation | n2=en:cns component | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cns infarctions
n1=en:retardation | n2=en:cns infarctions | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cns stimulation (finding)
n1=en:retardation | n2=en:cns stimulation (finding) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cns venous malformations
n1=en:retardation | n2=en:cns venous malformations | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:coach syndrome
n1=en:retardation | n2=en:coach syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:coarctation
n1=en:retardation | n2=en:coarctation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:coarse tremors
n1=en:retardation | n2=en:coarse tremors | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:coarsened pattern of sulci and gyri
n1=en:retardation | n2=en:coarsened pattern of sulci and gyri | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cobblestone lissencephaly
n1=en:retardation | n2=en:cobblestone lissencephaly | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cobblestone lissencephaly (1 patient)
n1=en:retardation | n2=en:cobblestone lissencephaly (1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cobblestone lissencephaly (posterior brain regions more affected than anterior regions)
n1=en:retardation | n2=en:cobblestone lissencephaly (posterior brain regions more affected than anterior regions) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cobblestone lissencephaly, posterior frontal and parietal regions
n1=en:retardation | n2=en:cobblestone lissencephaly, posterior frontal and parietal regions | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cobblestone lissencephaly, type ii
n1=en:retardation | n2=en:cobblestone lissencephaly, type ii | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cobblestone lissencephaly, type ii (wws)
n1=en:retardation | n2=en:cobblestone lissencephaly, type ii (wws) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cockayne syndrome, type i
n1=en:retardation | n2=en:cockayne syndrome, type i | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cockayne syndrome, type ii
n1=en:retardation | n2=en:cockayne syndrome, type ii | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:coenzyme q10 deficiency, primary, 1
n1=en:retardation | n2=en:coenzyme q10 deficiency, primary, 1 | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:coffin-lowry syndrome
n1=en:retardation | n2=en:coffin-lowry syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:coffin-siris syndrome
n1=en:retardation | n2=en:coffin-siris syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cognition is preserved
n1=en:retardation | n2=en:cognition is preserved | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cognition is spared
n1=en:retardation | n2=en:cognition is spared | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cognitive and attention disorders and disturbances
n1=en:retardation | n2=en:cognitive and attention disorders and disturbances | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cognitive decline (1 family)
n1=en:retardation | n2=en:cognitive decline (1 family) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cognitive decline (1 patient)
n1=en:retardation | n2=en:cognitive decline (1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cognitive decline (in some patients)
n1=en:retardation | n2=en:cognitive decline (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cognitive decline (later in life)
n1=en:retardation | n2=en:cognitive decline (later in life) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cognitive decline (rare)
n1=en:retardation | n2=en:cognitive decline (rare) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cognitive decline in adulthood
n1=en:retardation | n2=en:cognitive decline in adulthood | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cognitive decline in older patients
n1=en:retardation | n2=en:cognitive decline in older patients | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cognitive decline, rapid
n1=en:retardation | n2=en:cognitive decline, rapid | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cognitive defects (rare)
n1=en:retardation | n2=en:cognitive defects (rare) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cognitive defects (variable from mild to severe)
n1=en:retardation | n2=en:cognitive defects (variable from mild to severe) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cognitive defects develop later in the disease
n1=en:retardation | n2=en:cognitive defects develop later in the disease | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cognitive defects in executive function and attention
n1=en:retardation | n2=en:cognitive defects in executive function and attention | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cognitive deficits (less common)
n1=en:retardation | n2=en:cognitive deficits (less common) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cognitive deficits may occur
n1=en:retardation | n2=en:cognitive deficits may occur | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cognitive deficits, mild (in some patients)
n1=en:retardation | n2=en:cognitive deficits, mild (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cognitive delay
n1=en:retardation | n2=en:cognitive delay | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cognitive delay, mild (1 patient)
n1=en:retardation | n2=en:cognitive delay, mild (1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cognitive delay, mild to severe
n1=en:retardation | n2=en:cognitive delay, mild to severe | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cognitive deterioration
n1=en:retardation | n2=en:cognitive deterioration | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cognitive disorder
n1=en:retardation | n2=en:cognitive disorder | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cognitive dysfunction
n1=en:retardation | n2=en:cognitive dysfunction | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cognitive dysfunction (in some patients)
n1=en:retardation | n2=en:cognitive dysfunction (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cognitive dysfunction (rare)
n1=en:retardation | n2=en:cognitive dysfunction (rare) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cognitive function, variable
n1=en:retardation | n2=en:cognitive function, variable | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cognitive impairment
n1=en:retardation | n2=en:cognitive impairment | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cognitive impairment (1 family)
n1=en:retardation | n2=en:cognitive impairment (1 family) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cognitive impairment (1 patient)
n1=en:retardation | n2=en:cognitive impairment (1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cognitive impairment (3 patients)
n1=en:retardation | n2=en:cognitive impairment (3 patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cognitive impairment (cvs+)
n1=en:retardation | n2=en:cognitive impairment (cvs+) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cognitive impairment (in 1 of 3 patients)
n1=en:retardation | n2=en:cognitive impairment (in 1 of 3 patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cognitive impairment (in some patients)
n1=en:retardation | n2=en:cognitive impairment (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cognitive impairment (rare)
n1=en:retardation | n2=en:cognitive impairment (rare) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cognitive impairment, gradual onset
n1=en:retardation | n2=en:cognitive impairment, gradual onset | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cognitive impairment, mild (1 patient)
n1=en:retardation | n2=en:cognitive impairment, mild (1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cognitive impairment, mild (44%)
n1=en:retardation | n2=en:cognitive impairment, mild (44%) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cognitive impairment, mild (in 2 of 3 patients)
n1=en:retardation | n2=en:cognitive impairment, mild (in 2 of 3 patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cognitive impairment, mild to moderate
n1=en:retardation | n2=en:cognitive impairment, mild to moderate | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cognitive impairment, mild to severe
n1=en:retardation | n2=en:cognitive impairment, mild to severe | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cognitive motor disorder
n1=en:retardation | n2=en:cognitive motor disorder | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cognitive regression
n1=en:retardation | n2=en:cognitive regression | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cognitive regression, mild
n1=en:retardation | n2=en:cognitive regression, mild | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cogwheel rigidities
n1=en:retardation | n2=en:cogwheel rigidities | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cogwheel rigidity (in some patients)
n1=en:retardation | n2=en:cogwheel rigidity (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cohen syndrome
n1=en:retardation | n2=en:cohen syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:coloboma, ocular, and ichthyosis, brain malformations, and endocrine abnormalities
n1=en:retardation | n2=en:coloboma, ocular, and ichthyosis, brain malformations, and endocrine abnormalities | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:colpocephaly
n1=en:retardation | n2=en:colpocephaly | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:coma
n1=en:retardation | n2=en:coma | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:coma (if untreated)
n1=en:retardation | n2=en:coma (if untreated) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:coma (in up to 33% of patients)
n1=en:retardation | n2=en:coma (in up to 33% of patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:coma (less common)
n1=en:retardation | n2=en:coma (less common) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:coma during episodes (in some patients)
n1=en:retardation | n2=en:coma during episodes (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:coma may occur after force feeding of high protein diet
n1=en:retardation | n2=en:coma may occur after force feeding of high protein diet | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:common atrioventricular orifice in double inlet ventricle
n1=en:retardation | n2=en:common atrioventricular orifice in double inlet ventricle | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:communicating hydrocephalus
n1=en:retardation | n2=en:communicating hydrocephalus | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:communication defects
n1=en:retardation | n2=en:communication defects | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:communication disorder
n1=en:retardation | n2=en:communication disorder | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:complete or partial absence of the corpus callosum
n1=en:retardation | n2=en:complete or partial absence of the corpus callosum | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:complete or partial absence of the corpus callosum (wws)
n1=en:retardation | n2=en:complete or partial absence of the corpus callosum (wws) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:complete trisomy 18 syndrome
n1=en:retardation | n2=en:complete trisomy 18 syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:complex motor behavior such as sleep walking
n1=en:retardation | n2=en:complex motor behavior such as sleep walking | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:complex partial seizure with impairment of consciousness
n1=en:retardation | n2=en:complex partial seizure with impairment of consciousness | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:complex partial seizures
n1=en:retardation | n2=en:complex partial seizures | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:complex partial seizures (in some patients)
n1=en:retardation | n2=en:complex partial seizures (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:complex partial seizures, often with secondary generalization, are the most common type
n1=en:retardation | n2=en:complex partial seizures, often with secondary generalization, are the most common type | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:complicated delivery deadborn
n1=en:retardation | n2=en:complicated delivery deadborn | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:complicated delivery liveborn
n1=en:retardation | n2=en:complicated delivery liveborn | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:complication of surgical and medical care, unspecified
n1=en:retardation | n2=en:complication of surgical and medical care, unspecified | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:compromised expressive language development, severe
n1=en:retardation | n2=en:compromised expressive language development, severe | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:concentration impairment
n1=en:retardation | n2=en:concentration impairment | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:concern sexual preference
n1=en:retardation | n2=en:concern sexual preference | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:concussion
n1=en:retardation | n2=en:concussion | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:conduct disorder
n1=en:retardation | n2=en:conduct disorder | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:condylomata acuminata in men
n1=en:retardation | n2=en:condylomata acuminata in men | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:condylomata acuminata in women
n1=en:retardation | n2=en:condylomata acuminata in women | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:confirmation of pregnancy
n1=en:retardation | n2=en:confirmation of pregnancy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:confusion
n1=en:retardation | n2=en:confusion | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:confusion (later-onset)
n1=en:retardation | n2=en:confusion (later-onset) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:confusion adverse event
n1=en:retardation | n2=en:confusion adverse event | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:confusion, paroxysmal
n1=en:retardation | n2=en:confusion, paroxysmal | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:congenital
n1=en:retardation | n2=en:congenital | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:congenital abnormal communication
n1=en:retardation | n2=en:congenital abnormal communication | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:congenital abnormal fusion
n1=en:retardation | n2=en:congenital abnormal fusion | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:congenital abnormality
n1=en:retardation | n2=en:congenital abnormality | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:congenital abnormality of lower limb and/or pelvic girdle
n1=en:retardation | n2=en:congenital abnormality of lower limb and/or pelvic girdle | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:congenital absence of the vermis
n1=en:retardation | n2=en:congenital absence of the vermis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:congenital anomalies of fetus
n1=en:retardation | n2=en:congenital anomalies of fetus | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:congenital anomalies of mother
n1=en:retardation | n2=en:congenital anomalies of mother | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:congenital anomaly of back
n1=en:retardation | n2=en:congenital anomaly of back | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:congenital anomaly of body wall
n1=en:retardation | n2=en:congenital anomaly of body wall | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:congenital anomaly of brain
n1=en:retardation | n2=en:congenital anomaly of brain | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:congenital anomaly of central nervous system
n1=en:retardation | n2=en:congenital anomaly of central nervous system | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:congenital anomaly of endocrine gland
n1=en:retardation | n2=en:congenital anomaly of endocrine gland | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:congenital anomaly of face
n1=en:retardation | n2=en:congenital anomaly of face | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:congenital anomaly of female genital system
n1=en:retardation | n2=en:congenital anomaly of female genital system | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:congenital anomaly of gastrointestinal tract
n1=en:retardation | n2=en:congenital anomaly of gastrointestinal tract | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:congenital anomaly of head
n1=en:retardation | n2=en:congenital anomaly of head | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:congenital anomaly of male genital system
n1=en:retardation | n2=en:congenital anomaly of male genital system | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:congenital anomaly of neck
n1=en:retardation | n2=en:congenital anomaly of neck | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:congenital anomaly of skeletal bone
n1=en:retardation | n2=en:congenital anomaly of skeletal bone | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:congenital anomaly of skull
n1=en:retardation | n2=en:congenital anomaly of skull | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:congenital anomaly of spine
n1=en:retardation | n2=en:congenital anomaly of spine | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:congenital anomaly of the hematopoietic system
n1=en:retardation | n2=en:congenital anomaly of the hematopoietic system | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:congenital anomaly of trunk
n1=en:retardation | n2=en:congenital anomaly of trunk | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:congenital anomaly of visual system
n1=en:retardation | n2=en:congenital anomaly of visual system | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:congenital cardiovascular abnormality
n1=en:retardation | n2=en:congenital cardiovascular abnormality | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:congenital cardiovascular malformation
n1=en:retardation | n2=en:congenital cardiovascular malformation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:congenital cataracts, facial dysmorphism, and neuropathy
n1=en:retardation | n2=en:congenital cataracts, facial dysmorphism, and neuropathy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:congenital cavitation
n1=en:retardation | n2=en:congenital cavitation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:congenital cerebellar hypoplasia
n1=en:retardation | n2=en:congenital cerebellar hypoplasia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:congenital deformity of ankle joint
n1=en:retardation | n2=en:congenital deformity of ankle joint | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:congenital deformity of chest wall
n1=en:retardation | n2=en:congenital deformity of chest wall | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:congenital deformity of clavicle
n1=en:retardation | n2=en:congenital deformity of clavicle | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:congenital deformity of hip
n1=en:retardation | n2=en:congenital deformity of hip | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:congenital deformity of knee joint
n1=en:retardation | n2=en:congenital deformity of knee joint | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:congenital deformity of labyrinth
n1=en:retardation | n2=en:congenital deformity of labyrinth | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:congenital deformity of mitral valve annulus
n1=en:retardation | n2=en:congenital deformity of mitral valve annulus | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:congenital deformity of pharynx
n1=en:retardation | n2=en:congenital deformity of pharynx | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:congenital deformity of pinna
n1=en:retardation | n2=en:congenital deformity of pinna | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:congenital deformity of scapula
n1=en:retardation | n2=en:congenital deformity of scapula | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:congenital diaphragmatic hernia
n1=en:retardation | n2=en:congenital diaphragmatic hernia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:congenital disorder of glycosylation type 1i
n1=en:retardation | n2=en:congenital disorder of glycosylation type 1i | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:congenital disorder of glycosylation type ij
n1=en:retardation | n2=en:congenital disorder of glycosylation type ij | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:congenital disruption
n1=en:retardation | n2=en:congenital disruption | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:congenital dysplasia
n1=en:retardation | n2=en:congenital dysplasia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:congenital ear anomaly nos (disorder)
n1=en:retardation | n2=en:congenital ear anomaly nos (disorder) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:congenital enlargement
n1=en:retardation | n2=en:congenital enlargement | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:congenital extension deformity
n1=en:retardation | n2=en:congenital extension deformity | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:congenital eye disorder
n1=en:retardation | n2=en:congenital eye disorder | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:congenital failure of fusion
n1=en:retardation | n2=en:congenital failure of fusion | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:congenital flat back deformity
n1=en:retardation | n2=en:congenital flat back deformity | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:congenital flexion deformity
n1=en:retardation | n2=en:congenital flexion deformity | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:congenital foot deformity
n1=en:retardation | n2=en:congenital foot deformity | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:congenital functional anomaly
n1=en:retardation | n2=en:congenital functional anomaly | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:congenital genitourinary abnormality
n1=en:retardation | n2=en:congenital genitourinary abnormality | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:congenital growth alteration
n1=en:retardation | n2=en:congenital growth alteration | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:congenital hallux valgus
n1=en:retardation | n2=en:congenital hallux valgus | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:congenital hamartoma
n1=en:retardation | n2=en:congenital hamartoma | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:congenital hand and foot deformity
n1=en:retardation | n2=en:congenital hand and foot deformity | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:congenital hernia
n1=en:retardation | n2=en:congenital hernia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:congenital hyperextension of limb
n1=en:retardation | n2=en:congenital hyperextension of limb | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:congenital hyperflexion of limb
n1=en:retardation | n2=en:congenital hyperflexion of limb | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:congenital hypoplasia of genital tubercle
n1=en:retardation | n2=en:congenital hypoplasia of genital tubercle | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:congenital hypothyroidism
n1=en:retardation | n2=en:congenital hypothyroidism | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:congenital hypotonia, axial or generalized
n1=en:retardation | n2=en:congenital hypotonia, axial or generalized | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:congenital hypotonia, mild
n1=en:retardation | n2=en:congenital hypotonia, mild | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:congenital infundibular stenosis
n1=en:retardation | n2=en:congenital infundibular stenosis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:congenital insensitivity to pain with anhidrosis
n1=en:retardation | n2=en:congenital insensitivity to pain with anhidrosis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:congenital keratoglobus
n1=en:retardation | n2=en:congenital keratoglobus | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:congenital macrocephaly
n1=en:retardation | n2=en:congenital macrocephaly | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:congenital malformation of genital organs
n1=en:retardation | n2=en:congenital malformation of genital organs | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:congenital malformation syndrome
n1=en:retardation | n2=en:congenital malformation syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:congenital malformation syndrome related to known exogenous cause
n1=en:retardation | n2=en:congenital malformation syndrome related to known exogenous cause | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:congenital malposition
n1=en:retardation | n2=en:congenital malposition | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:congenital melanosis
n1=en:retardation | n2=en:congenital melanosis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:congenital metabolic disorder
n1=en:retardation | n2=en:congenital metabolic disorder | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:congenital microtia
n1=en:retardation | n2=en:congenital microtia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:congenital morphologic anomaly
n1=en:retardation | n2=en:congenital morphologic anomaly | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:congenital muscular dystrophy-dystroglycanopathy with mental retardation type b2
n1=en:retardation | n2=en:congenital muscular dystrophy-dystroglycanopathy with mental retardation type b2 | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:congenital musculoskeletal defect
n1=en:retardation | n2=en:congenital musculoskeletal defect | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:congenital nervous system disorder
n1=en:retardation | n2=en:congenital nervous system disorder | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:congenital opacity
n1=en:retardation | n2=en:congenital opacity | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:congenital pigmentation
n1=en:retardation | n2=en:congenital pigmentation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:congenital porencephaly
n1=en:retardation | n2=en:congenital porencephaly | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:congenital red cell hypoplasia
n1=en:retardation | n2=en:congenital red cell hypoplasia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:congenital respiratory system disorder
n1=en:retardation | n2=en:congenital respiratory system disorder | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:congenital septation
n1=en:retardation | n2=en:congenital septation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:congenital sequestration
n1=en:retardation | n2=en:congenital sequestration | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:congenital skin disorder
n1=en:retardation | n2=en:congenital skin disorder | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:congenital stenosis
n1=en:retardation | n2=en:congenital stenosis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:congenital systemic disorder
n1=en:retardation | n2=en:congenital systemic disorder | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:congenital urinary system abnormality
n1=en:retardation | n2=en:congenital urinary system abnormality | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:congenital vascular anomaly
n1=en:retardation | n2=en:congenital vascular anomaly | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:congenital vena cava abnormality
n1=en:retardation | n2=en:congenital vena cava abnormality | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:congenital visceral anomaly
n1=en:retardation | n2=en:congenital visceral anomaly | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:conjoined twins
n1=en:retardation | n2=en:conjoined twins | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:connatal disorder
n1=en:retardation | n2=en:connatal disorder | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:connective and soft tissue injury
n1=en:retardation | n2=en:connective and soft tissue injury | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:consciousness fluctuating
n1=en:retardation | n2=en:consciousness fluctuating | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:constructional apraxia (in a subset of patients)
n1=en:retardation | n2=en:constructional apraxia (in a subset of patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:contact dermatitis and other eczema
n1=en:retardation | n2=en:contact dermatitis and other eczema | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:continuous spike-wave discharges during sleep
n1=en:retardation | n2=en:continuous spike-wave discharges during sleep | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:continuous spike-waves during slow-wave sleep
n1=en:retardation | n2=en:continuous spike-waves during slow-wave sleep | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:contractures (older children and adolescents)
n1=en:retardation | n2=en:contractures (older children and adolescents) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:contralateral hemiparesis, congenital
n1=en:retardation | n2=en:contralateral hemiparesis, congenital | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:contusion/hemorrhage eye
n1=en:retardation | n2=en:contusion/hemorrhage eye | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:convulsions, febrile (in some patients)
n1=en:retardation | n2=en:convulsions, febrile (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:convulsive seizures
n1=en:retardation | n2=en:convulsive seizures | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cor pulmonale
n1=en:retardation | n2=en:cor pulmonale | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:corneal ulcer
n1=en:retardation | n2=en:corneal ulcer | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:corprolalia
n1=en:retardation | n2=en:corprolalia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:corpus callosum abnormalities (in some patients)
n1=en:retardation | n2=en:corpus callosum abnormalities (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:corpus callosum agenesis
n1=en:retardation | n2=en:corpus callosum agenesis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:corpus callosum lipoma
n1=en:retardation | n2=en:corpus callosum lipoma | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:corpus callosum, agenesis of (in some patients)
n1=en:retardation | n2=en:corpus callosum, agenesis of (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:corpus callosum, agenesis of, with mental retardation, ocular coloboma, and micrognathia
n1=en:retardation | n2=en:corpus callosum, agenesis of, with mental retardation, ocular coloboma, and micrognathia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:corpus callosum, thin (rare)
n1=en:retardation | n2=en:corpus callosum, thin (rare) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cortada kousseff matsumoto syndrome
n1=en:retardation | n2=en:cortada kousseff matsumoto syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cortical and brainstem neuronal loss
n1=en:retardation | n2=en:cortical and brainstem neuronal loss | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cortical and subcortical atrophy (1 patient)
n1=en:retardation | n2=en:cortical and subcortical atrophy (1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cortical and subcortical hyperintensities
n1=en:retardation | n2=en:cortical and subcortical hyperintensities | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cortical and subcortical neuronal loss in the frontal and temporal regions
n1=en:retardation | n2=en:cortical and subcortical neuronal loss in the frontal and temporal regions | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cortical and subcortical regions involved
n1=en:retardation | n2=en:cortical and subcortical regions involved | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cortical atrophy (43%)
n1=en:retardation | n2=en:cortical atrophy (43%) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cortical atrophy (frontal area)
n1=en:retardation | n2=en:cortical atrophy (frontal area) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cortical atrophy (in 2 siblings)
n1=en:retardation | n2=en:cortical atrophy (in 2 siblings) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cortical atrophy (in some patients)
n1=en:retardation | n2=en:cortical atrophy (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cortical atrophy (rare)
n1=en:retardation | n2=en:cortical atrophy (rare) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cortical atrophy with loss of pyramidal neurons in the motor cortex
n1=en:retardation | n2=en:cortical atrophy with loss of pyramidal neurons in the motor cortex | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cortical atrophy, progressive
n1=en:retardation | n2=en:cortical atrophy, progressive | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cortical blindness (in 1 moroccan patient)
n1=en:retardation | n2=en:cortical blindness (in 1 moroccan patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cortical cytotoxic edema
n1=en:retardation | n2=en:cortical cytotoxic edema | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cortical degeneration
n1=en:retardation | n2=en:cortical degeneration | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cortical dysgenesis
n1=en:retardation | n2=en:cortical dysgenesis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cortical dysgenesis, complex
n1=en:retardation | n2=en:cortical dysgenesis, complex | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cortical dysplasia
n1=en:retardation | n2=en:cortical dysplasia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cortical dysplasia (1 patient)
n1=en:retardation | n2=en:cortical dysplasia (1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cortical dysplasia (2 patients)
n1=en:retardation | n2=en:cortical dysplasia (2 patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cortical dysplasia, focal (1 patient)
n1=en:retardation | n2=en:cortical dysplasia, focal (1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cortical dysplasia, focal (in some patients)
n1=en:retardation | n2=en:cortical dysplasia, focal (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cortical gyral simplification
n1=en:retardation | n2=en:cortical gyral simplification | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cortical hypergyria (in some patients)
n1=en:retardation | n2=en:cortical hypergyria (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cortical malformations
n1=en:retardation | n2=en:cortical malformations | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cortical myoclonic tremors characterized by 8 to 10-hz discharges
n1=en:retardation | n2=en:cortical myoclonic tremors characterized by 8 to 10-hz discharges | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cortical neuronal loss
n1=en:retardation | n2=en:cortical neuronal loss | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cortical origin of the tremor
n1=en:retardation | n2=en:cortical origin of the tremor | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cortical reflex myoclonus
n1=en:retardation | n2=en:cortical reflex myoclonus | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cortical simplification
n1=en:retardation | n2=en:cortical simplification | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cortical thinning
n1=en:retardation | n2=en:cortical thinning | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cortical tubers
n1=en:retardation | n2=en:cortical tubers | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cortical venous thromboses
n1=en:retardation | n2=en:cortical venous thromboses | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:corticobasal degeneration (in some patients)
n1=en:retardation | n2=en:corticobasal degeneration (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:corticospinal signs (87% of patients in 1 report)
n1=en:retardation | n2=en:corticospinal signs (87% of patients in 1 report) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:corticospinal tract atrophy
n1=en:retardation | n2=en:corticospinal tract atrophy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:corticospinal tract disease in lower limbs (in adulthood)
n1=en:retardation | n2=en:corticospinal tract disease in lower limbs (in adulthood) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:corticospinal tract hypoplasia
n1=en:retardation | n2=en:corticospinal tract hypoplasia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:corticospinal tracts with decreased myelin staining
n1=en:retardation | n2=en:corticospinal tracts with decreased myelin staining | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:costello syndrome
n1=en:retardation | n2=en:costello syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cranial nerve anomalies
n1=en:retardation | n2=en:cranial nerve anomalies | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cranial nerve dysfunction
n1=en:retardation | n2=en:cranial nerve dysfunction | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cranial nerve palsies can arise with head and neck paragangliomas
n1=en:retardation | n2=en:cranial nerve palsies can arise with head and neck paragangliomas | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cranial nerve palsy
n1=en:retardation | n2=en:cranial nerve palsy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cranial nerve palsy, intermittent, transient
n1=en:retardation | n2=en:cranial nerve palsy, intermittent, transient | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:craniofacial dyssynostosis
n1=en:retardation | n2=en:craniofacial dyssynostosis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:craniofenestria
n1=en:retardation | n2=en:craniofenestria | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cranioschisis
n1=en:retardation | n2=en:cranioschisis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:craniostenosis with congenital heart disease mental retardation
n1=en:retardation | n2=en:craniostenosis with congenital heart disease mental retardation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:craniosynostosis
n1=en:retardation | n2=en:craniosynostosis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:crawling and standing not achieved
n1=en:retardation | n2=en:crawling and standing not achieved | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cri du chat syndrome
n1=en:retardation | n2=en:cri du chat syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:crowding of the posterior fossa
n1=en:retardation | n2=en:crowding of the posterior fossa | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cryptophthalmia
n1=en:retardation | n2=en:cryptophthalmia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cryptorchidism arachnodactyly mental retardation
n1=en:retardation | n2=en:cryptorchidism arachnodactyly mental retardation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ct scan shows dense calcifications in the basal ganglia
n1=en:retardation | n2=en:ct scan shows dense calcifications in the basal ganglia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cutaneous mastocytosis, conductive hearing loss and microtia
n1=en:retardation | n2=en:cutaneous mastocytosis, conductive hearing loss and microtia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cutis laxa, autosomal recessive, type iia
n1=en:retardation | n2=en:cutis laxa, autosomal recessive, type iia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cutis verticis gyrata, retinitis pigmentosa, and sensorineural deafness
n1=en:retardation | n2=en:cutis verticis gyrata, retinitis pigmentosa, and sensorineural deafness | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cyclopia
n1=en:retardation | n2=en:cyclopia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cyst of septum pellucidum
n1=en:retardation | n2=en:cyst of septum pellucidum | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cyst of septum pellucidum (in some patients)
n1=en:retardation | n2=en:cyst of septum pellucidum (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cystathionine beta-synthase deficiency disease
n1=en:retardation | n2=en:cystathionine beta-synthase deficiency disease | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cystic cavitation of the white matter
n1=en:retardation | n2=en:cystic cavitation of the white matter | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cystic degeneration of cerebral white matter with preserved cortex
n1=en:retardation | n2=en:cystic degeneration of cerebral white matter with preserved cortex | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cystic degeneration of the white matter
n1=en:retardation | n2=en:cystic degeneration of the white matter | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cystic destruction of brain tissue, including basal ganglia
n1=en:retardation | n2=en:cystic destruction of brain tissue, including basal ganglia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cystic lesions consistent with leigh syndrome (256000)
n1=en:retardation | n2=en:cystic lesions consistent with leigh syndrome (256000) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cystic lesions in the basal ganglia, brainstem, and cerebral hemispheres similar to leigh syndrome (256000)
n1=en:retardation | n2=en:cystic lesions in the basal ganglia, brainstem, and cerebral hemispheres similar to leigh syndrome (256000) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cystic lysis of the deep white matter
n1=en:retardation | n2=en:cystic lysis of the deep white matter | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cystitis/other urinary infection nos
n1=en:retardation | n2=en:cystitis/other urinary infection nos | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cysts tend to enlarge with age
n1=en:retardation | n2=en:cysts tend to enlarge with age | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cytochrome-c oxidase deficiency
n1=en:retardation | n2=en:cytochrome-c oxidase deficiency | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cytogenetic abnormality
n1=en:retardation | n2=en:cytogenetic abnormality | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:cytopathic effect
n1=en:retardation | n2=en:cytopathic effect | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:d-2-hydroxyglutaric aciduria 1
n1=en:retardation | n2=en:d-2-hydroxyglutaric aciduria 1 | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:d-glyceric aciduria
n1=en:retardation | n2=en:d-glyceric aciduria | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dandy walker variant
n1=en:retardation | n2=en:dandy walker variant | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dandy-walker malformation
n1=en:retardation | n2=en:dandy-walker malformation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dandy-walker malformation (1 patient)
n1=en:retardation | n2=en:dandy-walker malformation (1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dandy-walker malformation (in 1 of 4 patients)
n1=en:retardation | n2=en:dandy-walker malformation (in 1 of 4 patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dandy-walker malformation (in some patients)
n1=en:retardation | n2=en:dandy-walker malformation (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dandy-walker malformation (rare)
n1=en:retardation | n2=en:dandy-walker malformation (rare) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dandy-walker malformation (variable)
n1=en:retardation | n2=en:dandy-walker malformation (variable) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dandy-walker malformation (wws)
n1=en:retardation | n2=en:dandy-walker malformation (wws) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:deafness
n1=en:retardation | n2=en:deafness | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:death
n1=en:retardation | n2=en:death | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:decerebrate or decorticate posturing late
n1=en:retardation | n2=en:decerebrate or decorticate posturing late | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:decerebrate posturings
n1=en:retardation | n2=en:decerebrate posturings | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:decorticate posture
n1=en:retardation | n2=en:decorticate posture | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:decrease in abstract thinking
n1=en:retardation | n2=en:decrease in abstract thinking | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:decreased active movements
n1=en:retardation | n2=en:decreased active movements | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:decreased amount of myelin-specific lipids
n1=en:retardation | n2=en:decreased amount of myelin-specific lipids | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:decreased amount of myelin-specific proteins
n1=en:retardation | n2=en:decreased amount of myelin-specific proteins | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:decreased brain volume (female)
n1=en:retardation | n2=en:decreased brain volume (female) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:decreased brain weight
n1=en:retardation | n2=en:decreased brain weight | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:decreased cerebellar folia
n1=en:retardation | n2=en:decreased cerebellar folia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:decreased cerebral volume, especially of the frontal lobes
n1=en:retardation | n2=en:decreased cerebral volume, especially of the frontal lobes | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:decreased cognition (later-onset)
n1=en:retardation | n2=en:decreased cognition (later-onset) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:decreased core body temperature
n1=en:retardation | n2=en:decreased core body temperature | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:decreased creatine signal seen on magnetic resonance spectroscopy
n1=en:retardation | n2=en:decreased creatine signal seen on magnetic resonance spectroscopy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:decreased csf volume in posterior fossa
n1=en:retardation | n2=en:decreased csf volume in posterior fossa | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:decreased delineation of the basal ganglia (in some patients)
n1=en:retardation | n2=en:decreased delineation of the basal ganglia (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:decreased fine motor coordination
n1=en:retardation | n2=en:decreased fine motor coordination | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:decreased iq
n1=en:retardation | n2=en:decreased iq | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:decreased iq (1 patient)
n1=en:retardation | n2=en:decreased iq (1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:decreased iq (some patients)
n1=en:retardation | n2=en:decreased iq (some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:decreased iron content in the substantia nigra
n1=en:retardation | n2=en:decreased iron content in the substantia nigra | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:decreased libido
n1=en:retardation | n2=en:decreased libido | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:decreased mental processing speed
n1=en:retardation | n2=en:decreased mental processing speed | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:decreased mitochondrial respiratory chain complex activity
n1=en:retardation | n2=en:decreased mitochondrial respiratory chain complex activity | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:decreased motor nerve conduction velocity
n1=en:retardation | n2=en:decreased motor nerve conduction velocity | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:decreased myelin
n1=en:retardation | n2=en:decreased myelin | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:decreased myelination seen on mri
n1=en:retardation | n2=en:decreased myelination seen on mri | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:decreased n-acetylaspartate
n1=en:retardation | n2=en:decreased n-acetylaspartate | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:decreased need for sleep
n1=en:retardation | n2=en:decreased need for sleep | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:decreased nonverbal iq
n1=en:retardation | n2=en:decreased nonverbal iq | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:decreased numbers of astrocytes
n1=en:retardation | n2=en:decreased numbers of astrocytes | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:decreased or absent gyri (in some patients)
n1=en:retardation | n2=en:decreased or absent gyri (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:decreased or absent motor evoked potentials (mep), indicating dysfunction of the corticospinal tracts
n1=en:retardation | n2=en:decreased or absent motor evoked potentials (mep), indicating dysfunction of the corticospinal tracts | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:decreased pain response
n1=en:retardation | n2=en:decreased pain response | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:decreased pyramidal cells
n1=en:retardation | n2=en:decreased pyramidal cells | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:decreased rapid automatized naming (ran) speed
n1=en:retardation | n2=en:decreased rapid automatized naming (ran) speed | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:decreased reflexes (in some patients)
n1=en:retardation | n2=en:decreased reflexes (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:decreased sleep latency
n1=en:retardation | n2=en:decreased sleep latency | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:decreased somatosensory-evoked potentials
n1=en:retardation | n2=en:decreased somatosensory-evoked potentials | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:decreased speech
n1=en:retardation | n2=en:decreased speech | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:decreased spontaneous movements at birth
n1=en:retardation | n2=en:decreased spontaneous movements at birth | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:decreased supratentorial volume
n1=en:retardation | n2=en:decreased supratentorial volume | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:decreased tendon reflex
n1=en:retardation | n2=en:decreased tendon reflex | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:decreased upper extremity reflexes
n1=en:retardation | n2=en:decreased upper extremity reflexes | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:decreased vibration sense, suggesting posterior column involvement
n1=en:retardation | n2=en:decreased vibration sense, suggesting posterior column involvement | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:decreased vibratory sense
n1=en:retardation | n2=en:decreased vibratory sense | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:decreased volume of the cerebral white matter
n1=en:retardation | n2=en:decreased volume of the cerebral white matter | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:decreased volume of the posterior cranial fossa with normal hindbrain volume
n1=en:retardation | n2=en:decreased volume of the posterior cranial fossa with normal hindbrain volume | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:decreased white matter
n1=en:retardation | n2=en:decreased white matter | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:decreased white matter volume
n1=en:retardation | n2=en:decreased white matter volume | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:decreasing responsiveness
n1=en:retardation | n2=en:decreasing responsiveness | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:deep hypointensities (mri, t2) suggestive of past microbleeds
n1=en:retardation | n2=en:deep hypointensities (mri, t2) suggestive of past microbleeds | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:deep interpeduncular fossa
n1=en:retardation | n2=en:deep interpeduncular fossa | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:deep posterior interpeduncular fossa
n1=en:retardation | n2=en:deep posterior interpeduncular fossa | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:deep white matter changes
n1=en:retardation | n2=en:deep white matter changes | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:deep white matter hypodensities
n1=en:retardation | n2=en:deep white matter hypodensities | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:deep white matter lesions, particularly affecting the frontal and parietal lobes
n1=en:retardation | n2=en:deep white matter lesions, particularly affecting the frontal and parietal lobes | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:defect in axonal guidance
n1=en:retardation | n2=en:defect in axonal guidance | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:defect in morphosyntactic rules
n1=en:retardation | n2=en:defect in morphosyntactic rules | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:defective myelination of the deep white matter
n1=en:retardation | n2=en:defective myelination of the deep white matter | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:defective opercularization
n1=en:retardation | n2=en:defective opercularization | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:defects in auditory cue processing
n1=en:retardation | n2=en:defects in auditory cue processing | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:defects in fine motor skills
n1=en:retardation | n2=en:defects in fine motor skills | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:defects in visual cue processing
n1=en:retardation | n2=en:defects in visual cue processing | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:deficient myelination
n1=en:retardation | n2=en:deficient myelination | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:deficit in basic reading
n1=en:retardation | n2=en:deficit in basic reading | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:deficit in expressive language
n1=en:retardation | n2=en:deficit in expressive language | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:deficit in nonword repetition (nwr)
n1=en:retardation | n2=en:deficit in nonword repetition (nwr) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:deficit in phonologic short-term memory
n1=en:retardation | n2=en:deficit in phonologic short-term memory | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:deficit in reading comprehension
n1=en:retardation | n2=en:deficit in reading comprehension | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:deficit in spelling
n1=en:retardation | n2=en:deficit in spelling | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:deficits in abstraction
n1=en:retardation | n2=en:deficits in abstraction | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:deficits in language expression
n1=en:retardation | n2=en:deficits in language expression | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:deformed temporal lobes
n1=en:retardation | n2=en:deformed temporal lobes | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:degeneration of anterior horn cells
n1=en:retardation | n2=en:degeneration of anterior horn cells | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:degeneration of purkinje cells in the cerebellum
n1=en:retardation | n2=en:degeneration of purkinje cells in the cerebellum | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:degeneration of the dentatorubral and pallidoluysian systems
n1=en:retardation | n2=en:degeneration of the dentatorubral and pallidoluysian systems | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:degeneration of the lateral corticospinal tracts
n1=en:retardation | n2=en:degeneration of the lateral corticospinal tracts | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:deja vu feeling
n1=en:retardation | n2=en:deja vu feeling | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:delay in gross motor development due to weakness
n1=en:retardation | n2=en:delay in gross motor development due to weakness | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:delay of gross motor function
n1=en:retardation | n2=en:delay of gross motor function | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:delayed adaptive hand use
n1=en:retardation | n2=en:delayed adaptive hand use | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:delayed ambulation
n1=en:retardation | n2=en:delayed ambulation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:delayed brainstem development (in some patients)
n1=en:retardation | n2=en:delayed brainstem development (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:delayed cerebellar development (in some patients)
n1=en:retardation | n2=en:delayed cerebellar development (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:delayed cerebral myelination
n1=en:retardation | n2=en:delayed cerebral myelination | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:delayed cognitive development (in some patients)
n1=en:retardation | n2=en:delayed cognitive development (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:delayed cognitive development, mild (reported in 1 family)
n1=en:retardation | n2=en:delayed cognitive development, mild (reported in 1 family) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:delayed cognitive development/learning disabilities (93%)
n1=en:retardation | n2=en:delayed cognitive development/learning disabilities (93%) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:delayed development (1 family)
n1=en:retardation | n2=en:delayed development (1 family) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:delayed development (about 25%)
n1=en:retardation | n2=en:delayed development (about 25%) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:delayed development (in some patients)
n1=en:retardation | n2=en:delayed development (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:delayed development (in some)
n1=en:retardation | n2=en:delayed development (in some) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:delayed development if untreated
n1=en:retardation | n2=en:delayed development if untreated | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:delayed development in early childhood (in some patients)
n1=en:retardation | n2=en:delayed development in early childhood (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:delayed development may occur
n1=en:retardation | n2=en:delayed development may occur | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:delayed development, after 8-15 months
n1=en:retardation | n2=en:delayed development, after 8-15 months | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:delayed development, ranging from mild to severe
n1=en:retardation | n2=en:delayed development, ranging from mild to severe | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:delayed development, severe
n1=en:retardation | n2=en:delayed development, severe | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:delayed development, variable (in some patients)
n1=en:retardation | n2=en:delayed development, variable (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:delayed development, variable severity, from birth in some patients
n1=en:retardation | n2=en:delayed development, variable severity, from birth in some patients | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:delayed developmental milestones
n1=en:retardation | n2=en:delayed developmental milestones | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:delayed epiphyseal fusion
n1=en:retardation | n2=en:delayed epiphyseal fusion | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:delayed gross motor development (in some patients)
n1=en:retardation | n2=en:delayed gross motor development (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:delayed gyration
n1=en:retardation | n2=en:delayed gyration | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:delayed independent walking
n1=en:retardation | n2=en:delayed independent walking | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:delayed intellectual development
n1=en:retardation | n2=en:delayed intellectual development | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:delayed motor and speech development, mild (1 family)
n1=en:retardation | n2=en:delayed motor and speech development, mild (1 family) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:delayed motor development (1 patient)
n1=en:retardation | n2=en:delayed motor development (1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:delayed motor development (secondary to skeletal abnormalities)
n1=en:retardation | n2=en:delayed motor development (secondary to skeletal abnormalities) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:delayed motor development due to muscle weakness
n1=en:retardation | n2=en:delayed motor development due to muscle weakness | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:delayed motor development, mild, transient
n1=en:retardation | n2=en:delayed motor development, mild, transient | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:delayed motor development, severe
n1=en:retardation | n2=en:delayed motor development, severe | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:delayed motor milestones due to muscle weakness
n1=en:retardation | n2=en:delayed motor milestones due to muscle weakness | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:delayed myelination
n1=en:retardation | n2=en:delayed myelination | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:delayed myelination (1 patient)
n1=en:retardation | n2=en:delayed myelination (1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:delayed myelination (1/4 patients)
n1=en:retardation | n2=en:delayed myelination (1/4 patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:delayed myelination (in some patients)
n1=en:retardation | n2=en:delayed myelination (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:delayed myelination (reported in 1 patient)
n1=en:retardation | n2=en:delayed myelination (reported in 1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:delayed myelination on brain mri (reported in 1 patient)
n1=en:retardation | n2=en:delayed myelination on brain mri (reported in 1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:delayed myelination seen on mri
n1=en:retardation | n2=en:delayed myelination seen on mri | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:delayed myelination, mild
n1=en:retardation | n2=en:delayed myelination, mild | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:delayed myelinization (in some patients)
n1=en:retardation | n2=en:delayed myelinization (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:delayed onset of phrase speech (> 36 months)
n1=en:retardation | n2=en:delayed onset of phrase speech (> 36 months) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:delayed opercularization
n1=en:retardation | n2=en:delayed opercularization | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:delayed or absent independent walking
n1=en:retardation | n2=en:delayed or absent independent walking | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:delayed psychomotor development (1 patient)
n1=en:retardation | n2=en:delayed psychomotor development (1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:delayed psychomotor development (in 1 family)
n1=en:retardation | n2=en:delayed psychomotor development (in 1 family) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:delayed psychomotor development (in most patients)
n1=en:retardation | n2=en:delayed psychomotor development (in most patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:delayed psychomotor development (in severe cases)
n1=en:retardation | n2=en:delayed psychomotor development (in severe cases) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:delayed psychomotor development (in some patients)
n1=en:retardation | n2=en:delayed psychomotor development (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:delayed psychomotor development (in some)
n1=en:retardation | n2=en:delayed psychomotor development (in some) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:delayed psychomotor development (mild to severe)
n1=en:retardation | n2=en:delayed psychomotor development (mild to severe) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:delayed psychomotor development (stops at development levels of 1-2 years)
n1=en:retardation | n2=en:delayed psychomotor development (stops at development levels of 1-2 years) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:delayed psychomotor development after onset of seizures
n1=en:retardation | n2=en:delayed psychomotor development after onset of seizures | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:delayed psychomotor development, mild
n1=en:retardation | n2=en:delayed psychomotor development, mild | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:delayed psychomotor development, mild (in 3 of 5 patients)
n1=en:retardation | n2=en:delayed psychomotor development, mild (in 3 of 5 patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:delayed psychomotor development, mild (in some patients)
n1=en:retardation | n2=en:delayed psychomotor development, mild (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:delayed psychomotor development, moderate to severe
n1=en:retardation | n2=en:delayed psychomotor development, moderate to severe | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:delayed psychomotor development, profound
n1=en:retardation | n2=en:delayed psychomotor development, profound | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:delayed psychomotor development, profound (1 patient)
n1=en:retardation | n2=en:delayed psychomotor development, profound (1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:delayed psychomotor development, profound (patient a)
n1=en:retardation | n2=en:delayed psychomotor development, profound (patient a) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:delayed psychomotor development, severe
n1=en:retardation | n2=en:delayed psychomotor development, severe | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:delayed psychomotor development, severe (> 90%)
n1=en:retardation | n2=en:delayed psychomotor development, severe (> 90%) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:delayed psychomotor development, severe (in 2 of 6 patients)
n1=en:retardation | n2=en:delayed psychomotor development, severe (in 2 of 6 patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:delayed psychomotor development, severe to profound
n1=en:retardation | n2=en:delayed psychomotor development, severe to profound | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:delayed psychomotor development, variable
n1=en:retardation | n2=en:delayed psychomotor development, variable | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:delayed puberty
n1=en:retardation | n2=en:delayed puberty | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:delayed speech and language development
n1=en:retardation | n2=en:delayed speech and language development | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:delayed speech development, severe
n1=en:retardation | n2=en:delayed speech development, severe | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:delayed walking (1 family)
n1=en:retardation | n2=en:delayed walking (1 family) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:delayed walking (less common)
n1=en:retardation | n2=en:delayed walking (less common) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:delayed walking (rare)
n1=en:retardation | n2=en:delayed walking (rare) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:delayed walking and running in early childhood
n1=en:retardation | n2=en:delayed walking and running in early childhood | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:delayed walking, mild (in some patients)
n1=en:retardation | n2=en:delayed walking, mild (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:deletion 18p syndrome
n1=en:retardation | n2=en:deletion 18p syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:deliria (incl confusion)
n1=en:retardation | n2=en:deliria (incl confusion) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:delirium
n1=en:retardation | n2=en:delirium | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:delirium (later-onset)
n1=en:retardation | n2=en:delirium (later-onset) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:delirium dementia and amnestic and other cognitive disorders
n1=en:retardation | n2=en:delirium dementia and amnestic and other cognitive disorders | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:delusion
n1=en:retardation | n2=en:delusion | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:delusional disorder
n1=en:retardation | n2=en:delusional disorder | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dementia
n1=en:retardation | n2=en:dementia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dementia (<20%)
n1=en:retardation | n2=en:dementia (<20%) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dementia (1 family)
n1=en:retardation | n2=en:dementia (1 family) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dementia (5%)
n1=en:retardation | n2=en:dementia (5%) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dementia (in some patients)
n1=en:retardation | n2=en:dementia (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dementia (later-onset)
n1=en:retardation | n2=en:dementia (later-onset) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dementia (onset in fifth decade)
n1=en:retardation | n2=en:dementia (onset in fifth decade) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dementia (subtype 3a)
n1=en:retardation | n2=en:dementia (subtype 3a) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dementia and amnestic conditions
n1=en:retardation | n2=en:dementia and amnestic conditions | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dementia in a subset of patients
n1=en:retardation | n2=en:dementia in a subset of patients | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dementia may occur
n1=en:retardation | n2=en:dementia may occur | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dementia of frontal lobe type
n1=en:retardation | n2=en:dementia of frontal lobe type | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dementia senile/alzheimer
n1=en:retardation | n2=en:dementia senile/alzheimer | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dementia, presenile, progressive, beginning around age 30 years
n1=en:retardation | n2=en:dementia, presenile, progressive, beginning around age 30 years | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dementia, progressive (more common in males)
n1=en:retardation | n2=en:dementia, progressive (more common in males) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dementia, progressive, with onset of disease
n1=en:retardation | n2=en:dementia, progressive, with onset of disease | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dementia, rapidly progressive
n1=en:retardation | n2=en:dementia, rapidly progressive | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:demyelination
n1=en:retardation | n2=en:demyelination | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:demyelination of the posterior and lateral columns of the spinal cord
n1=en:retardation | n2=en:demyelination of the posterior and lateral columns of the spinal cord | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:demyelination with white matter disease in internal capsule, external capsule, genu of corpus callosum, subcortical white matter, and posterior fossa
n1=en:retardation | n2=en:demyelination with white matter disease in internal capsule, external capsule, genu of corpus callosum, subcortical white matter, and posterior fossa | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:demyelination, symmetric
n1=en:retardation | n2=en:demyelination, symmetric | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:demyelinization
n1=en:retardation | n2=en:demyelinization | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:denervation seen on emg
n1=en:retardation | n2=en:denervation seen on emg | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dense calcifications in the cerebellar dentate nucleus
n1=en:retardation | n2=en:dense calcifications in the cerebellar dentate nucleus | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:depersonalization
n1=en:retardation | n2=en:depersonalization | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:depressed mood disorders and disturbances
n1=en:retardation | n2=en:depressed mood disorders and disturbances | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:depression
n1=en:retardation | n2=en:depression | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:depression, psychotic
n1=en:retardation | n2=en:depression, psychotic | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:depressive disorder
n1=en:retardation | n2=en:depressive disorder | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dermatophytosis
n1=en:retardation | n2=en:dermatophytosis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dermoid cyst
n1=en:retardation | n2=en:dermoid cyst | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:deterioration of motor development
n1=en:retardation | n2=en:deterioration of motor development | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:development varies from normal to retarded
n1=en:retardation | n2=en:development varies from normal to retarded | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:developmental agnosias
n1=en:retardation | n2=en:developmental agnosias | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:developmental arithmetic disorder
n1=en:retardation | n2=en:developmental arithmetic disorder | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:developmental arrest, 2nd year of life
n1=en:retardation | n2=en:developmental arrest, 2nd year of life | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:developmental coordination disorder
n1=en:retardation | n2=en:developmental coordination disorder | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:developmental delay
n1=en:retardation | n2=en:developmental delay | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:developmental delay (1 family)
n1=en:retardation | n2=en:developmental delay (1 family) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:developmental delay (1 patient)
n1=en:retardation | n2=en:developmental delay (1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:developmental delay (100%)
n1=en:retardation | n2=en:developmental delay (100%) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:developmental delay (20%)
n1=en:retardation | n2=en:developmental delay (20%) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:developmental delay (apparent after the first year of life)
n1=en:retardation | n2=en:developmental delay (apparent after the first year of life) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:developmental delay (female)
n1=en:retardation | n2=en:developmental delay (female) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:developmental delay (homozygote)
n1=en:retardation | n2=en:developmental delay (homozygote) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:developmental delay (in most patients)
n1=en:retardation | n2=en:developmental delay (in most patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:developmental delay (in some patients who survive infancy)
n1=en:retardation | n2=en:developmental delay (in some patients who survive infancy) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:developmental delay (in some patients)
n1=en:retardation | n2=en:developmental delay (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:developmental delay (in some)
n1=en:retardation | n2=en:developmental delay (in some) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:developmental delay (microdeletion patients only)
n1=en:retardation | n2=en:developmental delay (microdeletion patients only) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:developmental delay (mild-severe)
n1=en:retardation | n2=en:developmental delay (mild-severe) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:developmental delay (rare)
n1=en:retardation | n2=en:developmental delay (rare) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:developmental delay (seen in recessive form)
n1=en:retardation | n2=en:developmental delay (seen in recessive form) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:developmental delay (type ii)
n1=en:retardation | n2=en:developmental delay (type ii) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:developmental delay (uncommon)
n1=en:retardation | n2=en:developmental delay (uncommon) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:developmental delay evident by 12-24 months of age
n1=en:retardation | n2=en:developmental delay evident by 12-24 months of age | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:developmental delay if undiagnosed or untreated
n1=en:retardation | n2=en:developmental delay if undiagnosed or untreated | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:developmental delay or regression
n1=en:retardation | n2=en:developmental delay or regression | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:developmental delay, mild
n1=en:retardation | n2=en:developmental delay, mild | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:developmental delay, mild (in some patients)
n1=en:retardation | n2=en:developmental delay, mild (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:developmental delay, mild (in some)
n1=en:retardation | n2=en:developmental delay, mild (in some) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:developmental delay, mild to moderate
n1=en:retardation | n2=en:developmental delay, mild to moderate | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:developmental delay, moderate (in some patients)
n1=en:retardation | n2=en:developmental delay, moderate (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:developmental delay, primarily motor, resolves in childhood
n1=en:retardation | n2=en:developmental delay, primarily motor, resolves in childhood | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:developmental delay, profound
n1=en:retardation | n2=en:developmental delay, profound | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:developmental delay, progressive
n1=en:retardation | n2=en:developmental delay, progressive | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:developmental delay, severe
n1=en:retardation | n2=en:developmental delay, severe | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:developmental delay, severe (2p21del)
n1=en:retardation | n2=en:developmental delay, severe (2p21del) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:developmental delay, significant
n1=en:retardation | n2=en:developmental delay, significant | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:developmental delay, variable
n1=en:retardation | n2=en:developmental delay, variable | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:developmental delay, variable severity
n1=en:retardation | n2=en:developmental delay, variable severity | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:developmental disease/disorder
n1=en:retardation | n2=en:developmental disease/disorder | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:developmental dislocation
n1=en:retardation | n2=en:developmental dislocation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:developmental disorder
n1=en:retardation | n2=en:developmental disorder | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:developmental disorders nec
n1=en:retardation | n2=en:developmental disorders nec | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:developmental expressive writing disorder
n1=en:retardation | n2=en:developmental expressive writing disorder | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:developmental failure of fusion
n1=en:retardation | n2=en:developmental failure of fusion | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:developmental hereditary disorder
n1=en:retardation | n2=en:developmental hereditary disorder | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:developmental immaturity
n1=en:retardation | n2=en:developmental immaturity | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:developmental language impairment
n1=en:retardation | n2=en:developmental language impairment | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:developmental malformation of branchial arch
n1=en:retardation | n2=en:developmental malformation of branchial arch | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:developmental reading disorder
n1=en:retardation | n2=en:developmental reading disorder | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:developmental regression
n1=en:retardation | n2=en:developmental regression | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:developmental regression (in some patients)
n1=en:retardation | n2=en:developmental regression (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:developmental regression after age 2 years
n1=en:retardation | n2=en:developmental regression after age 2 years | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:developmental regression after onset of seizures
n1=en:retardation | n2=en:developmental regression after onset of seizures | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:developmental regression after the first year
n1=en:retardation | n2=en:developmental regression after the first year | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:developmental regression before age 6 months
n1=en:retardation | n2=en:developmental regression before age 6 months | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:developmental regression in about 50% of patients
n1=en:retardation | n2=en:developmental regression in about 50% of patients | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:developmental regression in affected children
n1=en:retardation | n2=en:developmental regression in affected children | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:developmental regression, after age 2 years (some)
n1=en:retardation | n2=en:developmental regression, after age 2 years (some) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:developmental regression, severe
n1=en:retardation | n2=en:developmental regression, severe | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:developmental retardation (in some patients)
n1=en:retardation | n2=en:developmental retardation (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:developmental retardation, profound
n1=en:retardation | n2=en:developmental retardation, profound | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:developmental retardation, severe
n1=en:retardation | n2=en:developmental retardation, severe | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:developmental stagnation
n1=en:retardation | n2=en:developmental stagnation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:developmental stagnation at onset of seizures
n1=en:retardation | n2=en:developmental stagnation at onset of seizures | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:developmental stricture
n1=en:retardation | n2=en:developmental stricture | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:developmentally disabled (finding)
n1=en:retardation | n2=en:developmentally disabled (finding) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:diabetes mellitus
n1=en:retardation | n2=en:diabetes mellitus | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:diabetes with coma (disorder)
n1=en:retardation | n2=en:diabetes with coma (disorder) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:diagnosis/diseases component
n1=en:retardation | n2=en:diagnosis/diseases component | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:diaper dermatitis
n1=en:retardation | n2=en:diaper dermatitis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:difficulties in fine bimanual activities
n1=en:retardation | n2=en:difficulties in fine bimanual activities | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:difficulties in fine movement of the hands
n1=en:retardation | n2=en:difficulties in fine movement of the hands | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:difficulties with equilibrium
n1=en:retardation | n2=en:difficulties with equilibrium | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:difficulties with fine motor skills and coordination
n1=en:retardation | n2=en:difficulties with fine motor skills and coordination | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:difficulty in phonologic coding
n1=en:retardation | n2=en:difficulty in phonologic coding | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:difficulty in spelling
n1=en:retardation | n2=en:difficulty in spelling | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:difficulty reading
n1=en:retardation | n2=en:difficulty reading | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:difficulty running
n1=en:retardation | n2=en:difficulty running | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:difficulty running and climbing stairs
n1=en:retardation | n2=en:difficulty running and climbing stairs | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:difficulty sleeping
n1=en:retardation | n2=en:difficulty sleeping | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:difficulty speaking during seizures
n1=en:retardation | n2=en:difficulty speaking during seizures | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:difficulty standing
n1=en:retardation | n2=en:difficulty standing | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:difficulty standing alone
n1=en:retardation | n2=en:difficulty standing alone | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:difficulty walking and climbing stairs
n1=en:retardation | n2=en:difficulty walking and climbing stairs | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:difficulty walking in childhood
n1=en:retardation | n2=en:difficulty walking in childhood | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:difficulty walking, running
n1=en:retardation | n2=en:difficulty walking, running | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:difficulty with writing and drawing
n1=en:retardation | n2=en:difficulty with writing and drawing | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:difficulty writing
n1=en:retardation | n2=en:difficulty writing | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:diffuse atrophy of cerebral hemispheres, corpus callosum, and brainstem
n1=en:retardation | n2=en:diffuse atrophy of cerebral hemispheres, corpus callosum, and brainstem | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:diffuse axonal swelling
n1=en:retardation | n2=en:diffuse axonal swelling | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:diffuse brain and spinal cord atrophy on brain ct/mri
n1=en:retardation | n2=en:diffuse brain and spinal cord atrophy on brain ct/mri | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:diffuse brain swelling occurs during coma
n1=en:retardation | n2=en:diffuse brain swelling occurs during coma | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:diffuse cerebellar atrophy
n1=en:retardation | n2=en:diffuse cerebellar atrophy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:diffuse cerebral atrophy on ct and mri
n1=en:retardation | n2=en:diffuse cerebral atrophy on ct and mri | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:diffuse cerebral atrophy seen on mri
n1=en:retardation | n2=en:diffuse cerebral atrophy seen on mri | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:diffuse cerebral gliosis
n1=en:retardation | n2=en:diffuse cerebral gliosis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:diffuse demyelination (increased signal intensity in t2-weighted images, especially frontal lobes)
n1=en:retardation | n2=en:diffuse demyelination (increased signal intensity in t2-weighted images, especially frontal lobes) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:diffuse enlargement of subarachnoid spaces and lateral ventricles (rare)
n1=en:retardation | n2=en:diffuse enlargement of subarachnoid spaces and lateral ventricles (rare) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:diffuse fibrillar astrocytosis (in type iib)
n1=en:retardation | n2=en:diffuse fibrillar astrocytosis (in type iib) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:diffuse hyperintense signal abnormalities in the white matter (in children)
n1=en:retardation | n2=en:diffuse hyperintense signal abnormalities in the white matter (in children) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:diffuse hypomyelination
n1=en:retardation | n2=en:diffuse hypomyelination | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:diffuse hyporeflexia (later)
n1=en:retardation | n2=en:diffuse hyporeflexia (later) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:diffuse hypotonia
n1=en:retardation | n2=en:diffuse hypotonia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:diffuse leptomeningeal enhancement seen on mri
n1=en:retardation | n2=en:diffuse leptomeningeal enhancement seen on mri | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:diffuse leukoencephalopathy
n1=en:retardation | n2=en:diffuse leukoencephalopathy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:diffuse lewy bodies throughout the brain (cortical and subcortical regions)
n1=en:retardation | n2=en:diffuse lewy bodies throughout the brain (cortical and subcortical regions) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:diffuse lewy body pathology
n1=en:retardation | n2=en:diffuse lewy body pathology | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:diffuse paroxysmal discharges
n1=en:retardation | n2=en:diffuse paroxysmal discharges | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:diffuse periventricular leukoencephalopathy
n1=en:retardation | n2=en:diffuse periventricular leukoencephalopathy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:diffuse signal abnormality of central white matter
n1=en:retardation | n2=en:diffuse signal abnormality of central white matter | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:diffuse slowing
n1=en:retardation | n2=en:diffuse slowing | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:diffuse slowing of background
n1=en:retardation | n2=en:diffuse slowing of background | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:diffuse spongiform leukoencephalopathy
n1=en:retardation | n2=en:diffuse spongiform leukoencephalopathy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:diffuse swelling of cerebral white matter
n1=en:retardation | n2=en:diffuse swelling of cerebral white matter | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:diffuse white matter abnormalities on brain mri
n1=en:retardation | n2=en:diffuse white matter abnormalities on brain mri | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:diffuse white matter abnormalities seen on brain mri
n1=en:retardation | n2=en:diffuse white matter abnormalities seen on brain mri | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:diffuse white matter changes (meb)
n1=en:retardation | n2=en:diffuse white matter changes (meb) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:diffuse white matter dysmyelination
n1=en:retardation | n2=en:diffuse white matter dysmyelination | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:diffuse white matter hyperintensities on t2-weighed imaging
n1=en:retardation | n2=en:diffuse white matter hyperintensities on t2-weighed imaging | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:diffuse white matter loss
n1=en:retardation | n2=en:diffuse white matter loss | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:diffuse, severe neuronal loss
n1=en:retardation | n2=en:diffuse, severe neuronal loss | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:digeorge syndrome
n1=en:retardation | n2=en:digeorge syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:digitorenocerebral syndrome
n1=en:retardation | n2=en:digitorenocerebral syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dihydropyrimidine dehydrogenase deficiency
n1=en:retardation | n2=en:dihydropyrimidine dehydrogenase deficiency | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dilatation of the 3rd ventricle (in one family)
n1=en:retardation | n2=en:dilatation of the 3rd ventricle (in one family) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dilatation of the lateral and third ventricles
n1=en:retardation | n2=en:dilatation of the lateral and third ventricles | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dilatation of the lateral ventricles (in one family)
n1=en:retardation | n2=en:dilatation of the lateral ventricles (in one family) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dilated fourth ventricle
n1=en:retardation | n2=en:dilated fourth ventricle | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dilated lateral ventricles (1 patient)
n1=en:retardation | n2=en:dilated lateral ventricles (1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dilated perivascular spaces
n1=en:retardation | n2=en:dilated perivascular spaces | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dilated venous sinuses
n1=en:retardation | n2=en:dilated venous sinuses | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dilated ventricles (finding)
n1=en:retardation | n2=en:dilated ventricles (finding) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dilation of cerebral ventricles
n1=en:retardation | n2=en:dilation of cerebral ventricles | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dilation of lateral ventricles
n1=en:retardation | n2=en:dilation of lateral ventricles | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dilation of lateral ventricles (in some patients)
n1=en:retardation | n2=en:dilation of lateral ventricles (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:diminished visual activity
n1=en:retardation | n2=en:diminished visual activity | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:diplegia
n1=en:retardation | n2=en:diplegia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:disability
n1=en:retardation | n2=en:disability | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:disability - moderate
n1=en:retardation | n2=en:disability - moderate | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:disability - severe
n1=en:retardation | n2=en:disability - severe | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:disability - slight
n1=en:retardation | n2=en:disability - slight | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:disability affecting daily living
n1=en:retardation | n2=en:disability affecting daily living | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:disability evaluation, normal, no disability, no impairment
n1=en:retardation | n2=en:disability evaluation, normal, no disability, no impairment | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:disability of lower limb
n1=en:retardation | n2=en:disability of lower limb | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:disability of upper limb
n1=en:retardation | n2=en:disability of upper limb | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:disability percentage
n1=en:retardation | n2=en:disability percentage | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:disabled population
n1=en:retardation | n2=en:disabled population | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:discrepancy between verbal and nonverbal abilities
n1=en:retardation | n2=en:discrepancy between verbal and nonverbal abilities | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:disdiadochokinesia
n1=en:retardation | n2=en:disdiadochokinesia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:disease of mouth/tongue/lips
n1=en:retardation | n2=en:disease of mouth/tongue/lips | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:disease of teeth/gums
n1=en:retardation | n2=en:disease of teeth/gums | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:disease or disorder
n1=en:retardation | n2=en:disease or disorder | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dislocation
n1=en:retardation | n2=en:dislocation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:disorder of branched-chain amino acid metabolism
n1=en:retardation | n2=en:disorder of branched-chain amino acid metabolism | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:disorder of higher mental process
n1=en:retardation | n2=en:disorder of higher mental process | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:disorder of psychological development
n1=en:retardation | n2=en:disorder of psychological development | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:disorder of stature
n1=en:retardation | n2=en:disorder of stature | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:disordered myelination
n1=en:retardation | n2=en:disordered myelination | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:disordered sleep pattern (in some patients)
n1=en:retardation | n2=en:disordered sleep pattern (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:disordered thinking
n1=en:retardation | n2=en:disordered thinking | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:disorders of cutaneous image and perception
n1=en:retardation | n2=en:disorders of cutaneous image and perception | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:disorganised speech
n1=en:retardation | n2=en:disorganised speech | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:disorganization of the anterior cerebellar vermis
n1=en:retardation | n2=en:disorganization of the anterior cerebellar vermis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:disorganized brain cytoarchitecture
n1=en:retardation | n2=en:disorganized brain cytoarchitecture | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:disorganized cortical architecture
n1=en:retardation | n2=en:disorganized cortical architecture | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:disorganized eeg
n1=en:retardation | n2=en:disorganized eeg | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:disorganized slow background activity seen on eeg
n1=en:retardation | n2=en:disorganized slow background activity seen on eeg | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:disorientation
n1=en:retardation | n2=en:disorientation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:disproportionately small cerebral cortex
n1=en:retardation | n2=en:disproportionately small cerebral cortex | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dissociative disorder
n1=en:retardation | n2=en:dissociative disorder | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:distal amyotrophy
n1=en:retardation | n2=en:distal amyotrophy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:distal muscle weakness
n1=en:retardation | n2=en:distal muscle weakness | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:distal muscle weakness and atrophy due to motor neuronopathy
n1=en:retardation | n2=en:distal muscle weakness and atrophy due to motor neuronopathy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:distal muscle weakness, upper and lower limbs
n1=en:retardation | n2=en:distal muscle weakness, upper and lower limbs | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:distal sensory impairment
n1=en:retardation | n2=en:distal sensory impairment | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:distal sensory loss to all modalities, lower limbs more affected than upper limbs
n1=en:retardation | n2=en:distal sensory loss to all modalities, lower limbs more affected than upper limbs | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:distal tapering of the carotid, cerebellar, and meningeal arteries
n1=en:retardation | n2=en:distal tapering of the carotid, cerebellar, and meningeal arteries | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:distal weakness occurs later
n1=en:retardation | n2=en:distal weakness occurs later | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:disturbance of attention
n1=en:retardation | n2=en:disturbance of attention | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:disturbance of consciousness
n1=en:retardation | n2=en:disturbance of consciousness | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:disturbances in thinking and perception
n1=en:retardation | n2=en:disturbances in thinking and perception | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:disturbed equilibrium
n1=en:retardation | n2=en:disturbed equilibrium | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:disturbed gait
n1=en:retardation | n2=en:disturbed gait | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:disturbed myelination affecting the periventricular and subcortical white matter
n1=en:retardation | n2=en:disturbed myelination affecting the periventricular and subcortical white matter | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:disturbed sleep-wake cycle
n1=en:retardation | n2=en:disturbed sleep-wake cycle | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:diurnal fluctuations of symptoms (in a subset of patients)
n1=en:retardation | n2=en:diurnal fluctuations of symptoms (in a subset of patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:diverticulosis
n1=en:retardation | n2=en:diverticulosis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dizziness
n1=en:retardation | n2=en:dizziness | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dizziness adverse event
n1=en:retardation | n2=en:dizziness adverse event | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dizziness may occur
n1=en:retardation | n2=en:dizziness may occur | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dizziness, episodic
n1=en:retardation | n2=en:dizziness, episodic | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dopamine-responsive parkinsonism
n1=en:retardation | n2=en:dopamine-responsive parkinsonism | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dopaminergic fiber systems in the brain
n1=en:retardation | n2=en:dopaminergic fiber systems in the brain | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:double cortex syndrome
n1=en:retardation | n2=en:double cortex syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:down syndrome
n1=en:retardation | n2=en:down syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dream disorder
n1=en:retardation | n2=en:dream disorder | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dream enactment
n1=en:retardation | n2=en:dream enactment | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dressing disability
n1=en:retardation | n2=en:dressing disability | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:drooling
n1=en:retardation | n2=en:drooling | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:drop attack
n1=en:retardation | n2=en:drop attack | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:drug abuse
n1=en:retardation | n2=en:drug abuse | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:drug dependence
n1=en:retardation | n2=en:drug dependence | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:drug-resistent seizures (rare)
n1=en:retardation | n2=en:drug-resistent seizures (rare) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dubowitz syndrome
n1=en:retardation | n2=en:dubowitz syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:duodenal ulcer
n1=en:retardation | n2=en:duodenal ulcer | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dural and choroid plexus calcifications
n1=en:retardation | n2=en:dural and choroid plexus calcifications | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dural ectasia
n1=en:retardation | n2=en:dural ectasia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dwarfism
n1=en:retardation | n2=en:dwarfism | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dysarthria
n1=en:retardation | n2=en:dysarthria | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dysarthria (1 family)
n1=en:retardation | n2=en:dysarthria (1 family) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dysarthria (1 patient)
n1=en:retardation | n2=en:dysarthria (1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dysarthria (74%)
n1=en:retardation | n2=en:dysarthria (74%) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dysarthria (in some patients)
n1=en:retardation | n2=en:dysarthria (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dysarthria (less common)
n1=en:retardation | n2=en:dysarthria (less common) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dysarthria (mild)
n1=en:retardation | n2=en:dysarthria (mild) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dysarthria (most common presenting symptom)
n1=en:retardation | n2=en:dysarthria (most common presenting symptom) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dysarthria (onset in third decade)
n1=en:retardation | n2=en:dysarthria (onset in third decade) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dysarthria may occur
n1=en:retardation | n2=en:dysarthria may occur | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dysarthria, mild (1 family)
n1=en:retardation | n2=en:dysarthria, mild (1 family) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dysarthria, mild (in some patients)
n1=en:retardation | n2=en:dysarthria, mild (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dysarthria, slowly progressive
n1=en:retardation | n2=en:dysarthria, slowly progressive | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dysarthrias, spastic
n1=en:retardation | n2=en:dysarthrias, spastic | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dysautonomia
n1=en:retardation | n2=en:dysautonomia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dysautonomia may occur
n1=en:retardation | n2=en:dysautonomia may occur | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dyscalculia
n1=en:retardation | n2=en:dyscalculia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dysdiadochokinesis
n1=en:retardation | n2=en:dysdiadochokinesis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dysdiadochokinesis (1 family)
n1=en:retardation | n2=en:dysdiadochokinesis (1 family) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dysdiadochokinesis (63%)
n1=en:retardation | n2=en:dysdiadochokinesis (63%) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dysequilibrium syndrome
n1=en:retardation | n2=en:dysequilibrium syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dysfunction of lateral corticospinal tracts
n1=en:retardation | n2=en:dysfunction of lateral corticospinal tracts | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dysfunction of the autonomic nervous system
n1=en:retardation | n2=en:dysfunction of the autonomic nervous system | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dysgenesis of corpus callosum
n1=en:retardation | n2=en:dysgenesis of corpus callosum | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dysgenesis of the anterior commissure (in some)
n1=en:retardation | n2=en:dysgenesis of the anterior commissure (in some) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dysgenesis of the corpus callosum (1 patient)
n1=en:retardation | n2=en:dysgenesis of the corpus callosum (1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dysgenesis or agenesis of the cerebellar vermis
n1=en:retardation | n2=en:dysgenesis or agenesis of the cerebellar vermis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dysgenesis or agenesis of the corpus callosum (in some)
n1=en:retardation | n2=en:dysgenesis or agenesis of the corpus callosum (in some) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dysgraphias
n1=en:retardation | n2=en:dysgraphias | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dyshidrosis [pompholyx]
n1=en:retardation | n2=en:dyshidrosis [pompholyx] | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dyskinesia
n1=en:retardation | n2=en:dyskinesia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dyskinesia buccoglossal
n1=en:retardation | n2=en:dyskinesia buccoglossal | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dyskinesia, episodic
n1=en:retardation | n2=en:dyskinesia, episodic | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dyskinesia, limb, exertion-induced
n1=en:retardation | n2=en:dyskinesia, limb, exertion-induced | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dyskinetic movements
n1=en:retardation | n2=en:dyskinetic movements | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dyslexia
n1=en:retardation | n2=en:dyslexia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dysmetria (1 family)
n1=en:retardation | n2=en:dysmetria (1 family) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dysmetria (1 patient)
n1=en:retardation | n2=en:dysmetria (1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dysmetria (in 1 of 3 families)
n1=en:retardation | n2=en:dysmetria (in 1 of 3 families) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dysmetria (in some patients)
n1=en:retardation | n2=en:dysmetria (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dysmetria (type i)
n1=en:retardation | n2=en:dysmetria (type i) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dysmetria, mild
n1=en:retardation | n2=en:dysmetria, mild | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dysmetrias, cerebellar
n1=en:retardation | n2=en:dysmetrias, cerebellar | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dysmetric saccades
n1=en:retardation | n2=en:dysmetric saccades | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dysmorphic basal ganglia
n1=en:retardation | n2=en:dysmorphic basal ganglia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dysmorphic basal ganglia (1 patient)
n1=en:retardation | n2=en:dysmorphic basal ganglia (1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dysmorphic basal ganglia (in some patients)
n1=en:retardation | n2=en:dysmorphic basal ganglia (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dysmorphic basal ganglia (in some)
n1=en:retardation | n2=en:dysmorphic basal ganglia (in some) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dysmorphic corpus callosum
n1=en:retardation | n2=en:dysmorphic corpus callosum | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dysmorphism
n1=en:retardation | n2=en:dysmorphism | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dysmyelinating leukodystrophy
n1=en:retardation | n2=en:dysmyelinating leukodystrophy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dysmyelination of the brain and spinal cord
n1=en:retardation | n2=en:dysmyelination of the brain and spinal cord | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dysmyelination of the brain, myelin is not formed properly
n1=en:retardation | n2=en:dysmyelination of the brain, myelin is not formed properly | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dysmyelination with jaundice
n1=en:retardation | n2=en:dysmyelination with jaundice | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dysosteosclerosis
n1=en:retardation | n2=en:dysosteosclerosis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dysphagia
n1=en:retardation | n2=en:dysphagia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dysphasia
n1=en:retardation | n2=en:dysphasia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dysphonia
n1=en:retardation | n2=en:dysphonia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dysplasia of the cerebellar hemispheres
n1=en:retardation | n2=en:dysplasia of the cerebellar hemispheres | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dysplastic basal ganglia
n1=en:retardation | n2=en:dysplastic basal ganglia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dysplastic c-shaped inferior olivary nuclei
n1=en:retardation | n2=en:dysplastic c-shaped inferior olivary nuclei | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dysplastic cerebellar gangliocytoma
n1=en:retardation | n2=en:dysplastic cerebellar gangliocytoma | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dysplastic cerebellar vermis
n1=en:retardation | n2=en:dysplastic cerebellar vermis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dysplastic cerebellum
n1=en:retardation | n2=en:dysplastic cerebellum | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dysplastic pons
n1=en:retardation | n2=en:dysplastic pons | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dysplastic superior cerebellar vermis
n1=en:retardation | n2=en:dysplastic superior cerebellar vermis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dystonia
n1=en:retardation | n2=en:dystonia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dystonia (<20%) (finding)
n1=en:retardation | n2=en:dystonia (<20%) (finding) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dystonia (1 family)
n1=en:retardation | n2=en:dystonia (1 family) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dystonia (1 patient)
n1=en:retardation | n2=en:dystonia (1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dystonia (14% of patients)
n1=en:retardation | n2=en:dystonia (14% of patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dystonia (57%)
n1=en:retardation | n2=en:dystonia (57%) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dystonia (in 2 patients)
n1=en:retardation | n2=en:dystonia (in 2 patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dystonia (in severe cases)
n1=en:retardation | n2=en:dystonia (in severe cases) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dystonia (in some patients)
n1=en:retardation | n2=en:dystonia (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dystonia (less common)
n1=en:retardation | n2=en:dystonia (less common) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dystonia (may spontaneously remit in childhood or adolescence)
n1=en:retardation | n2=en:dystonia (may spontaneously remit in childhood or adolescence) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dystonia 18 (disorder)
n1=en:retardation | n2=en:dystonia 18 (disorder) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dystonia at onset (16%)
n1=en:retardation | n2=en:dystonia at onset (16%) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dystonia disorders
n1=en:retardation | n2=en:dystonia disorders | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dystonia may become generalized
n1=en:retardation | n2=en:dystonia may become generalized | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dystonia with diurnal variation
n1=en:retardation | n2=en:dystonia with diurnal variation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dystonia, episodic, primary affects hands and feet
n1=en:retardation | n2=en:dystonia, episodic, primary affects hands and feet | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dystonia, focal (at onset)
n1=en:retardation | n2=en:dystonia, focal (at onset) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dystonia, focal, limited to orbicularis oculi muscle (blepharospasm)
n1=en:retardation | n2=en:dystonia, focal, limited to orbicularis oculi muscle (blepharospasm) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dystonia, generalized, dopa-unresponsive
n1=en:retardation | n2=en:dystonia, generalized, dopa-unresponsive | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dystonia, limb, exercise-induced
n1=en:retardation | n2=en:dystonia, limb, exercise-induced | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dystonia, progressive
n1=en:retardation | n2=en:dystonia, progressive | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dystonia, severe (in all limbs)
n1=en:retardation | n2=en:dystonia, severe (in all limbs) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dystonia, trunk and limbs (upper and lower)
n1=en:retardation | n2=en:dystonia, trunk and limbs (upper and lower) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dystonic hand posturing (44% of patients)
n1=en:retardation | n2=en:dystonic hand posturing (44% of patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dystonic movements (in 1 of 6 patients)
n1=en:retardation | n2=en:dystonic movements (in 1 of 6 patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dystonic posture
n1=en:retardation | n2=en:dystonic posture | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dystonic posturing (rare)
n1=en:retardation | n2=en:dystonic posturing (rare) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dystonic posturing of the hands
n1=en:retardation | n2=en:dystonic posturing of the hands | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dystonic tongue protrusion
n1=en:retardation | n2=en:dystonic tongue protrusion | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dystonic tremor
n1=en:retardation | n2=en:dystonic tremor | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dystonic vocal tremor
n1=en:retardation | n2=en:dystonic vocal tremor | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dystonic writer's cramp
n1=en:retardation | n2=en:dystonic writer's cramp | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:dystrophic neurites
n1=en:retardation | n2=en:dystrophic neurites | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ear neoplasm
n1=en:retardation | n2=en:ear neoplasm | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ear, face and neck congenital anomalies
n1=en:retardation | n2=en:ear, face and neck congenital anomalies | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ear, patella, short stature syndrome
n1=en:retardation | n2=en:ear, patella, short stature syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:earlier sleep-offset time (earlier awakening)
n1=en:retardation | n2=en:earlier sleep-offset time (earlier awakening) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:early and severe foot extensor muscle involvement
n1=en:retardation | n2=en:early and severe foot extensor muscle involvement | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:early childhood developmental disability
n1=en:retardation | n2=en:early childhood developmental disability | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:early involvement of the corticospinal pathways
n1=en:retardation | n2=en:early involvement of the corticospinal pathways | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:early severe fetal akinesia sequence
n1=en:retardation | n2=en:early severe fetal akinesia sequence | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:early-onset myoclonic seizures
n1=en:retardation | n2=en:early-onset myoclonic seizures | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:eating disorder
n1=en:retardation | n2=en:eating disorder | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:eating problems in children
n1=en:retardation | n2=en:eating problems in children | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:echolalia
n1=en:retardation | n2=en:echolalia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ectodermal dysplasia
n1=en:retardation | n2=en:ectodermal dysplasia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ectopia
n1=en:retardation | n2=en:ectopia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ectopia cordis
n1=en:retardation | n2=en:ectopia cordis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ectopic dorsal pontine transverse bundle of fibers forms the 'cap'
n1=en:retardation | n2=en:ectopic dorsal pontine transverse bundle of fibers forms the 'cap' | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ectopic posterior pituitary
n1=en:retardation | n2=en:ectopic posterior pituitary | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ectopic posterior pituitary (in some patients)
n1=en:retardation | n2=en:ectopic posterior pituitary (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ectopic pregnancy
n1=en:retardation | n2=en:ectopic pregnancy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ectromelia
n1=en:retardation | n2=en:ectromelia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:educationally subnormal
n1=en:retardation | n2=en:educationally subnormal | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:eeg - alpha abolished, continuous spike waves, intense myoclonus on photic stimulation (stage 3)
n1=en:retardation | n2=en:eeg - alpha abolished, continuous spike waves, intense myoclonus on photic stimulation (stage 3) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:eeg - alpha slowing, 4-6 hz spike waves, myoclonus on photic stimulation (stage 2)
n1=en:retardation | n2=en:eeg - alpha slowing, 4-6 hz spike waves, myoclonus on photic stimulation (stage 2) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:eeg - polyspike on photic stimulation (stage 1)
n1=en:retardation | n2=en:eeg - polyspike on photic stimulation (stage 1) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:eeg abnormalities - slow waking background, intermittent rhythmical slowing (3-5hz), epileptiform discharges
n1=en:retardation | n2=en:eeg abnormalities - slow waking background, intermittent rhythmical slowing (3-5hz), epileptiform discharges | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:eeg abnormalities in 20-50%
n1=en:retardation | n2=en:eeg abnormalities in 20-50% | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:eeg abnormalities in 20-50% impaired language development
n1=en:retardation | n2=en:eeg abnormalities in 20-50% impaired language development | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:eeg and symptomatology suggest mesial temporal origin
n1=en:retardation | n2=en:eeg and symptomatology suggest mesial temporal origin | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:eeg during episodes shows desynchronization
n1=en:retardation | n2=en:eeg during episodes shows desynchronization | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:eeg is slowed with polyspike wave discharges
n1=en:retardation | n2=en:eeg is slowed with polyspike wave discharges | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:eeg is usually normal
n1=en:retardation | n2=en:eeg is usually normal | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:eeg later shows generalized spike or polyspike waves and focal spikes
n1=en:retardation | n2=en:eeg later shows generalized spike or polyspike waves and focal spikes | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:eeg may be normal at first
n1=en:retardation | n2=en:eeg may be normal at first | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:eeg may show migrating focal or multifocal origin (in severe cases)
n1=en:retardation | n2=en:eeg may show migrating focal or multifocal origin (in severe cases) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:eeg shows 3-4-hz spike and multispike slow wave complexes
n1=en:retardation | n2=en:eeg shows 3-4-hz spike and multispike slow wave complexes | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:eeg shows 3-4-hz spike waves
n1=en:retardation | n2=en:eeg shows 3-4-hz spike waves | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:eeg shows 3-hz spike-wave discharges
n1=en:retardation | n2=en:eeg shows 3-hz spike-wave discharges | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:eeg shows abundant slow waves and fast spike activity
n1=en:retardation | n2=en:eeg shows abundant slow waves and fast spike activity | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:eeg shows active generalized spike and wave and polyspike pattern
n1=en:retardation | n2=en:eeg shows active generalized spike and wave and polyspike pattern | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:eeg shows burst suppression
n1=en:retardation | n2=en:eeg shows burst suppression | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:eeg shows centrotemporal spike-wave discharges
n1=en:retardation | n2=en:eeg shows centrotemporal spike-wave discharges | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:eeg shows epileptiform activity
n1=en:retardation | n2=en:eeg shows epileptiform activity | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:eeg shows epileptiform discharges
n1=en:retardation | n2=en:eeg shows epileptiform discharges | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:eeg shows frontal lobe origin
n1=en:retardation | n2=en:eeg shows frontal lobe origin | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:eeg shows generalized polyspike and wave discharges (4-5 hz)
n1=en:retardation | n2=en:eeg shows generalized polyspike and wave discharges (4-5 hz) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:eeg shows generalized polyspike and wave discharges (4-6 hz)
n1=en:retardation | n2=en:eeg shows generalized polyspike and wave discharges (4-6 hz) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:eeg shows generalized, bilateral, synchronous, symmetrical discharge
n1=en:retardation | n2=en:eeg shows generalized, bilateral, synchronous, symmetrical discharge | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:eeg shows hypsarrhythmia
n1=en:retardation | n2=en:eeg shows hypsarrhythmia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:eeg shows hypsarrhythmia (in 1 of 6 patients)
n1=en:retardation | n2=en:eeg shows hypsarrhythmia (in 1 of 6 patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:eeg shows multifocal discharges
n1=en:retardation | n2=en:eeg shows multifocal discharges | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:eeg shows multifocal epileptic activity
n1=en:retardation | n2=en:eeg shows multifocal epileptic activity | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:eeg shows nonspecific slow-wave paroxysms
n1=en:retardation | n2=en:eeg shows nonspecific slow-wave paroxysms | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:eeg shows photosensitivity
n1=en:retardation | n2=en:eeg shows photosensitivity | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:eeg shows rolandic sharp waves and spikes
n1=en:retardation | n2=en:eeg shows rolandic sharp waves and spikes | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:eeg shows slow frequency high amplitude waves with high frequency polyspikes
n1=en:retardation | n2=en:eeg shows slow frequency high amplitude waves with high frequency polyspikes | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:eeg shows slowed dysrhythmia and multifocal discharges
n1=en:retardation | n2=en:eeg shows slowed dysrhythmia and multifocal discharges | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:eeg shows spike and multispike waves, 3-4 hz
n1=en:retardation | n2=en:eeg shows spike and multispike waves, 3-4 hz | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:eeg shows spike and wave or polyspike and wave discharges
n1=en:retardation | n2=en:eeg shows spike and wave or polyspike and wave discharges | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:eeg shows suppression with ictal burst activities
n1=en:retardation | n2=en:eeg shows suppression with ictal burst activities | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:eeg shows suppression-burst pattern
n1=en:retardation | n2=en:eeg shows suppression-burst pattern | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:eeg shows unilateral centrotemporal spikes
n1=en:retardation | n2=en:eeg shows unilateral centrotemporal spikes | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:eeg shows with a multifocal pattern with spikes and sharp waves
n1=en:retardation | n2=en:eeg shows with a multifocal pattern with spikes and sharp waves | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:eeg with burst suppression
n1=en:retardation | n2=en:eeg with burst suppression | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:eeg with focal discharge
n1=en:retardation | n2=en:eeg with focal discharge | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:eeg with paroxysmal activity
n1=en:retardation | n2=en:eeg with paroxysmal activity | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:eeg with photoparoxysmal response
n1=en:retardation | n2=en:eeg with photoparoxysmal response | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:effaced gyral pattern
n1=en:retardation | n2=en:effaced gyral pattern | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:effect prosthetic device
n1=en:retardation | n2=en:effect prosthetic device | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ehlers-danlos syndrome, beasley cohen type
n1=en:retardation | n2=en:ehlers-danlos syndrome, beasley cohen type | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:electroencephalogram (eeg) abnormalities
n1=en:retardation | n2=en:electroencephalogram (eeg) abnormalities | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:electroencephalogram abnormal
n1=en:retardation | n2=en:electroencephalogram abnormal | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:electrophysiologic studies indicate cortical origin
n1=en:retardation | n2=en:electrophysiologic studies indicate cortical origin | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:elejalde disease
n1=en:retardation | n2=en:elejalde disease | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:elevated interferon levels in cerebrospinal fluid
n1=en:retardation | n2=en:elevated interferon levels in cerebrospinal fluid | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:elevated pterin levels (tetrahydrobiopterin, neopterin) in cerebrospinal fluid
n1=en:retardation | n2=en:elevated pterin levels (tetrahydrobiopterin, neopterin) in cerebrospinal fluid | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:elevated white cell count in cerebrospinal fluid
n1=en:retardation | n2=en:elevated white cell count in cerebrospinal fluid | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:elevation and splaying of the superior cerebellar peduncles
n1=en:retardation | n2=en:elevation and splaying of the superior cerebellar peduncles | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:elimination disorders
n1=en:retardation | n2=en:elimination disorders | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:elongated superior cerebellar peduncles
n1=en:retardation | n2=en:elongated superior cerebellar peduncles | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:emanuel syndrome
n1=en:retardation | n2=en:emanuel syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:embolism, cerebral
n1=en:retardation | n2=en:embolism, cerebral | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:embryological remnant
n1=en:retardation | n2=en:embryological remnant | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:embryonal rest and/or persistent embryonic structure
n1=en:retardation | n2=en:embryonal rest and/or persistent embryonic structure | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:embryonic cyst
n1=en:retardation | n2=en:embryonic cyst | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:emg shows bursts of activity originating in the masseter muscle and spreading to the orbicularis oris and oculi muscles
n1=en:retardation | n2=en:emg shows bursts of activity originating in the masseter muscle and spreading to the orbicularis oris and oculi muscles | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:emg shows continuous motor unit firing at rest
n1=en:retardation | n2=en:emg shows continuous motor unit firing at rest | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:emg shows evidence of denervation
n1=en:retardation | n2=en:emg shows evidence of denervation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:emg shows fibrillation potentials and mixed myopathic and neurogenic motor unit potentials
n1=en:retardation | n2=en:emg shows fibrillation potentials and mixed myopathic and neurogenic motor unit potentials | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:emg shows fibrillations and fasiculations
n1=en:retardation | n2=en:emg shows fibrillations and fasiculations | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:emg shows involuntary continuous motor activity at rest
n1=en:retardation | n2=en:emg shows involuntary continuous motor activity at rest | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:emg shows neurogenic abnormalities
n1=en:retardation | n2=en:emg shows neurogenic abnormalities | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:emg shows neurogenic changes
n1=en:retardation | n2=en:emg shows neurogenic changes | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:emg shows neurogenic changes and denervation
n1=en:retardation | n2=en:emg shows neurogenic changes and denervation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:emg shows neurogenic findings
n1=en:retardation | n2=en:emg shows neurogenic findings | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:emg with spontaneous discharge of normal motor unit potentials
n1=en:retardation | n2=en:emg with spontaneous discharge of normal motor unit potentials | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:empty sella syndrome
n1=en:retardation | n2=en:empty sella syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:encephalitis
n1=en:retardation | n2=en:encephalitis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:encephalocele
n1=en:retardation | n2=en:encephalocele | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:encephalocele (1 patient)
n1=en:retardation | n2=en:encephalocele (1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:encephalocele (rare)
n1=en:retardation | n2=en:encephalocele (rare) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:encephalocele (single case)
n1=en:retardation | n2=en:encephalocele (single case) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:encephalocele (uncommon)
n1=en:retardation | n2=en:encephalocele (uncommon) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:encephalocele of orbit
n1=en:retardation | n2=en:encephalocele of orbit | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:encephaloceles, frontal
n1=en:retardation | n2=en:encephaloceles, frontal | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:encephalomyelopathy
n1=en:retardation | n2=en:encephalomyelopathy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:encephalomyopathy
n1=en:retardation | n2=en:encephalomyopathy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:encephalopathic attacks, episodic, associated with infection
n1=en:retardation | n2=en:encephalopathic attacks, episodic, associated with infection | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:encephalopathic episodes, often associated with infection
n1=en:retardation | n2=en:encephalopathic episodes, often associated with infection | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:encephalopathy
n1=en:retardation | n2=en:encephalopathy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:encephalopathy (in 1 patient)
n1=en:retardation | n2=en:encephalopathy (in 1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:encephalopathy (in some patients)
n1=en:retardation | n2=en:encephalopathy (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:encephalopathy adverse event
n1=en:retardation | n2=en:encephalopathy adverse event | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:encephalopathy associated with hypoglycemia
n1=en:retardation | n2=en:encephalopathy associated with hypoglycemia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:encephalopathy during episodes
n1=en:retardation | n2=en:encephalopathy during episodes | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:encephalopathy, acute-onset
n1=en:retardation | n2=en:encephalopathy, acute-onset | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:encephalopathy, acute, episodic
n1=en:retardation | n2=en:encephalopathy, acute, episodic | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:encephalopathy, acute, sudden-onset after febrile illness
n1=en:retardation | n2=en:encephalopathy, acute, sudden-onset after febrile illness | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:encephalopathy, acute, sudden-onset during febrile illness
n1=en:retardation | n2=en:encephalopathy, acute, sudden-onset during febrile illness | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:encephalopathy, episodic
n1=en:retardation | n2=en:encephalopathy, episodic | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:encephalopathy, episodic, associated with febrile illnesses
n1=en:retardation | n2=en:encephalopathy, episodic, associated with febrile illnesses | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:encephalopathy, severe, neonatal
n1=en:retardation | n2=en:encephalopathy, severe, neonatal | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:encopresis
n1=en:retardation | n2=en:encopresis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:end-position nystagmus
n1=en:retardation | n2=en:end-position nystagmus | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:endocrine infection
n1=en:retardation | n2=en:endocrine infection | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:endothelial intracytoplasmic globular inclusions
n1=en:retardation | n2=en:endothelial intracytoplasmic globular inclusions | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:enhancement of the c-reflex
n1=en:retardation | n2=en:enhancement of the c-reflex | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:enlarged cerebellar cistern
n1=en:retardation | n2=en:enlarged cerebellar cistern | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:enlarged cerebellum
n1=en:retardation | n2=en:enlarged cerebellum | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:enlarged cisterna magna
n1=en:retardation | n2=en:enlarged cisterna magna | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:enlarged cisterna magna (in some patients)
n1=en:retardation | n2=en:enlarged cisterna magna (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:enlarged corpus callosum
n1=en:retardation | n2=en:enlarged corpus callosum | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:enlarged extraaxial space on brain imaging
n1=en:retardation | n2=en:enlarged extraaxial space on brain imaging | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:enlarged fourth ventricle, mild
n1=en:retardation | n2=en:enlarged fourth ventricle, mild | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:enlarged lateral and third ventricles
n1=en:retardation | n2=en:enlarged lateral and third ventricles | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:enlarged lateral ventricles (occipital>frontal)
n1=en:retardation | n2=en:enlarged lateral ventricles (occipital>frontal) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:enlarged motor unit action potentials
n1=en:retardation | n2=en:enlarged motor unit action potentials | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:enlarged or prominent ventricles (in some patients)
n1=en:retardation | n2=en:enlarged or prominent ventricles (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:enlarged ventricles (1 patient)
n1=en:retardation | n2=en:enlarged ventricles (1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:enlarged ventricles (in some patients)
n1=en:retardation | n2=en:enlarged ventricles (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:enlarged ventricles (in some)
n1=en:retardation | n2=en:enlarged ventricles (in some) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:enlarged white matter
n1=en:retardation | n2=en:enlarged white matter | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:entire brain
n1=en:retardation | n2=en:entire brain | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:entire central nervous system
n1=en:retardation | n2=en:entire central nervous system | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:entire nucleus of brain
n1=en:retardation | n2=en:entire nucleus of brain | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:eosinophilic 'cotton wool' plaques without dense congophilic core in various brain regions
n1=en:retardation | n2=en:eosinophilic 'cotton wool' plaques without dense congophilic core in various brain regions | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ependymitis
n1=en:retardation | n2=en:ependymitis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:epididymo-orchitis
n1=en:retardation | n2=en:epididymo-orchitis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:epilepsia partialis continua
n1=en:retardation | n2=en:epilepsia partialis continua | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:epilepsies, myoclonic
n1=en:retardation | n2=en:epilepsies, myoclonic | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:epilepsy (in 2 of 3 patients)
n1=en:retardation | n2=en:epilepsy (in 2 of 3 patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:epilepsy (in some patients)
n1=en:retardation | n2=en:epilepsy (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:epilepsy, frontal lobe
n1=en:retardation | n2=en:epilepsy, frontal lobe | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:epilepsy, multifocal, intractable
n1=en:retardation | n2=en:epilepsy, multifocal, intractable | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:epilepsy, myoclonic astatic
n1=en:retardation | n2=en:epilepsy, myoclonic astatic | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:epilepsy, progressive myoclonic 3
n1=en:retardation | n2=en:epilepsy, progressive myoclonic 3 | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:epilepsy, progressive myoclonic, 8
n1=en:retardation | n2=en:epilepsy, progressive myoclonic, 8 | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:epilepsy, pyridoxine-dependent
n1=en:retardation | n2=en:epilepsy, pyridoxine-dependent | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:epilepsy, refractory (onset in adolescence or young adulthood)
n1=en:retardation | n2=en:epilepsy, refractory (onset in adolescence or young adulthood) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:epilepsy, rolandic
n1=en:retardation | n2=en:epilepsy, rolandic | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:epilepsy, temporal lobe
n1=en:retardation | n2=en:epilepsy, temporal lobe | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:epileptic drop attack
n1=en:retardation | n2=en:epileptic drop attack | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:epileptic encephalopathy
n1=en:retardation | n2=en:epileptic encephalopathy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:epileptic encephalopathy (in 2 of 3 patients)
n1=en:retardation | n2=en:epileptic encephalopathy (in 2 of 3 patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:epileptic encephalopathy (in some patients)
n1=en:retardation | n2=en:epileptic encephalopathy (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:epileptic encephalopathy with psychomotor retardation (rare)
n1=en:retardation | n2=en:epileptic encephalopathy with psychomotor retardation (rare) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:epileptic encephalopathy, childhood-onset
n1=en:retardation | n2=en:epileptic encephalopathy, childhood-onset | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:epileptic encephalopathy, early infantile, 1
n1=en:retardation | n2=en:epileptic encephalopathy, early infantile, 1 | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:epileptic encephalopathy, early infantile, 7
n1=en:retardation | n2=en:epileptic encephalopathy, early infantile, 7 | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:epiphyseal dysplasia hearing loss dysmorphism
n1=en:retardation | n2=en:epiphyseal dysplasia hearing loss dysmorphism | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:episodes begin with muscle tightening
n1=en:retardation | n2=en:episodes begin with muscle tightening | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:episodes last up to 2 minutes
n1=en:retardation | n2=en:episodes last up to 2 minutes | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:episodes may last less than 30 minutes or greater than several hours
n1=en:retardation | n2=en:episodes may last less than 30 minutes or greater than several hours | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:episodes of decreased alertness, hypotonia, and poor respiration requiring mechanical ventilation
n1=en:retardation | n2=en:episodes of decreased alertness, hypotonia, and poor respiration requiring mechanical ventilation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:episodes of weakness can last 1 day to several weeks and can occur 1-3 times per month
n1=en:retardation | n2=en:episodes of weakness can last 1 day to several weeks and can occur 1-3 times per month | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:episodes typically occur several times a week
n1=en:retardation | n2=en:episodes typically occur several times a week | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:episodic absence-like spells
n1=en:retardation | n2=en:episodic absence-like spells | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:episodic acute neurologic deterioration/encephalopathy, recurrent
n1=en:retardation | n2=en:episodic acute neurologic deterioration/encephalopathy, recurrent | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:episodic ataxia
n1=en:retardation | n2=en:episodic ataxia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:episodic confusion
n1=en:retardation | n2=en:episodic confusion | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:episodic generalized skeletal muscle contractions
n1=en:retardation | n2=en:episodic generalized skeletal muscle contractions | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:episodic hemiplegia
n1=en:retardation | n2=en:episodic hemiplegia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:episodic subtype, headaches occur in clusters
n1=en:retardation | n2=en:episodic subtype, headaches occur in clusters | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:episodic sudden headache
n1=en:retardation | n2=en:episodic sudden headache | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:episodic vomiting
n1=en:retardation | n2=en:episodic vomiting | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:equivocal plantar response
n1=en:retardation | n2=en:equivocal plantar response | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:erythrokeratodermia variabilis 3 (disorder)
n1=en:retardation | n2=en:erythrokeratodermia variabilis 3 (disorder) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:esophageal disorder
n1=en:retardation | n2=en:esophageal disorder | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:essential tremor
n1=en:retardation | n2=en:essential tremor | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:essential tremor (1 family)
n1=en:retardation | n2=en:essential tremor (1 family) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ethmocephaly
n1=en:retardation | n2=en:ethmocephaly | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ethylmalonic encephalopathy
n1=en:retardation | n2=en:ethylmalonic encephalopathy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:euphoric mood
n1=en:retardation | n2=en:euphoric mood | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:eustachian tube salpingitis
n1=en:retardation | n2=en:eustachian tube salpingitis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:evolution to severe encephalopathy
n1=en:retardation | n2=en:evolution to severe encephalopathy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:exaggerated acoustic startle response
n1=en:retardation | n2=en:exaggerated acoustic startle response | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:exaggerated moro reflex
n1=en:retardation | n2=en:exaggerated moro reflex | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:exaggerated startle response
n1=en:retardation | n2=en:exaggerated startle response | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:exaggerated startle response to tactile or acoustic stimuli
n1=en:retardation | n2=en:exaggerated startle response to tactile or acoustic stimuli | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:excessive cerumen
n1=en:retardation | n2=en:excessive cerumen | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:excessive daytime somnolence
n1=en:retardation | n2=en:excessive daytime somnolence | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:exencephaly
n1=en:retardation | n2=en:exencephaly | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:expressive aphasia
n1=en:retardation | n2=en:expressive aphasia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:expressive language delay
n1=en:retardation | n2=en:expressive language delay | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:expressive language disorder
n1=en:retardation | n2=en:expressive language disorder | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:expressive speech absent
n1=en:retardation | n2=en:expressive speech absent | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:expressive speech deficit
n1=en:retardation | n2=en:expressive speech deficit | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:exstrophy
n1=en:retardation | n2=en:exstrophy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:extensive melanosis of leptomeninges, amygdala, and cerebellar hemispheres
n1=en:retardation | n2=en:extensive melanosis of leptomeninges, amygdala, and cerebellar hemispheres | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:extensor plantar responses (1 family)
n1=en:retardation | n2=en:extensor plantar responses (1 family) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:extensor plantar responses (1 patient)
n1=en:retardation | n2=en:extensor plantar responses (1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:extensor plantar responses (early-on)
n1=en:retardation | n2=en:extensor plantar responses (early-on) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:extensor plantar responses (in some patients)
n1=en:retardation | n2=en:extensor plantar responses (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:extensor plantar responses (later)
n1=en:retardation | n2=en:extensor plantar responses (later) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:extensor plantar responses (reported in 1 family)
n1=en:retardation | n2=en:extensor plantar responses (reported in 1 family) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:extensor plantar responses (reported in 1 patient)
n1=en:retardation | n2=en:extensor plantar responses (reported in 1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:extensor plantar responses (variable)
n1=en:retardation | n2=en:extensor plantar responses (variable) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:extensor posturing
n1=en:retardation | n2=en:extensor posturing | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:external capsule and claustrum may be involved
n1=en:retardation | n2=en:external capsule and claustrum may be involved | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:extra superior temporal gyrus (female)
n1=en:retardation | n2=en:extra superior temporal gyrus (female) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:extraneuronal accumulation of autofluorescent pigmented material in various brain regions
n1=en:retardation | n2=en:extraneuronal accumulation of autofluorescent pigmented material in various brain regions | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:extrapyramidal disorder
n1=en:retardation | n2=en:extrapyramidal disorder | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:extrapyramidal dyskinesia
n1=en:retardation | n2=en:extrapyramidal dyskinesia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:extrapyramidal dyskinesias (1 patient)
n1=en:retardation | n2=en:extrapyramidal dyskinesias (1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:extrapyramidal features
n1=en:retardation | n2=en:extrapyramidal features | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:extrapyramidal muscular rigidity
n1=en:retardation | n2=en:extrapyramidal muscular rigidity | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:extrapyramidal sign
n1=en:retardation | n2=en:extrapyramidal sign | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:extrapyramidal signs (in 1 patient)
n1=en:retardation | n2=en:extrapyramidal signs (in 1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:extrapyramidal signs (in some patients) thinning of the corpus callosum
n1=en:retardation | n2=en:extrapyramidal signs (in some patients) thinning of the corpus callosum | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:extrapyramidal signs (less common)
n1=en:retardation | n2=en:extrapyramidal signs (less common) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:extrapyramidal signs may develop
n1=en:retardation | n2=en:extrapyramidal signs may develop | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:extrapyramidal signs, mild
n1=en:retardation | n2=en:extrapyramidal signs, mild | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:extrapyramidal symptoms (later-onset)
n1=en:retardation | n2=en:extrapyramidal symptoms (later-onset) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:extrapyramidal symptoms may occur
n1=en:retardation | n2=en:extrapyramidal symptoms may occur | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:extremity ataxia
n1=en:retardation | n2=en:extremity ataxia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:eye
n1=en:retardation | n2=en:eye | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:facial cleft
n1=en:retardation | n2=en:facial cleft | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:facial muscle sparing
n1=en:retardation | n2=en:facial muscle sparing | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:facial muscle weakness
n1=en:retardation | n2=en:facial muscle weakness | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:facial muscle weakness of muscles innervated by cn vii
n1=en:retardation | n2=en:facial muscle weakness of muscles innervated by cn vii | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:facial myokymia, mild
n1=en:retardation | n2=en:facial myokymia, mild | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:facial myokymias
n1=en:retardation | n2=en:facial myokymias | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:facial nerve palsy
n1=en:retardation | n2=en:facial nerve palsy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:facial nerve weakness
n1=en:retardation | n2=en:facial nerve weakness | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:facial palsy secondary to cranial hyperostosis
n1=en:retardation | n2=en:facial palsy secondary to cranial hyperostosis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:facial paralysis
n1=en:retardation | n2=en:facial paralysis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:facial paresis, congenital bilateral
n1=en:retardation | n2=en:facial paresis, congenital bilateral | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:facial-faucial-finger mini-myoclonus (fff)
n1=en:retardation | n2=en:facial-faucial-finger mini-myoclonus (fff) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:facial-lingual fasciculations
n1=en:retardation | n2=en:facial-lingual fasciculations | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:facial, pharyngeal, and masticatory muscle diplegia
n1=en:retardation | n2=en:facial, pharyngeal, and masticatory muscle diplegia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:faciocardiomelic syndrome
n1=en:retardation | n2=en:faciocardiomelic syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:faciomandibular myoclonus, nocturnal
n1=en:retardation | n2=en:faciomandibular myoclonus, nocturnal | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:factitious disorder
n1=en:retardation | n2=en:factitious disorder | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:failure of opercularization of the frontal and temporal lobes on ct
n1=en:retardation | n2=en:failure of opercularization of the frontal and temporal lobes on ct | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:failure to achieve sitting or walking (severe form)
n1=en:retardation | n2=en:failure to achieve sitting or walking (severe form) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:fall
n1=en:retardation | n2=en:fall | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:falx cerebri, precocious calcification of
n1=en:retardation | n2=en:falx cerebri, precocious calcification of | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:familial scaphocephaly syndrome
n1=en:retardation | n2=en:familial scaphocephaly syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:family history of mental retardation
n1=en:retardation | n2=en:family history of mental retardation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:fasciculation
n1=en:retardation | n2=en:fasciculation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:fasciculation-like movements
n1=en:retardation | n2=en:fasciculation-like movements | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:fasciculations (after long disease duration)
n1=en:retardation | n2=en:fasciculations (after long disease duration) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:fasciculations, tongue
n1=en:retardation | n2=en:fasciculations, tongue | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:fatal subacute encephalopathy (1 family)
n1=en:retardation | n2=en:fatal subacute encephalopathy (1 family) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:fatigue
n1=en:retardation | n2=en:fatigue | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:favorable response to levodopa
n1=en:retardation | n2=en:favorable response to levodopa | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:fear of mental disorder
n1=en:retardation | n2=en:fear of mental disorder | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:fearful expression
n1=en:retardation | n2=en:fearful expression | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:febrile seizure
n1=en:retardation | n2=en:febrile seizure | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:febrile seizures (1 patient)
n1=en:retardation | n2=en:febrile seizures (1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:febrile seizures (in some)
n1=en:retardation | n2=en:febrile seizures (in some) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:febrile seizures (reported in 1 patient)
n1=en:retardation | n2=en:febrile seizures (reported in 1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:febrile seizures (usually remit by age 6 years)
n1=en:retardation | n2=en:febrile seizures (usually remit by age 6 years) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:febrile seizures in infancy
n1=en:retardation | n2=en:febrile seizures in infancy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:febrile seizures may occur
n1=en:retardation | n2=en:febrile seizures may occur | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:feeding and eating disorders
n1=en:retardation | n2=en:feeding and eating disorders | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:feeding disability
n1=en:retardation | n2=en:feeding disability | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:feeding problem
n1=en:retardation | n2=en:feeding problem | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:feeling anxious/nervous/tense
n1=en:retardation | n2=en:feeling anxious/nervous/tense | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:feeling depressed
n1=en:retardation | n2=en:feeling depressed | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:feeling/behaving irritable
n1=en:retardation | n2=en:feeling/behaving irritable | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:feeling/behaving old/senile
n1=en:retardation | n2=en:feeling/behaving old/senile | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:feingold syndrome
n1=en:retardation | n2=en:feingold syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:feingold syndrome 2
n1=en:retardation | n2=en:feingold syndrome 2 | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:female genital injuries
n1=en:retardation | n2=en:female genital injuries | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:femur fracture
n1=en:retardation | n2=en:femur fracture | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:fenestrated basilar artery
n1=en:retardation | n2=en:fenestrated basilar artery | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:festinating (parkinsonian) gait
n1=en:retardation | n2=en:festinating (parkinsonian) gait | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:fetal akinesia deformation sequence
n1=en:retardation | n2=en:fetal akinesia deformation sequence | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:fetal alcohol syndrome
n1=en:retardation | n2=en:fetal alcohol syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:fetal postural deformity
n1=en:retardation | n2=en:fetal postural deformity | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:fg syndrome
n1=en:retardation | n2=en:fg syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:fibrillary plaques in the cerebellar cortex
n1=en:retardation | n2=en:fibrillary plaques in the cerebellar cortex | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:fibrillation
n1=en:retardation | n2=en:fibrillation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:fibroid/myoma (uterus/cervix)
n1=en:retardation | n2=en:fibroid/myoma (uterus/cervix) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:fibrous astrocyte
n1=en:retardation | n2=en:fibrous astrocyte | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:fifth ventricle
n1=en:retardation | n2=en:fifth ventricle | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:fine motor delay
n1=en:retardation | n2=en:fine motor delay | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:fine motor disability
n1=en:retardation | n2=en:fine motor disability | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:fine motor impairment
n1=en:retardation | n2=en:fine motor impairment | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:fine motor skills delayed
n1=en:retardation | n2=en:fine motor skills delayed | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:fine motor task disruption
n1=en:retardation | n2=en:fine motor task disruption | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:fine motor/coordination problems (12%)
n1=en:retardation | n2=en:fine motor/coordination problems (12%) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:fine rapid hand tremor, 4-12 hz
n1=en:retardation | n2=en:fine rapid hand tremor, 4-12 hz | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:fine tremors
n1=en:retardation | n2=en:fine tremors | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:finger dysmetria
n1=en:retardation | n2=en:finger dysmetria | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:finger twitching
n1=en:retardation | n2=en:finger twitching | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:first dorsal interossei muscle atrophy
n1=en:retardation | n2=en:first dorsal interossei muscle atrophy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:first dorsal interossei muscle weakness
n1=en:retardation | n2=en:first dorsal interossei muscle weakness | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:flaccidity, episodic
n1=en:retardation | n2=en:flaccidity, episodic | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:flat pons
n1=en:retardation | n2=en:flat pons | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:flattening of the caudate
n1=en:retardation | n2=en:flattening of the caudate | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:flattening of the pons
n1=en:retardation | n2=en:flattening of the pons | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:flexor plantar response
n1=en:retardation | n2=en:flexor plantar response | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:floppiness
n1=en:retardation | n2=en:floppiness | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:floppy infant
n1=en:retardation | n2=en:floppy infant | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:fluctuating neurologic signs
n1=en:retardation | n2=en:fluctuating neurologic signs | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:fluctuations in consciousness
n1=en:retardation | n2=en:fluctuations in consciousness | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:fluid filled posterior fossa
n1=en:retardation | n2=en:fluid filled posterior fossa | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:fluid-filled cavity within the cerebral hemispheres, can be unilateral or bilateral and may or may not communicate with cerebrospinal fluid (csf) spaces
n1=en:retardation | n2=en:fluid-filled cavity within the cerebral hemispheres, can be unilateral or bilateral and may or may not communicate with cerebrospinal fluid (csf) spaces | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:focal cerebellar dysplasia
n1=en:retardation | n2=en:focal cerebellar dysplasia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:focal clonic seizure
n1=en:retardation | n2=en:focal clonic seizure | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:focal cortical dysplasia
n1=en:retardation | n2=en:focal cortical dysplasia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:focal discharges
n1=en:retardation | n2=en:focal discharges | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:focal dyscognitive seizures
n1=en:retardation | n2=en:focal dyscognitive seizures | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:focal dystonia (adult onset)
n1=en:retardation | n2=en:focal dystonia (adult onset) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:focal dystonia (e.g., writer's cramp)
n1=en:retardation | n2=en:focal dystonia (e.g., writer's cramp) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:focal dystonia (rare)
n1=en:retardation | n2=en:focal dystonia (rare) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:focal dystonia, upper limb
n1=en:retardation | n2=en:focal dystonia, upper limb | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:focal dystonia, usually of the hands
n1=en:retardation | n2=en:focal dystonia, usually of the hands | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:focal dystonias
n1=en:retardation | n2=en:focal dystonias | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:focal hyperplasia of the choroid plexus
n1=en:retardation | n2=en:focal hyperplasia of the choroid plexus | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:focal interhemispheric fusion
n1=en:retardation | n2=en:focal interhemispheric fusion | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:focal lissencephaly
n1=en:retardation | n2=en:focal lissencephaly | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:focal microgyria
n1=en:retardation | n2=en:focal microgyria | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:focal neurologic deficit
n1=en:retardation | n2=en:focal neurologic deficit | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:focal neurologic deficits (i.e., hemiparesis)
n1=en:retardation | n2=en:focal neurologic deficits (i.e., hemiparesis) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:focal neurologic signs
n1=en:retardation | n2=en:focal neurologic signs | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:focal nodular heterotopia
n1=en:retardation | n2=en:focal nodular heterotopia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:focal pachygyria
n1=en:retardation | n2=en:focal pachygyria | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:focal parietal pachygyria
n1=en:retardation | n2=en:focal parietal pachygyria | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:focal paroxysmal discharges
n1=en:retardation | n2=en:focal paroxysmal discharges | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:focal thickening of the cortex on mri (in type iib)
n1=en:retardation | n2=en:focal thickening of the cortex on mri (in type iib) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:focal tremor
n1=en:retardation | n2=en:focal tremor | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:focal white matter lesions (in type iib)
n1=en:retardation | n2=en:focal white matter lesions (in type iib) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:focal, segmental or multifocal dystonia
n1=en:retardation | n2=en:focal, segmental or multifocal dystonia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:foot-drop
n1=en:retardation | n2=en:foot-drop | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:forebrain
n1=en:retardation | n2=en:forebrain | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:forebrain defects
n1=en:retardation | n2=en:forebrain defects | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:foreign body in auditory canal
n1=en:retardation | n2=en:foreign body in auditory canal | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:foreign body nose/larynx/bronchus
n1=en:retardation | n2=en:foreign body nose/larynx/bronchus | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:four-repeat tau plaques in the striatum
n1=en:retardation | n2=en:four-repeat tau plaques in the striatum | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:fracture hand/foot bones
n1=en:retardation | n2=en:fracture hand/foot bones | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:fracture of radius and ulna
n1=en:retardation | n2=en:fracture of radius and ulna | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:fracture of tibia and fibula
n1=en:retardation | n2=en:fracture of tibia and fibula | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:fracture other
n1=en:retardation | n2=en:fracture other | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:fragile x syndrome
n1=en:retardation | n2=en:fragile x syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:fraser syndrome
n1=en:retardation | n2=en:fraser syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:frequency 3.5 hz in midline
n1=en:retardation | n2=en:frequency 3.5 hz in midline | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:frequency 6 hz in lateral gaze
n1=en:retardation | n2=en:frequency 6 hz in lateral gaze | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:frequency of 1 to 20 episodes per day
n1=en:retardation | n2=en:frequency of 1 to 20 episodes per day | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:frequent falls
n1=en:retardation | n2=en:frequent falls | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:frequent falls with preservation of consciousness
n1=en:retardation | n2=en:frequent falls with preservation of consciousness | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:frequent headache
n1=en:retardation | n2=en:frequent headache | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:frightening sensation
n1=en:retardation | n2=en:frightening sensation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:frohlich syndrome
n1=en:retardation | n2=en:frohlich syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:frontal cortical atophy
n1=en:retardation | n2=en:frontal cortical atophy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:frontal lobe
n1=en:retardation | n2=en:frontal lobe | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:frontal lobe atrophy
n1=en:retardation | n2=en:frontal lobe atrophy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:frontal lobe hypoplasia
n1=en:retardation | n2=en:frontal lobe hypoplasia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:frontal lobe origin
n1=en:retardation | n2=en:frontal lobe origin | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:frontal lobe syndrome
n1=en:retardation | n2=en:frontal lobe syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:frontal release signs
n1=en:retardation | n2=en:frontal release signs | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:frontolimbic dementia
n1=en:retardation | n2=en:frontolimbic dementia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:frontometaphyseal dysplasia
n1=en:retardation | n2=en:frontometaphyseal dysplasia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:frontonasal dysplasia
n1=en:retardation | n2=en:frontonasal dysplasia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:frontoparietal polymicrogyria
n1=en:retardation | n2=en:frontoparietal polymicrogyria | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:frontotemporal atrophy
n1=en:retardation | n2=en:frontotemporal atrophy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:frontotemporal atrophy, mild, seen on mri
n1=en:retardation | n2=en:frontotemporal atrophy, mild, seen on mri | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:frontotemporal dementia
n1=en:retardation | n2=en:frontotemporal dementia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:frontotemporal dementia (1 patient)
n1=en:retardation | n2=en:frontotemporal dementia (1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:frontotemporal dementia (in 30% of patients)
n1=en:retardation | n2=en:frontotemporal dementia (in 30% of patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:frontotemporal dementia, variable severity
n1=en:retardation | n2=en:frontotemporal dementia, variable severity | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:frontotemporal hypoplasia
n1=en:retardation | n2=en:frontotemporal hypoplasia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:frontotemporal leukoencephalopathy
n1=en:retardation | n2=en:frontotemporal leukoencephalopathy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:frontotemporal lobar atrophy
n1=en:retardation | n2=en:frontotemporal lobar atrophy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:frontotemporal lobar atrophy with 'knife-edge' distinction
n1=en:retardation | n2=en:frontotemporal lobar atrophy with 'knife-edge' distinction | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:frontotemporal pachygyria (1 patient)
n1=en:retardation | n2=en:frontotemporal pachygyria (1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:frontotemporal polymicrogyria
n1=en:retardation | n2=en:frontotemporal polymicrogyria | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:frontotemporal/subcortical dementia
n1=en:retardation | n2=en:frontotemporal/subcortical dementia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:frontotemporoparietal cortical dysplasia
n1=en:retardation | n2=en:frontotemporoparietal cortical dysplasia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:fucosidosis
n1=en:retardation | n2=en:fucosidosis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:functional quadriplegia
n1=en:retardation | n2=en:functional quadriplegia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:funnel-shaped signal tapering from subcortical white matter to ventricle (in some type iib patients)
n1=en:retardation | n2=en:funnel-shaped signal tapering from subcortical white matter to ventricle (in some type iib patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:fused hemispheres (wws)
n1=en:retardation | n2=en:fused hemispheres (wws) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:fusion of the basal ganglia
n1=en:retardation | n2=en:fusion of the basal ganglia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:fusion of the cerebellar hemispheres
n1=en:retardation | n2=en:fusion of the cerebellar hemispheres | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:fusion of the dentate nuclei and the superior cerebellar peduncles
n1=en:retardation | n2=en:fusion of the dentate nuclei and the superior cerebellar peduncles | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:fusion of the left and right thalami
n1=en:retardation | n2=en:fusion of the left and right thalami | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:gait abnormalities (in some patients)
n1=en:retardation | n2=en:gait abnormalities (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:gait abnormalities (less common)
n1=en:retardation | n2=en:gait abnormalities (less common) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:gait abnormalities due to muscle weakness
n1=en:retardation | n2=en:gait abnormalities due to muscle weakness | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:gait abnormalities may occur
n1=en:retardation | n2=en:gait abnormalities may occur | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:gait and limb ataxia
n1=en:retardation | n2=en:gait and limb ataxia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:gait apraxia
n1=en:retardation | n2=en:gait apraxia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:gait ataxia (in some patients)
n1=en:retardation | n2=en:gait ataxia (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:gait ataxias, cerebellar
n1=en:retardation | n2=en:gait ataxias, cerebellar | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:gait difficulties due to contractures of the lower limbs
n1=en:retardation | n2=en:gait difficulties due to contractures of the lower limbs | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:gait difficulties, late-onset
n1=en:retardation | n2=en:gait difficulties, late-onset | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:gait disability
n1=en:retardation | n2=en:gait disability | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:gait disturbance
n1=en:retardation | n2=en:gait disturbance | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:gait disturbance (ataxia)
n1=en:retardation | n2=en:gait disturbance (ataxia) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:gait imbalance
n1=en:retardation | n2=en:gait imbalance | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:gait impairment
n1=en:retardation | n2=en:gait impairment | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:gait impairment (55%)
n1=en:retardation | n2=en:gait impairment (55%) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:gait instability, worse in the dark
n1=en:retardation | n2=en:gait instability, worse in the dark | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:gait unsteady
n1=en:retardation | n2=en:gait unsteady | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:gait, drop foot
n1=en:retardation | n2=en:gait, drop foot | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:gait, rigid
n1=en:retardation | n2=en:gait, rigid | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:galactosemia
n1=en:retardation | n2=en:galactosemia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:galloway mowat syndrome
n1=en:retardation | n2=en:galloway mowat syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:game friedman paradice syndrome
n1=en:retardation | n2=en:game friedman paradice syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ganglion joint/tendon
n1=en:retardation | n2=en:ganglion joint/tendon | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:gangliosidosis, generalized gm1, type 1 (disorder)
n1=en:retardation | n2=en:gangliosidosis, generalized gm1, type 1 (disorder) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:gastroenteritis presumed infectious
n1=en:retardation | n2=en:gastroenteritis presumed infectious | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:gastroschisis
n1=en:retardation | n2=en:gastroschisis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:gaucher disease
n1=en:retardation | n2=en:gaucher disease | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:gaze deviation
n1=en:retardation | n2=en:gaze deviation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:general clinical state
n1=en:retardation | n2=en:general clinical state | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:generalized amyotrophy
n1=en:retardation | n2=en:generalized amyotrophy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:generalized and focal spike and wave complexes seen on eeg
n1=en:retardation | n2=en:generalized and focal spike and wave complexes seen on eeg | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:generalized cerebral hypoplasia/atrophy (45%)
n1=en:retardation | n2=en:generalized cerebral hypoplasia/atrophy (45%) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:generalized cerebral, cerebellar, and brainstem atrophy, progressive
n1=en:retardation | n2=en:generalized cerebral, cerebellar, and brainstem atrophy, progressive | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:generalized clonic or tonic-clonic seizures
n1=en:retardation | n2=en:generalized clonic or tonic-clonic seizures | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:generalized cortical atrophy (in one patient)
n1=en:retardation | n2=en:generalized cortical atrophy (in one patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:generalized cortical atrophy, most prominent in the frontal and parietal lobes
n1=en:retardation | n2=en:generalized cortical atrophy, most prominent in the frontal and parietal lobes | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:generalized dystonia
n1=en:retardation | n2=en:generalized dystonia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:generalized hypotonia
n1=en:retardation | n2=en:generalized hypotonia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:generalized myelin loss
n1=en:retardation | n2=en:generalized myelin loss | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:generalized seizures
n1=en:retardation | n2=en:generalized seizures | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:generalized slowing
n1=en:retardation | n2=en:generalized slowing | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:generalized slowing seen on eeg
n1=en:retardation | n2=en:generalized slowing seen on eeg | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:generalized spike wave discharges
n1=en:retardation | n2=en:generalized spike wave discharges | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:generalized spike-wave activity seen on eeg
n1=en:retardation | n2=en:generalized spike-wave activity seen on eeg | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:generalized spike-wave discharges see on eeg
n1=en:retardation | n2=en:generalized spike-wave discharges see on eeg | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:generalized stiffening
n1=en:retardation | n2=en:generalized stiffening | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:generalized tonic-clonic seizures (gtcs) (in most patients)
n1=en:retardation | n2=en:generalized tonic-clonic seizures (gtcs) (in most patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:generalized tonic-clonic seizures (gtcs) on awakening
n1=en:retardation | n2=en:generalized tonic-clonic seizures (gtcs) on awakening | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:generalized tonic-clonic seizures (often develop in adolescence)
n1=en:retardation | n2=en:generalized tonic-clonic seizures (often develop in adolescence) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:generalized tonic-clonic seizures (rare)
n1=en:retardation | n2=en:generalized tonic-clonic seizures (rare) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:generalized tonic-clonic seizures (stage 2 and 3)
n1=en:retardation | n2=en:generalized tonic-clonic seizures (stage 2 and 3) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:generalized tonic-clonic seizures in 50%
n1=en:retardation | n2=en:generalized tonic-clonic seizures in 50% | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:generalized tonic-clonic seizures on awakening
n1=en:retardation | n2=en:generalized tonic-clonic seizures on awakening | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:genital herpes in men
n1=en:retardation | n2=en:genital herpes in men | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:genital herpes in women
n1=en:retardation | n2=en:genital herpes in women | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:germinal cysts over the caudate
n1=en:retardation | n2=en:germinal cysts over the caudate | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:geroderma osteodysplastica
n1=en:retardation | n2=en:geroderma osteodysplastica | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:giant cortical somatosensory evoked potentials (seps)
n1=en:retardation | n2=en:giant cortical somatosensory evoked potentials (seps) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:giant granules in schwann cells
n1=en:retardation | n2=en:giant granules in schwann cells | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:gilles de la tourette syndrome (reported in 1 patient)
n1=en:retardation | n2=en:gilles de la tourette syndrome (reported in 1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:gingival cyst of newborn
n1=en:retardation | n2=en:gingival cyst of newborn | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:glaucoma
n1=en:retardation | n2=en:glaucoma | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:glial activation
n1=en:retardation | n2=en:glial activation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:glial cell
n1=en:retardation | n2=en:glial cell | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:glial inclusions
n1=en:retardation | n2=en:glial inclusions | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:gliosis
n1=en:retardation | n2=en:gliosis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:gliosis (27%)
n1=en:retardation | n2=en:gliosis (27%) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:gliosis (patient a)
n1=en:retardation | n2=en:gliosis (patient a) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:gliosis in the brainstem
n1=en:retardation | n2=en:gliosis in the brainstem | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:gliosis in the striatum, medial thalamic nuclei, and inferior olives
n1=en:retardation | n2=en:gliosis in the striatum, medial thalamic nuclei, and inferior olives | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:gliosis of the white matter
n1=en:retardation | n2=en:gliosis of the white matter | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:gliosis, necrosis, neuronal loss in basal ganglia, brainstem, and spinal cord
n1=en:retardation | n2=en:gliosis, necrosis, neuronal loss in basal ganglia, brainstem, and spinal cord | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:global and focal neurologic abnormalities (less than 30%)
n1=en:retardation | n2=en:global and focal neurologic abnormalities (less than 30%) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:global brain atrophy
n1=en:retardation | n2=en:global brain atrophy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:global cerebral atrophy, mild (in some patients)
n1=en:retardation | n2=en:global cerebral atrophy, mild (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:global developmental delay
n1=en:retardation | n2=en:global developmental delay | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:global developmental delay if untreated
n1=en:retardation | n2=en:global developmental delay if untreated | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:global developmental delay, variable severity
n1=en:retardation | n2=en:global developmental delay, variable severity | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:global hypotonia
n1=en:retardation | n2=en:global hypotonia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:global reduction in cerebral blood flow on pet scan
n1=en:retardation | n2=en:global reduction in cerebral blood flow on pet scan | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:globally delayed development
n1=en:retardation | n2=en:globally delayed development | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:globular basal ganglia (1 patient)
n1=en:retardation | n2=en:globular basal ganglia (1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:globular thalamus (1 patient)
n1=en:retardation | n2=en:globular thalamus (1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:glomeruloid vascular proliferation in brain and spinal cord
n1=en:retardation | n2=en:glomeruloid vascular proliferation in brain and spinal cord | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:glomerulonephritis/nephrosis
n1=en:retardation | n2=en:glomerulonephritis/nephrosis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:glut1 deficiency syndrome
n1=en:retardation | n2=en:glut1 deficiency syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:glycine encephalopathy
n1=en:retardation | n2=en:glycine encephalopathy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:glycosuria, renal
n1=en:retardation | n2=en:glycosuria, renal | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:goiter
n1=en:retardation | n2=en:goiter | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:goldberg-shprintzen megacolon syndrome
n1=en:retardation | n2=en:goldberg-shprintzen megacolon syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:goldenhar syndrome
n1=en:retardation | n2=en:goldenhar syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:gonadal dysgenesis
n1=en:retardation | n2=en:gonadal dysgenesis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:goniodysgenesis-mental retardation-short stature syndrome
n1=en:retardation | n2=en:goniodysgenesis-mental retardation-short stature syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:gonorrhea female
n1=en:retardation | n2=en:gonorrhea female | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:gonorrhea male
n1=en:retardation | n2=en:gonorrhea male | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:gout
n1=en:retardation | n2=en:gout | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:gowers sign
n1=en:retardation | n2=en:gowers sign | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:grand mal epilepsy
n1=en:retardation | n2=en:grand mal epilepsy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:grand mal seizure
n1=en:retardation | n2=en:grand mal seizure | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:granular material in neurons
n1=en:retardation | n2=en:granular material in neurons | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:granular osmiophilic cytoplasmic deposits in schwann cells
n1=en:retardation | n2=en:granular osmiophilic cytoplasmic deposits in schwann cells | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:granulovacuolar degeneration
n1=en:retardation | n2=en:granulovacuolar degeneration | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:gray matter
n1=en:retardation | n2=en:gray matter | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:gray matter appears relatively unaffected
n1=en:retardation | n2=en:gray matter appears relatively unaffected | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:gray matter heterotopia (in some patients)
n1=en:retardation | n2=en:gray matter heterotopia (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:gray matter structure of central nervous system
n1=en:retardation | n2=en:gray matter structure of central nervous system | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:greig syndrome
n1=en:retardation | n2=en:greig syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:grimaces
n1=en:retardation | n2=en:grimaces | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:griscelli syndrome, type 1
n1=en:retardation | n2=en:griscelli syndrome, type 1 | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:gross motor delay
n1=en:retardation | n2=en:gross motor delay | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:gross motor delay (in one family)
n1=en:retardation | n2=en:gross motor delay (in one family) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:gross motor delay, mild
n1=en:retardation | n2=en:gross motor delay, mild | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:gross motor disability
n1=en:retardation | n2=en:gross motor disability | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:gross motor skill delay (infancy)
n1=en:retardation | n2=en:gross motor skill delay (infancy) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:growth and development disorder
n1=en:retardation | n2=en:growth and development disorder | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:growth deficiency and mental retardation with facial dysmorphism
n1=en:retardation | n2=en:growth deficiency and mental retardation with facial dysmorphism | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:growth retardation
n1=en:retardation | n2=en:growth retardation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:gtcs during 'leisure' time (evening)
n1=en:retardation | n2=en:gtcs during 'leisure' time (evening) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:guanidinoacetate methyltransferase deficiency
n1=en:retardation | n2=en:guanidinoacetate methyltransferase deficiency | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:gurgling or drooling during seizures
n1=en:retardation | n2=en:gurgling or drooling during seizures | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:gyral disorganization
n1=en:retardation | n2=en:gyral disorganization | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:gyral simplification
n1=en:retardation | n2=en:gyral simplification | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hadziselimovic syndrome
n1=en:retardation | n2=en:hadziselimovic syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hall riggs mental retardation syndrome
n1=en:retardation | n2=en:hall riggs mental retardation syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hallucination
n1=en:retardation | n2=en:hallucination | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hallucinations (rare)
n1=en:retardation | n2=en:hallucinations (rare) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hamartoma
n1=en:retardation | n2=en:hamartoma | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hamartomatous lesions of the brain
n1=en:retardation | n2=en:hamartomatous lesions of the brain | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hand function disability
n1=en:retardation | n2=en:hand function disability | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hand muscle atrophy
n1=en:retardation | n2=en:hand muscle atrophy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hand muscle weakness
n1=en:retardation | n2=en:hand muscle weakness | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hand tremor (in some patients)
n1=en:retardation | n2=en:hand tremor (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:handicapping condition
n1=en:retardation | n2=en:handicapping condition | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:has tingling sensation
n1=en:retardation | n2=en:has tingling sensation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:haspeslagh fryns muelenaere syndrome
n1=en:retardation | n2=en:haspeslagh fryns muelenaere syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:head 'tilt' in infancy
n1=en:retardation | n2=en:head 'tilt' in infancy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:head bobbing
n1=en:retardation | n2=en:head bobbing | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:head lag
n1=en:retardation | n2=en:head lag | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:head movements abnormal
n1=en:retardation | n2=en:head movements abnormal | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:head oscillations
n1=en:retardation | n2=en:head oscillations | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:head titubation
n1=en:retardation | n2=en:head titubation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:head titubations
n1=en:retardation | n2=en:head titubations | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:head tremor
n1=en:retardation | n2=en:head tremor | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:head tremor (14% of patients)
n1=en:retardation | n2=en:head tremor (14% of patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:head tremor (in some patients)
n1=en:retardation | n2=en:head tremor (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:head tremor, mild
n1=en:retardation | n2=en:head tremor, mild | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:head-rolling movements
n1=en:retardation | n2=en:head-rolling movements | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:headache
n1=en:retardation | n2=en:headache | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:headache (with pheochromocytoma)
n1=en:retardation | n2=en:headache (with pheochromocytoma) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:headache is unilateral
n1=en:retardation | n2=en:headache is unilateral | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:headache is usually not a symptom
n1=en:retardation | n2=en:headache is usually not a symptom | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:headache recurrent
n1=en:retardation | n2=en:headache recurrent | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:headache, episodic
n1=en:retardation | n2=en:headache, episodic | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:headache, suboccipital, migraine-like (most common symptom) precipitated by coughing, sneezing, bending forward, lifting, neck extension
n1=en:retardation | n2=en:headache, suboccipital, migraine-like (most common symptom) precipitated by coughing, sneezing, bending forward, lifting, neck extension | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:headaches, severe, unilateral
n1=en:retardation | n2=en:headaches, severe, unilateral | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:heart failure
n1=en:retardation | n2=en:heart failure | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:heart malformation
n1=en:retardation | n2=en:heart malformation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:heart murmur
n1=en:retardation | n2=en:heart murmur | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:heightened sensitivity to external stimuli
n1=en:retardation | n2=en:heightened sensitivity to external stimuli | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hemangiomas and lymphangiomas of any site
n1=en:retardation | n2=en:hemangiomas and lymphangiomas of any site | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hemiclonic seizures
n1=en:retardation | n2=en:hemiclonic seizures | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hemihypertrophy
n1=en:retardation | n2=en:hemihypertrophy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hemihypoasthesia
n1=en:retardation | n2=en:hemihypoasthesia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hemimegalencephaly
n1=en:retardation | n2=en:hemimegalencephaly | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hemiparesis
n1=en:retardation | n2=en:hemiparesis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hemiparesis (in some patients)
n1=en:retardation | n2=en:hemiparesis (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hemiparesis, paroxysmal
n1=en:retardation | n2=en:hemiparesis, paroxysmal | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hemiplegia
n1=en:retardation | n2=en:hemiplegia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hemiplegia (rare)
n1=en:retardation | n2=en:hemiplegia (rare) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hemiplegic migraine
n1=en:retardation | n2=en:hemiplegic migraine | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hemiplegic migraine in some patients
n1=en:retardation | n2=en:hemiplegic migraine in some patients | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hemisensory attacks
n1=en:retardation | n2=en:hemisensory attacks | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hemispheric atrophy
n1=en:retardation | n2=en:hemispheric atrophy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hemivertebra
n1=en:retardation | n2=en:hemivertebra | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hemorrhage
n1=en:retardation | n2=en:hemorrhage | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hemorrhagic cerebrovascular accident
n1=en:retardation | n2=en:hemorrhagic cerebrovascular accident | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hemorrhoid
n1=en:retardation | n2=en:hemorrhoid | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hemosiderin deposition
n1=en:retardation | n2=en:hemosiderin deposition | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hepatic coma
n1=en:retardation | n2=en:hepatic coma | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hepatic encephalopathy
n1=en:retardation | n2=en:hepatic encephalopathy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hepatomegaly
n1=en:retardation | n2=en:hepatomegaly | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hereditary elliptocytosis
n1=en:retardation | n2=en:hereditary elliptocytosis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hereditary hemolytic anemia
n1=en:retardation | n2=en:hereditary hemolytic anemia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hermaphrodite
n1=en:retardation | n2=en:hermaphrodite | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:herniation and elongation of the cerebellar tonsils, cerebellar vermis, brainstem, and fourth ventricle through the foramen magnum
n1=en:retardation | n2=en:herniation and elongation of the cerebellar tonsils, cerebellar vermis, brainstem, and fourth ventricle through the foramen magnum | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:herniation of the cerebellar tonsils through the foramen magnum 5 mm or greater
n1=en:retardation | n2=en:herniation of the cerebellar tonsils through the foramen magnum 5 mm or greater | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:herpes simplex infections
n1=en:retardation | n2=en:herpes simplex infections | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:herpes zoster
n1=en:retardation | n2=en:herpes zoster | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:heterotopic neurons in the white matter (36%)
n1=en:retardation | n2=en:heterotopic neurons in the white matter (36%) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hiatal hernia
n1=en:retardation | n2=en:hiatal hernia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hiccough
n1=en:retardation | n2=en:hiccough | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:high intensity area in white matter on head mri
n1=en:retardation | n2=en:high intensity area in white matter on head mri | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:high pain threshold
n1=en:retardation | n2=en:high pain threshold | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:high risk pregnancy
n1=en:retardation | n2=en:high risk pregnancy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:high signal intensities at gray/white matter junction
n1=en:retardation | n2=en:high signal intensities at gray/white matter junction | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:high signal intensities in periventricular white matter
n1=en:retardation | n2=en:high signal intensities in periventricular white matter | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:high voltage spikes over the temporal and central regions seen on eeg
n1=en:retardation | n2=en:high voltage spikes over the temporal and central regions seen on eeg | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:high voltage, fast rhythms seen on eeg
n1=en:retardation | n2=en:high voltage, fast rhythms seen on eeg | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:high-steppage gait
n1=en:retardation | n2=en:high-steppage gait | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:high-stepping gait
n1=en:retardation | n2=en:high-stepping gait | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hindbrain and midbrain
n1=en:retardation | n2=en:hindbrain and midbrain | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hip osteoarthritis
n1=en:retardation | n2=en:hip osteoarthritis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hippocampal atrophy (1 patient)
n1=en:retardation | n2=en:hippocampal atrophy (1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hippocampal atrophy (in 2 siblings)
n1=en:retardation | n2=en:hippocampal atrophy (in 2 siblings) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hippocampal hypoplasia
n1=en:retardation | n2=en:hippocampal hypoplasia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:histidinemia
n1=en:retardation | n2=en:histidinemia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hiv/aids
n1=en:retardation | n2=en:hiv/aids | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hodgkin lymphoma
n1=en:retardation | n2=en:hodgkin lymphoma | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:holoprosencephaly
n1=en:retardation | n2=en:holoprosencephaly | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:holoprosencephaly (1 patient)
n1=en:retardation | n2=en:holoprosencephaly (1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:holoprosencephaly (100%)
n1=en:retardation | n2=en:holoprosencephaly (100%) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:holoprosencephaly (less common)
n1=en:retardation | n2=en:holoprosencephaly (less common) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:holoprosencephaly (variable)
n1=en:retardation | n2=en:holoprosencephaly (variable) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:holoprosencephaly 10
n1=en:retardation | n2=en:holoprosencephaly 10 | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:holoprosencephaly type 2
n1=en:retardation | n2=en:holoprosencephaly type 2 | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:holoprosencephaly type 5
n1=en:retardation | n2=en:holoprosencephaly type 5 | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:homocystinuria
n1=en:retardation | n2=en:homocystinuria | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hooked aspect of the frontal horn of the lateral ventricles due to abnormally shaped basal ganglia
n1=en:retardation | n2=en:hooked aspect of the frontal horn of the lateral ventricles due to abnormally shaped basal ganglia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:horner syndrome
n1=en:retardation | n2=en:horner syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hostility
n1=en:retardation | n2=en:hostility | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hunger and thirst disturbances (in some patients)
n1=en:retardation | n2=en:hunger and thirst disturbances (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:huntington's disease
n1=en:retardation | n2=en:huntington's disease | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:huntington's disease pathway
n1=en:retardation | n2=en:huntington's disease pathway | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hurler syndrome
n1=en:retardation | n2=en:hurler syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hydranencephaly
n1=en:retardation | n2=en:hydranencephaly | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hydrocephalus
n1=en:retardation | n2=en:hydrocephalus | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hydrocephalus (11%)
n1=en:retardation | n2=en:hydrocephalus (11%) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hydrocephalus (12%)
n1=en:retardation | n2=en:hydrocephalus (12%) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hydrocephalus (in 1 patient)
n1=en:retardation | n2=en:hydrocephalus (in 1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hydrocephalus (in 2 patients)
n1=en:retardation | n2=en:hydrocephalus (in 2 patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hydrocephalus (in some patients)
n1=en:retardation | n2=en:hydrocephalus (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hydrocephalus (less common)
n1=en:retardation | n2=en:hydrocephalus (less common) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hydrocephalus (rare)
n1=en:retardation | n2=en:hydrocephalus (rare) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hydrocephalus (uncommon)
n1=en:retardation | n2=en:hydrocephalus (uncommon) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hydrocephalus (variable)
n1=en:retardation | n2=en:hydrocephalus (variable) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hydrocephalus, nonsyndromic, autosomal recessive 1
n1=en:retardation | n2=en:hydrocephalus, nonsyndromic, autosomal recessive 1 | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hydrocephalus, normal pressure
n1=en:retardation | n2=en:hydrocephalus, normal pressure | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hydrocephalus, occasional
n1=en:retardation | n2=en:hydrocephalus, occasional | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hydrocephaly, mild
n1=en:retardation | n2=en:hydrocephaly, mild | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hydroxyacyl-coa dehydrogenase, type 2, deficiency
n1=en:retardation | n2=en:hydroxyacyl-coa dehydrogenase, type 2, deficiency | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hyperactive brainstem reflexes (head retraction, palmomental, snout)
n1=en:retardation | n2=en:hyperactive brainstem reflexes (head retraction, palmomental, snout) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hyperactive deep tendon reflexes
n1=en:retardation | n2=en:hyperactive deep tendon reflexes | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hyperactive deep tendon reflexes in early stage
n1=en:retardation | n2=en:hyperactive deep tendon reflexes in early stage | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hyperactive startle reflex
n1=en:retardation | n2=en:hyperactive startle reflex | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hyperactivity
n1=en:retardation | n2=en:hyperactivity | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hyperekplexia (rare)
n1=en:retardation | n2=en:hyperekplexia (rare) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hyperexplexia
n1=en:retardation | n2=en:hyperexplexia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hyperextension of the neck
n1=en:retardation | n2=en:hyperextension of the neck | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hyperintense lesions in the basal ganglia on mri
n1=en:retardation | n2=en:hyperintense lesions in the basal ganglia on mri | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hyperintense lesions of the globi pallidi
n1=en:retardation | n2=en:hyperintense lesions of the globi pallidi | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hyperintensities in the basal ganglia (rare)
n1=en:retardation | n2=en:hyperintensities in the basal ganglia (rare) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hyperintensities in the basal ganglia and/or thalamus
n1=en:retardation | n2=en:hyperintensities in the basal ganglia and/or thalamus | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hyperirritability
n1=en:retardation | n2=en:hyperirritability | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hyperkinesia
n1=en:retardation | n2=en:hyperkinesia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hyperkinetic involuntary movements
n1=en:retardation | n2=en:hyperkinetic involuntary movements | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypermetric saccades
n1=en:retardation | n2=en:hypermetric saccades | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypermotor automatisms
n1=en:retardation | n2=en:hypermotor automatisms | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypermotor behavior
n1=en:retardation | n2=en:hypermotor behavior | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hyperphenylalaninemia, bh4-deficient, b
n1=en:retardation | n2=en:hyperphenylalaninemia, bh4-deficient, b | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hyperphenylalaninemia, non phenylketonuric
n1=en:retardation | n2=en:hyperphenylalaninemia, non phenylketonuric | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hyperphosphatasia with mental retardation
n1=en:retardation | n2=en:hyperphosphatasia with mental retardation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hyperprolinemia type 2
n1=en:retardation | n2=en:hyperprolinemia type 2 | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hyperreflexia
n1=en:retardation | n2=en:hyperreflexia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hyperreflexia (2 patients)
n1=en:retardation | n2=en:hyperreflexia (2 patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hyperreflexia (33%)
n1=en:retardation | n2=en:hyperreflexia (33%) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hyperreflexia (70%)
n1=en:retardation | n2=en:hyperreflexia (70%) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hyperreflexia (early)
n1=en:retardation | n2=en:hyperreflexia (early) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hyperreflexia (later)
n1=en:retardation | n2=en:hyperreflexia (later) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hyperreflexia (less common)
n1=en:retardation | n2=en:hyperreflexia (less common) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hyperreflexia (particularly in lower extremities, more prevalent in adolescents and adults)
n1=en:retardation | n2=en:hyperreflexia (particularly in lower extremities, more prevalent in adolescents and adults) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hyperreflexia (some patients)
n1=en:retardation | n2=en:hyperreflexia (some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hyperreflexia (type i)
n1=en:retardation | n2=en:hyperreflexia (type i) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hyperreflexia in some
n1=en:retardation | n2=en:hyperreflexia in some | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hyperreflexia in the lower limbs (in some patients)
n1=en:retardation | n2=en:hyperreflexia in the lower limbs (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hyperreflexia may occur
n1=en:retardation | n2=en:hyperreflexia may occur | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hyperreflexia proximally
n1=en:retardation | n2=en:hyperreflexia proximally | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hyperreflexia, especially of the lower limbs
n1=en:retardation | n2=en:hyperreflexia, especially of the lower limbs | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hyperreflexia, lower limbs more than upper limbs
n1=en:retardation | n2=en:hyperreflexia, lower limbs more than upper limbs | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hyperreflexia, lower limbs, mild
n1=en:retardation | n2=en:hyperreflexia, lower limbs, mild | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypersensitive to stimuli
n1=en:retardation | n2=en:hypersensitive to stimuli | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypersensitivity to sound
n1=en:retardation | n2=en:hypersensitivity to sound | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypersomnia disorder related to another mental disorder
n1=en:retardation | n2=en:hypersomnia disorder related to another mental disorder | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypersomnolent
n1=en:retardation | n2=en:hypersomnolent | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypertelorism
n1=en:retardation | n2=en:hypertelorism | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypertension with involvement target organs
n1=en:retardation | n2=en:hypertension with involvement target organs | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypertensive encephalopathy
n1=en:retardation | n2=en:hypertensive encephalopathy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hyperthermia
n1=en:retardation | n2=en:hyperthermia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hyperthyroidism, nonautoimmune
n1=en:retardation | n2=en:hyperthyroidism, nonautoimmune | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypertonia
n1=en:retardation | n2=en:hypertonia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypertonia (after age 2 years)
n1=en:retardation | n2=en:hypertonia (after age 2 years) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypertonia (childhood)
n1=en:retardation | n2=en:hypertonia (childhood) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypertonia (in some patients)
n1=en:retardation | n2=en:hypertonia (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypertonia (older children and adolescents)
n1=en:retardation | n2=en:hypertonia (older children and adolescents) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypertonia (type ii)
n1=en:retardation | n2=en:hypertonia (type ii) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypertonia and rigidity during seizures
n1=en:retardation | n2=en:hypertonia and rigidity during seizures | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypertonia in early stage
n1=en:retardation | n2=en:hypertonia in early stage | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypertonia in neonatal period
n1=en:retardation | n2=en:hypertonia in neonatal period | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypertonia late
n1=en:retardation | n2=en:hypertonia late | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypertonia of lower limbs, later
n1=en:retardation | n2=en:hypertonia of lower limbs, later | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypertonia of the extremities
n1=en:retardation | n2=en:hypertonia of the extremities | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypertonia, mild, transient
n1=en:retardation | n2=en:hypertonia, mild, transient | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypertonia, peripheral dystonia
n1=en:retardation | n2=en:hypertonia, peripheral dystonia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypertonic seizures
n1=en:retardation | n2=en:hypertonic seizures | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypertonicity
n1=en:retardation | n2=en:hypertonicity | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypertrophy of clitoris
n1=en:retardation | n2=en:hypertrophy of clitoris | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypertrophy of tonsils and adenoids
n1=en:retardation | n2=en:hypertrophy of tonsils and adenoids | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hyperventilation
n1=en:retardation | n2=en:hyperventilation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypnagogic hallucinations
n1=en:retardation | n2=en:hypnagogic hallucinations | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypnapompic hallucinations
n1=en:retardation | n2=en:hypnapompic hallucinations | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypo- and demyelination of the brain
n1=en:retardation | n2=en:hypo- and demyelination of the brain | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypocalcemic seizures
n1=en:retardation | n2=en:hypocalcemic seizures | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypocalcemic tetany
n1=en:retardation | n2=en:hypocalcemic tetany | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypodensity of caudate
n1=en:retardation | n2=en:hypodensity of caudate | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypodensity of cerebral white matter seen on mri
n1=en:retardation | n2=en:hypodensity of cerebral white matter seen on mri | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypodensity of lenticular nuclei
n1=en:retardation | n2=en:hypodensity of lenticular nuclei | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypodensity of the white matter
n1=en:retardation | n2=en:hypodensity of the white matter | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypodysplasia of the corpus callosum
n1=en:retardation | n2=en:hypodysplasia of the corpus callosum | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypogenesis of the corpus callosum
n1=en:retardation | n2=en:hypogenesis of the corpus callosum | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypoglycemia
n1=en:retardation | n2=en:hypoglycemia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypoglycemia-related seizures
n1=en:retardation | n2=en:hypoglycemia-related seizures | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypoglycemia, leucine-induced
n1=en:retardation | n2=en:hypoglycemia, leucine-induced | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypoglycemic coma
n1=en:retardation | n2=en:hypoglycemic coma | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypoglycemic encephalopathy
n1=en:retardation | n2=en:hypoglycemic encephalopathy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypoglycemic seizures
n1=en:retardation | n2=en:hypoglycemic seizures | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypokinesia
n1=en:retardation | n2=en:hypokinesia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypokinesia in infancy
n1=en:retardation | n2=en:hypokinesia in infancy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypokinetic movements
n1=en:retardation | n2=en:hypokinetic movements | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypometabolism of the frontal lobe and thalamic regions
n1=en:retardation | n2=en:hypometabolism of the frontal lobe and thalamic regions | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypomimia
n1=en:retardation | n2=en:hypomimia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypomyelinating leukoencephalopathy
n1=en:retardation | n2=en:hypomyelinating leukoencephalopathy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypomyelination
n1=en:retardation | n2=en:hypomyelination | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypomyelination (1 patient)
n1=en:retardation | n2=en:hypomyelination (1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypomyelination (patient a) metabolic : hypochloremia metabolic alkalosis (patient a)
n1=en:retardation | n2=en:hypomyelination (patient a) metabolic : hypochloremia metabolic alkalosis (patient a) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypomyelination of the brain white matter, diffuse
n1=en:retardation | n2=en:hypomyelination of the brain white matter, diffuse | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypoparathyroidism-retardation-dysmorphism syndrome
n1=en:retardation | n2=en:hypoparathyroidism-retardation-dysmorphism syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypoplasia
n1=en:retardation | n2=en:hypoplasia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypoplasia and displacement of the corticospinal fibers within the brainstem
n1=en:retardation | n2=en:hypoplasia and displacement of the corticospinal fibers within the brainstem | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypoplasia of anterior or entire pituitary gland (frequent)
n1=en:retardation | n2=en:hypoplasia of anterior or entire pituitary gland (frequent) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypoplasia of corpus callosum
n1=en:retardation | n2=en:hypoplasia of corpus callosum | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypoplasia of corpus callosum and cerebellar vermis
n1=en:retardation | n2=en:hypoplasia of corpus callosum and cerebellar vermis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypoplasia of dentate nucleus
n1=en:retardation | n2=en:hypoplasia of dentate nucleus | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypoplasia of olfactory tract
n1=en:retardation | n2=en:hypoplasia of olfactory tract | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypoplasia of septum pellucidum
n1=en:retardation | n2=en:hypoplasia of septum pellucidum | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypoplasia of the brainstem
n1=en:retardation | n2=en:hypoplasia of the brainstem | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypoplasia of the corpus callosum (2 patients)
n1=en:retardation | n2=en:hypoplasia of the corpus callosum (2 patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypoplasia of the hypothalamus
n1=en:retardation | n2=en:hypoplasia of the hypothalamus | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypoplasia of the medulla oblongata
n1=en:retardation | n2=en:hypoplasia of the medulla oblongata | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypoplasia of the mesencephalic tectum
n1=en:retardation | n2=en:hypoplasia of the mesencephalic tectum | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypoplasia of the optic chiasm
n1=en:retardation | n2=en:hypoplasia of the optic chiasm | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypoplasia of the optic tract
n1=en:retardation | n2=en:hypoplasia of the optic tract | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypoplasia of the pons
n1=en:retardation | n2=en:hypoplasia of the pons | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypoplasia of the posterior corpus callosum (in some patients)
n1=en:retardation | n2=en:hypoplasia of the posterior corpus callosum (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypoplasia of the pyramidal tract
n1=en:retardation | n2=en:hypoplasia of the pyramidal tract | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypoplasia of the ventral pons
n1=en:retardation | n2=en:hypoplasia of the ventral pons | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypoplasia or dysgenesis of the corpus callosum (in some patients)
n1=en:retardation | n2=en:hypoplasia or dysgenesis of the corpus callosum (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypoplastic anterior pituitary (in some patients)
n1=en:retardation | n2=en:hypoplastic anterior pituitary (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypoplastic anterior pituitary gland
n1=en:retardation | n2=en:hypoplastic anterior pituitary gland | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypoplastic brainstem with loss of demarcation at the pontomedullary junction
n1=en:retardation | n2=en:hypoplastic brainstem with loss of demarcation at the pontomedullary junction | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypoplastic cerebellar vermis (rare)
n1=en:retardation | n2=en:hypoplastic cerebellar vermis (rare) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypoplastic cerebrum
n1=en:retardation | n2=en:hypoplastic cerebrum | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypoplastic corpus callosum (1 patient)
n1=en:retardation | n2=en:hypoplastic corpus callosum (1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypoplastic corpus callosum (in some patients)
n1=en:retardation | n2=en:hypoplastic corpus callosum (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypoplastic corpus callosum (in some)
n1=en:retardation | n2=en:hypoplastic corpus callosum (in some) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypoplastic corpus callosum (rare)
n1=en:retardation | n2=en:hypoplastic corpus callosum (rare) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypoplastic internal capsule (in some)
n1=en:retardation | n2=en:hypoplastic internal capsule (in some) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypoplastic olfactory lobes
n1=en:retardation | n2=en:hypoplastic olfactory lobes | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypoplastic or absent middle cerebellar peduncles
n1=en:retardation | n2=en:hypoplastic or absent middle cerebellar peduncles | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypoplastic or absent optic chiasm
n1=en:retardation | n2=en:hypoplastic or absent optic chiasm | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypoplastic pituitary gland (in some patients)
n1=en:retardation | n2=en:hypoplastic pituitary gland (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypoplastic pons
n1=en:retardation | n2=en:hypoplastic pons | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypoplastic/atrophic corpus callosum (55%)
n1=en:retardation | n2=en:hypoplastic/atrophic corpus callosum (55%) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hyporeflexia
n1=en:retardation | n2=en:hyporeflexia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hyporeflexia (early)
n1=en:retardation | n2=en:hyporeflexia (early) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hyporeflexia (occurs later)
n1=en:retardation | n2=en:hyporeflexia (occurs later) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hyporeflexia of lower limbs
n1=en:retardation | n2=en:hyporeflexia of lower limbs | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hyporeflexia or areflexia
n1=en:retardation | n2=en:hyporeflexia or areflexia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hyporeflexia to hyperreflexia
n1=en:retardation | n2=en:hyporeflexia to hyperreflexia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hyposmia/anosmia
n1=en:retardation | n2=en:hyposmia/anosmia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hyposmia/anosmia (in some patients)
n1=en:retardation | n2=en:hyposmia/anosmia (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hyposomnia co-occurrent and due to psychological disorder
n1=en:retardation | n2=en:hyposomnia co-occurrent and due to psychological disorder | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypospadias
n1=en:retardation | n2=en:hypospadias | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypothalamic hamartoma
n1=en:retardation | n2=en:hypothalamic hamartoma | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypothalamus
n1=en:retardation | n2=en:hypothalamus | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypotonia
n1=en:retardation | n2=en:hypotonia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypotonia (1 patient)
n1=en:retardation | n2=en:hypotonia (1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypotonia (93%)
n1=en:retardation | n2=en:hypotonia (93%) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypotonia (96%)
n1=en:retardation | n2=en:hypotonia (96%) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypotonia (congenital form)
n1=en:retardation | n2=en:hypotonia (congenital form) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypotonia (early infancy)
n1=en:retardation | n2=en:hypotonia (early infancy) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypotonia (early-onset form)
n1=en:retardation | n2=en:hypotonia (early-onset form) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypotonia (hcs and 2p21del)
n1=en:retardation | n2=en:hypotonia (hcs and 2p21del) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypotonia (in 1/4 patients)
n1=en:retardation | n2=en:hypotonia (in 1/4 patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypotonia (in males)
n1=en:retardation | n2=en:hypotonia (in males) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypotonia (in some patients)
n1=en:retardation | n2=en:hypotonia (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypotonia (less common)
n1=en:retardation | n2=en:hypotonia (less common) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypotonia (newborn)
n1=en:retardation | n2=en:hypotonia (newborn) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypotonia (rare)
n1=en:retardation | n2=en:hypotonia (rare) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypotonia (type i and type ii, infantile)
n1=en:retardation | n2=en:hypotonia (type i and type ii, infantile) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypotonia at birth
n1=en:retardation | n2=en:hypotonia at birth | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypotonia changing to hypertonia
n1=en:retardation | n2=en:hypotonia changing to hypertonia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypotonia in infancy and early childhood
n1=en:retardation | n2=en:hypotonia in infancy and early childhood | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypotonia in later stages
n1=en:retardation | n2=en:hypotonia in later stages | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypotonia progressing to hypertonia
n1=en:retardation | n2=en:hypotonia progressing to hypertonia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypotonia, axial, severe
n1=en:retardation | n2=en:hypotonia, axial, severe | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypotonia, global, severe
n1=en:retardation | n2=en:hypotonia, global, severe | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypotonia, mild
n1=en:retardation | n2=en:hypotonia, mild | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypotonia, mild, transient
n1=en:retardation | n2=en:hypotonia, mild, transient | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypotonia, neonatal (> 90%)
n1=en:retardation | n2=en:hypotonia, neonatal (> 90%) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypotonia, poor moro reflex
n1=en:retardation | n2=en:hypotonia, poor moro reflex | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypotonia, profound muscular (in some patients)
n1=en:retardation | n2=en:hypotonia, profound muscular (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypotonia, proximal, severe
n1=en:retardation | n2=en:hypotonia, proximal, severe | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypotonia, severe (rare)
n1=en:retardation | n2=en:hypotonia, severe (rare) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypotonic
n1=en:retardation | n2=en:hypotonic | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypotonic seizures
n1=en:retardation | n2=en:hypotonic seizures | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypotonicity (in some patients)
n1=en:retardation | n2=en:hypotonicity (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypotrophic brainstem
n1=en:retardation | n2=en:hypotrophic brainstem | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypoxic convulsions
n1=en:retardation | n2=en:hypoxic convulsions | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypperreflexia
n1=en:retardation | n2=en:hypperreflexia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypsarrhythmia
n1=en:retardation | n2=en:hypsarrhythmia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypsarrhythmia (1 patient)
n1=en:retardation | n2=en:hypsarrhythmia (1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypsarrhythmia (in some patients)
n1=en:retardation | n2=en:hypsarrhythmia (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypsarrhythmia or severe multifocal epileptic abnormalities with poor background activity on eeg
n1=en:retardation | n2=en:hypsarrhythmia or severe multifocal epileptic abnormalities with poor background activity on eeg | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hypsarrhythmia seen on eeg
n1=en:retardation | n2=en:hypsarrhythmia seen on eeg | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hysteria
n1=en:retardation | n2=en:hysteria | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:hysterical/hypochondriacal disease
n1=en:retardation | n2=en:hysterical/hypochondriacal disease | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ichthyosiform erythroderma, corneal involvement, deafness
n1=en:retardation | n2=en:ichthyosiform erythroderma, corneal involvement, deafness | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ichthyosis follicularis atrichia photophobia syndrome
n1=en:retardation | n2=en:ichthyosis follicularis atrichia photophobia syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ictal eeg showed partial seizures with frontal lobe origin
n1=en:retardation | n2=en:ictal eeg showed partial seizures with frontal lobe origin | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ictal eeg shows diffuse slow delta and theta activity
n1=en:retardation | n2=en:ictal eeg shows diffuse slow delta and theta activity | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ictal eeg shows focal onset in central, parietal, or temporal regions
n1=en:retardation | n2=en:ictal eeg shows focal onset in central, parietal, or temporal regions | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ictal eeg shows focal onset, often posterior region of brain
n1=en:retardation | n2=en:ictal eeg shows focal onset, often posterior region of brain | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ictal eeg shows focal, temporal, unilateral, rhythmic slow wave activity of high amplitude
n1=en:retardation | n2=en:ictal eeg shows focal, temporal, unilateral, rhythmic slow wave activity of high amplitude | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ictal eeg with bisynchronous spike waves
n1=en:retardation | n2=en:ictal eeg with bisynchronous spike waves | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:identity problem
n1=en:retardation | n2=en:identity problem | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:idiopathic generalized epilepsy in childhood (homozygous patient)
n1=en:retardation | n2=en:idiopathic generalized epilepsy in childhood (homozygous patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:idiopathic torsion dystonia
n1=en:retardation | n2=en:idiopathic torsion dystonia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:idiot
n1=en:retardation | n2=en:idiot | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:illegible handwriting
n1=en:retardation | n2=en:illegible handwriting | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:imaging shows noncalcified subependymal periventricular heterotopic nodules of gray matter
n1=en:retardation | n2=en:imaging shows noncalcified subependymal periventricular heterotopic nodules of gray matter | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:imaging shows signal abnormalities in basal ganglia
n1=en:retardation | n2=en:imaging shows signal abnormalities in basal ganglia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:imbalance
n1=en:retardation | n2=en:imbalance | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:imbecility
n1=en:retardation | n2=en:imbecility | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:immature brain with no gyral development
n1=en:retardation | n2=en:immature brain with no gyral development | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:immature myelination
n1=en:retardation | n2=en:immature myelination | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:immobile
n1=en:retardation | n2=en:immobile | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:immunodeficiency-centromeric instability-facial anomalies syndrome 2
n1=en:retardation | n2=en:immunodeficiency-centromeric instability-facial anomalies syndrome 2 | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:impaired ambulation due to muscle weakness
n1=en:retardation | n2=en:impaired ambulation due to muscle weakness | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:impaired balance
n1=en:retardation | n2=en:impaired balance | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:impaired balance (2 patients)
n1=en:retardation | n2=en:impaired balance (2 patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:impaired cognition (in some patients)
n1=en:retardation | n2=en:impaired cognition (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:impaired executive function (in some patients)
n1=en:retardation | n2=en:impaired executive function (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:impaired expression of language
n1=en:retardation | n2=en:impaired expression of language | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:impaired expressive speech
n1=en:retardation | n2=en:impaired expressive speech | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:impaired fine motor skills
n1=en:retardation | n2=en:impaired fine motor skills | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:impaired gait due to peripheral neuropathy
n1=en:retardation | n2=en:impaired gait due to peripheral neuropathy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:impaired horizontal smooth pursuit
n1=en:retardation | n2=en:impaired horizontal smooth pursuit | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:impaired insight
n1=en:retardation | n2=en:impaired insight | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:impaired language development
n1=en:retardation | n2=en:impaired language development | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:impaired long-term verbal memory
n1=en:retardation | n2=en:impaired long-term verbal memory | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:impaired motor control, mild
n1=en:retardation | n2=en:impaired motor control, mild | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:impaired processing of language
n1=en:retardation | n2=en:impaired processing of language | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:impaired proprioception
n1=en:retardation | n2=en:impaired proprioception | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:impaired psychomotor development
n1=en:retardation | n2=en:impaired psychomotor development | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:impaired tandem gait
n1=en:retardation | n2=en:impaired tandem gait | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:impaired use of nonverbal behaviors, such as eye-to-eye gaze, facial expression, body posture, and gestures
n1=en:retardation | n2=en:impaired use of nonverbal behaviors, such as eye-to-eye gaze, facial expression, body posture, and gestures | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:impaired vertical visual pursuit
n1=en:retardation | n2=en:impaired vertical visual pursuit | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:impaired vibration sensation at ankles
n1=en:retardation | n2=en:impaired vibration sensation at ankles | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:impaired vibration sensation in the lower limbs
n1=en:retardation | n2=en:impaired vibration sensation in the lower limbs | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:impaired visuospatial skills
n1=en:retardation | n2=en:impaired visuospatial skills | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:impaired voluntary movement
n1=en:retardation | n2=en:impaired voluntary movement | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:impaired walking ability (in some patients)
n1=en:retardation | n2=en:impaired walking ability (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:impairment of balance
n1=en:retardation | n2=en:impairment of balance | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:impairment of gross and fine motor coordination
n1=en:retardation | n2=en:impairment of gross and fine motor coordination | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:imperforate anus
n1=en:retardation | n2=en:imperforate anus | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:impetigo
n1=en:retardation | n2=en:impetigo | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:impulse control disorder nec (disorder) in snomedct_us_2016_03_01
n1=en:retardation | n2=en:impulse control disorder nec (disorder) in snomedct_us_2016_03_01 | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:impulse-control disorder
n1=en:retardation | n2=en:impulse-control disorder | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:inability to communicate
n1=en:retardation | n2=en:inability to communicate | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:inability to generate syntactic grammar rules (i.e., tense, gender, number)
n1=en:retardation | n2=en:inability to generate syntactic grammar rules (i.e., tense, gender, number) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:inability to hold head
n1=en:retardation | n2=en:inability to hold head | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:inability to hold head up
n1=en:retardation | n2=en:inability to hold head up | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:inability to hold neck up ('limber neck') onset at 6 months
n1=en:retardation | n2=en:inability to hold neck up ('limber neck') onset at 6 months | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:inability to reach
n1=en:retardation | n2=en:inability to reach | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:inability to run
n1=en:retardation | n2=en:inability to run | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:inability to run (in some patients)
n1=en:retardation | n2=en:inability to run (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:inability to sit
n1=en:retardation | n2=en:inability to sit | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:inability to sit or control head
n1=en:retardation | n2=en:inability to sit or control head | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:inability to sit or stand independently
n1=en:retardation | n2=en:inability to sit or stand independently | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:inability to sit or walk independently
n1=en:retardation | n2=en:inability to sit or walk independently | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:inability to stand on toes
n1=en:retardation | n2=en:inability to stand on toes | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:inability to stand without assistance
n1=en:retardation | n2=en:inability to stand without assistance | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:inability to walk independently
n1=en:retardation | n2=en:inability to walk independently | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:inability to walk unaided
n1=en:retardation | n2=en:inability to walk unaided | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:inability to walk unsupported
n1=en:retardation | n2=en:inability to walk unsupported | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:inarticulate speech delayed gross motor skills
n1=en:retardation | n2=en:inarticulate speech delayed gross motor skills | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:incomplete anencephaly, hemicrania
n1=en:retardation | n2=en:incomplete anencephaly, hemicrania | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:incomplete myelination
n1=en:retardation | n2=en:incomplete myelination | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:incomprehensible speech
n1=en:retardation | n2=en:incomprehensible speech | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:incontinentia pigmenti, familial male-lethal type
n1=en:retardation | n2=en:incontinentia pigmenti, familial male-lethal type | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:incoordination of the hands
n1=en:retardation | n2=en:incoordination of the hands | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:incoordination of trunk and limbs
n1=en:retardation | n2=en:incoordination of trunk and limbs | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:increase in blood pressure
n1=en:retardation | n2=en:increase in blood pressure | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:increased activity period
n1=en:retardation | n2=en:increased activity period | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:increased cerebral lactate
n1=en:retardation | n2=en:increased cerebral lactate | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:increased csf lactate
n1=en:retardation | n2=en:increased csf lactate | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:increased csf protein
n1=en:retardation | n2=en:increased csf protein | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:increased csf protein with normal cell count
n1=en:retardation | n2=en:increased csf protein with normal cell count | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:increased deep tendon reflexes (if left untreated)
n1=en:retardation | n2=en:increased deep tendon reflexes (if left untreated) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:increased falls
n1=en:retardation | n2=en:increased falls | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:increased intracranial pressure preoperatively (in some patients)
n1=en:retardation | n2=en:increased intracranial pressure preoperatively (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:increased iron deposition in the basal ganglia
n1=en:retardation | n2=en:increased iron deposition in the basal ganglia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:increased iron deposition in the basal ganglia (40%)
n1=en:retardation | n2=en:increased iron deposition in the basal ganglia (40%) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:increased lactate in the brain
n1=en:retardation | n2=en:increased lactate in the brain | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:increased muscle tone in the lower limbs
n1=en:retardation | n2=en:increased muscle tone in the lower limbs | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:increased neurologic sequelae of infections (rare)
n1=en:retardation | n2=en:increased neurologic sequelae of infections (rare) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:increased risk of seizures in childhood or adulthood (11-16%)
n1=en:retardation | n2=en:increased risk of seizures in childhood or adulthood (11-16%) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:increased signal intensity on t(2)-weighted scans in the periventricular and centrum ovale area
n1=en:retardation | n2=en:increased signal intensity on t(2)-weighted scans in the periventricular and centrum ovale area | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:increased startle response
n1=en:retardation | n2=en:increased startle response | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:increased subdural space around frontal lobes
n1=en:retardation | n2=en:increased subdural space around frontal lobes | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:increased t2 signal intensities in the middle cerebellar peduncles
n1=en:retardation | n2=en:increased t2 signal intensities in the middle cerebellar peduncles | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:increased tone in the upper limbs (occur later)
n1=en:retardation | n2=en:increased tone in the upper limbs (occur later) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:increased white matter abnormalities on t2 signalling (in type iib)
n1=en:retardation | n2=en:increased white matter abnormalities on t2 signalling (in type iib) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:independent walking never achieved
n1=en:retardation | n2=en:independent walking never achieved | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:indication for modification of patient status
n1=en:retardation | n2=en:indication for modification of patient status | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:individuals can stand or walk with support by 4 to 6 years of age
n1=en:retardation | n2=en:individuals can stand or walk with support by 4 to 6 years of age | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:individuals require less sleep in a 24-hour period compared to age-matched controls
n1=en:retardation | n2=en:individuals require less sleep in a 24-hour period compared to age-matched controls | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:induced abortion finding
n1=en:retardation | n2=en:induced abortion finding | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:infantile encephalopathy
n1=en:retardation | n2=en:infantile encephalopathy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:infantile encephalopathy, progressive
n1=en:retardation | n2=en:infantile encephalopathy, progressive | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:infantile hemiplegias
n1=en:retardation | n2=en:infantile hemiplegias | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:infantile irritability (if left untreated)
n1=en:retardation | n2=en:infantile irritability (if left untreated) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:infantile muscular hypotonia
n1=en:retardation | n2=en:infantile muscular hypotonia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:infantile neuroaxonal dystrophy
n1=en:retardation | n2=en:infantile neuroaxonal dystrophy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:infantile nystagmus
n1=en:retardation | n2=en:infantile nystagmus | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:infantile seizures
n1=en:retardation | n2=en:infantile seizures | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:infantile seizures (approximately 80% of patients)
n1=en:retardation | n2=en:infantile seizures (approximately 80% of patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:infantile seizures, afebrile, with no neurologic sequelae (in 40% of patients)
n1=en:retardation | n2=en:infantile seizures, afebrile, with no neurologic sequelae (in 40% of patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:infantile spasm
n1=en:retardation | n2=en:infantile spasm | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:infantilism
n1=en:retardation | n2=en:infantilism | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:infarction
n1=en:retardation | n2=en:infarction | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:infections of musculoskeletal system
n1=en:retardation | n2=en:infections of musculoskeletal system | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:infectious conjunctivitis
n1=en:retardation | n2=en:infectious conjunctivitis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:infectious diarrhea/dysentery
n1=en:retardation | n2=en:infectious diarrhea/dysentery | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:infectious disease circulatory system
n1=en:retardation | n2=en:infectious disease circulatory system | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:infectious mononucleosis
n1=en:retardation | n2=en:infectious mononucleosis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:inferior olivary nuclei show fetal pattern
n1=en:retardation | n2=en:inferior olivary nuclei show fetal pattern | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:inferior vermis hypoplasia
n1=en:retardation | n2=en:inferior vermis hypoplasia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:inflexible adherence to routines or rituals
n1=en:retardation | n2=en:inflexible adherence to routines or rituals | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:influenza (proven) without pneumonia
n1=en:retardation | n2=en:influenza (proven) without pneumonia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:infrequent generalized seizures
n1=en:retardation | n2=en:infrequent generalized seizures | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ingrown toenail/other disease of nail
n1=en:retardation | n2=en:ingrown toenail/other disease of nail | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:inguinal hernia
n1=en:retardation | n2=en:inguinal hernia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:inhibition/loss sexual fulfillment
n1=en:retardation | n2=en:inhibition/loss sexual fulfillment | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:initial hypotonia, followed by spasticity
n1=en:retardation | n2=en:initial hypotonia, followed by spasticity | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:initial normal development
n1=en:retardation | n2=en:initial normal development | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:injuries complicating pregnancy
n1=en:retardation | n2=en:injuries complicating pregnancy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:insomnia
n1=en:retardation | n2=en:insomnia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:insomnia adverse event
n1=en:retardation | n2=en:insomnia adverse event | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:insomnia related to...[indicate the axis i or axis ii disorder]
n1=en:retardation | n2=en:insomnia related to...[indicate the axis i or axis ii disorder] | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:insomnia, refractory
n1=en:retardation | n2=en:insomnia, refractory | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:insulin-like growth factor i deficiency
n1=en:retardation | n2=en:insulin-like growth factor i deficiency | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:intellect high (in some patients)
n1=en:retardation | n2=en:intellect high (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:intellectual delay
n1=en:retardation | n2=en:intellectual delay | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:intellectual development
n1=en:retardation | n2=en:intellectual development | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:intellectual disabilities (in 1 family)
n1=en:retardation | n2=en:intellectual disabilities (in 1 family) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:intellectual disability (in 1 ashkenazi patient)
n1=en:retardation | n2=en:intellectual disability (in 1 ashkenazi patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:intellectual disability (in most patients)
n1=en:retardation | n2=en:intellectual disability (in most patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:intellectual disability (in some patients)
n1=en:retardation | n2=en:intellectual disability (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:intellectual disability, mild (1 patient)
n1=en:retardation | n2=en:intellectual disability, mild (1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:intellectual disability, mild (in some patients)
n1=en:retardation | n2=en:intellectual disability, mild (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:intellectual disability, mild (uncommon)
n1=en:retardation | n2=en:intellectual disability, mild (uncommon) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:intellectual disability, mild to moderate
n1=en:retardation | n2=en:intellectual disability, mild to moderate | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:intellectual disability, mild to moderate (in homozygotes)
n1=en:retardation | n2=en:intellectual disability, mild to moderate (in homozygotes) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:intellectual disability, mild to severe
n1=en:retardation | n2=en:intellectual disability, mild to severe | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:intellectual disability, moderate (in some patients)
n1=en:retardation | n2=en:intellectual disability, moderate (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:intellectual disability, moderate to severe
n1=en:retardation | n2=en:intellectual disability, moderate to severe | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:intellectual disability, progressive
n1=en:retardation | n2=en:intellectual disability, progressive | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:intellectual function may be high in milder cases
n1=en:retardation | n2=en:intellectual function may be high in milder cases | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:intellectual impairment (rare)
n1=en:retardation | n2=en:intellectual impairment (rare) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:intellectual impairment, mild
n1=en:retardation | n2=en:intellectual impairment, mild | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:intellectual impairment, mild (in some patients)
n1=en:retardation | n2=en:intellectual impairment, mild (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:intelligence
n1=en:retardation | n2=en:intelligence | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:intelligence and ability
n1=en:retardation | n2=en:intelligence and ability | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:intensive care psychiatric disorder
n1=en:retardation | n2=en:intensive care psychiatric disorder | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:intention tremor (1 patient)
n1=en:retardation | n2=en:intention tremor (1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:intention tremor (in some patients)
n1=en:retardation | n2=en:intention tremor (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:intention tremor in those who survive
n1=en:retardation | n2=en:intention tremor in those who survive | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:intentional trauma
n1=en:retardation | n2=en:intentional trauma | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:interhemispheric cysts
n1=en:retardation | n2=en:interhemispheric cysts | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:interhemispheric lipoma
n1=en:retardation | n2=en:interhemispheric lipoma | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:interictal ataxia may occur later in disease course
n1=en:retardation | n2=en:interictal ataxia may occur later in disease course | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:interictal downbeat nystagmus
n1=en:retardation | n2=en:interictal downbeat nystagmus | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:interictal dystonia may occur later in disease course
n1=en:retardation | n2=en:interictal dystonia may occur later in disease course | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:interictal eeg is usually normal
n1=en:retardation | n2=en:interictal eeg is usually normal | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:interictal eeg may be normal or abnormal
n1=en:retardation | n2=en:interictal eeg may be normal or abnormal | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:interictal eeg may show nonspecific changes in 15 to 20%
n1=en:retardation | n2=en:interictal eeg may show nonspecific changes in 15 to 20% | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:interictal eeg shows 3-4 hz general spike-wave complexes
n1=en:retardation | n2=en:interictal eeg shows 3-4 hz general spike-wave complexes | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:interictal neurologic impairment
n1=en:retardation | n2=en:interictal neurologic impairment | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:interictal periods of normal health
n1=en:retardation | n2=en:interictal periods of normal health | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:intermittent episodes associated with lethargy, vomiting
n1=en:retardation | n2=en:intermittent episodes associated with lethargy, vomiting | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:intermittent migraine headaches
n1=en:retardation | n2=en:intermittent migraine headaches | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:intermittent wheelchair dependence (stage 3)
n1=en:retardation | n2=en:intermittent wheelchair dependence (stage 3) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:intermittent, transient episodes of worsening of ataxia
n1=en:retardation | n2=en:intermittent, transient episodes of worsening of ataxia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:interosseus muscle atrophy
n1=en:retardation | n2=en:interosseus muscle atrophy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:interventricular cysts
n1=en:retardation | n2=en:interventricular cysts | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:intestinal malrotation
n1=en:retardation | n2=en:intestinal malrotation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:intracellular accumulation of material resulting in curvilinear profiles on ultrastructural analysis
n1=en:retardation | n2=en:intracellular accumulation of material resulting in curvilinear profiles on ultrastructural analysis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:intracellular accumulation of material resulting in fingerprint profiles on ultrastructural analysis
n1=en:retardation | n2=en:intracellular accumulation of material resulting in fingerprint profiles on ultrastructural analysis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:intracellular accumulation of material resulting in rectilinear profiles on ultrastructural analysis
n1=en:retardation | n2=en:intracellular accumulation of material resulting in rectilinear profiles on ultrastructural analysis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:intracellular lewy bodies
n1=en:retardation | n2=en:intracellular lewy bodies | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:intracellular pas-positive polyglucosan inclusion bodies ('lafora' bodies)
n1=en:retardation | n2=en:intracellular pas-positive polyglucosan inclusion bodies ('lafora' bodies) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:intracerebral calcifications (in some patients)
n1=en:retardation | n2=en:intracerebral calcifications (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:intracerebral cysts (in some patients)
n1=en:retardation | n2=en:intracerebral cysts (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:intracerebral periventricular calcifications
n1=en:retardation | n2=en:intracerebral periventricular calcifications | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:intracranial bleeding (1 patient)
n1=en:retardation | n2=en:intracranial bleeding (1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:intracranial calcification affecting the basal ganglia (in some patients)
n1=en:retardation | n2=en:intracranial calcification affecting the basal ganglia (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:intracranial calcification by x-ray or ct
n1=en:retardation | n2=en:intracranial calcification by x-ray or ct | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:intracranial calcifications (1 patient)
n1=en:retardation | n2=en:intracranial calcifications (1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:intracranial calcifications (in some patients)
n1=en:retardation | n2=en:intracranial calcifications (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:intracranial calcifications in the anterior mesial temporal lobes
n1=en:retardation | n2=en:intracranial calcifications in the anterior mesial temporal lobes | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:intracranial calcifications, band-like, particularly periventricular and in the basal ganglia and thalamus
n1=en:retardation | n2=en:intracranial calcifications, band-like, particularly periventricular and in the basal ganglia and thalamus | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:intracranial cysts
n1=en:retardation | n2=en:intracranial cysts | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:intracranial hemorrhage
n1=en:retardation | n2=en:intracranial hemorrhage | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:intracranial hypertension
n1=en:retardation | n2=en:intracranial hypertension | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:intracranial lipoma (cerebello-pontine)
n1=en:retardation | n2=en:intracranial lipoma (cerebello-pontine) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:intracranial thin-walled sinusoidal vessel (cavernous) malformations
n1=en:retardation | n2=en:intracranial thin-walled sinusoidal vessel (cavernous) malformations | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:intractable epilepsy
n1=en:retardation | n2=en:intractable epilepsy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:intraneuronal inclusions
n1=en:retardation | n2=en:intraneuronal inclusions | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:intraparenchymal brain hemorrhage, multifocal
n1=en:retardation | n2=en:intraparenchymal brain hemorrhage, multifocal | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:intraspinal neoplasm
n1=en:retardation | n2=en:intraspinal neoplasm | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:invalidism
n1=en:retardation | n2=en:invalidism | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:involuntary dystonic or choreiform movements
n1=en:retardation | n2=en:involuntary dystonic or choreiform movements | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:involuntary jerking movements
n1=en:retardation | n2=en:involuntary jerking movements | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:involuntary movement and habit disorder
n1=en:retardation | n2=en:involuntary movement and habit disorder | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:involuntary movements
n1=en:retardation | n2=en:involuntary movements | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:involuntary movements may be precipitated by exertion or anxiety
n1=en:retardation | n2=en:involuntary movements may be precipitated by exertion or anxiety | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:involuntary movements of extremities, neck, trunk, and/or face
n1=en:retardation | n2=en:involuntary movements of extremities, neck, trunk, and/or face | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:involuntary movements, asymmetric
n1=en:retardation | n2=en:involuntary movements, asymmetric | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:involuntary repetitive movements
n1=en:retardation | n2=en:involuntary repetitive movements | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:involuntary rhythmic myoclonic movements ('tremor') of the distal extremities, usually fingers
n1=en:retardation | n2=en:involuntary rhythmic myoclonic movements ('tremor') of the distal extremities, usually fingers | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:involuntary rhythmic myoclonic movements ('tremor'), upper extremities
n1=en:retardation | n2=en:involuntary rhythmic myoclonic movements ('tremor'), upper extremities | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:involuntary writhing movements
n1=en:retardation | n2=en:involuntary writhing movements | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ipsilateral brain hypoplasia
n1=en:retardation | n2=en:ipsilateral brain hypoplasia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ipsilateral cranial nerve hypoplasia
n1=en:retardation | n2=en:ipsilateral cranial nerve hypoplasia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:iq 85-115 (female)
n1=en:retardation | n2=en:iq 85-115 (female) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:iron accumulation in the basal ganglia seen on mri
n1=en:retardation | n2=en:iron accumulation in the basal ganglia seen on mri | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:iron accumulation in the globus pallidus and substantia nigra seen on mri
n1=en:retardation | n2=en:iron accumulation in the globus pallidus and substantia nigra seen on mri | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:iron deposition in pallidal nuclei
n1=en:retardation | n2=en:iron deposition in pallidal nuclei | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:iron deposition in the basal ganglia (in some patients)
n1=en:retardation | n2=en:iron deposition in the basal ganglia (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:iron deposition in the globus pallidus (variable)
n1=en:retardation | n2=en:iron deposition in the globus pallidus (variable) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:iron deposition in the globus pallidus and substantia nigra seen on mri
n1=en:retardation | n2=en:iron deposition in the globus pallidus and substantia nigra seen on mri | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:iron deposits in the globus pallidus, caudate, and substantia nigra
n1=en:retardation | n2=en:iron deposits in the globus pallidus, caudate, and substantia nigra | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:iron-containing deposits in various brain regions
n1=en:retardation | n2=en:iron-containing deposits in various brain regions | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:iron-deficiency anemia
n1=en:retardation | n2=en:iron-deficiency anemia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:irregular cortical ribbon
n1=en:retardation | n2=en:irregular cortical ribbon | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:irregular folding of the cortex
n1=en:retardation | n2=en:irregular folding of the cortex | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:irregular spike and slow waves
n1=en:retardation | n2=en:irregular spike and slow waves | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:irresistible desire to move the legs
n1=en:retardation | n2=en:irresistible desire to move the legs | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:irritable bowel syndrome
n1=en:retardation | n2=en:irritable bowel syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:irritation
n1=en:retardation | n2=en:irritation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ischemic cerebrovascular accident
n1=en:retardation | n2=en:ischemic cerebrovascular accident | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ischemic infarct of brain
n1=en:retardation | n2=en:ischemic infarct of brain | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ischemic infarction (rare)
n1=en:retardation | n2=en:ischemic infarction (rare) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ischemic necrotic lesions
n1=en:retardation | n2=en:ischemic necrotic lesions | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ischemic stroke (in some patients)
n1=en:retardation | n2=en:ischemic stroke (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ischemic stroke in the basal ganglia (rare)
n1=en:retardation | n2=en:ischemic stroke in the basal ganglia (rare) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:isolated absence of pain sensation
n1=en:retardation | n2=en:isolated absence of pain sensation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:isolated focal dystonia may occur
n1=en:retardation | n2=en:isolated focal dystonia may occur | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:jacksonian seizure
n1=en:retardation | n2=en:jacksonian seizure | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:jacobsen syndrome
n1=en:retardation | n2=en:jacobsen syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:jerk-locked premyoclonus spikes
n1=en:retardation | n2=en:jerk-locked premyoclonus spikes | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:jerking may be unidirectional, periodically alternating, or mixed pendular and jerk-like
n1=en:retardation | n2=en:jerking may be unidirectional, periodically alternating, or mixed pendular and jerk-like | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:jerking movements
n1=en:retardation | n2=en:jerking movements | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:jerky head movements
n1=en:retardation | n2=en:jerky head movements | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:jerky limb movements
n1=en:retardation | n2=en:jerky limb movements | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:jerky movements in infancy
n1=en:retardation | n2=en:jerky movements in infancy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:johanson-blizzard syndrome
n1=en:retardation | n2=en:johanson-blizzard syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:joubert syndrome
n1=en:retardation | n2=en:joubert syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:joubert syndrome 15
n1=en:retardation | n2=en:joubert syndrome 15 | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:joubert syndrome 18
n1=en:retardation | n2=en:joubert syndrome 18 | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:joubert syndrome 2
n1=en:retardation | n2=en:joubert syndrome 2 | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:joubert syndrome 21
n1=en:retardation | n2=en:joubert syndrome 21 | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:joubert syndrome 3
n1=en:retardation | n2=en:joubert syndrome 3 | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:joubert syndrome 5
n1=en:retardation | n2=en:joubert syndrome 5 | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:joubert syndrome 6
n1=en:retardation | n2=en:joubert syndrome 6 | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:kabuki syndrome
n1=en:retardation | n2=en:kabuki syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:kaufman oculocerebrofacial syndrome
n1=en:retardation | n2=en:kaufman oculocerebrofacial syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:kbg syndrome
n1=en:retardation | n2=en:kbg syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:kearns-sayre syndrome (530000), in a subset of patients
n1=en:retardation | n2=en:kearns-sayre syndrome (530000), in a subset of patients | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:kernicterus
n1=en:retardation | n2=en:kernicterus | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:klinefelter syndrome
n1=en:retardation | n2=en:klinefelter syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:klippel-trenaunay-weber syndrome
n1=en:retardation | n2=en:klippel-trenaunay-weber syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:knee and ankle clonus
n1=en:retardation | n2=en:knee and ankle clonus | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:known or suspected fetal abnormality affecting management of mother
n1=en:retardation | n2=en:known or suspected fetal abnormality affecting management of mother | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:kuzniecky syndrome
n1=en:retardation | n2=en:kuzniecky syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lack of bunina bodies
n1=en:retardation | n2=en:lack of bunina bodies | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lack of communication
n1=en:retardation | n2=en:lack of communication | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lack of development
n1=en:retardation | n2=en:lack of development | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lack of developmental development
n1=en:retardation | n2=en:lack of developmental development | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lack of developmental milestones
n1=en:retardation | n2=en:lack of developmental milestones | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lack of ependymal cells
n1=en:retardation | n2=en:lack of ependymal cells | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lack of expressive speech
n1=en:retardation | n2=en:lack of expressive speech | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lack of head control
n1=en:retardation | n2=en:lack of head control | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lack of head or postural control (in severe cases)
n1=en:retardation | n2=en:lack of head or postural control (in severe cases) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lack of independent ambulation
n1=en:retardation | n2=en:lack of independent ambulation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lack of independent ambulation (1 patient)
n1=en:retardation | n2=en:lack of independent ambulation (1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lack of independent sitting or walking
n1=en:retardation | n2=en:lack of independent sitting or walking | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lack of independent walking (in some patients)
n1=en:retardation | n2=en:lack of independent walking (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lack of inflammatory infiltrate
n1=en:retardation | n2=en:lack of inflammatory infiltrate | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lack of motor development
n1=en:retardation | n2=en:lack of motor development | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lack of motor development (wws)
n1=en:retardation | n2=en:lack of motor development (wws) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lack of motor milestones
n1=en:retardation | n2=en:lack of motor milestones | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lack of neurologic development
n1=en:retardation | n2=en:lack of neurologic development | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lack of peer relationships
n1=en:retardation | n2=en:lack of peer relationships | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lack of psychomotor development (1 patient)
n1=en:retardation | n2=en:lack of psychomotor development (1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lack of psychomotor development (severe connatal form)
n1=en:retardation | n2=en:lack of psychomotor development (severe connatal form) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lack of skein-like inclusions
n1=en:retardation | n2=en:lack of skein-like inclusions | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lack of speech (in severe cases)
n1=en:retardation | n2=en:lack of speech (in severe cases) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lack of speech acquisition
n1=en:retardation | n2=en:lack of speech acquisition | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lack of speech development
n1=en:retardation | n2=en:lack of speech development | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lack of speech development (some patients)
n1=en:retardation | n2=en:lack of speech development (some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lack of speech or only a few words
n1=en:retardation | n2=en:lack of speech or only a few words | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lack of speech or poor speech
n1=en:retardation | n2=en:lack of speech or poor speech | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lack of spontaneous movement
n1=en:retardation | n2=en:lack of spontaneous movement | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lack of spontaneous play
n1=en:retardation | n2=en:lack of spontaneous play | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lack of upper motor neuron signs
n1=en:retardation | n2=en:lack of upper motor neuron signs | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lack of verbal communication
n1=en:retardation | n2=en:lack of verbal communication | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lack of visual attention
n1=en:retardation | n2=en:lack of visual attention | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lack of volitional movement
n1=en:retardation | n2=en:lack of volitional movement | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lacunar infarcts develop after age 40 years
n1=en:retardation | n2=en:lacunar infarcts develop after age 40 years | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lacunar infarcts in the deep-brain nuclei, brainstem, internal capsule seen on imaging
n1=en:retardation | n2=en:lacunar infarcts in the deep-brain nuclei, brainstem, internal capsule seen on imaging | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:laminar necrosis
n1=en:retardation | n2=en:laminar necrosis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:language acquisition difficulties (in some patients)
n1=en:retardation | n2=en:language acquisition difficulties (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:language delay
n1=en:retardation | n2=en:language delay | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:language delay (55%)
n1=en:retardation | n2=en:language delay (55%) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:language delay/disorder
n1=en:retardation | n2=en:language delay/disorder | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:language development limited to a few words
n1=en:retardation | n2=en:language development limited to a few words | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:language disorder
n1=en:retardation | n2=en:language disorder | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:language or speech disorder
n1=en:retardation | n2=en:language or speech disorder | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:large basal ganglia
n1=en:retardation | n2=en:large basal ganglia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:large cavum vergae
n1=en:retardation | n2=en:large cavum vergae | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:large cerebellum, progressive
n1=en:retardation | n2=en:large cerebellum, progressive | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:large sella turcica
n1=en:retardation | n2=en:large sella turcica | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:large subcortical cysts in frontal and temporal lobes
n1=en:retardation | n2=en:large subcortical cysts in frontal and temporal lobes | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:larnygeotracheoesophageal cleft
n1=en:retardation | n2=en:larnygeotracheoesophageal cleft | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:larsen syndrome
n1=en:retardation | n2=en:larsen syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:laryngeal atresia
n1=en:retardation | n2=en:laryngeal atresia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:laryngocele
n1=en:retardation | n2=en:laryngocele | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:late ambulation
n1=en:retardation | n2=en:late ambulation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:late diaphragmatic involvement
n1=en:retardation | n2=en:late diaphragmatic involvement | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:late effect of trauma
n1=en:retardation | n2=en:late effect of trauma | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:late-onset spinocerebellar degeneration
n1=en:retardation | n2=en:late-onset spinocerebellar degeneration | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lateral corticospinal tracts show atrophy, pallor, and degeneration
n1=en:retardation | n2=en:lateral corticospinal tracts show atrophy, pallor, and degeneration | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lateral epicondylitis
n1=en:retardation | n2=en:lateral epicondylitis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lathosterolosis
n1=en:retardation | n2=en:lathosterolosis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:laurence-moon syndrome
n1=en:retardation | n2=en:laurence-moon syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:learning and developmental delay (in some patients)
n1=en:retardation | n2=en:learning and developmental delay (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:learning difficulties
n1=en:retardation | n2=en:learning difficulties | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:learning difficulties (in 1 patient)
n1=en:retardation | n2=en:learning difficulties (in 1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:learning difficulties (in some patients)
n1=en:retardation | n2=en:learning difficulties (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:learning difficulties (less common)
n1=en:retardation | n2=en:learning difficulties (less common) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:learning difficulties (seen in recessive form)
n1=en:retardation | n2=en:learning difficulties (seen in recessive form) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:learning difficulties in affected females
n1=en:retardation | n2=en:learning difficulties in affected females | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:learning difficulties, mild (1 family)
n1=en:retardation | n2=en:learning difficulties, mild (1 family) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:learning disabilities
n1=en:retardation | n2=en:learning disabilities | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:learning disabilities (1 family)
n1=en:retardation | n2=en:learning disabilities (1 family) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:learning disabilities (30%)
n1=en:retardation | n2=en:learning disabilities (30%) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:learning disabilities (in females)
n1=en:retardation | n2=en:learning disabilities (in females) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:learning disabilities (in some patients)
n1=en:retardation | n2=en:learning disabilities (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:learning disabilities (in some)
n1=en:retardation | n2=en:learning disabilities (in some) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:learning disabilities (major)
n1=en:retardation | n2=en:learning disabilities (major) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:learning disability (90% patients)
n1=en:retardation | n2=en:learning disability (90% patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:learning disability (early in life)
n1=en:retardation | n2=en:learning disability (early in life) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:learning disorder
n1=en:retardation | n2=en:learning disorder | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:learning problems
n1=en:retardation | n2=en:learning problems | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:leber optic atrophy and dystonia
n1=en:retardation | n2=en:leber optic atrophy and dystonia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:leg cramp
n1=en:retardation | n2=en:leg cramp | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:leg pain
n1=en:retardation | n2=en:leg pain | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:leg stiffness
n1=en:retardation | n2=en:leg stiffness | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:leigh disease
n1=en:retardation | n2=en:leigh disease | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:leigh syndrome (245000), in a subset of patients
n1=en:retardation | n2=en:leigh syndrome (245000), in a subset of patients | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:leigh syndrome (in some patients)
n1=en:retardation | n2=en:leigh syndrome (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:leptomeningeal melanocytosis (in some patients)
n1=en:retardation | n2=en:leptomeningeal melanocytosis (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:leptomeningeal thickening
n1=en:retardation | n2=en:leptomeningeal thickening | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lesch-nyhan syndrome
n1=en:retardation | n2=en:lesch-nyhan syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lesions are symmetrical
n1=en:retardation | n2=en:lesions are symmetrical | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lesions characterized by demyelination, necrosis, gliosis, spongiosis, and capillary proliferation
n1=en:retardation | n2=en:lesions characterized by demyelination, necrosis, gliosis, spongiosis, and capillary proliferation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lesions in basal ganglia, brainstem, cerebellum, thalamus, spinal cord
n1=en:retardation | n2=en:lesions in basal ganglia, brainstem, cerebellum, thalamus, spinal cord | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lesions in basal ganglia, brainstem, cerebellum, thalamus, spinal cord characterized by demyelination, necrosis, gliosis, spongiosis, and capillary proliferation
n1=en:retardation | n2=en:lesions in basal ganglia, brainstem, cerebellum, thalamus, spinal cord characterized by demyelination, necrosis, gliosis, spongiosis, and capillary proliferation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lesions in the anterior pituitary (less common)
n1=en:retardation | n2=en:lesions in the anterior pituitary (less common) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lesions in the basal ganglia
n1=en:retardation | n2=en:lesions in the basal ganglia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lesions in the caudate and putamen
n1=en:retardation | n2=en:lesions in the caudate and putamen | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lesions in the caudate and putamen seen on mri
n1=en:retardation | n2=en:lesions in the caudate and putamen seen on mri | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lesions in the internal capsule after age 40 years
n1=en:retardation | n2=en:lesions in the internal capsule after age 40 years | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lesions show signal increase on t2- and signal decrease on t1-weighted images
n1=en:retardation | n2=en:lesions show signal increase on t2- and signal decrease on t1-weighted images | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lethargy
n1=en:retardation | n2=en:lethargy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lethargy associated with hypoglycemia
n1=en:retardation | n2=en:lethargy associated with hypoglycemia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lethargy, neonatal
n1=en:retardation | n2=en:lethargy, neonatal | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:leukemia
n1=en:retardation | n2=en:leukemia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:leukoaraiosis
n1=en:retardation | n2=en:leukoaraiosis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:leukodystrophy
n1=en:retardation | n2=en:leukodystrophy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:leukodystrophy (in 1 of 2 patients)
n1=en:retardation | n2=en:leukodystrophy (in 1 of 2 patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:leukodystrophy (in some patients)
n1=en:retardation | n2=en:leukodystrophy (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:leukodystrophy and white matter changes, which improve with age
n1=en:retardation | n2=en:leukodystrophy and white matter changes, which improve with age | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:leukodystrophy, demyelinating
n1=en:retardation | n2=en:leukodystrophy, demyelinating | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:leukodystrophy, hypomyelinating
n1=en:retardation | n2=en:leukodystrophy, hypomyelinating | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:leukoencephalopathy
n1=en:retardation | n2=en:leukoencephalopathy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:leukoencephalopathy in the frontal and parietal lobes (later)
n1=en:retardation | n2=en:leukoencephalopathy in the frontal and parietal lobes (later) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:leukoencephalopathy in the periventricular and deep white matter and brainstem, cerebellum, and spinal cord tracts
n1=en:retardation | n2=en:leukoencephalopathy in the periventricular and deep white matter and brainstem, cerebellum, and spinal cord tracts | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:leukoencephalopathy on ct and mri
n1=en:retardation | n2=en:leukoencephalopathy on ct and mri | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:leukoencephalopathy with metaphyseal chondrodysplasia
n1=en:retardation | n2=en:leukoencephalopathy with metaphyseal chondrodysplasia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:leukoencephalopathy, severe
n1=en:retardation | n2=en:leukoencephalopathy, severe | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:leukomalacia (rare)
n1=en:retardation | n2=en:leukomalacia (rare) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lewy bodies
n1=en:retardation | n2=en:lewy bodies | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lewy bodies (not always present)
n1=en:retardation | n2=en:lewy bodies (not always present) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lewy bodies in the substantia nigra
n1=en:retardation | n2=en:lewy bodies in the substantia nigra | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lewy bodies throughout the brain
n1=en:retardation | n2=en:lewy bodies throughout the brain | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:light-induced sneezing
n1=en:retardation | n2=en:light-induced sneezing | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lightheadedness
n1=en:retardation | n2=en:lightheadedness | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:limb ataxia, progressive
n1=en:retardation | n2=en:limb ataxia, progressive | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:limb deformities, congenital
n1=en:retardation | n2=en:limb deformities, congenital | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:limb dysmetria
n1=en:retardation | n2=en:limb dysmetria | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:limb dystonia
n1=en:retardation | n2=en:limb dystonia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:limb dystonia (18%)
n1=en:retardation | n2=en:limb dystonia (18%) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:limb fasciculations
n1=en:retardation | n2=en:limb fasciculations | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:limb hypertonia
n1=en:retardation | n2=en:limb hypertonia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:limb hypertonia (in some patients)
n1=en:retardation | n2=en:limb hypertonia (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:limb incoordination (in some patients)
n1=en:retardation | n2=en:limb incoordination (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:limb muscle stiffness is often asymmetric
n1=en:retardation | n2=en:limb muscle stiffness is often asymmetric | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:limb muscle weakness (distal greater than proximal)
n1=en:retardation | n2=en:limb muscle weakness (distal greater than proximal) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:limb posturing (if left untreated)
n1=en:retardation | n2=en:limb posturing (if left untreated) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:limb spasticity
n1=en:retardation | n2=en:limb spasticity | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:limb-girdle muscular dystrophy type 2p
n1=en:retardation | n2=en:limb-girdle muscular dystrophy type 2p | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:limbic malformations
n1=en:retardation | n2=en:limbic malformations | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:limbic system
n1=en:retardation | n2=en:limbic system | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:limited expressive language
n1=en:retardation | n2=en:limited expressive language | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:limited memory, attention, language
n1=en:retardation | n2=en:limited memory, attention, language | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:limited psychological function
n1=en:retardation | n2=en:limited psychological function | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:limited verbal comprehension
n1=en:retardation | n2=en:limited verbal comprehension | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:limited walking ability
n1=en:retardation | n2=en:limited walking ability | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lingual-facial-buccal dyskinesia
n1=en:retardation | n2=en:lingual-facial-buccal dyskinesia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lipid metabolism disorder
n1=en:retardation | n2=en:lipid metabolism disorder | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lipodystrophy, generalized, with mental retardation, deafness, short stature, and slender bones
n1=en:retardation | n2=en:lipodystrophy, generalized, with mental retardation, deafness, short stature, and slender bones | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lipoidosis
n1=en:retardation | n2=en:lipoidosis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lipoma
n1=en:retardation | n2=en:lipoma | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lipoma, anterior sacral
n1=en:retardation | n2=en:lipoma, anterior sacral | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lipomyelocystoceles
n1=en:retardation | n2=en:lipomyelocystoceles | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lissencephaly
n1=en:retardation | n2=en:lissencephaly | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lissencephaly (anterior to posterior decreasing gradient of severity, more prominent in anterior brain regions)
n1=en:retardation | n2=en:lissencephaly (anterior to posterior decreasing gradient of severity, more prominent in anterior brain regions) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lissencephaly (anterior to posterior increasing gradient of severity and more prominent in posterior brain regions)
n1=en:retardation | n2=en:lissencephaly (anterior to posterior increasing gradient of severity and more prominent in posterior brain regions) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lissencephaly (reported in 1 patient)
n1=en:retardation | n2=en:lissencephaly (reported in 1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lissencephaly, posterior to anterior gradient
n1=en:retardation | n2=en:lissencephaly, posterior to anterior gradient | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lithium induced birth defect
n1=en:retardation | n2=en:lithium induced birth defect | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:little or no speech acquisition
n1=en:retardation | n2=en:little or no speech acquisition | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:little polarity in remaining neurons
n1=en:retardation | n2=en:little polarity in remaining neurons | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:little spontaneous limb movement
n1=en:retardation | n2=en:little spontaneous limb movement | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:little spontaneous movement
n1=en:retardation | n2=en:little spontaneous movement | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lobar dysmorphism
n1=en:retardation | n2=en:lobar dysmorphism | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lobar holoprosencephalies
n1=en:retardation | n2=en:lobar holoprosencephalies | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lobar hpe shows clear interhemispheric fissure and 2 lateral ventricles
n1=en:retardation | n2=en:lobar hpe shows clear interhemispheric fissure and 2 lateral ventricles | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:locomotor delay (early-onset form)
n1=en:retardation | n2=en:locomotor delay (early-onset form) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:long perforating arteries of the brain are affected
n1=en:retardation | n2=en:long perforating arteries of the brain are affected | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:long-tract signs
n1=en:retardation | n2=en:long-tract signs | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:long, thickened cerebellar peduncles
n1=en:retardation | n2=en:long, thickened cerebellar peduncles | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:loss of ability to walk
n1=en:retardation | n2=en:loss of ability to walk | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:loss of ability to walk in first decade
n1=en:retardation | n2=en:loss of ability to walk in first decade | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:loss of ability to walk later
n1=en:retardation | n2=en:loss of ability to walk later | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:loss of ambulation
n1=en:retardation | n2=en:loss of ambulation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:loss of ankle reflexes
n1=en:retardation | n2=en:loss of ankle reflexes | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:loss of anterior horn cells and gliosis in the spinal cord
n1=en:retardation | n2=en:loss of anterior horn cells and gliosis in the spinal cord | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:loss of any acquired abilities in early childhood
n1=en:retardation | n2=en:loss of any acquired abilities in early childhood | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:loss of balance may occur
n1=en:retardation | n2=en:loss of balance may occur | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:loss of cerebellar granular cells
n1=en:retardation | n2=en:loss of cerebellar granular cells | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:loss of cerebellar purkinje cells
n1=en:retardation | n2=en:loss of cerebellar purkinje cells | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:loss of cerebral white matter (in 1 of 3 patients)
n1=en:retardation | n2=en:loss of cerebral white matter (in 1 of 3 patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:loss of consciousness
n1=en:retardation | n2=en:loss of consciousness | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:loss of consciousness (1 patient)
n1=en:retardation | n2=en:loss of consciousness (1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:loss of coordination
n1=en:retardation | n2=en:loss of coordination | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:loss of deep tendon reflexes (later)
n1=en:retardation | n2=en:loss of deep tendon reflexes (later) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:loss of developmental milestones
n1=en:retardation | n2=en:loss of developmental milestones | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:loss of dopaminergic neurons
n1=en:retardation | n2=en:loss of dopaminergic neurons | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:loss of dopaminergic neurons in the substantia nigra
n1=en:retardation | n2=en:loss of dopaminergic neurons in the substantia nigra | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:loss of dorsal root ganglion cells
n1=en:retardation | n2=en:loss of dorsal root ganglion cells | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:loss of executive functions
n1=en:retardation | n2=en:loss of executive functions | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:loss of fine motor skills
n1=en:retardation | n2=en:loss of fine motor skills | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:loss of gait (in some)
n1=en:retardation | n2=en:loss of gait (in some) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:loss of hypocretin (orexin)-secreting neurons in the hypothalamus
n1=en:retardation | n2=en:loss of hypocretin (orexin)-secreting neurons in the hypothalamus | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:loss of independent ambulation
n1=en:retardation | n2=en:loss of independent ambulation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:loss of independent ambulation (in some patients)
n1=en:retardation | n2=en:loss of independent ambulation (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:loss of independent ambulation approximately 30 years after onset
n1=en:retardation | n2=en:loss of independent ambulation approximately 30 years after onset | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:loss of independent ambulation by age 10 years
n1=en:retardation | n2=en:loss of independent ambulation by age 10 years | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:loss of independent ambulation within a few years
n1=en:retardation | n2=en:loss of independent ambulation within a few years | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:loss of language ability
n1=en:retardation | n2=en:loss of language ability | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:loss of lower alpha-motor neurons in the anterior horn of the spinal cord and lower brainstem
n1=en:retardation | n2=en:loss of lower alpha-motor neurons in the anterior horn of the spinal cord and lower brainstem | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:loss of motor functions
n1=en:retardation | n2=en:loss of motor functions | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:loss of motor milestones
n1=en:retardation | n2=en:loss of motor milestones | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:loss of motor neurons in the anterior horn of the spinal cord
n1=en:retardation | n2=en:loss of motor neurons in the anterior horn of the spinal cord | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:loss of motor neurons in the spinal cord
n1=en:retardation | n2=en:loss of motor neurons in the spinal cord | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:loss of motor skills
n1=en:retardation | n2=en:loss of motor skills | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:loss of myelin
n1=en:retardation | n2=en:loss of myelin | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:loss of myelin and oligodendroglia
n1=en:retardation | n2=en:loss of myelin and oligodendroglia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:loss of myelin in the cerebral and cerebellar white matter
n1=en:retardation | n2=en:loss of myelin in the cerebral and cerebellar white matter | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:loss of myelin in the descending lateral spinal cord tracts
n1=en:retardation | n2=en:loss of myelin in the descending lateral spinal cord tracts | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:loss of myelin in the pyramidal tracts
n1=en:retardation | n2=en:loss of myelin in the pyramidal tracts | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:loss of myelinated fibers in spinal cord roots
n1=en:retardation | n2=en:loss of myelinated fibers in spinal cord roots | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:loss of myelinated fibers with regenerative clusters on biopsy
n1=en:retardation | n2=en:loss of myelinated fibers with regenerative clusters on biopsy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:loss of neurons affecting all cortical layers
n1=en:retardation | n2=en:loss of neurons affecting all cortical layers | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:loss of neurons and gliosis in basal ganglia, cranial nerve nuclei, and spinal cord
n1=en:retardation | n2=en:loss of neurons and gliosis in basal ganglia, cranial nerve nuclei, and spinal cord | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:loss of pain and temperature in a cape-like distribution
n1=en:retardation | n2=en:loss of pain and temperature in a cape-like distribution | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:loss of pigmented neurons in the substantia nigra
n1=en:retardation | n2=en:loss of pigmented neurons in the substantia nigra | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:loss of postural tone
n1=en:retardation | n2=en:loss of postural tone | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:loss of primary reflexes
n1=en:retardation | n2=en:loss of primary reflexes | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:loss of purkinje cells
n1=en:retardation | n2=en:loss of purkinje cells | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:loss of purkinje cells in the cerebellar vermis
n1=en:retardation | n2=en:loss of purkinje cells in the cerebellar vermis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:loss of purkinje cells in the cerebellum
n1=en:retardation | n2=en:loss of purkinje cells in the cerebellum | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:loss of purposeful hand movements
n1=en:retardation | n2=en:loss of purposeful hand movements | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:loss of reflexes due to myopathy
n1=en:retardation | n2=en:loss of reflexes due to myopathy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:loss of speech
n1=en:retardation | n2=en:loss of speech | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:loss of speech (1 patient)
n1=en:retardation | n2=en:loss of speech (1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:loss of speech development
n1=en:retardation | n2=en:loss of speech development | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:loss of spontaneous movements
n1=en:retardation | n2=en:loss of spontaneous movements | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:loss of very early milestones
n1=en:retardation | n2=en:loss of very early milestones | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:loss of white matter
n1=en:retardation | n2=en:loss of white matter | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:low apparent diffusion coefficient (adc) values
n1=en:retardation | n2=en:low apparent diffusion coefficient (adc) values | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:low densities in the basal ganglia similar to leigh syndrome (256000)
n1=en:retardation | n2=en:low densities in the basal ganglia similar to leigh syndrome (256000) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:low density white matter on ct scan
n1=en:retardation | n2=en:low density white matter on ct scan | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:low iq
n1=en:retardation | n2=en:low iq | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:low-lying cerebellar tonsils
n1=en:retardation | n2=en:low-lying cerebellar tonsils | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:low-normal intelligence
n1=en:retardation | n2=en:low-normal intelligence | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:low-normal iq
n1=en:retardation | n2=en:low-normal iq | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lower extremity weakness with febrile episodes (rare)
n1=en:retardation | n2=en:lower extremity weakness with febrile episodes (rare) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lower limb atrophy
n1=en:retardation | n2=en:lower limb atrophy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lower limb dystonia
n1=en:retardation | n2=en:lower limb dystonia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lower limb hyperreflexia
n1=en:retardation | n2=en:lower limb hyperreflexia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lower limb hyperreflexia (reported in 1 patient)
n1=en:retardation | n2=en:lower limb hyperreflexia (reported in 1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lower limb hypertonia
n1=en:retardation | n2=en:lower limb hypertonia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lower limb hypotrophy
n1=en:retardation | n2=en:lower limb hypotrophy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lower limb muscle atrophy
n1=en:retardation | n2=en:lower limb muscle atrophy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lower limb muscle weakness (occurs later)
n1=en:retardation | n2=en:lower limb muscle weakness (occurs later) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lower limb spasticity
n1=en:retardation | n2=en:lower limb spasticity | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lower limb spasticity, mild
n1=en:retardation | n2=en:lower limb spasticity, mild | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lower limb weakness, proximal
n1=en:retardation | n2=en:lower limb weakness, proximal | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lower limbs affected before upper limbs
n1=en:retardation | n2=en:lower limbs affected before upper limbs | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lower limbs weakness and atrophy, distal
n1=en:retardation | n2=en:lower limbs weakness and atrophy, distal | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lower motor neuron degeneration
n1=en:retardation | n2=en:lower motor neuron degeneration | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lower motor neuron disease affecting upper and lower limbs
n1=en:retardation | n2=en:lower motor neuron disease affecting upper and lower limbs | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lower motor neuron dysfunction
n1=en:retardation | n2=en:lower motor neuron dysfunction | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lower motor neuron dysfunction involving upper and lower limbs
n1=en:retardation | n2=en:lower motor neuron dysfunction involving upper and lower limbs | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lower motor neuron involvement after long disease duration
n1=en:retardation | n2=en:lower motor neuron involvement after long disease duration | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lower motor neuron involvement, mild, seen on emg (in some patients)
n1=en:retardation | n2=en:lower motor neuron involvement, mild, seen on emg (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lower motor neuron signs, later
n1=en:retardation | n2=en:lower motor neuron signs, later | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lower motor neuron symptoms
n1=en:retardation | n2=en:lower motor neuron symptoms | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lower motor signs
n1=en:retardation | n2=en:lower motor signs | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lumbar disc lesion/radiation
n1=en:retardation | n2=en:lumbar disc lesion/radiation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lumbar paraspinal rigidity causes exaggerated lumbar lordosis
n1=en:retardation | n2=en:lumbar paraspinal rigidity causes exaggerated lumbar lordosis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lumbosacral meningocele
n1=en:retardation | n2=en:lumbosacral meningocele | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lymphatic abnormalities
n1=en:retardation | n2=en:lymphatic abnormalities | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:lymphocytic infiltration of the brain
n1=en:retardation | n2=en:lymphocytic infiltration of the brain | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:macrocephaly (due to dandy-walker malformation)
n1=en:retardation | n2=en:macrocephaly (due to dandy-walker malformation) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:macroencephaly
n1=en:retardation | n2=en:macroencephaly | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:macrosomia obesity macrocephaly ocular abnormalities
n1=en:retardation | n2=en:macrosomia obesity macrocephaly ocular abnormalities | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:macular degeneration
n1=en:retardation | n2=en:macular degeneration | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:madokoro ohdo sonoda syndrome
n1=en:retardation | n2=en:madokoro ohdo sonoda syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:magnetic resonance spectroscopy (mrs) shows decreased n-acetylaspartic acid in unaffected white matter
n1=en:retardation | n2=en:magnetic resonance spectroscopy (mrs) shows decreased n-acetylaspartic acid in unaffected white matter | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:magnetic resonance spectroscopy (mrs) shows increased lactate in the central nervous system
n1=en:retardation | n2=en:magnetic resonance spectroscopy (mrs) shows increased lactate in the central nervous system | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:magnetic resonance spectroscopy shows increased lactate in white matter
n1=en:retardation | n2=en:magnetic resonance spectroscopy shows increased lactate in white matter | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:major congenital anomaly
n1=en:retardation | n2=en:major congenital anomaly | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:major developmental delay
n1=en:retardation | n2=en:major developmental delay | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:major developmental milestones are not attained
n1=en:retardation | n2=en:major developmental milestones are not attained | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:malaria
n1=en:retardation | n2=en:malaria | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:male genital injuries
n1=en:retardation | n2=en:male genital injuries | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:malformation of the insula
n1=en:retardation | n2=en:malformation of the insula | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:malformation, cerebral arteriovenous
n1=en:retardation | n2=en:malformation, cerebral arteriovenous | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:malformations of cortical development
n1=en:retardation | n2=en:malformations of cortical development | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:malformations of cortical development, variable
n1=en:retardation | n2=en:malformations of cortical development, variable | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:malformations of the mid- and hindbrain
n1=en:retardation | n2=en:malformations of the mid- and hindbrain | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:malignant bladder neoplasm
n1=en:retardation | n2=en:malignant bladder neoplasm | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:malignant cervical neoplasm
n1=en:retardation | n2=en:malignant cervical neoplasm | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:malignant gastric neoplasm
n1=en:retardation | n2=en:malignant gastric neoplasm | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:malignant kidney neoplasm
n1=en:retardation | n2=en:malignant kidney neoplasm | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:malignant neoplasm of colon with rectum
n1=en:retardation | n2=en:malignant neoplasm of colon with rectum | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:malignant neoplasm of female breast
n1=en:retardation | n2=en:malignant neoplasm of female breast | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:malignant neoplasm other/unspecified
n1=en:retardation | n2=en:malignant neoplasm other/unspecified | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:malignant neoplasm: bronchus or lung, unspecified
n1=en:retardation | n2=en:malignant neoplasm: bronchus or lung, unspecified | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:malignant nervous system neoplasm
n1=en:retardation | n2=en:malignant nervous system neoplasm | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:malignant obstetric neoplasm
n1=en:retardation | n2=en:malignant obstetric neoplasm | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:malignant pancreatic neoplasm
n1=en:retardation | n2=en:malignant pancreatic neoplasm | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:malignant prostate neoplasm
n1=en:retardation | n2=en:malignant prostate neoplasm | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:malignant skin neoplasm
n1=en:retardation | n2=en:malignant skin neoplasm | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:malignant thyroid gland neoplasm
n1=en:retardation | n2=en:malignant thyroid gland neoplasm | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:malpuech facial clefting syndrome
n1=en:retardation | n2=en:malpuech facial clefting syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mandibular cleft
n1=en:retardation | n2=en:mandibular cleft | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:manic and bipolar mood disorders and disturbances
n1=en:retardation | n2=en:manic and bipolar mood disorders and disturbances | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:manic psychosis
n1=en:retardation | n2=en:manic psychosis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mannosidosis
n1=en:retardation | n2=en:mannosidosis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:maple syrup urine disease
n1=en:retardation | n2=en:maple syrup urine disease | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:markedly delayed nerve conduction velocities
n1=en:retardation | n2=en:markedly delayed nerve conduction velocities | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:marshall-smith syndrome
n1=en:retardation | n2=en:marshall-smith syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:masa syndrome (disorder)
n1=en:retardation | n2=en:masa syndrome (disorder) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mask-like facies
n1=en:retardation | n2=en:mask-like facies | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mastitis, postpartum
n1=en:retardation | n2=en:mastitis, postpartum | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mean sleep latency is less than 5 to 8 minutes
n1=en:retardation | n2=en:mean sleep latency is less than 5 to 8 minutes | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:measles
n1=en:retardation | n2=en:measles | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:medical history:find:pt:^patient:nom:phenx
n1=en:retardation | n2=en:medical history:find:pt:^patient:nom:phenx | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:medication abuse
n1=en:retardation | n2=en:medication abuse | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:medulloblastoma
n1=en:retardation | n2=en:medulloblastoma | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mega cisterna magna
n1=en:retardation | n2=en:mega cisterna magna | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mega-aeroesophagus sign
n1=en:retardation | n2=en:mega-aeroesophagus sign | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:megacisterna magna (in some patients)
n1=en:retardation | n2=en:megacisterna magna (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:megacisterna magna (rare)
n1=en:retardation | n2=en:megacisterna magna (rare) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:megalencephalic leukoencephalopathy with subcortical cysts 2a
n1=en:retardation | n2=en:megalencephalic leukoencephalopathy with subcortical cysts 2a | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:megalencephaly cutis marmorata telangiectatica congenita
n1=en:retardation | n2=en:megalencephaly cutis marmorata telangiectatica congenita | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:memory defects
n1=en:retardation | n2=en:memory defects | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:memory dysfunction
n1=en:retardation | n2=en:memory dysfunction | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:memory impairment
n1=en:retardation | n2=en:memory impairment | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:memory impairment, progressive
n1=en:retardation | n2=en:memory impairment, progressive | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:memory loss
n1=en:retardation | n2=en:memory loss | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:meninges
n1=en:retardation | n2=en:meninges | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:meningioma
n1=en:retardation | n2=en:meningioma | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:meningioma (in some patients)
n1=en:retardation | n2=en:meningioma (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:meningitis
n1=en:retardation | n2=en:meningitis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:meningitis/encephalitis
n1=en:retardation | n2=en:meningitis/encephalitis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:meningoceles, multiple, lateral
n1=en:retardation | n2=en:meningoceles, multiple, lateral | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:meningoencephalitis
n1=en:retardation | n2=en:meningoencephalitis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:meningoencephalocele (wws)
n1=en:retardation | n2=en:meningoencephalocele (wws) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:menkes disease
n1=en:retardation | n2=en:menkes disease | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental aberration
n1=en:retardation | n2=en:mental aberration | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental abnormality acute transient
n1=en:retardation | n2=en:mental abnormality acute transient | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental and behavioural disorders
n1=en:retardation | n2=en:mental and behavioural disorders | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental and behavioural disorders due to psychoactive substance use
n1=en:retardation | n2=en:mental and behavioural disorders due to psychoactive substance use | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental delay or retardation (uncommon)
n1=en:retardation | n2=en:mental delay or retardation (uncommon) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental deterioration beginning 2 to 5 years after onset of seizures
n1=en:retardation | n2=en:mental deterioration beginning 2 to 5 years after onset of seizures | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental deterioration in a subset of patients
n1=en:retardation | n2=en:mental deterioration in a subset of patients | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental deterioration in childhood
n1=en:retardation | n2=en:mental deterioration in childhood | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental disorder and/or culture bound syndrome
n1=en:retardation | n2=en:mental disorder and/or culture bound syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental disorder diagnosis
n1=en:retardation | n2=en:mental disorder diagnosis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental disorder due to a general medical condition
n1=en:retardation | n2=en:mental disorder due to a general medical condition | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental disorder due to drug
n1=en:retardation | n2=en:mental disorder due to drug | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental disorder in mother complicating childbirth
n1=en:retardation | n2=en:mental disorder in mother complicating childbirth | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental disorder transient
n1=en:retardation | n2=en:mental disorder transient | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental disorder usually first evident in infancy, childhood and/or adolescence
n1=en:retardation | n2=en:mental disorder usually first evident in infancy, childhood and/or adolescence | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental disorders complicating pregnancy, childbirth, or the puerperium
n1=en:retardation | n2=en:mental disorders complicating pregnancy, childbirth, or the puerperium | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental disorders during pregnancy, childbirth and the puerperium
n1=en:retardation | n2=en:mental disorders during pregnancy, childbirth and the puerperium | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental disorders of mother
n1=en:retardation | n2=en:mental disorders of mother | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental disorders of mother, antepartum condition or complication
n1=en:retardation | n2=en:mental disorders of mother, antepartum condition or complication | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental disorders of mother, delivered, with mention of postpartum complication
n1=en:retardation | n2=en:mental disorders of mother, delivered, with mention of postpartum complication | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental disorders of mother, delivered, with or without mention of antepartum condition
n1=en:retardation | n2=en:mental disorders of mother, delivered, with or without mention of antepartum condition | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental disorders of mother, postpartum condition or complication
n1=en:retardation | n2=en:mental disorders of mother, postpartum condition or complication | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental disorders of mother, unspecified as to episode of care or not applicable
n1=en:retardation | n2=en:mental disorders of mother, unspecified as to episode of care or not applicable | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental dysequilibrium
n1=en:retardation | n2=en:mental dysequilibrium | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental impairment
n1=en:retardation | n2=en:mental impairment | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental impairment may develop with repeated acute episodes
n1=en:retardation | n2=en:mental impairment may develop with repeated acute episodes | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental impairment, mild to moderate
n1=en:retardation | n2=en:mental impairment, mild to moderate | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental lethargy
n1=en:retardation | n2=en:mental lethargy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation (1 family)
n1=en:retardation | n2=en:mental retardation (1 family) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation (15%)
n1=en:retardation | n2=en:mental retardation (15%) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation (18% of patients)
n1=en:retardation | n2=en:mental retardation (18% of patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation (2 patients)
n1=en:retardation | n2=en:mental retardation (2 patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation (2/3 patients)
n1=en:retardation | n2=en:mental retardation (2/3 patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation (20%)
n1=en:retardation | n2=en:mental retardation (20%) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation (25%)
n1=en:retardation | n2=en:mental retardation (25%) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation (3 patients)
n1=en:retardation | n2=en:mental retardation (3 patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation (30%)
n1=en:retardation | n2=en:mental retardation (30%) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation (31%)
n1=en:retardation | n2=en:mental retardation (31%) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation (38%)
n1=en:retardation | n2=en:mental retardation (38%) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation (47%)
n1=en:retardation | n2=en:mental retardation (47%) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation (50% patients)
n1=en:retardation | n2=en:mental retardation (50% patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation (6%)
n1=en:retardation | n2=en:mental retardation (6%) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation (7%)
n1=en:retardation | n2=en:mental retardation (7%) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation (70%)
n1=en:retardation | n2=en:mental retardation (70%) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation (about 40%)
n1=en:retardation | n2=en:mental retardation (about 40%) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation (average iq 51)
n1=en:retardation | n2=en:mental retardation (average iq 51) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation (average iq 56)
n1=en:retardation | n2=en:mental retardation (average iq 56) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation (cvs+)
n1=en:retardation | n2=en:mental retardation (cvs+) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation (develops later)
n1=en:retardation | n2=en:mental retardation (develops later) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation (early-onset form)
n1=en:retardation | n2=en:mental retardation (early-onset form) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation (if left untreated)
n1=en:retardation | n2=en:mental retardation (if left untreated) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation (if untreated in infancy)
n1=en:retardation | n2=en:mental retardation (if untreated in infancy) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation (in 2 of 6 patients)
n1=en:retardation | n2=en:mental retardation (in 2 of 6 patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation (in 2 patients) learning disability (in 1 patient)
n1=en:retardation | n2=en:mental retardation (in 2 patients) learning disability (in 1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation (in a subset of patients)
n1=en:retardation | n2=en:mental retardation (in a subset of patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation (in most patients)
n1=en:retardation | n2=en:mental retardation (in most patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation (in most)
n1=en:retardation | n2=en:mental retardation (in most) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation (in some cases)
n1=en:retardation | n2=en:mental retardation (in some cases) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation (in some patients)
n1=en:retardation | n2=en:mental retardation (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation (in some)
n1=en:retardation | n2=en:mental retardation (in some) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation (in type iia)
n1=en:retardation | n2=en:mental retardation (in type iia) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation (iq 20-78)
n1=en:retardation | n2=en:mental retardation (iq 20-78) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation (iq 24-85) (variable)
n1=en:retardation | n2=en:mental retardation (iq 24-85) (variable) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation (iq 45-75)
n1=en:retardation | n2=en:mental retardation (iq 45-75) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation (iq 50-60 combined griffiths and stanford-binet scale)
n1=en:retardation | n2=en:mental retardation (iq 50-60 combined griffiths and stanford-binet scale) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation (less common)
n1=en:retardation | n2=en:mental retardation (less common) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation (males)
n1=en:retardation | n2=en:mental retardation (males) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation (moderate to severe in males)
n1=en:retardation | n2=en:mental retardation (moderate to severe in males) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation (one patient)
n1=en:retardation | n2=en:mental retardation (one patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation (one-third)
n1=en:retardation | n2=en:mental retardation (one-third) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation (range mild to severe)
n1=en:retardation | n2=en:mental retardation (range mild to severe) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation (rare less than 1% of cases)
n1=en:retardation | n2=en:mental retardation (rare less than 1% of cases) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation (rare)
n1=en:retardation | n2=en:mental retardation (rare) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation (rarely noted)
n1=en:retardation | n2=en:mental retardation (rarely noted) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation (reported in 1 family)
n1=en:retardation | n2=en:mental retardation (reported in 1 family) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation (reported in 1 patient)
n1=en:retardation | n2=en:mental retardation (reported in 1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation (secondary to intracranial bleed)
n1=en:retardation | n2=en:mental retardation (secondary to intracranial bleed) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation (seen in hhs variant)
n1=en:retardation | n2=en:mental retardation (seen in hhs variant) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation (some)
n1=en:retardation | n2=en:mental retardation (some) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation (sometimes)
n1=en:retardation | n2=en:mental retardation (sometimes) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation (type i)
n1=en:retardation | n2=en:mental retardation (type i) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation (uncommon)
n1=en:retardation | n2=en:mental retardation (uncommon) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation (untreated hypothyroidism)
n1=en:retardation | n2=en:mental retardation (untreated hypothyroidism) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation (variable expression)
n1=en:retardation | n2=en:mental retardation (variable expression) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation by age 30 years
n1=en:retardation | n2=en:mental retardation by age 30 years | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation by the age of 7 years
n1=en:retardation | n2=en:mental retardation by the age of 7 years | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation can occur in patients with repeated episodes of dehydration
n1=en:retardation | n2=en:mental retardation can occur in patients with repeated episodes of dehydration | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation due to repeated episodes of hypoglycemia
n1=en:retardation | n2=en:mental retardation due to repeated episodes of hypoglycemia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation from rapid mental regression
n1=en:retardation | n2=en:mental retardation from rapid mental regression | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation has been reported
n1=en:retardation | n2=en:mental retardation has been reported | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation if untreated
n1=en:retardation | n2=en:mental retardation if untreated | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation in 5-13%
n1=en:retardation | n2=en:mental retardation in 5-13% | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation in 75%
n1=en:retardation | n2=en:mental retardation in 75% | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation in survivors
n1=en:retardation | n2=en:mental retardation in survivors | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation may occur
n1=en:retardation | n2=en:mental retardation may occur | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation screen
n1=en:retardation | n2=en:mental retardation screen | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation severity unspecified
n1=en:retardation | n2=en:mental retardation severity unspecified | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation with psychosis, pyramidal signs, and macroorchidism
n1=en:retardation | n2=en:mental retardation with psychosis, pyramidal signs, and macroorchidism | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation with spastic paraplegia
n1=en:retardation | n2=en:mental retardation with spastic paraplegia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation wolff type
n1=en:retardation | n2=en:mental retardation wolff type | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation, autosomal dominant 1
n1=en:retardation | n2=en:mental retardation, autosomal dominant 1 | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation, autosomal dominant 22
n1=en:retardation | n2=en:mental retardation, autosomal dominant 22 | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation, autosomal recessive 36
n1=en:retardation | n2=en:mental retardation, autosomal recessive 36 | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation, autosomal recessive 38
n1=en:retardation | n2=en:mental retardation, autosomal recessive 38 | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation, autosomal recessive 40
n1=en:retardation | n2=en:mental retardation, autosomal recessive 40 | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation, autosomal recessive 46
n1=en:retardation | n2=en:mental retardation, autosomal recessive 46 | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation, borderline (1 patient)
n1=en:retardation | n2=en:mental retardation, borderline (1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation, borderline to severe
n1=en:retardation | n2=en:mental retardation, borderline to severe | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation, borderline-mild in carrier females
n1=en:retardation | n2=en:mental retardation, borderline-mild in carrier females | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation, buenos aires type
n1=en:retardation | n2=en:mental retardation, buenos aires type | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation, fra12a type
n1=en:retardation | n2=en:mental retardation, fra12a type | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation, in subgroup of patients
n1=en:retardation | n2=en:mental retardation, in subgroup of patients | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation, microcephaly, growth retardation, joint contractures, and facial dysmorphism
n1=en:retardation | n2=en:mental retardation, microcephaly, growth retardation, joint contractures, and facial dysmorphism | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation, mild (1 family)
n1=en:retardation | n2=en:mental retardation, mild (1 family) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation, mild (1 patient)
n1=en:retardation | n2=en:mental retardation, mild (1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation, mild (10%)
n1=en:retardation | n2=en:mental retardation, mild (10%) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation, mild (11%)
n1=en:retardation | n2=en:mental retardation, mild (11%) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation, mild (18%)
n1=en:retardation | n2=en:mental retardation, mild (18%) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation, mild (2 families)
n1=en:retardation | n2=en:mental retardation, mild (2 families) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation, mild (20% have more severe mental retardation)
n1=en:retardation | n2=en:mental retardation, mild (20% have more severe mental retardation) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation, mild (carrier females)
n1=en:retardation | n2=en:mental retardation, mild (carrier females) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation, mild (in some females)
n1=en:retardation | n2=en:mental retardation, mild (in some females) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation, mild (in some patients)
n1=en:retardation | n2=en:mental retardation, mild (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation, mild (iq range from 50 to 70)
n1=en:retardation | n2=en:mental retardation, mild (iq range from 50 to 70) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation, mild (rare)
n1=en:retardation | n2=en:mental retardation, mild (rare) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation, mild to moderate
n1=en:retardation | n2=en:mental retardation, mild to moderate | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation, mild to moderate (20% of patients)
n1=en:retardation | n2=en:mental retardation, mild to moderate (20% of patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation, mild to moderate (in 12%)
n1=en:retardation | n2=en:mental retardation, mild to moderate (in 12%) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation, mild to moderate (in some patients)
n1=en:retardation | n2=en:mental retardation, mild to moderate (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation, mild to moderate (iq 30-76)
n1=en:retardation | n2=en:mental retardation, mild to moderate (iq 30-76) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation, mild to profound
n1=en:retardation | n2=en:mental retardation, mild to profound | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation, mild to severe
n1=en:retardation | n2=en:mental retardation, mild to severe | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation, mild-borderline, nonprogressive
n1=en:retardation | n2=en:mental retardation, mild-borderline, nonprogressive | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation, mild-moderate (28%, usually in males)
n1=en:retardation | n2=en:mental retardation, mild-moderate (28%, usually in males) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation, mild-moderate (some)
n1=en:retardation | n2=en:mental retardation, mild-moderate (some) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation, mild, in most carrier females
n1=en:retardation | n2=en:mental retardation, mild, in most carrier females | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation, mild, some patients (iq 70-80)
n1=en:retardation | n2=en:mental retardation, mild, some patients (iq 70-80) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation, moderate (apparent by age 4 years)
n1=en:retardation | n2=en:mental retardation, moderate (apparent by age 4 years) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation, moderate (in 1 patient)
n1=en:retardation | n2=en:mental retardation, moderate (in 1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation, moderate (in sister)
n1=en:retardation | n2=en:mental retardation, moderate (in sister) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation, moderate (in some patients)
n1=en:retardation | n2=en:mental retardation, moderate (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation, moderate to profound
n1=en:retardation | n2=en:mental retardation, moderate to profound | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation, moderate to severe
n1=en:retardation | n2=en:mental retardation, moderate to severe | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation, moderate to severe (10-15% of patients)
n1=en:retardation | n2=en:mental retardation, moderate to severe (10-15% of patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation, moderate to severe (in some patients)
n1=en:retardation | n2=en:mental retardation, moderate to severe (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation, moderate to severe (iq 35-50)
n1=en:retardation | n2=en:mental retardation, moderate to severe (iq 35-50) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation, moderate to severe (iq 40 to 60)
n1=en:retardation | n2=en:mental retardation, moderate to severe (iq 40 to 60) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation, moderate to severe (type ii, infantile and juvenile)
n1=en:retardation | n2=en:mental retardation, moderate to severe (type ii, infantile and juvenile) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation, moderate-severe (2p21del)
n1=en:retardation | n2=en:mental retardation, moderate-severe (2p21del) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation, occasional
n1=en:retardation | n2=en:mental retardation, occasional | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation, profound (wws)
n1=en:retardation | n2=en:mental retardation, profound (wws) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation, progressive (50% of patients)
n1=en:retardation | n2=en:mental retardation, progressive (50% of patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation, residual mild-to-severe (in some patients)
n1=en:retardation | n2=en:mental retardation, residual mild-to-severe (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation, severe (if untreated)
n1=en:retardation | n2=en:mental retardation, severe (if untreated) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation, severe (meb)
n1=en:retardation | n2=en:mental retardation, severe (meb) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation, severe in some patients
n1=en:retardation | n2=en:mental retardation, severe in some patients | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation, severe to profound
n1=en:retardation | n2=en:mental retardation, severe to profound | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation, severe, profound
n1=en:retardation | n2=en:mental retardation, severe, profound | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation, variable (in some patients)
n1=en:retardation | n2=en:mental retardation, variable (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation, variable degree (in some patients)
n1=en:retardation | n2=en:mental retardation, variable degree (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation, variable severity
n1=en:retardation | n2=en:mental retardation, variable severity | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation, x-linked
n1=en:retardation | n2=en:mental retardation, x-linked | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation, x-linked 101
n1=en:retardation | n2=en:mental retardation, x-linked 101 | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation, x-linked 3
n1=en:retardation | n2=en:mental retardation, x-linked 3 | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation, x-linked 93 (disorder)
n1=en:retardation | n2=en:mental retardation, x-linked 93 (disorder) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation, x-linked 98
n1=en:retardation | n2=en:mental retardation, x-linked 98 | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation, x-linked 99
n1=en:retardation | n2=en:mental retardation, x-linked 99 | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation, x-linked, syndromic 17
n1=en:retardation | n2=en:mental retardation, x-linked, syndromic 17 | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation, x-linked, syndromic, nascimento type
n1=en:retardation | n2=en:mental retardation, x-linked, syndromic, nascimento type | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation, x-linked, with epilepsy
n1=en:retardation | n2=en:mental retardation, x-linked, with epilepsy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation, x-linked, with short stature (disorder)
n1=en:retardation | n2=en:mental retardation, x-linked, with short stature (disorder) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental retardation, x-linked, with short stature, hypogonadism, and abnormal gait
n1=en:retardation | n2=en:mental retardation, x-linked, with short stature, hypogonadism, and abnormal gait | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental state abnormal aggravated
n1=en:retardation | n2=en:mental state abnormal aggravated | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mental symptom
n1=en:retardation | n2=en:mental symptom | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mentally disabled persons
n1=en:retardation | n2=en:mentally disabled persons | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mentally late developer
n1=en:retardation | n2=en:mentally late developer | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mesial temporal brain malformations
n1=en:retardation | n2=en:mesial temporal brain malformations | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mesial temporal sclerosis (in 1 patient)
n1=en:retardation | n2=en:mesial temporal sclerosis (in 1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:metaphyseal acroscyphodysplasia
n1=en:retardation | n2=en:metaphyseal acroscyphodysplasia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:methylcrotonyl-coa carboxylase deficiency
n1=en:retardation | n2=en:methylcrotonyl-coa carboxylase deficiency | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:methylmalonic acidemia with homocystinuria
n1=en:retardation | n2=en:methylmalonic acidemia with homocystinuria | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:methylmalonic aciduria and homocystinuria, cbld type
n1=en:retardation | n2=en:methylmalonic aciduria and homocystinuria, cbld type | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mevalonic aciduria
n1=en:retardation | n2=en:mevalonic aciduria | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:microbleeds
n1=en:retardation | n2=en:microbleeds | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:microbleeds (most smaller than 5 mm) occur after age 40 years
n1=en:retardation | n2=en:microbleeds (most smaller than 5 mm) occur after age 40 years | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:microcephalic osteodysplastic primordial dwarfism, type 3
n1=en:retardation | n2=en:microcephalic osteodysplastic primordial dwarfism, type 3 | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:microcephalic osteodysplastic primordial dwarfism, type i
n1=en:retardation | n2=en:microcephalic osteodysplastic primordial dwarfism, type i | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:microcephalic osteodysplastic primordial dwarfism, type ii
n1=en:retardation | n2=en:microcephalic osteodysplastic primordial dwarfism, type ii | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:microcephalic primordial dwarfism toriello type
n1=en:retardation | n2=en:microcephalic primordial dwarfism toriello type | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:microcephaly
n1=en:retardation | n2=en:microcephaly | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:microcephaly and chorioretinopathy, autosomal recessive, 1
n1=en:retardation | n2=en:microcephaly and chorioretinopathy, autosomal recessive, 1 | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:microcephaly and chorioretinopathy, autosomal recessive, 2
n1=en:retardation | n2=en:microcephaly and chorioretinopathy, autosomal recessive, 2 | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:microcephaly with mental retardation and digital anomalies
n1=en:retardation | n2=en:microcephaly with mental retardation and digital anomalies | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:microcephaly, primary autosomal recessive, 2 (disorder)
n1=en:retardation | n2=en:microcephaly, primary autosomal recessive, 2 (disorder) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:microcephaly, short stature, and impaired glucose metabolism
n1=en:retardation | n2=en:microcephaly, short stature, and impaired glucose metabolism | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:microcystic degeneration
n1=en:retardation | n2=en:microcystic degeneration | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:micrographia
n1=en:retardation | n2=en:micrographia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:microgyria
n1=en:retardation | n2=en:microgyria | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:microlissencephalies
n1=en:retardation | n2=en:microlissencephalies | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:microphthalmia, syndromic 13
n1=en:retardation | n2=en:microphthalmia, syndromic 13 | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:microvacuolation
n1=en:retardation | n2=en:microvacuolation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:microvascular spaces, dilated
n1=en:retardation | n2=en:microvascular spaces, dilated | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:midbrain atrophy
n1=en:retardation | n2=en:midbrain atrophy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:midline brain calcifications
n1=en:retardation | n2=en:midline brain calcifications | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:midline forebrain defects
n1=en:retardation | n2=en:midline forebrain defects | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:migraine
n1=en:retardation | n2=en:migraine | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:migraine (40% of patients)
n1=en:retardation | n2=en:migraine (40% of patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:migraine (in affected males)
n1=en:retardation | n2=en:migraine (in affected males) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:migraine (in some patients)
n1=en:retardation | n2=en:migraine (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:migraine (uncommon)
n1=en:retardation | n2=en:migraine (uncommon) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:migraine headache (less common)
n1=en:retardation | n2=en:migraine headache (less common) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:migraine headaches (cvs+)
n1=en:retardation | n2=en:migraine headaches (cvs+) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:migraine headaches (ipsilateral to facial hemangioma)
n1=en:retardation | n2=en:migraine headaches (ipsilateral to facial hemangioma) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:migraine headaches (onset in adolescence)
n1=en:retardation | n2=en:migraine headaches (onset in adolescence) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:migraine with aura
n1=en:retardation | n2=en:migraine with aura | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:migraine with aura, usually visual (in 50% of patients)
n1=en:retardation | n2=en:migraine with aura, usually visual (in 50% of patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:migraine without aura
n1=en:retardation | n2=en:migraine without aura | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:migraine, with or without aura
n1=en:retardation | n2=en:migraine, with or without aura | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:migraines (less common)
n1=en:retardation | n2=en:migraines (less common) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:migrating clonic jerks (in some patients)
n1=en:retardation | n2=en:migrating clonic jerks (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:migrating discharges from one cortical region to another seen on eeg (in some patients)
n1=en:retardation | n2=en:migrating discharges from one cortical region to another seen on eeg (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:migrating focal discharges from one cortical region to another seen on eeg
n1=en:retardation | n2=en:migrating focal discharges from one cortical region to another seen on eeg | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:migrating partial seizures
n1=en:retardation | n2=en:migrating partial seizures | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mild brain anomalies on mri (e.g., dilated ventricles) (in some patients)
n1=en:retardation | n2=en:mild brain anomalies on mri (e.g., dilated ventricles) (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mild cerebellar hypoplasia
n1=en:retardation | n2=en:mild cerebellar hypoplasia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mild cognitive decline (1 patient)
n1=en:retardation | n2=en:mild cognitive decline (1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mild cognitive deterioration in adults
n1=en:retardation | n2=en:mild cognitive deterioration in adults | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mild cognitive disorder
n1=en:retardation | n2=en:mild cognitive disorder | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mild cognitive impairment (in 2 patients)
n1=en:retardation | n2=en:mild cognitive impairment (in 2 patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mild cognitive impairment (in some patients)
n1=en:retardation | n2=en:mild cognitive impairment (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mild cognitive impairment (less common)
n1=en:retardation | n2=en:mild cognitive impairment (less common) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mild cortical atrophy (in 1 patient)
n1=en:retardation | n2=en:mild cortical atrophy (in 1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mild cortical atrophy on ct or mri
n1=en:retardation | n2=en:mild cortical atrophy on ct or mri | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mild distal sensory deficits
n1=en:retardation | n2=en:mild distal sensory deficits | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mild global developmental delay
n1=en:retardation | n2=en:mild global developmental delay | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mild loss of neurons in the cerebellum
n1=en:retardation | n2=en:mild loss of neurons in the cerebellum | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mild memory loss
n1=en:retardation | n2=en:mild memory loss | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mild mental decline
n1=en:retardation | n2=en:mild mental decline | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mild mental deterioration
n1=en:retardation | n2=en:mild mental deterioration | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mild mental retardation
n1=en:retardation | n2=en:mild mental retardation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mild mental retardation (39%) feeding problems/weak suck (43%)
n1=en:retardation | n2=en:mild mental retardation (39%) feeding problems/weak suck (43%) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mild mental retardation (in 1/4 patients)
n1=en:retardation | n2=en:mild mental retardation (in 1/4 patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mild mental retardation (some)
n1=en:retardation | n2=en:mild mental retardation (some) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mild motor development delay
n1=en:retardation | n2=en:mild motor development delay | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mild paraparesis
n1=en:retardation | n2=en:mild paraparesis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mild psychomotor delay
n1=en:retardation | n2=en:mild psychomotor delay | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mild pyramidal signs (variable expression)
n1=en:retardation | n2=en:mild pyramidal signs (variable expression) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mild sensorimotor neuropathy
n1=en:retardation | n2=en:mild sensorimotor neuropathy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mild spasticity
n1=en:retardation | n2=en:mild spasticity | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mild structural abnormalities seen mri (in some patients)
n1=en:retardation | n2=en:mild structural abnormalities seen mri (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mild to moderate learning difficulties
n1=en:retardation | n2=en:mild to moderate learning difficulties | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mild to severe mental retardation (24%)
n1=en:retardation | n2=en:mild to severe mental retardation (24%) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mild upper limb involvement
n1=en:retardation | n2=en:mild upper limb involvement | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mild-moderate mental retardation (80% affected males)
n1=en:retardation | n2=en:mild-moderate mental retardation (80% affected males) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mild-moderate ventricular dilatation
n1=en:retardation | n2=en:mild-moderate ventricular dilatation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mild-severe mental retardation (20%)
n1=en:retardation | n2=en:mild-severe mental retardation (20%) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:milder cases have isolated recurrent daytime sleepiness and/or lapses into sleep without cataplexy
n1=en:retardation | n2=en:milder cases have isolated recurrent daytime sleepiness and/or lapses into sleep without cataplexy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mildly decreased intelligence has been reported
n1=en:retardation | n2=en:mildly decreased intelligence has been reported | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mildly delayed developmental milestones
n1=en:retardation | n2=en:mildly delayed developmental milestones | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mildly delayed motor development
n1=en:retardation | n2=en:mildly delayed motor development | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mildly delayed motor development due to vestibular dysfunction
n1=en:retardation | n2=en:mildly delayed motor development due to vestibular dysfunction | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mildly enlarged ventricles
n1=en:retardation | n2=en:mildly enlarged ventricles | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mildly thin corpus callosum
n1=en:retardation | n2=en:mildly thin corpus callosum | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:miller-dieker syndrome
n1=en:retardation | n2=en:miller-dieker syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:minimal brain dysfunction
n1=en:retardation | n2=en:minimal brain dysfunction | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:minimal gliosis
n1=en:retardation | n2=en:minimal gliosis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:minimal or lack of speech
n1=en:retardation | n2=en:minimal or lack of speech | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:minimal to absent speech
n1=en:retardation | n2=en:minimal to absent speech | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:minor motor impairment (stage 2)
n1=en:retardation | n2=en:minor motor impairment (stage 2) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mirror hand movements (bimanual synkinesis, in some patients)
n1=en:retardation | n2=en:mirror hand movements (bimanual synkinesis, in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mirror movements disorder
n1=en:retardation | n2=en:mirror movements disorder | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mirror movements, involuntary, affecting the hand and fingers
n1=en:retardation | n2=en:mirror movements, involuntary, affecting the hand and fingers | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mirror movements, involuntary, usually of the upper limb and hand
n1=en:retardation | n2=en:mirror movements, involuntary, usually of the upper limb and hand | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:miscellaneous mental disorders
n1=en:retardation | n2=en:miscellaneous mental disorders | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:misorientation of pyramidal fibers
n1=en:retardation | n2=en:misorientation of pyramidal fibers | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:misshapen posterior fossa
n1=en:retardation | n2=en:misshapen posterior fossa | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mitochondrial complex iii deficiency, nuclear type 1
n1=en:retardation | n2=en:mitochondrial complex iii deficiency, nuclear type 1 | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mitochondrial dna depletion in brain tissue
n1=en:retardation | n2=en:mitochondrial dna depletion in brain tissue | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mitochondrial dna depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria)
n1=en:retardation | n2=en:mitochondrial dna depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mitochondrial dna depletion syndrome 8a (encephalomyopathic type with renal tubulopathy)
n1=en:retardation | n2=en:mitochondrial dna depletion syndrome 8a (encephalomyopathic type with renal tubulopathy) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mitochondrial encephalopathy
n1=en:retardation | n2=en:mitochondrial encephalopathy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mixed cerebellar/pseudobulbar dysarthria
n1=en:retardation | n2=en:mixed cerebellar/pseudobulbar dysarthria | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mixed developmental disorder
n1=en:retardation | n2=en:mixed developmental disorder | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mobility poor
n1=en:retardation | n2=en:mobility poor | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mobius syndrome
n1=en:retardation | n2=en:mobius syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:moderate cortical atrophy (in some patients)
n1=en:retardation | n2=en:moderate cortical atrophy (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:moderate learning difficulties
n1=en:retardation | n2=en:moderate learning difficulties | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:moderate mental retardation (i.q. 35-49)
n1=en:retardation | n2=en:moderate mental retardation (i.q. 35-49) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:moderate to severe hypotonia
n1=en:retardation | n2=en:moderate to severe hypotonia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:moderately thickened cortex
n1=en:retardation | n2=en:moderately thickened cortex | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:molar tooth sign on brain mri
n1=en:retardation | n2=en:molar tooth sign on brain mri | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:molar tooth sign on brain mri (subset of patients)
n1=en:retardation | n2=en:molar tooth sign on brain mri (subset of patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:molar tooth sign on mri
n1=en:retardation | n2=en:molar tooth sign on mri | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:molar tooth sign seen on mri
n1=en:retardation | n2=en:molar tooth sign seen on mri | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:molluscum contagiosum
n1=en:retardation | n2=en:molluscum contagiosum | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:momes syndrome
n1=en:retardation | n2=en:momes syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:moniliasis genital female
n1=en:retardation | n2=en:moniliasis genital female | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:moniliasis/candida (excluding x72 y75)
n1=en:retardation | n2=en:moniliasis/candida (excluding x72 y75) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:monopareses
n1=en:retardation | n2=en:monopareses | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:monotone speech
n1=en:retardation | n2=en:monotone speech | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:monotonous speech
n1=en:retardation | n2=en:monotonous speech | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:monster (disorder)
n1=en:retardation | n2=en:monster (disorder) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mood disorder
n1=en:retardation | n2=en:mood disorder | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mood disorders and disturbances nec
n1=en:retardation | n2=en:mood disorders and disturbances nec | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mood lability
n1=en:retardation | n2=en:mood lability | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:morning myoclonic jerks
n1=en:retardation | n2=en:morning myoclonic jerks | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:moro reflex absent
n1=en:retardation | n2=en:moro reflex absent | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:moronity
n1=en:retardation | n2=en:moronity | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:most never acquire independent ambulation
n1=en:retardation | n2=en:most never acquire independent ambulation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:most patients achieve walking with aid
n1=en:retardation | n2=en:most patients achieve walking with aid | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:most patients are wheelchair-bound
n1=en:retardation | n2=en:most patients are wheelchair-bound | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:most patients do not achieve independent sitting or walking
n1=en:retardation | n2=en:most patients do not achieve independent sitting or walking | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:most patients remain stable or improve in years after the abrupt onset of symptoms
n1=en:retardation | n2=en:most patients remain stable or improve in years after the abrupt onset of symptoms | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mosy patients become wheelchair-bound after 10 years
n1=en:retardation | n2=en:mosy patients become wheelchair-bound after 10 years | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:motor abnormalities
n1=en:retardation | n2=en:motor abnormalities | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:motor and intellectual disability, severe
n1=en:retardation | n2=en:motor and intellectual disability, severe | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:motor and vocal tics
n1=en:retardation | n2=en:motor and vocal tics | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:motor automatisms
n1=en:retardation | n2=en:motor automatisms | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:motor delay (in one patient)
n1=en:retardation | n2=en:motor delay (in one patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:motor deterioration
n1=en:retardation | n2=en:motor deterioration | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:motor deterioration in second decade
n1=en:retardation | n2=en:motor deterioration in second decade | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:motor development delay (83%)
n1=en:retardation | n2=en:motor development delay (83%) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:motor development delayed (in some patients)
n1=en:retardation | n2=en:motor development delayed (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:motor developmental delay
n1=en:retardation | n2=en:motor developmental delay | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:motor developmental delay, severe
n1=en:retardation | n2=en:motor developmental delay, severe | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:motor disorders
n1=en:retardation | n2=en:motor disorders | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:motor disturbances
n1=en:retardation | n2=en:motor disturbances | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:motor dysfunction
n1=en:retardation | n2=en:motor dysfunction | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:motor dyspraxia
n1=en:retardation | n2=en:motor dyspraxia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:motor incoordination
n1=en:retardation | n2=en:motor incoordination | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:motor neuron disease
n1=en:retardation | n2=en:motor neuron disease | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:motor neuron disease (less common)
n1=en:retardation | n2=en:motor neuron disease (less common) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:motor neuron disease, lower
n1=en:retardation | n2=en:motor neuron disease, lower | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:motor regression
n1=en:retardation | n2=en:motor regression | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:motor retardation, mild
n1=en:retardation | n2=en:motor retardation, mild | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:motor seizures, nocturnal, usually occur in clusters (up to 8 per night) during dozing or on awakening
n1=en:retardation | n2=en:motor seizures, nocturnal, usually occur in clusters (up to 8 per night) during dozing or on awakening | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:motor stereotypy
n1=en:retardation | n2=en:motor stereotypy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:motor symptoms may be present
n1=en:retardation | n2=en:motor symptoms may be present | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:motor tic
n1=en:retardation | n2=en:motor tic | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mouth movements
n1=en:retardation | n2=en:mouth movements | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:movement abnormalities of the extremities
n1=en:retardation | n2=en:movement abnormalities of the extremities | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:movement disorder
n1=en:retardation | n2=en:movement disorder | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:movement of visual image - finding
n1=en:retardation | n2=en:movement of visual image - finding | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:movements ('tremors') characterized by 8 to 10-hz discharges
n1=en:retardation | n2=en:movements ('tremors') characterized by 8 to 10-hz discharges | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:movements are exacerbated by anxiety
n1=en:retardation | n2=en:movements are exacerbated by anxiety | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:moyamoya disease
n1=en:retardation | n2=en:moyamoya disease | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mr spectroscopy shows decreased n-acetyl aspartate
n1=en:retardation | n2=en:mr spectroscopy shows decreased n-acetyl aspartate | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mri - diffuse or focal cerebral and cerebellar white matter disease
n1=en:retardation | n2=en:mri - diffuse or focal cerebral and cerebellar white matter disease | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mri imaging shows cavitation of the basal ganglia
n1=en:retardation | n2=en:mri imaging shows cavitation of the basal ganglia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mri is best imaging modality to detect lesions
n1=en:retardation | n2=en:mri is best imaging modality to detect lesions | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mri may be normal, especially in type iib
n1=en:retardation | n2=en:mri may be normal, especially in type iib | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mri may show atrophy of the cerebrum
n1=en:retardation | n2=en:mri may show atrophy of the cerebrum | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mri may show lesions in basal ganglia, thalamus, and white matter
n1=en:retardation | n2=en:mri may show lesions in basal ganglia, thalamus, and white matter | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mri shows absence of the facial nerve
n1=en:retardation | n2=en:mri shows absence of the facial nerve | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mri shows atretic occipital cephalocele with bony skull defect
n1=en:retardation | n2=en:mri shows atretic occipital cephalocele with bony skull defect | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mri shows brain asymmetry
n1=en:retardation | n2=en:mri shows brain asymmetry | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mri shows brainstem hypoplasia
n1=en:retardation | n2=en:mri shows brainstem hypoplasia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mri shows cerebellar atrophy
n1=en:retardation | n2=en:mri shows cerebellar atrophy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mri shows cerebral atrophy
n1=en:retardation | n2=en:mri shows cerebral atrophy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mri shows congenital abnormalities of the posterior fossa
n1=en:retardation | n2=en:mri shows congenital abnormalities of the posterior fossa | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mri shows decreased signal intensities in the basal ganglia
n1=en:retardation | n2=en:mri shows decreased signal intensities in the basal ganglia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mri shows decreased signal intensity in the pallidal nuclei with central hyperintensity ('eye of the tiger' sign)
n1=en:retardation | n2=en:mri shows decreased signal intensity in the pallidal nuclei with central hyperintensity ('eye of the tiger' sign) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mri shows defects of the corpus callosum
n1=en:retardation | n2=en:mri shows defects of the corpus callosum | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mri shows delayed myelination (1 of 6 patients)
n1=en:retardation | n2=en:mri shows delayed myelination (1 of 6 patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mri shows diffuse white matter hyperintensities on t2-weighted imaging
n1=en:retardation | n2=en:mri shows diffuse white matter hyperintensities on t2-weighted imaging | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mri shows dysmyelination
n1=en:retardation | n2=en:mri shows dysmyelination | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mri shows frontal and temporal cortical atrophy
n1=en:retardation | n2=en:mri shows frontal and temporal cortical atrophy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mri shows generalized atrophy
n1=en:retardation | n2=en:mri shows generalized atrophy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mri shows global lack of myelination in the cerebral hemispheres
n1=en:retardation | n2=en:mri shows global lack of myelination in the cerebral hemispheres | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mri shows globus pallidus signal abnormalities
n1=en:retardation | n2=en:mri shows globus pallidus signal abnormalities | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mri shows high signal intensity of the white matter later
n1=en:retardation | n2=en:mri shows high signal intensity of the white matter later | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mri shows hypointensity of the thalami early-on
n1=en:retardation | n2=en:mri shows hypointensity of the thalami early-on | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mri shows increased t2-weighted signals in the globus pallidi
n1=en:retardation | n2=en:mri shows increased t2-weighted signals in the globus pallidi | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mri shows leukoencephalopathy
n1=en:retardation | n2=en:mri shows leukoencephalopathy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mri shows no normal myelination
n1=en:retardation | n2=en:mri shows no normal myelination | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mri shows short, thick corpus callosum
n1=en:retardation | n2=en:mri shows short, thick corpus callosum | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mri shows subcortical leukoencephalopathy with cavitation
n1=en:retardation | n2=en:mri shows subcortical leukoencephalopathy with cavitation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mri shows symmetric lesions of the basal ganglia (particularly caudate and putamen)
n1=en:retardation | n2=en:mri shows symmetric lesions of the basal ganglia (particularly caudate and putamen) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mri shows symmetric, diffuse lesions with csf-like signal intensity
n1=en:retardation | n2=en:mri shows symmetric, diffuse lesions with csf-like signal intensity | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mri shows t2-weighted signals in the basal ganglia
n1=en:retardation | n2=en:mri shows t2-weighted signals in the basal ganglia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mri shows white matter lesions
n1=en:retardation | n2=en:mri shows white matter lesions | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mrs shows decreased choline in affected white matter
n1=en:retardation | n2=en:mrs shows decreased choline in affected white matter | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mrs shows decreased creatine in white matter
n1=en:retardation | n2=en:mrs shows decreased creatine in white matter | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mrx78 gene
n1=en:retardation | n2=en:mrx78 gene | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mucolipidosis type iv
n1=en:retardation | n2=en:mucolipidosis type iv | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mucopolysaccharidosis type iiia
n1=en:retardation | n2=en:mucopolysaccharidosis type iiia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mucopolysaccharidosis type iiib
n1=en:retardation | n2=en:mucopolysaccharidosis type iiib | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mucopolysaccharidosis type iiic
n1=en:retardation | n2=en:mucopolysaccharidosis type iiic | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mucopolysaccharidosis type iiid
n1=en:retardation | n2=en:mucopolysaccharidosis type iiid | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:muenke syndrome
n1=en:retardation | n2=en:muenke syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:multifocal areas of laminar dysmorphic neurons (in type iia)
n1=en:retardation | n2=en:multifocal areas of laminar dysmorphic neurons (in type iia) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:multifocal cerebral white matter abnormalities
n1=en:retardation | n2=en:multifocal cerebral white matter abnormalities | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:multifocal discharges
n1=en:retardation | n2=en:multifocal discharges | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:multifocal discharges associated with contralateral jerky movements
n1=en:retardation | n2=en:multifocal discharges associated with contralateral jerky movements | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:multifocal discharges seen on eeg (in some patients)
n1=en:retardation | n2=en:multifocal discharges seen on eeg (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:multifocal epileptic activity
n1=en:retardation | n2=en:multifocal epileptic activity | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:multifocal epileptiform discharges on diffuse slow background
n1=en:retardation | n2=en:multifocal epileptiform discharges on diffuse slow background | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:multifocal epileptiform spikes seen on eeg
n1=en:retardation | n2=en:multifocal epileptiform spikes seen on eeg | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:multifocal intractable seizures
n1=en:retardation | n2=en:multifocal intractable seizures | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:multifocal seizure
n1=en:retardation | n2=en:multifocal seizure | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:multifocal spike and wave activity
n1=en:retardation | n2=en:multifocal spike and wave activity | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:multifocal spike waves
n1=en:retardation | n2=en:multifocal spike waves | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:multifocal spikes
n1=en:retardation | n2=en:multifocal spikes | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:multifocal spikes and progressive slowing of background activity seen on eeg
n1=en:retardation | n2=en:multifocal spikes and progressive slowing of background activity seen on eeg | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:multifocal white matter lesions
n1=en:retardation | n2=en:multifocal white matter lesions | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:multiple aneurysms
n1=en:retardation | n2=en:multiple aneurysms | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:multiple congenital anomalies
n1=en:retardation | n2=en:multiple congenital anomalies | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:multiple disability
n1=en:retardation | n2=en:multiple disability | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:multiple independent spike foci
n1=en:retardation | n2=en:multiple independent spike foci | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:multiple lesions in the white matter
n1=en:retardation | n2=en:multiple lesions in the white matter | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:multiple sclerosis
n1=en:retardation | n2=en:multiple sclerosis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:multiple sclerosis-like illness (516003.0001)
n1=en:retardation | n2=en:multiple sclerosis-like illness (516003.0001) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:multiple sulfatase deficiency disease
n1=en:retardation | n2=en:multiple sulfatase deficiency disease | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:multiple trauma/internal injury
n1=en:retardation | n2=en:multiple trauma/internal injury | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mumps
n1=en:retardation | n2=en:mumps | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:muscle atrophy
n1=en:retardation | n2=en:muscle atrophy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:muscle biopsy shows neurogenic changes
n1=en:retardation | n2=en:muscle biopsy shows neurogenic changes | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:muscle cramp
n1=en:retardation | n2=en:muscle cramp | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:muscle stiffness and rigidity, chronic, fluctuating
n1=en:retardation | n2=en:muscle stiffness and rigidity, chronic, fluctuating | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:muscle weakness
n1=en:retardation | n2=en:muscle weakness | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:muscle weakness lower limb
n1=en:retardation | n2=en:muscle weakness lower limb | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:muscle weakness of limb
n1=en:retardation | n2=en:muscle weakness of limb | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:muscle weakness, distal (lower limbs more affected than upper limbs), due to motor neuronopathy
n1=en:retardation | n2=en:muscle weakness, distal (lower limbs more affected than upper limbs), due to motor neuronopathy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:muscle weakness, distal, upper and lower
n1=en:retardation | n2=en:muscle weakness, distal, upper and lower | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:muscle weakness, proximal, due to neuronopathy begins in the lower limbs and then progresses to upper limbs
n1=en:retardation | n2=en:muscle weakness, proximal, due to neuronopathy begins in the lower limbs and then progresses to upper limbs | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:muscle weakness, proximal, symmetric (lower limbs more affected than upper limbs) due to motor neuronopathy
n1=en:retardation | n2=en:muscle weakness, proximal, symmetric (lower limbs more affected than upper limbs) due to motor neuronopathy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:muscle weakness, symmetric, proximal due to motor neuronopathy
n1=en:retardation | n2=en:muscle weakness, symmetric, proximal due to motor neuronopathy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) type a, 4
n1=en:retardation | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) type a, 4 | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) type a, 6
n1=en:retardation | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) type a, 6 | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 3
n1=en:retardation | n2=en:muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 3 | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:muscular dystrophy, congenital, 1c
n1=en:retardation | n2=en:muscular dystrophy, congenital, 1c | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:muscular dystrophy, congenital, megaconial type
n1=en:retardation | n2=en:muscular dystrophy, congenital, megaconial type | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:muscular hypotonia of the trunk
n1=en:retardation | n2=en:muscular hypotonia of the trunk | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:muscular rigidity
n1=en:retardation | n2=en:muscular rigidity | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:musician's cramp
n1=en:retardation | n2=en:musician's cramp | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:mutism
n1=en:retardation | n2=en:mutism | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:myclonus (rare)
n1=en:retardation | n2=en:myclonus (rare) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:myelin loss in the corticospinal tracts
n1=en:retardation | n2=en:myelin loss in the corticospinal tracts | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:myelin microvacuolation
n1=en:retardation | n2=en:myelin microvacuolation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:myelin-like lamellar structures in schwann cells
n1=en:retardation | n2=en:myelin-like lamellar structures in schwann cells | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:myelination defect
n1=en:retardation | n2=en:myelination defect | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:myelination defects (type ii)
n1=en:retardation | n2=en:myelination defects (type ii) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:myelomeningocele
n1=en:retardation | n2=en:myelomeningocele | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:myelomeningocele (less common)
n1=en:retardation | n2=en:myelomeningocele (less common) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:myelomeningocele (rare)
n1=en:retardation | n2=en:myelomeningocele (rare) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:myhre syndrome
n1=en:retardation | n2=en:myhre syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:myoclonic epilepsy (1 patient)
n1=en:retardation | n2=en:myoclonic epilepsy (1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:myoclonic jerk
n1=en:retardation | n2=en:myoclonic jerk | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:myoclonic jerks (less common)
n1=en:retardation | n2=en:myoclonic jerks (less common) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:myoclonic jerks (rare)
n1=en:retardation | n2=en:myoclonic jerks (rare) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:myoclonic seizure, refractory
n1=en:retardation | n2=en:myoclonic seizure, refractory | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:myoclonic seizures (1 patient)
n1=en:retardation | n2=en:myoclonic seizures (1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:myoclonic seizures (subtype 3a)
n1=en:retardation | n2=en:myoclonic seizures (subtype 3a) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:myoclonic seizures may occur
n1=en:retardation | n2=en:myoclonic seizures may occur | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:myoclonic seizures, frequent, long-lasting (many hours)
n1=en:retardation | n2=en:myoclonic seizures, frequent, long-lasting (many hours) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:myoclonic seizures, progressive
n1=en:retardation | n2=en:myoclonic seizures, progressive | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:myoclonic spasms, superimposed episodic, severe, painful (characterized by activation of antagonistic muscle pairs, may involve facial muscles)
n1=en:retardation | n2=en:myoclonic spasms, superimposed episodic, severe, painful (characterized by activation of antagonistic muscle pairs, may involve facial muscles) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:myoclonic-astatic seizures
n1=en:retardation | n2=en:myoclonic-astatic seizures | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:myoclonus (in 1 family)
n1=en:retardation | n2=en:myoclonus (in 1 family) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:myoclonus (in a subset of patients)
n1=en:retardation | n2=en:myoclonus (in a subset of patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:myoclonus (less common)
n1=en:retardation | n2=en:myoclonus (less common) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:myoclonus (subtype 3a)
n1=en:retardation | n2=en:myoclonus (subtype 3a) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:myoclonus (type i and type ii, infantile and juvenile)
n1=en:retardation | n2=en:myoclonus (type i and type ii, infantile and juvenile) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:myoclonus, axial (predominantly in upper limbs, occurs at rest and increases with activity or changes in posture)
n1=en:retardation | n2=en:myoclonus, axial (predominantly in upper limbs, occurs at rest and increases with activity or changes in posture) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:myoclonus, cortical, multifocal
n1=en:retardation | n2=en:myoclonus, cortical, multifocal | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:myoclonus, paroxysmal
n1=en:retardation | n2=en:myoclonus, paroxysmal | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:myokymia
n1=en:retardation | n2=en:myokymia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:myokymia (in some patients)
n1=en:retardation | n2=en:myokymia (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:myokymia, especially facial
n1=en:retardation | n2=en:myokymia, especially facial | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:myopathy
n1=en:retardation | n2=en:myopathy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:myotonia
n1=en:retardation | n2=en:myotonia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:myotonia (in 1 patient)
n1=en:retardation | n2=en:myotonia (in 1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:myotonic seizures
n1=en:retardation | n2=en:myotonic seizures | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:myxedema
n1=en:retardation | n2=en:myxedema | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:narcolepsy
n1=en:retardation | n2=en:narcolepsy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neck drop
n1=en:retardation | n2=en:neck drop | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neck pain
n1=en:retardation | n2=en:neck pain | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:necrotic process
n1=en:retardation | n2=en:necrotic process | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:necrotic white matter lesions throughout the brain and brainstem
n1=en:retardation | n2=en:necrotic white matter lesions throughout the brain and brainstem | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neocortical atrophy
n1=en:retardation | n2=en:neocortical atrophy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neocortical dysplasia (27%)
n1=en:retardation | n2=en:neocortical dysplasia (27%) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neonatal deformity
n1=en:retardation | n2=en:neonatal deformity | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neonatal epileptic encephalopathy (nee)
n1=en:retardation | n2=en:neonatal epileptic encephalopathy (nee) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neonatal hearing impairment
n1=en:retardation | n2=en:neonatal hearing impairment | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neonatal hypotonia
n1=en:retardation | n2=en:neonatal hypotonia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neonatal irresponsiveness
n1=en:retardation | n2=en:neonatal irresponsiveness | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neonatal irritability
n1=en:retardation | n2=en:neonatal irritability | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neonatal jaundice
n1=en:retardation | n2=en:neonatal jaundice | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neonatal/early-infantile onset encephalopathy
n1=en:retardation | n2=en:neonatal/early-infantile onset encephalopathy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neoplasm
n1=en:retardation | n2=en:neoplasm | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neoplasm of ocular adnexa
n1=en:retardation | n2=en:neoplasm of ocular adnexa | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:nerve cells show ballooning with membrane-bound vesicles with reticulogranular pattern
n1=en:retardation | n2=en:nerve cells show ballooning with membrane-bound vesicles with reticulogranular pattern | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:nerve degeneration
n1=en:retardation | n2=en:nerve degeneration | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:nerve paralysis
n1=en:retardation | n2=en:nerve paralysis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:nervous breakdown
n1=en:retardation | n2=en:nervous breakdown | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:nervousness
n1=en:retardation | n2=en:nervousness | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neuhauser syndrome
n1=en:retardation | n2=en:neuhauser syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neural tube defect
n1=en:retardation | n2=en:neural tube defect | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neural tube defect (in some patients)
n1=en:retardation | n2=en:neural tube defect (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neural tube defects (4%)
n1=en:retardation | n2=en:neural tube defects (4%) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neural tube defects may occur
n1=en:retardation | n2=en:neural tube defects may occur | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neurasthenia/surmenage
n1=en:retardation | n2=en:neurasthenia/surmenage | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neuroaxonal abnormalities
n1=en:retardation | n2=en:neuroaxonal abnormalities | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neuroaxonal dystrophies
n1=en:retardation | n2=en:neuroaxonal dystrophies | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neuroaxonal spheroids
n1=en:retardation | n2=en:neuroaxonal spheroids | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neurobehavioral changes associated with hyperammonemia
n1=en:retardation | n2=en:neurobehavioral changes associated with hyperammonemia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neurocognitive disorders
n1=en:retardation | n2=en:neurocognitive disorders | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neurocognitive impairment, mild (homozygous patient)
n1=en:retardation | n2=en:neurocognitive impairment, mild (homozygous patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neurodegeneration (patient a)
n1=en:retardation | n2=en:neurodegeneration (patient a) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neurodegeneration in the basal ganglia
n1=en:retardation | n2=en:neurodegeneration in the basal ganglia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neurodegeneration in the cerebellum
n1=en:retardation | n2=en:neurodegeneration in the cerebellum | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neurodegeneration in the substantia nigra
n1=en:retardation | n2=en:neurodegeneration in the substantia nigra | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neurodegeneration leading to profound mental retardation
n1=en:retardation | n2=en:neurodegeneration leading to profound mental retardation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neurodegeneration with brain iron accumulation 5
n1=en:retardation | n2=en:neurodegeneration with brain iron accumulation 5 | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neurodevelopmental anomaly
n1=en:retardation | n2=en:neurodevelopmental anomaly | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neurodevelopmental disorder
n1=en:retardation | n2=en:neurodevelopmental disorder | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neurodevelopmental impairment (early-onset form)
n1=en:retardation | n2=en:neurodevelopmental impairment (early-onset form) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neurodevelopmental regression
n1=en:retardation | n2=en:neurodevelopmental regression | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neurofibrillary degeneration (morphologic abnormality)
n1=en:retardation | n2=en:neurofibrillary degeneration (morphologic abnormality) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neurofibrillary mapt (tau)-positive tangles
n1=en:retardation | n2=en:neurofibrillary mapt (tau)-positive tangles | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neurofibrillary tangles composed of disordered microtubules
n1=en:retardation | n2=en:neurofibrillary tangles composed of disordered microtubules | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neurofibrillary tangles may be present
n1=en:retardation | n2=en:neurofibrillary tangles may be present | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neurofibromas can occur at cervical, thoracic, lumbar, and sacral levels
n1=en:retardation | n2=en:neurofibromas can occur at cervical, thoracic, lumbar, and sacral levels | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neurogenic bladder
n1=en:retardation | n2=en:neurogenic bladder | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neurogenic muscle atrophy, especially in the lower limbs
n1=en:retardation | n2=en:neurogenic muscle atrophy, especially in the lower limbs | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neuroimaging shows cortical atrophy
n1=en:retardation | n2=en:neuroimaging shows cortical atrophy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neurologic abnormalities in about 7%
n1=en:retardation | n2=en:neurologic abnormalities in about 7% | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neurologic crises with coma (in some patients)
n1=en:retardation | n2=en:neurologic crises with coma (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neurologic decompensation
n1=en:retardation | n2=en:neurologic decompensation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neurologic degeneration
n1=en:retardation | n2=en:neurologic degeneration | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neurologic deterioration in longterm survivors
n1=en:retardation | n2=en:neurologic deterioration in longterm survivors | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neurologic dysfunction, progressive
n1=en:retardation | n2=en:neurologic dysfunction, progressive | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neurologic involvement (in some patients)
n1=en:retardation | n2=en:neurologic involvement (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neurologic involvement is rare
n1=en:retardation | n2=en:neurologic involvement is rare | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neurologic regression
n1=en:retardation | n2=en:neurologic regression | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neurologic regression after age 2 years
n1=en:retardation | n2=en:neurologic regression after age 2 years | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neurologic regression after prolonged episodes
n1=en:retardation | n2=en:neurologic regression after prolonged episodes | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neurologic regression around age 3 months
n1=en:retardation | n2=en:neurologic regression around age 3 months | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neurologic regression following seizure onset
n1=en:retardation | n2=en:neurologic regression following seizure onset | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neurologic sequelae not always present
n1=en:retardation | n2=en:neurologic sequelae not always present | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neurologic sequelae of stroke
n1=en:retardation | n2=en:neurologic sequelae of stroke | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neurologic symptoms, if present, usually result from associated syringomyelia
n1=en:retardation | n2=en:neurologic symptoms, if present, usually result from associated syringomyelia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neurological development terminology
n1=en:retardation | n2=en:neurological development terminology | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neuromuscular disturbances, progressive
n1=en:retardation | n2=en:neuromuscular disturbances, progressive | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neuron apoptotic process
n1=en:retardation | n2=en:neuron apoptotic process | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neuron loss
n1=en:retardation | n2=en:neuron loss | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neuronal and vascular calcifications
n1=en:retardation | n2=en:neuronal and vascular calcifications | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neuronal ceroid lipofuscinosis
n1=en:retardation | n2=en:neuronal ceroid lipofuscinosis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neuronal ceroid lipofuscinosis type 3
n1=en:retardation | n2=en:neuronal ceroid lipofuscinosis type 3 | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neuronal heterotopia
n1=en:retardation | n2=en:neuronal heterotopia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neuronal inclusion bodies stain for neuroserpin
n1=en:retardation | n2=en:neuronal inclusion bodies stain for neuroserpin | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neuronal loss (patient a)
n1=en:retardation | n2=en:neuronal loss (patient a) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neuronal loss and gliosis in caudate and putamen
n1=en:retardation | n2=en:neuronal loss and gliosis in caudate and putamen | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neuronal loss and gliosis in the cerebral cortex
n1=en:retardation | n2=en:neuronal loss and gliosis in the cerebral cortex | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neuronal loss and gliosis in the dentate nucleus
n1=en:retardation | n2=en:neuronal loss and gliosis in the dentate nucleus | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neuronal loss and gliosis in the inferior olives
n1=en:retardation | n2=en:neuronal loss and gliosis in the inferior olives | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neuronal loss and gliosis in the substantia nigra pars compacta
n1=en:retardation | n2=en:neuronal loss and gliosis in the substantia nigra pars compacta | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neuronal loss in basal ganglia
n1=en:retardation | n2=en:neuronal loss in basal ganglia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neuronal loss in central nervous system
n1=en:retardation | n2=en:neuronal loss in central nervous system | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neuronal loss in the brainstem
n1=en:retardation | n2=en:neuronal loss in the brainstem | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neuronal loss in the cerebral cortex
n1=en:retardation | n2=en:neuronal loss in the cerebral cortex | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neuronal loss in the cerebrum and cerebellum
n1=en:retardation | n2=en:neuronal loss in the cerebrum and cerebellum | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neuronal loss in the dentate nuclei
n1=en:retardation | n2=en:neuronal loss in the dentate nuclei | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neuronal loss in the hippocampus
n1=en:retardation | n2=en:neuronal loss in the hippocampus | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neuronal loss in the inferior olives
n1=en:retardation | n2=en:neuronal loss in the inferior olives | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neuronal loss in the locus ceruleus
n1=en:retardation | n2=en:neuronal loss in the locus ceruleus | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neuronal loss in the purkinje cell layer of the cerebellar vermis
n1=en:retardation | n2=en:neuronal loss in the purkinje cell layer of the cerebellar vermis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neuronal loss in the striatum, cerebral cortex, and cerebellum (in some patients)
n1=en:retardation | n2=en:neuronal loss in the striatum, cerebral cortex, and cerebellum (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neuronal loss in the striatum, medial thalamic nuclei, and inferior olives
n1=en:retardation | n2=en:neuronal loss in the striatum, medial thalamic nuclei, and inferior olives | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neuronal loss in the substantia nigra
n1=en:retardation | n2=en:neuronal loss in the substantia nigra | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neuronal loss, diffuse
n1=en:retardation | n2=en:neuronal loss, diffuse | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neuronal loss, particularly of cerebellar purkinje cells
n1=en:retardation | n2=en:neuronal loss, particularly of cerebellar purkinje cells | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neuronal migration defect
n1=en:retardation | n2=en:neuronal migration defect | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neuronal migration disorder
n1=en:retardation | n2=en:neuronal migration disorder | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neuropathologic examination shows calcification of the small brain vessels
n1=en:retardation | n2=en:neuropathologic examination shows calcification of the small brain vessels | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neuropathologic examination shows extensive spongiosis and gliosis
n1=en:retardation | n2=en:neuropathologic examination shows extensive spongiosis and gliosis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neuropathologic examination shows severe demyelination
n1=en:retardation | n2=en:neuropathologic examination shows severe demyelination | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neuropathologic findings include leukoencephalopathy, predominantly in the upper corticospinal tract and cerebellar peduncles (initially)
n1=en:retardation | n2=en:neuropathologic findings include leukoencephalopathy, predominantly in the upper corticospinal tract and cerebellar peduncles (initially) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neuropathology shows alpha-synuclein-containing cytoplasmic inclusions in glial cells
n1=en:retardation | n2=en:neuropathology shows alpha-synuclein-containing cytoplasmic inclusions in glial cells | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neuropathology shows diffuse demyelination of the cerebral white matter
n1=en:retardation | n2=en:neuropathology shows diffuse demyelination of the cerebral white matter | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neuropathology shows fmr1 mrna-positive inclusions in neurons and astrocytes
n1=en:retardation | n2=en:neuropathology shows fmr1 mrna-positive inclusions in neurons and astrocytes | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neuropathology shows neuronal degeneration
n1=en:retardation | n2=en:neuropathology shows neuronal degeneration | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neuropathology shows neuronal loss in basal ganglia, brainstem, and cerebellum
n1=en:retardation | n2=en:neuropathology shows neuronal loss in basal ganglia, brainstem, and cerebellum | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neuropathology shows severe neuronal loss in the inner granular layer of the cerebellum
n1=en:retardation | n2=en:neuropathology shows severe neuronal loss in the inner granular layer of the cerebellum | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neurophysiologic abnormalities (eeg, sep, vep)
n1=en:retardation | n2=en:neurophysiologic abnormalities (eeg, sep, vep) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neurophysiologic abnormalities (eeg, vep, sep)
n1=en:retardation | n2=en:neurophysiologic abnormalities (eeg, vep, sep) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neurophysiologic studies show evidence of denervation and renervation
n1=en:retardation | n2=en:neurophysiologic studies show evidence of denervation and renervation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neuropil
n1=en:retardation | n2=en:neuropil | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neuropsychologic cognitive abnormalities
n1=en:retardation | n2=en:neuropsychologic cognitive abnormalities | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neuropsychologic impairment
n1=en:retardation | n2=en:neuropsychologic impairment | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neurosarcoidosis (5-16% of patients)
n1=en:retardation | n2=en:neurosarcoidosis (5-16% of patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neurosis
n1=en:retardation | n2=en:neurosis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neurotic, personality, or other mental disorder
n1=en:retardation | n2=en:neurotic, personality, or other mental disorder | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:neurotic, stress-related and somatoform disorders
n1=en:retardation | n2=en:neurotic, stress-related and somatoform disorders | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:never able to walk
n1=en:retardation | n2=en:never able to walk | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:never learn to walk (some patients)
n1=en:retardation | n2=en:never learn to walk (some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:nevus of ito
n1=en:retardation | n2=en:nevus of ito | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:nevus/mole
n1=en:retardation | n2=en:nevus/mole | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:nicolaides baraitser syndrome
n1=en:retardation | n2=en:nicolaides baraitser syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:niemann-pick disease, type a
n1=en:retardation | n2=en:niemann-pick disease, type a | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:nigrostriatal degeneration
n1=en:retardation | n2=en:nigrostriatal degeneration | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:no amyloid plaques
n1=en:retardation | n2=en:no amyloid plaques | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:no autistic features
n1=en:retardation | n2=en:no autistic features | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:no bulbar involvement
n1=en:retardation | n2=en:no bulbar involvement | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:no central nervous system abnormalities
n1=en:retardation | n2=en:no central nervous system abnormalities | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:no cerebellar signs
n1=en:retardation | n2=en:no cerebellar signs | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:no cerebellar vermis aplasia/hypoplasia
n1=en:retardation | n2=en:no cerebellar vermis aplasia/hypoplasia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:no cognitive decline
n1=en:retardation | n2=en:no cognitive decline | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:no dementia
n1=en:retardation | n2=en:no dementia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:no development
n1=en:retardation | n2=en:no development | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:no developmental progress
n1=en:retardation | n2=en:no developmental progress | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:no disease
n1=en:retardation | n2=en:no disease | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:no gaze contact
n1=en:retardation | n2=en:no gaze contact | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:no head control
n1=en:retardation | n2=en:no head control | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:no hippocampal sclerosis
n1=en:retardation | n2=en:no hippocampal sclerosis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:no hydrocephalus
n1=en:retardation | n2=en:no hydrocephalus | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:no language
n1=en:retardation | n2=en:no language | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:no language development
n1=en:retardation | n2=en:no language development | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:no lewy bodies
n1=en:retardation | n2=en:no lewy bodies | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:no mental retardation
n1=en:retardation | n2=en:no mental retardation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:no motor skills acquired (in some)
n1=en:retardation | n2=en:no motor skills acquired (in some) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:no myoclonus
n1=en:retardation | n2=en:no myoclonus | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:no neurofibrillary tangles
n1=en:retardation | n2=en:no neurofibrillary tangles | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:no neurofibromas
n1=en:retardation | n2=en:no neurofibromas | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:no other neurologic deficits
n1=en:retardation | n2=en:no other neurologic deficits | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:no other neurologic disorder
n1=en:retardation | n2=en:no other neurologic disorder | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:no overt seizures
n1=en:retardation | n2=en:no overt seizures | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:no pick bodies or lewy bodies
n1=en:retardation | n2=en:no pick bodies or lewy bodies | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:no response to l-dopa treatment
n1=en:retardation | n2=en:no response to l-dopa treatment | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:no seizures
n1=en:retardation | n2=en:no seizures | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:no seizures (hcs)
n1=en:retardation | n2=en:no seizures (hcs) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:no sensory deficit
n1=en:retardation | n2=en:no sensory deficit | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:no sensory symptoms
n1=en:retardation | n2=en:no sensory symptoms | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:no speech acquisition
n1=en:retardation | n2=en:no speech acquisition | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:no speech development (in most patients)
n1=en:retardation | n2=en:no speech development (in most patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:no speech problem
n1=en:retardation | n2=en:no speech problem | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:no spontaneous movements
n1=en:retardation | n2=en:no spontaneous movements | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:no structural brain abnormalities seen on mri
n1=en:retardation | n2=en:no structural brain abnormalities seen on mri | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:no structural brain anomalies
n1=en:retardation | n2=en:no structural brain anomalies | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:no tau pathology
n1=en:retardation | n2=en:no tau pathology | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:no tremor
n1=en:retardation | n2=en:no tremor | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:no visual fixation
n1=en:retardation | n2=en:no visual fixation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:no voluntary movement
n1=en:retardation | n2=en:no voluntary movement | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:nocturnal enuresis
n1=en:retardation | n2=en:nocturnal enuresis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:nocturnal occurrence
n1=en:retardation | n2=en:nocturnal occurrence | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:nocturnal occurrence, usually during light sleep
n1=en:retardation | n2=en:nocturnal occurrence, usually during light sleep | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:nocturnal seizures
n1=en:retardation | n2=en:nocturnal seizures | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:nocturnal seizures (in some patients)
n1=en:retardation | n2=en:nocturnal seizures (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:nocturnal sleep disruption
n1=en:retardation | n2=en:nocturnal sleep disruption | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:nodding of head
n1=en:retardation | n2=en:nodding of head | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:nodular heterotopia
n1=en:retardation | n2=en:nodular heterotopia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:nodular heterotopia (in some patients)
n1=en:retardation | n2=en:nodular heterotopia (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:nodular heterotopia (less common)
n1=en:retardation | n2=en:nodular heterotopia (less common) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:nodular heterotopia (rare)
n1=en:retardation | n2=en:nodular heterotopia (rare) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:nodular heterotopia of the grey matter
n1=en:retardation | n2=en:nodular heterotopia of the grey matter | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:non-febrile seizures later
n1=en:retardation | n2=en:non-febrile seizures later | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:non-gonococcal urethritis
n1=en:retardation | n2=en:non-gonococcal urethritis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:non-purposeful arm movements, choreoathetoid-like
n1=en:retardation | n2=en:non-purposeful arm movements, choreoathetoid-like | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:non-rheum heart valve disease
n1=en:retardation | n2=en:non-rheum heart valve disease | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:nonprogressive cerebellar ataxia
n1=en:retardation | n2=en:nonprogressive cerebellar ataxia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:nonspecific leukoencephalopathy (52%)
n1=en:retardation | n2=en:nonspecific leukoencephalopathy (52%) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:nonspecific spongiform degeneration
n1=en:retardation | n2=en:nonspecific spongiform degeneration | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:nonverbal (in some patients)
n1=en:retardation | n2=en:nonverbal (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:noonan-like syndrome with loose anagen hair
n1=en:retardation | n2=en:noonan-like syndrome with loose anagen hair | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:normal brain mri or ct scan
n1=en:retardation | n2=en:normal brain mri or ct scan | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:normal cognition (1 patient)
n1=en:retardation | n2=en:normal cognition (1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:normal cognition (in some patients)
n1=en:retardation | n2=en:normal cognition (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:normal cognition (reported in 1 patient who survived to age 20 years)
n1=en:retardation | n2=en:normal cognition (reported in 1 patient who survived to age 20 years) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:normal cognition (reported in some patients)
n1=en:retardation | n2=en:normal cognition (reported in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:normal cognition and intellectual function
n1=en:retardation | n2=en:normal cognition and intellectual function | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:normal delivery deadborn
n1=en:retardation | n2=en:normal delivery deadborn | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:normal delivery liveborn
n1=en:retardation | n2=en:normal delivery liveborn | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:normal development
n1=en:retardation | n2=en:normal development | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:normal development (in 2 of 6 patients)
n1=en:retardation | n2=en:normal development (in 2 of 6 patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:normal development in some patients
n1=en:retardation | n2=en:normal development in some patients | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:normal development until 6-18 months
n1=en:retardation | n2=en:normal development until 6-18 months | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:normal early development
n1=en:retardation | n2=en:normal early development | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:normal early development, up to 8 to 15 months of age
n1=en:retardation | n2=en:normal early development, up to 8 to 15 months of age | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:normal early developmental milestones
n1=en:retardation | n2=en:normal early developmental milestones | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:normal early psychomotor development
n1=en:retardation | n2=en:normal early psychomotor development | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:normal fine motor activity
n1=en:retardation | n2=en:normal fine motor activity | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:normal initial psychomotor development
n1=en:retardation | n2=en:normal initial psychomotor development | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:normal intellectual development
n1=en:retardation | n2=en:normal intellectual development | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:normal intellectual function
n1=en:retardation | n2=en:normal intellectual function | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:normal intelligence (in some patients)
n1=en:retardation | n2=en:normal intelligence (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:normal intelligence (majority)
n1=en:retardation | n2=en:normal intelligence (majority) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:normal intelligence in carrier females
n1=en:retardation | n2=en:normal intelligence in carrier females | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:normal intelligence in iib
n1=en:retardation | n2=en:normal intelligence in iib | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:normal intelligence in majority
n1=en:retardation | n2=en:normal intelligence in majority | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:normal intelligence in most cases
n1=en:retardation | n2=en:normal intelligence in most cases | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:normal intelligence to mild or moderate mental retardation
n1=en:retardation | n2=en:normal intelligence to mild or moderate mental retardation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:normal interictal eeg
n1=en:retardation | n2=en:normal interictal eeg | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:normal interictal neurologic examination
n1=en:retardation | n2=en:normal interictal neurologic examination | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:normal iq in infancy, then iq drops with age
n1=en:retardation | n2=en:normal iq in infancy, then iq drops with age | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:normal mental development
n1=en:retardation | n2=en:normal mental development | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:normal motor conduction studies (initially)
n1=en:retardation | n2=en:normal motor conduction studies (initially) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:normal motor development
n1=en:retardation | n2=en:normal motor development | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:normal muscle strength
n1=en:retardation | n2=en:normal muscle strength | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:normal neurologic development in most cases
n1=en:retardation | n2=en:normal neurologic development in most cases | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:normal neurological development is possible
n1=en:retardation | n2=en:normal neurological development is possible | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:normal neuromuscular studies
n1=en:retardation | n2=en:normal neuromuscular studies | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:normal psychomotor development
n1=en:retardation | n2=en:normal psychomotor development | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:normal psychomotor development in most
n1=en:retardation | n2=en:normal psychomotor development in most | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:normal psychomotor development until age 2 to 3 years
n1=en:retardation | n2=en:normal psychomotor development until age 2 to 3 years | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:normal sleep-onset time (normal time of falling asleep)
n1=en:retardation | n2=en:normal sleep-onset time (normal time of falling asleep) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:normal to mild mental retardation
n1=en:retardation | n2=en:normal to mild mental retardation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:normal to mildly delayed development
n1=en:retardation | n2=en:normal to mildly delayed development | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:normal, timely language development
n1=en:retardation | n2=en:normal, timely language development | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:norrie syndrome
n1=en:retardation | n2=en:norrie syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:nuclear magnetic resonance imaging brain normal
n1=en:retardation | n2=en:nuclear magnetic resonance imaging brain normal | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:numbness
n1=en:retardation | n2=en:numbness | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:nystagmus
n1=en:retardation | n2=en:nystagmus | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:nystagmus decreases on convergence
n1=en:retardation | n2=en:nystagmus decreases on convergence | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:nystagmus is accentuated by fixation, lateral gaze, smooth pursuit
n1=en:retardation | n2=en:nystagmus is accentuated by fixation, lateral gaze, smooth pursuit | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:nystagmus, horizontal
n1=en:retardation | n2=en:nystagmus, horizontal | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:nystagmus, jerky, horizontal, congenital
n1=en:retardation | n2=en:nystagmus, jerky, horizontal, congenital | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:nystagmus, mild
n1=en:retardation | n2=en:nystagmus, mild | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:obsessive compulsive behavior
n1=en:retardation | n2=en:obsessive compulsive behavior | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:obstruction of the foramen of monro (variable)
n1=en:retardation | n2=en:obstruction of the foramen of monro (variable) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:obtundation
n1=en:retardation | n2=en:obtundation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:occasional degeneration of the globus pallidus
n1=en:retardation | n2=en:occasional degeneration of the globus pallidus | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:occipital dermal sinus tract
n1=en:retardation | n2=en:occipital dermal sinus tract | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:occipital encephalocele (in some patients)
n1=en:retardation | n2=en:occipital encephalocele (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:occipital encephalocele (wws)
n1=en:retardation | n2=en:occipital encephalocele (wws) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:occipital encephaloceles
n1=en:retardation | n2=en:occipital encephaloceles | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:occipital headache
n1=en:retardation | n2=en:occipital headache | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:occipital lobe
n1=en:retardation | n2=en:occipital lobe | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:occipital lobe atrophy
n1=en:retardation | n2=en:occipital lobe atrophy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:occipital lobe infarct (rare)
n1=en:retardation | n2=en:occipital lobe infarct (rare) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:occipital meningocele
n1=en:retardation | n2=en:occipital meningocele | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:occipital meningocele (less common)
n1=en:retardation | n2=en:occipital meningocele (less common) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:occipital myelomeningocele (less common)
n1=en:retardation | n2=en:occipital myelomeningocele (less common) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:occipital neural tube defects
n1=en:retardation | n2=en:occipital neural tube defects | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:occlusive hydrocephalus, congenital
n1=en:retardation | n2=en:occlusive hydrocephalus, congenital | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:occurs most often during the night or early morning
n1=en:retardation | n2=en:occurs most often during the night or early morning | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ocular foreign body
n1=en:retardation | n2=en:ocular foreign body | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ocular motility spared
n1=en:retardation | n2=en:ocular motility spared | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ocular muscle abnormalities
n1=en:retardation | n2=en:ocular muscle abnormalities | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ocular palsies
n1=en:retardation | n2=en:ocular palsies | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:oculocerebrocutaneous syndrome
n1=en:retardation | n2=en:oculocerebrocutaneous syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:oculocerebrorenal syndrome
n1=en:retardation | n2=en:oculocerebrorenal syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:oculogyric crisis
n1=en:retardation | n2=en:oculogyric crisis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:oculomotor apraxia
n1=en:retardation | n2=en:oculomotor apraxia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:odontogenic cyst
n1=en:retardation | n2=en:odontogenic cyst | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ohdo syndrome, maat-kievit-brunner type
n1=en:retardation | n2=en:ohdo syndrome, maat-kievit-brunner type | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:olfactory lobe agenesis
n1=en:retardation | n2=en:olfactory lobe agenesis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:olfactory or auditory hallucinations
n1=en:retardation | n2=en:olfactory or auditory hallucinations | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:oligodendrocytes with foamy cytoplasm
n1=en:retardation | n2=en:oligodendrocytes with foamy cytoplasm | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:oligophrenia
n1=en:retardation | n2=en:oligophrenia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:olivopontocerebellar atrophy
n1=en:retardation | n2=en:olivopontocerebellar atrophy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:olivopontocerebellar hypoplasia, fetal-onset
n1=en:retardation | n2=en:olivopontocerebellar hypoplasia, fetal-onset | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:olivopontocerebellar hypoplasia, severe
n1=en:retardation | n2=en:olivopontocerebellar hypoplasia, severe | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:omphalocele
n1=en:retardation | n2=en:omphalocele | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:onat syndrome
n1=en:retardation | n2=en:onat syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:only some achieve rolling or sitting
n1=en:retardation | n2=en:only some achieve rolling or sitting | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:only walking achieved
n1=en:retardation | n2=en:only walking achieved | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:onset may be triggered by emotional stress, fever, exercise, exposure to heat
n1=en:retardation | n2=en:onset may be triggered by emotional stress, fever, exercise, exposure to heat | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:open operculum
n1=en:retardation | n2=en:open operculum | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:open spina bifida (myelomeningocele, 182940)
n1=en:retardation | n2=en:open spina bifida (myelomeningocele, 182940) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:open sylvian fissures
n1=en:retardation | n2=en:open sylvian fissures | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:opisthotonic posturing
n1=en:retardation | n2=en:opisthotonic posturing | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:opisthotonos (type ii)
n1=en:retardation | n2=en:opisthotonos (type ii) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:opisthotonus
n1=en:retardation | n2=en:opisthotonus | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:opitz-g syndrome, type 2
n1=en:retardation | n2=en:opitz-g syndrome, type 2 | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:opsoclonus
n1=en:retardation | n2=en:opsoclonus | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:optic ataxia (in a subset of patients)
n1=en:retardation | n2=en:optic ataxia (in a subset of patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:optic nerve hypoplasia
n1=en:retardation | n2=en:optic nerve hypoplasia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:optic tract agenesis
n1=en:retardation | n2=en:optic tract agenesis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:optic tract and chiasm hypoplasia
n1=en:retardation | n2=en:optic tract and chiasm hypoplasia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:organic mental disorder
n1=en:retardation | n2=en:organic mental disorder | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:organic writer's cramp
n1=en:retardation | n2=en:organic writer's cramp | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:organic, including symptomatic, mental disorders
n1=en:retardation | n2=en:organic, including symptomatic, mental disorders | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:organoid nevus
n1=en:retardation | n2=en:organoid nevus | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ornithine carbamoyltransferase deficiency disease
n1=en:retardation | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:orofacial dyspraxia, linguistic and nonlinguistic
n1=en:retardation | n2=en:orofacial dyspraxia, linguistic and nonlinguistic | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:orofacial dystonia
n1=en:retardation | n2=en:orofacial dystonia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:orofaciodigital syndrome 11
n1=en:retardation | n2=en:orofaciodigital syndrome 11 | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:orofaciodigital syndrome 3
n1=en:retardation | n2=en:orofaciodigital syndrome 3 | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:orofaciodigital syndrome type 6
n1=en:retardation | n2=en:orofaciodigital syndrome type 6 | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:oromandibular dystonia
n1=en:retardation | n2=en:oromandibular dystonia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:orotic aciduria
n1=en:retardation | n2=en:orotic aciduria | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:orthostatic hypotension
n1=en:retardation | n2=en:orthostatic hypotension | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:orthostatic proteinuria
n1=en:retardation | n2=en:orthostatic proteinuria | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:osgood-schlatter's disease
n1=en:retardation | n2=en:osgood-schlatter's disease | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ossification of the faux cerebri (less common)
n1=en:retardation | n2=en:ossification of the faux cerebri (less common) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:osteoarthritis, knee
n1=en:retardation | n2=en:osteoarthritis, knee | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:osteoarthritis, spine
n1=en:retardation | n2=en:osteoarthritis, spine | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:osteolysis syndrome recessive
n1=en:retardation | n2=en:osteolysis syndrome recessive | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:osteoporosis
n1=en:retardation | n2=en:osteoporosis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:osteoporosis with pseudoglioma
n1=en:retardation | n2=en:osteoporosis with pseudoglioma | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:other abdominal hernia
n1=en:retardation | n2=en:other abdominal hernia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:other anaemias
n1=en:retardation | n2=en:other anaemias | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:other and unspecified congenital anomalies
n1=en:retardation | n2=en:other and unspecified congenital anomalies | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:other and unspecified disorders of the circulatory system
n1=en:retardation | n2=en:other and unspecified disorders of the circulatory system | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:other and unspecified special symptoms or syndromes, nec in mdr18_1
n1=en:retardation | n2=en:other and unspecified special symptoms or syndromes, nec in mdr18_1 | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:other arterial obstructive/peripheral vascular disease
n1=en:retardation | n2=en:other arterial obstructive/peripheral vascular disease | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:other auditory injuries
n1=en:retardation | n2=en:other auditory injuries | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:other auras may occur
n1=en:retardation | n2=en:other auras may occur | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:other benign neoplasm female genital
n1=en:retardation | n2=en:other benign neoplasm female genital | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:other benign neoplasm of skin, unspecified
n1=en:retardation | n2=en:other benign neoplasm of skin, unspecified | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:other complications of the puerperium
n1=en:retardation | n2=en:other complications of the puerperium | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:other concern behavior adolescence
n1=en:retardation | n2=en:other concern behavior adolescence | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:other concern behavior childhood
n1=en:retardation | n2=en:other concern behavior childhood | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:other congenital anomalies of limbs
n1=en:retardation | n2=en:other congenital anomalies of limbs | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:other congenital anomalies of nervous system
n1=en:retardation | n2=en:other congenital anomalies of nervous system | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:other congenital malformations of circulatory system
n1=en:retardation | n2=en:other congenital malformations of circulatory system | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:other congenital malformations of digestive system
n1=en:retardation | n2=en:other congenital malformations of digestive system | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:other congenital malformations of eye
n1=en:retardation | n2=en:other congenital malformations of eye | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:other congenital malformations of heart
n1=en:retardation | n2=en:other congenital malformations of heart | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:other congenital musculoskeletal deformities
n1=en:retardation | n2=en:other congenital musculoskeletal deformities | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:other congenital upper alimentary tract anomalies
n1=en:retardation | n2=en:other congenital upper alimentary tract anomalies | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:other cranial nerves may be involved
n1=en:retardation | n2=en:other cranial nerves may be involved | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:other dermatologic congenital anomalies
n1=en:retardation | n2=en:other dermatologic congenital anomalies | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:other digestive system injuries
n1=en:retardation | n2=en:other digestive system injuries | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:other disease blood/lymph/spleen
n1=en:retardation | n2=en:other disease blood/lymph/spleen | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:other disease male genital including breast
n1=en:retardation | n2=en:other disease male genital including breast | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:other disease of neurological system
n1=en:retardation | n2=en:other disease of neurological system | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:other disease of pregnancy/delivery/puerperium
n1=en:retardation | n2=en:other disease of pregnancy/delivery/puerperium | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:other diseases female genital system
n1=en:retardation | n2=en:other diseases female genital system | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:other diseases of digestive system
n1=en:retardation | n2=en:other diseases of digestive system | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:other diseases of ear/mastoid
n1=en:retardation | n2=en:other diseases of ear/mastoid | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:other disorders of eye
n1=en:retardation | n2=en:other disorders of eye | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:other disorders of the skin and subcutaneous tissue
n1=en:retardation | n2=en:other disorders of the skin and subcutaneous tissue | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:other disorders of urinary system
n1=en:retardation | n2=en:other disorders of urinary system | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:other endocrine or metabolic congenital anomalies
n1=en:retardation | n2=en:other endocrine or metabolic congenital anomalies | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:other endocrine/metabolic nutritional disease
n1=en:retardation | n2=en:other endocrine/metabolic nutritional disease | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:other female genital malignant neoplasms
n1=en:retardation | n2=en:other female genital malignant neoplasms | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:other forms of chronic ischaemic heart disease
n1=en:retardation | n2=en:other forms of chronic ischaemic heart disease | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:other forms of heart disease
n1=en:retardation | n2=en:other forms of heart disease | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:other general/unspecified diseases
n1=en:retardation | n2=en:other general/unspecified diseases | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:other head injury without skull fracture
n1=en:retardation | n2=en:other head injury without skull fracture | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:other hematologic congenital anomalies
n1=en:retardation | n2=en:other hematologic congenital anomalies | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:other hematologic injuries
n1=en:retardation | n2=en:other hematologic injuries | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:other hematologic malignant neoplasms
n1=en:retardation | n2=en:other hematologic malignant neoplasms | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:other hematological abnormality
n1=en:retardation | n2=en:other hematological abnormality | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:other infection neurological system
n1=en:retardation | n2=en:other infection neurological system | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:other infection/inflammation of eye (excluding herpes)
n1=en:retardation | n2=en:other infection/inflammation of eye (excluding herpes) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:other infections of respiratory system
n1=en:retardation | n2=en:other infections of respiratory system | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:other infectious diseases
n1=en:retardation | n2=en:other infectious diseases | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:other infectious skin disease
n1=en:retardation | n2=en:other infectious skin disease | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:other male genital malignant neoplasm
n1=en:retardation | n2=en:other male genital malignant neoplasm | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:other malignant neoplasm urinary tract
n1=en:retardation | n2=en:other malignant neoplasm urinary tract | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:other malignant respiratory neoplasm
n1=en:retardation | n2=en:other malignant respiratory neoplasm | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:other mental retardation
n1=en:retardation | n2=en:other mental retardation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:other mental/psychological disorders
n1=en:retardation | n2=en:other mental/psychological disorders | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:other musculoskeletal disorder
n1=en:retardation | n2=en:other musculoskeletal disorder | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:other neurologic injuries
n1=en:retardation | n2=en:other neurologic injuries | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:other neurotic disorders
n1=en:retardation | n2=en:other neurotic disorders | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:other non-obstetrical conditions
n1=en:retardation | n2=en:other non-obstetrical conditions | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:other ocular injuries
n1=en:retardation | n2=en:other ocular injuries | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:other organic psychosis
n1=en:retardation | n2=en:other organic psychosis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:other osteoarthritis
n1=en:retardation | n2=en:other osteoarthritis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:other peptic ulcers
n1=en:retardation | n2=en:other peptic ulcers | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:other peripheral neuritis
n1=en:retardation | n2=en:other peripheral neuritis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:other psychological symptom/complaint
n1=en:retardation | n2=en:other psychological symptom/complaint | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:other psychoses
n1=en:retardation | n2=en:other psychoses | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:other respiratory injuries
n1=en:retardation | n2=en:other respiratory injuries | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:other respiratory system diseases
n1=en:retardation | n2=en:other respiratory system diseases | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:other seizure types (in some patients)
n1=en:retardation | n2=en:other seizure types (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:other specified congenital malformations
n1=en:retardation | n2=en:other specified congenital malformations | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:other specified drug-induced mental disorders
n1=en:retardation | n2=en:other specified drug-induced mental disorders | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:other specified intellectual disabilities
n1=en:retardation | n2=en:other specified intellectual disabilities | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:other specified mental retardation
n1=en:retardation | n2=en:other specified mental retardation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:other specified psychophysiological malfunction
n1=en:retardation | n2=en:other specified psychophysiological malfunction | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:other specified transient mental disorders due to conditions classified elsewhere, other
n1=en:retardation | n2=en:other specified transient mental disorders due to conditions classified elsewhere, other | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:other viral disease with exanthems
n1=en:retardation | n2=en:other viral disease with exanthems | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:other viral diseases
n1=en:retardation | n2=en:other viral diseases | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:other/unspecified neoplasm female genital
n1=en:retardation | n2=en:other/unspecified neoplasm female genital | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:other/unspecified neoplasm skin
n1=en:retardation | n2=en:other/unspecified neoplasm skin | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:other/unspecified neoplasms
n1=en:retardation | n2=en:other/unspecified neoplasms | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:otitis externa
n1=en:retardation | n2=en:otitis externa | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:otocephaly
n1=en:retardation | n2=en:otocephaly | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:otopalatodigital syndrome, type ii
n1=en:retardation | n2=en:otopalatodigital syndrome, type ii | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:otosclerosis
n1=en:retardation | n2=en:otosclerosis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:over time, white matter vanishes and is replaced by csf
n1=en:retardation | n2=en:over time, white matter vanishes and is replaced by csf | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:overactive child/hyperkinetic
n1=en:retardation | n2=en:overactive child/hyperkinetic | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:overlapping lesion of brain
n1=en:retardation | n2=en:overlapping lesion of brain | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:overweight
n1=en:retardation | n2=en:overweight | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pachygyria (1 patient)
n1=en:retardation | n2=en:pachygyria (1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pachygyria (less common)
n1=en:retardation | n2=en:pachygyria (less common) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pachygyria (posterior-to-anterior gradient)
n1=en:retardation | n2=en:pachygyria (posterior-to-anterior gradient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pachygyria (rare)
n1=en:retardation | n2=en:pachygyria (rare) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pachygyria with preferential frontoparietal involvement (meb)
n1=en:retardation | n2=en:pachygyria with preferential frontoparietal involvement (meb) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pachygyria, bilateral frontotemporal
n1=en:retardation | n2=en:pachygyria, bilateral frontotemporal | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pachygyria, frontoparietal
n1=en:retardation | n2=en:pachygyria, frontoparietal | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pachygyria, most prominent in the frontal lobes
n1=en:retardation | n2=en:pachygyria, most prominent in the frontal lobes | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pachygyria, occipital
n1=en:retardation | n2=en:pachygyria, occipital | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pachygyria, usually posterior
n1=en:retardation | n2=en:pachygyria, usually posterior | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pachygyrias
n1=en:retardation | n2=en:pachygyrias | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pachymacrogyria
n1=en:retardation | n2=en:pachymacrogyria | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pachymeningitis cervicalis (cervical cord compression due to thickened dura)
n1=en:retardation | n2=en:pachymeningitis cervicalis (cervical cord compression due to thickened dura) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pain
n1=en:retardation | n2=en:pain | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pain (sharp, boring, drilling, piercing)
n1=en:retardation | n2=en:pain (sharp, boring, drilling, piercing) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pain affects upper body
n1=en:retardation | n2=en:pain affects upper body | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pain, episodic
n1=en:retardation | n2=en:pain, episodic | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:palatal myoclonus
n1=en:retardation | n2=en:palatal myoclonus | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pallidal degeneration
n1=en:retardation | n2=en:pallidal degeneration | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pallor of dorsal columns of the spinal cord
n1=en:retardation | n2=en:pallor of dorsal columns of the spinal cord | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:paradoxical cerebral emboli
n1=en:retardation | n2=en:paradoxical cerebral emboli | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:paralysis
n1=en:retardation | n2=en:paralysis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:paralysis, episodic, after strenuous exercise
n1=en:retardation | n2=en:paralysis, episodic, after strenuous exercise | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:paraneoplastic syndrome
n1=en:retardation | n2=en:paraneoplastic syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:paranoid reaction
n1=en:retardation | n2=en:paranoid reaction | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:paraparesis
n1=en:retardation | n2=en:paraparesis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:paraparesis, spastic
n1=en:retardation | n2=en:paraparesis, spastic | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:paraphilias
n1=en:retardation | n2=en:paraphilias | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:paraplegia
n1=en:retardation | n2=en:paraplegia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:paraplegia secondary to spinal cord compression due to severe kyphosis
n1=en:retardation | n2=en:paraplegia secondary to spinal cord compression due to severe kyphosis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:paraspinal masses
n1=en:retardation | n2=en:paraspinal masses | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:paraventricular cysts
n1=en:retardation | n2=en:paraventricular cysts | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:parenchymal neuromelanosis
n1=en:retardation | n2=en:parenchymal neuromelanosis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:paresis (hcp)
n1=en:retardation | n2=en:paresis (hcp) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:paresis of extensor muscles of the big toe is presenting symptom
n1=en:retardation | n2=en:paresis of extensor muscles of the big toe is presenting symptom | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:paresthesia
n1=en:retardation | n2=en:paresthesia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:parietal lobe
n1=en:retardation | n2=en:parietal lobe | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:parietal lobe epilepsy
n1=en:retardation | n2=en:parietal lobe epilepsy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:paris trousseau thrombocytopenia
n1=en:retardation | n2=en:paris trousseau thrombocytopenia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:parkinsonism
n1=en:retardation | n2=en:parkinsonism | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:parkinsonism (in some patients)
n1=en:retardation | n2=en:parkinsonism (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:parkinsonism (in some)
n1=en:retardation | n2=en:parkinsonism (in some) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:parkinsonism (later onset)
n1=en:retardation | n2=en:parkinsonism (later onset) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:parkinsonism (later)
n1=en:retardation | n2=en:parkinsonism (later) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:parkinsonism (less common)
n1=en:retardation | n2=en:parkinsonism (less common) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:parkinsonism has been described in 1 family
n1=en:retardation | n2=en:parkinsonism has been described in 1 family | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:parkinsonism may occur
n1=en:retardation | n2=en:parkinsonism may occur | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:parkinsonism, early-onset
n1=en:retardation | n2=en:parkinsonism, early-onset | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:parkinsonism, l-dopa responsive
n1=en:retardation | n2=en:parkinsonism, l-dopa responsive | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:parkinsonism, levodopa-responsive (occurs at later stages, may replace dystonia symptoms)
n1=en:retardation | n2=en:parkinsonism, levodopa-responsive (occurs at later stages, may replace dystonia symptoms) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:paroxysmal choreoathetosis
n1=en:retardation | n2=en:paroxysmal choreoathetosis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:paroxysmal dystonia
n1=en:retardation | n2=en:paroxysmal dystonia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:paroxysmal lethargy
n1=en:retardation | n2=en:paroxysmal lethargy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:paroxysmal nonkinesigenic dyskinesia
n1=en:retardation | n2=en:paroxysmal nonkinesigenic dyskinesia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:paroxysmal oculogyric crises
n1=en:retardation | n2=en:paroxysmal oculogyric crises | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:partial absence of the corpus callosum (in one patient)
n1=en:retardation | n2=en:partial absence of the corpus callosum (in one patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:partial agenesis of corpus callosum
n1=en:retardation | n2=en:partial agenesis of corpus callosum | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:partial agenesis of corpus callosum (rare, in males)
n1=en:retardation | n2=en:partial agenesis of corpus callosum (rare, in males) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:partial agenesis of the corpus callosum (in 1 of 2 sibs)
n1=en:retardation | n2=en:partial agenesis of the corpus callosum (in 1 of 2 sibs) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:partial agenesis of the corpus callosum (rare)
n1=en:retardation | n2=en:partial agenesis of the corpus callosum (rare) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:partial empty sella turcica
n1=en:retardation | n2=en:partial empty sella turcica | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:partial epilepsy
n1=en:retardation | n2=en:partial epilepsy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:partial migrating seizures seen on eeg (in some patients)
n1=en:retardation | n2=en:partial migrating seizures seen on eeg (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:partial or complete absence of the cerebellar vermis consistent with dandy walker malformation
n1=en:retardation | n2=en:partial or complete absence of the cerebellar vermis consistent with dandy walker malformation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:partial or complete agenesis of corpus callosum
n1=en:retardation | n2=en:partial or complete agenesis of corpus callosum | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:partial or total agenesis of the corpus callosum (33%)
n1=en:retardation | n2=en:partial or total agenesis of the corpus callosum (33%) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:partial pachygyria
n1=en:retardation | n2=en:partial pachygyria | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:partial response to pyridoxine
n1=en:retardation | n2=en:partial response to pyridoxine | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:partial seizure
n1=en:retardation | n2=en:partial seizure | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:partial seizures, simple and complex
n1=en:retardation | n2=en:partial seizures, simple and complex | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:partington x-linked mental retardation syndrome
n1=en:retardation | n2=en:partington x-linked mental retardation syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:patchy demyelination of subcortical white matter
n1=en:retardation | n2=en:patchy demyelination of subcortical white matter | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:patchy diffuse hyperintensities on t2-weighted mri
n1=en:retardation | n2=en:patchy diffuse hyperintensities on t2-weighted mri | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:patellar and ankle clonus
n1=en:retardation | n2=en:patellar and ankle clonus | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:patellar tendon reflexes hyperactive
n1=en:retardation | n2=en:patellar tendon reflexes hyperactive | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:patent ductus arteriosus - persisting type
n1=en:retardation | n2=en:patent ductus arteriosus - persisting type | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pathologic calcification, calcified structure
n1=en:retardation | n2=en:pathologic calcification, calcified structure | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pathologic changes in anterior horn cells and lateral corticospinal tracts
n1=en:retardation | n2=en:pathologic changes in anterior horn cells and lateral corticospinal tracts | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pathology includes spongiform changes, diffuse nerve cell degeneration and glial proliferation
n1=en:retardation | n2=en:pathology includes spongiform changes, diffuse nerve cell degeneration and glial proliferation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:patients 20-30 years old have hyperintense lesions on t2-weighted mri in the frontal and anterior temporal lobes
n1=en:retardation | n2=en:patients 20-30 years old have hyperintense lesions on t2-weighted mri in the frontal and anterior temporal lobes | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:patients 30-40 years old have hyperintense lesions in periventricular areas, the external capsule, basal ganglia, thalamus, and brainstem
n1=en:retardation | n2=en:patients 30-40 years old have hyperintense lesions in periventricular areas, the external capsule, basal ganglia, thalamus, and brainstem | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:patients achieve ambulation
n1=en:retardation | n2=en:patients achieve ambulation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:patients may develop a seizure disorder later in life
n1=en:retardation | n2=en:patients may develop a seizure disorder later in life | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:patients may have no structural abnormalities in the central nervous system
n1=en:retardation | n2=en:patients may have no structural abnormalities in the central nervous system | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:patients may only achieve sitting or walking
n1=en:retardation | n2=en:patients may only achieve sitting or walking | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:patients older than 50 years have hyperintensities, lacunar infarcts, and microbleeds
n1=en:retardation | n2=en:patients older than 50 years have hyperintensities, lacunar infarcts, and microbleeds | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:patients show normal psychomotor development
n1=en:retardation | n2=en:patients show normal psychomotor development | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:paucity of anterior horn motor neurons
n1=en:retardation | n2=en:paucity of anterior horn motor neurons | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:peak frequency of vomiting every 10 to 15 minutes
n1=en:retardation | n2=en:peak frequency of vomiting every 10 to 15 minutes | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:peculiar gait (if left untreated)
n1=en:retardation | n2=en:peculiar gait (if left untreated) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:peculiar stance and sitting posture (if left untreated)
n1=en:retardation | n2=en:peculiar stance and sitting posture (if left untreated) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pediatric adverse events terminology
n1=en:retardation | n2=en:pediatric adverse events terminology | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pediatric failure to thrive
n1=en:retardation | n2=en:pediatric failure to thrive | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pediatric immunization terminology
n1=en:retardation | n2=en:pediatric immunization terminology | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pediatric psychiatric disorder
n1=en:retardation | n2=en:pediatric psychiatric disorder | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pediatric terminology
n1=en:retardation | n2=en:pediatric terminology | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pediculosis/other skin infestation
n1=en:retardation | n2=en:pediculosis/other skin infestation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pelizaeus-merzbacher disease
n1=en:retardation | n2=en:pelizaeus-merzbacher disease | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pelvic inflammatory disease
n1=en:retardation | n2=en:pelvic inflammatory disease | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:perception disturbance
n1=en:retardation | n2=en:perception disturbance | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pericystic abnormal myelination
n1=en:retardation | n2=en:pericystic abnormal myelination | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:perinatal mortality
n1=en:retardation | n2=en:perinatal mortality | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:periodic paralysis (finding)
n1=en:retardation | n2=en:periodic paralysis (finding) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:periodic paralysis, usually hypokalemic
n1=en:retardation | n2=en:periodic paralysis, usually hypokalemic | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:periodic stiffness
n1=en:retardation | n2=en:periodic stiffness | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:peripheral demyelinating neuropathy, central dysmyelination, waardenburg syndrome, and hirschsprung disease
n1=en:retardation | n2=en:peripheral demyelinating neuropathy, central dysmyelination, waardenburg syndrome, and hirschsprung disease | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:peripheral hypertonia
n1=en:retardation | n2=en:peripheral hypertonia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:peripheral motor neuropathy
n1=en:retardation | n2=en:peripheral motor neuropathy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:peripheral nervous system disorder
n1=en:retardation | n2=en:peripheral nervous system disorder | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:peripheral sensory neuropathy
n1=en:retardation | n2=en:peripheral sensory neuropathy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:perisylvian polymicrogyria
n1=en:retardation | n2=en:perisylvian polymicrogyria | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:perivascular spaces
n1=en:retardation | n2=en:perivascular spaces | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:periventricular and subcortical white matter abnormalities
n1=en:retardation | n2=en:periventricular and subcortical white matter abnormalities | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:periventricular calcifications
n1=en:retardation | n2=en:periventricular calcifications | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:periventricular cysts
n1=en:retardation | n2=en:periventricular cysts | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:periventricular gray matter heterotopia
n1=en:retardation | n2=en:periventricular gray matter heterotopia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:periventricular hemorrhagic infarction
n1=en:retardation | n2=en:periventricular hemorrhagic infarction | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:periventricular leukomalacia
n1=en:retardation | n2=en:periventricular leukomalacia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:periventricular leukomalacia (reported in 2 patients)
n1=en:retardation | n2=en:periventricular leukomalacia (reported in 2 patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:periventricular nodular heterotopia
n1=en:retardation | n2=en:periventricular nodular heterotopia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:periventricular nodular heterotopia seen on mri
n1=en:retardation | n2=en:periventricular nodular heterotopia seen on mri | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:periventricular white matter abnormalities
n1=en:retardation | n2=en:periventricular white matter abnormalities | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:periventricular white matter abnormalities (in some patients)
n1=en:retardation | n2=en:periventricular white matter abnormalities (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:periventricular white matter changes
n1=en:retardation | n2=en:periventricular white matter changes | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:periventricular white matter changes (meb)
n1=en:retardation | n2=en:periventricular white matter changes (meb) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:periventricular white matter gliosis (in some patients)
n1=en:retardation | n2=en:periventricular white matter gliosis (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:periventricular white matter hyperintensities, bilateral
n1=en:retardation | n2=en:periventricular white matter hyperintensities, bilateral | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:periventricular white matter lesions
n1=en:retardation | n2=en:periventricular white matter lesions | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pernicious/folate deficiency anemias
n1=en:retardation | n2=en:pernicious/folate deficiency anemias | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:peroxisomal fatty acyl-coa reductase 1 disorder
n1=en:retardation | n2=en:peroxisomal fatty acyl-coa reductase 1 disorder | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:peroxisome biogenesis disorder 3b
n1=en:retardation | n2=en:peroxisome biogenesis disorder 3b | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:perseveration
n1=en:retardation | n2=en:perseveration | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:persistent cavum septum pellucidum
n1=en:retardation | n2=en:persistent cavum septum pellucidum | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:persistent cavus septum pellucidum
n1=en:retardation | n2=en:persistent cavus septum pellucidum | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:persistent cloaca
n1=en:retardation | n2=en:persistent cloaca | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:persistent falcine venous sinus
n1=en:retardation | n2=en:persistent falcine venous sinus | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:personal care disability
n1=en:retardation | n2=en:personal care disability | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:personal hygiene disability
n1=en:retardation | n2=en:personal hygiene disability | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:personality change
n1=en:retardation | n2=en:personality change | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:personality disorder
n1=en:retardation | n2=en:personality disorder | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:personality disorders and disturbances in behaviour
n1=en:retardation | n2=en:personality disorders and disturbances in behaviour | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pervasive developmental disorder
n1=en:retardation | n2=en:pervasive developmental disorder | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:petit mal epilepsy
n1=en:retardation | n2=en:petit mal epilepsy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pettigrew syndrome
n1=en:retardation | n2=en:pettigrew syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pharyngeal gag reflex negative
n1=en:retardation | n2=en:pharyngeal gag reflex negative | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:phase of life problem adult
n1=en:retardation | n2=en:phase of life problem adult | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:phenylketonuria
n1=en:retardation | n2=en:phenylketonuria | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:phenylketonuria ii
n1=en:retardation | n2=en:phenylketonuria ii | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:phlebitis and thrombophlebitis
n1=en:retardation | n2=en:phlebitis and thrombophlebitis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:phonology deficits
n1=en:retardation | n2=en:phonology deficits | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:phonophobia
n1=en:retardation | n2=en:phonophobia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:phosphoglycerate dehydrogenase deficiency
n1=en:retardation | n2=en:phosphoglycerate dehydrogenase deficiency | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:phosphoglycerate kinase 1 deficiency
n1=en:retardation | n2=en:phosphoglycerate kinase 1 deficiency | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:photoparoxysmal and photomyoclonic responses
n1=en:retardation | n2=en:photoparoxysmal and photomyoclonic responses | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:photoparoxysmal response (in some)
n1=en:retardation | n2=en:photoparoxysmal response (in some) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:photophobia
n1=en:retardation | n2=en:photophobia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:photosensitive tonic-clonic seizures
n1=en:retardation | n2=en:photosensitive tonic-clonic seizures | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:photosensitivity in one-third of patients
n1=en:retardation | n2=en:photosensitivity in one-third of patients | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:physical disability
n1=en:retardation | n2=en:physical disability | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pick bodies found in neocortical layers, granule cells of the dentate gyrus, and throughout the hippocampus
n1=en:retardation | n2=en:pick bodies found in neocortical layers, granule cells of the dentate gyrus, and throughout the hippocampus | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pigmentary loss in the substantia nigra
n1=en:retardation | n2=en:pigmentary loss in the substantia nigra | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pilonidal cyst/fistula
n1=en:retardation | n2=en:pilonidal cyst/fistula | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pineal gland
n1=en:retardation | n2=en:pineal gland | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pineal hypertrophy
n1=en:retardation | n2=en:pineal hypertrophy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pitt-hopkins syndrome
n1=en:retardation | n2=en:pitt-hopkins syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pituitary agenesis
n1=en:retardation | n2=en:pituitary agenesis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pituitary agenesis (rare)
n1=en:retardation | n2=en:pituitary agenesis (rare) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pituitary aplasia or dysplasia
n1=en:retardation | n2=en:pituitary aplasia or dysplasia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pituitary gland adenoma
n1=en:retardation | n2=en:pituitary gland adenoma | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pituitary gland hypoplasia
n1=en:retardation | n2=en:pituitary gland hypoplasia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pituitary hypoplasia (in some patients)
n1=en:retardation | n2=en:pituitary hypoplasia (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pityriasis rosea
n1=en:retardation | n2=en:pityriasis rosea | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:plaque, amyloid
n1=en:retardation | n2=en:plaque, amyloid | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:platybasia
n1=en:retardation | n2=en:platybasia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pleural effusion
n1=en:retardation | n2=en:pleural effusion | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pleurisy with pleural effusion
n1=en:retardation | n2=en:pleurisy with pleural effusion | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pneumonia
n1=en:retardation | n2=en:pneumonia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:poisoning by medical agent
n1=en:retardation | n2=en:poisoning by medical agent | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:poliomyelitis/other enterovirus
n1=en:retardation | n2=en:poliomyelitis/other enterovirus | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:polycystic kidney disease
n1=en:retardation | n2=en:polycystic kidney disease | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:polyglucosan bodies (round intracellular inclusions) found in neuronal and astrocytic processes
n1=en:retardation | n2=en:polyglucosan bodies (round intracellular inclusions) found in neuronal and astrocytic processes | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:polygyria
n1=en:retardation | n2=en:polygyria | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:polymicrogyria
n1=en:retardation | n2=en:polymicrogyria | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:polymicrogyria (64%)
n1=en:retardation | n2=en:polymicrogyria (64%) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:polymicrogyria (meb)
n1=en:retardation | n2=en:polymicrogyria (meb) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:polymicrogyria (rare)
n1=en:retardation | n2=en:polymicrogyria (rare) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:polymicrogyria (reported in 1 patient)
n1=en:retardation | n2=en:polymicrogyria (reported in 1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:polymicrogyria, anterior to posterior gradient
n1=en:retardation | n2=en:polymicrogyria, anterior to posterior gradient | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:polymicrogyria, asymmetric or symmetric
n1=en:retardation | n2=en:polymicrogyria, asymmetric or symmetric | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:polymicrogyria, bilateral frontoparietal
n1=en:retardation | n2=en:polymicrogyria, bilateral frontoparietal | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:polymicrogyria, diffuse, asymmetric
n1=en:retardation | n2=en:polymicrogyria, diffuse, asymmetric | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:polymicrogyria, frontal
n1=en:retardation | n2=en:polymicrogyria, frontal | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:polymicrogyria, most severe in the frontoparietal regions
n1=en:retardation | n2=en:polymicrogyria, most severe in the frontoparietal regions | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:polymicrogyria, occipital
n1=en:retardation | n2=en:polymicrogyria, occipital | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:polymicrogyria, predominantly frontal and perisylvian
n1=en:retardation | n2=en:polymicrogyria, predominantly frontal and perisylvian | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:polymicrogyria, symmetric or asymmetric
n1=en:retardation | n2=en:polymicrogyria, symmetric or asymmetric | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:polymicrogyria, temporo-occipital
n1=en:retardation | n2=en:polymicrogyria, temporo-occipital | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:polymicrogyria, usually frontal (in some patients)
n1=en:retardation | n2=en:polymicrogyria, usually frontal (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:polyneuropathies, motor
n1=en:retardation | n2=en:polyneuropathies, motor | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:polyneuropathy
n1=en:retardation | n2=en:polyneuropathy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:polysyndactyly
n1=en:retardation | n2=en:polysyndactyly | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pons damage
n1=en:retardation | n2=en:pons damage | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pontine atrophy
n1=en:retardation | n2=en:pontine atrophy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pontine dysraphia
n1=en:retardation | n2=en:pontine dysraphia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pontine hypoplasia (1 family)
n1=en:retardation | n2=en:pontine hypoplasia (1 family) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pontine hypoplasia, mild
n1=en:retardation | n2=en:pontine hypoplasia, mild | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pontocerebellar arachnoid cyst (reported in 2 patients)
n1=en:retardation | n2=en:pontocerebellar arachnoid cyst (reported in 2 patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pontocerebellar atrophy
n1=en:retardation | n2=en:pontocerebellar atrophy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pontocerebellar hypoplasia type 1
n1=en:retardation | n2=en:pontocerebellar hypoplasia type 1 | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pontocerebellar hypoplasia, type 8
n1=en:retardation | n2=en:pontocerebellar hypoplasia, type 8 | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pontoneocerebellar hypoplasia
n1=en:retardation | n2=en:pontoneocerebellar hypoplasia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:poor adaptation to disability
n1=en:retardation | n2=en:poor adaptation to disability | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:poor adaptive skills
n1=en:retardation | n2=en:poor adaptive skills | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:poor balance (finding)
n1=en:retardation | n2=en:poor balance (finding) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:poor cognition
n1=en:retardation | n2=en:poor cognition | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:poor communication
n1=en:retardation | n2=en:poor communication | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:poor concentration
n1=en:retardation | n2=en:poor concentration | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:poor coordination
n1=en:retardation | n2=en:poor coordination | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:poor coordination (83%)
n1=en:retardation | n2=en:poor coordination (83%) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:poor delineation of cerebral cortical regions
n1=en:retardation | n2=en:poor delineation of cerebral cortical regions | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:poor dendritic maturation
n1=en:retardation | n2=en:poor dendritic maturation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:poor differentiation of gray and white matter on t2-weighted mri
n1=en:retardation | n2=en:poor differentiation of gray and white matter on t2-weighted mri | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:poor eye contact
n1=en:retardation | n2=en:poor eye contact | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:poor feeding (congenital form form)
n1=en:retardation | n2=en:poor feeding (congenital form form) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:poor fine and gross motor coordination
n1=en:retardation | n2=en:poor fine and gross motor coordination | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:poor fine motor coordination
n1=en:retardation | n2=en:poor fine motor coordination | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:poor fine motor skills
n1=en:retardation | n2=en:poor fine motor skills | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:poor gross motor coordination
n1=en:retardation | n2=en:poor gross motor coordination | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:poor hand-eye coordination
n1=en:retardation | n2=en:poor hand-eye coordination | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:poor head and trunk control in infancy
n1=en:retardation | n2=en:poor head and trunk control in infancy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:poor head control
n1=en:retardation | n2=en:poor head control | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:poor language
n1=en:retardation | n2=en:poor language | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:poor language and speech development
n1=en:retardation | n2=en:poor language and speech development | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:poor motor coordination
n1=en:retardation | n2=en:poor motor coordination | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:poor motor development
n1=en:retardation | n2=en:poor motor development | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:poor myelination
n1=en:retardation | n2=en:poor myelination | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:poor neonatal suck and swallow reflexes
n1=en:retardation | n2=en:poor neonatal suck and swallow reflexes | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:poor or absent independent walking
n1=en:retardation | n2=en:poor or absent independent walking | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:poor or absent smooth pursuit
n1=en:retardation | n2=en:poor or absent smooth pursuit | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:poor or absent speech
n1=en:retardation | n2=en:poor or absent speech | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:poor or absent speech acquisition
n1=en:retardation | n2=en:poor or absent speech acquisition | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:poor or absent speech development
n1=en:retardation | n2=en:poor or absent speech development | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:poor responsiveness
n1=en:retardation | n2=en:poor responsiveness | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:poor school performance
n1=en:retardation | n2=en:poor school performance | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:poor speech
n1=en:retardation | n2=en:poor speech | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:poor speech or lack of speech development
n1=en:retardation | n2=en:poor speech or lack of speech development | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:poor speech or no speech
n1=en:retardation | n2=en:poor speech or no speech | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:poor spontaneous movements
n1=en:retardation | n2=en:poor spontaneous movements | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:poor vestibuloocular reflex
n1=en:retardation | n2=en:poor vestibuloocular reflex | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:poor visual-motor integration (range 41-80)
n1=en:retardation | n2=en:poor visual-motor integration (range 41-80) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:poor visual-spatial construction
n1=en:retardation | n2=en:poor visual-spatial construction | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:poor-absent neurologic development
n1=en:retardation | n2=en:poor-absent neurologic development | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:porencephalic changes
n1=en:retardation | n2=en:porencephalic changes | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:porencephalic cyst
n1=en:retardation | n2=en:porencephalic cyst | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:porencephaly (in some patients)
n1=en:retardation | n2=en:porencephaly (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:porencephaly, familial
n1=en:retardation | n2=en:porencephaly, familial | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:posterior column degeneration
n1=en:retardation | n2=en:posterior column degeneration | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:posterior column sensory loss
n1=en:retardation | n2=en:posterior column sensory loss | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:posterior fossa abnormalities (rare)
n1=en:retardation | n2=en:posterior fossa abnormalities (rare) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:posterior fossa arachnoid cyst
n1=en:retardation | n2=en:posterior fossa arachnoid cyst | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:posterior fossa compression syndrome
n1=en:retardation | n2=en:posterior fossa compression syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:posterior fossa crowding, progressive
n1=en:retardation | n2=en:posterior fossa crowding, progressive | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:posterior fossa cyst
n1=en:retardation | n2=en:posterior fossa cyst | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:posterior fossa cyst (in 1 of 2 patients)
n1=en:retardation | n2=en:posterior fossa cyst (in 1 of 2 patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:posterior fossa cyst continuous with the fourth ventricle
n1=en:retardation | n2=en:posterior fossa cyst continuous with the fourth ventricle | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:posterior fossa cysts (wws)
n1=en:retardation | n2=en:posterior fossa cysts (wws) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:posterior fossa malformations
n1=en:retardation | n2=en:posterior fossa malformations | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:posterior pachygyria
n1=en:retardation | n2=en:posterior pachygyria | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:posterior slow-wave activity on eeg
n1=en:retardation | n2=en:posterior slow-wave activity on eeg | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:posterior urethral valve
n1=en:retardation | n2=en:posterior urethral valve | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:postnatal development of hypertonic extremities
n1=en:retardation | n2=en:postnatal development of hypertonic extremities | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:postural dystonia (onset is restricted to 1 extremity, usually lower, with foot dystonia)
n1=en:retardation | n2=en:postural dystonia (onset is restricted to 1 extremity, usually lower, with foot dystonia) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:postural hand tremor
n1=en:retardation | n2=en:postural hand tremor | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:postural instability
n1=en:retardation | n2=en:postural instability | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:postural instability (63%)
n1=en:retardation | n2=en:postural instability (63%) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:postural tremor (later onset, spreads to all limbs and neck)
n1=en:retardation | n2=en:postural tremor (later onset, spreads to all limbs and neck) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:postural tremor, slow, irregular (in some patients)
n1=en:retardation | n2=en:postural tremor, slow, irregular (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:posturing
n1=en:retardation | n2=en:posturing | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:prader-willi syndrome
n1=en:retardation | n2=en:prader-willi syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:praxis
n1=en:retardation | n2=en:praxis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pre-senile dementia
n1=en:retardation | n2=en:pre-senile dementia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:precocious puberty
n1=en:retardation | n2=en:precocious puberty | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pregnancy complications, infectious
n1=en:retardation | n2=en:pregnancy complications, infectious | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:premature birth of newborn
n1=en:retardation | n2=en:premature birth of newborn | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:premature epiphyseal fusion
n1=en:retardation | n2=en:premature epiphyseal fusion | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:premature stroke
n1=en:retardation | n2=en:premature stroke | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:premenstrual tension
n1=en:retardation | n2=en:premenstrual tension | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:prenatal disorder
n1=en:retardation | n2=en:prenatal disorder | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:presbycusis
n1=en:retardation | n2=en:presbycusis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:presence of rosenthal fibers (eosinophilic bodies near astrocyte filaments)
n1=en:retardation | n2=en:presence of rosenthal fibers (eosinophilic bodies near astrocyte filaments) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:presenile and senile dementia
n1=en:retardation | n2=en:presenile and senile dementia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:preservation of u fibers
n1=en:retardation | n2=en:preservation of u fibers | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:prieto x-linked mental retardation syndrome
n1=en:retardation | n2=en:prieto x-linked mental retardation syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:primarily affects distal lower limbs
n1=en:retardation | n2=en:primarily affects distal lower limbs | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:primitive reflex
n1=en:retardation | n2=en:primitive reflex | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:primitive reflexes (in some patients)
n1=en:retardation | n2=en:primitive reflexes (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:primitive reflexes (palmomental, snout, glabellar)
n1=en:retardation | n2=en:primitive reflexes (palmomental, snout, glabellar) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:primitive sylvian fissures
n1=en:retardation | n2=en:primitive sylvian fissures | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:primrose syndrome
n1=en:retardation | n2=en:primrose syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:prion protein-positive senile plaques
n1=en:retardation | n2=en:prion protein-positive senile plaques | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:prnp-immunoreactive cerebral amyloid angiopathy (in some patients)
n1=en:retardation | n2=en:prnp-immunoreactive cerebral amyloid angiopathy (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:profound global developmental delay
n1=en:retardation | n2=en:profound global developmental delay | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:profound intellectual disabilities
n1=en:retardation | n2=en:profound intellectual disabilities | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:profound mental retardation and hypotonia in survivors
n1=en:retardation | n2=en:profound mental retardation and hypotonia in survivors | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:progression to paralysis and atrophy of distal lower limb muscles
n1=en:retardation | n2=en:progression to paralysis and atrophy of distal lower limb muscles | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:progression to tetraplegia and decerebrate state
n1=en:retardation | n2=en:progression to tetraplegia and decerebrate state | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:progressive ataxia (onset second year of life)
n1=en:retardation | n2=en:progressive ataxia (onset second year of life) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:progressive bulbar palsy
n1=en:retardation | n2=en:progressive bulbar palsy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:progressive cerebellar ataxia
n1=en:retardation | n2=en:progressive cerebellar ataxia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:progressive cerebellar degeneration
n1=en:retardation | n2=en:progressive cerebellar degeneration | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:progressive cerebral atrophy seen on mri
n1=en:retardation | n2=en:progressive cerebral atrophy seen on mri | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:progressive choreoathetosis
n1=en:retardation | n2=en:progressive choreoathetosis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:progressive cns degeneration
n1=en:retardation | n2=en:progressive cns degeneration | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:progressive cognitive decline following normal development in childhood (in some patients)
n1=en:retardation | n2=en:progressive cognitive decline following normal development in childhood (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:progressive encephalopathy
n1=en:retardation | n2=en:progressive encephalopathy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:progressive extrapyramidal movement disorder
n1=en:retardation | n2=en:progressive extrapyramidal movement disorder | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:progressive forgetfulness
n1=en:retardation | n2=en:progressive forgetfulness | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:progressive gait ataxia
n1=en:retardation | n2=en:progressive gait ataxia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:progressive impairment of gait
n1=en:retardation | n2=en:progressive impairment of gait | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:progressive inability to walk
n1=en:retardation | n2=en:progressive inability to walk | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:progressive intellectual decline
n1=en:retardation | n2=en:progressive intellectual decline | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:progressive language deterioration
n1=en:retardation | n2=en:progressive language deterioration | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:progressive leukoencephalopathy
n1=en:retardation | n2=en:progressive leukoencephalopathy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:progressive loss of movement control
n1=en:retardation | n2=en:progressive loss of movement control | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:progressive myoclonus epilepsy
n1=en:retardation | n2=en:progressive myoclonus epilepsy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:progressive neurologic deterioration
n1=en:retardation | n2=en:progressive neurologic deterioration | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:progressive psychomotor deterioration
n1=en:retardation | n2=en:progressive psychomotor deterioration | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:progressive pyramidal and cerebellar signs
n1=en:retardation | n2=en:progressive pyramidal and cerebellar signs | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:progressive spastic diplegia to quadriplegia
n1=en:retardation | n2=en:progressive spastic diplegia to quadriplegia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:progressive spastic paraplegia
n1=en:retardation | n2=en:progressive spastic paraplegia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:progressive spastic quadriplegia
n1=en:retardation | n2=en:progressive spastic quadriplegia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:progressive spasticity
n1=en:retardation | n2=en:progressive spasticity | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:progressive truncal ataxia
n1=en:retardation | n2=en:progressive truncal ataxia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:progressive ventriculomegaly
n1=en:retardation | n2=en:progressive ventriculomegaly | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:progressive white matter lesions in the brain
n1=en:retardation | n2=en:progressive white matter lesions in the brain | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:progressive, symmetric degeneration of the caudate and putamen
n1=en:retardation | n2=en:progressive, symmetric degeneration of the caudate and putamen | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:prolonged seizure
n1=en:retardation | n2=en:prolonged seizure | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:prolonged somatosensory evoked potentials (seps)
n1=en:retardation | n2=en:prolonged somatosensory evoked potentials (seps) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:prominent cortical sulci
n1=en:retardation | n2=en:prominent cortical sulci | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:prominent csf spaces (in some patients)
n1=en:retardation | n2=en:prominent csf spaces (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:prominent perivascular spaces
n1=en:retardation | n2=en:prominent perivascular spaces | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:prominent perivascular spaces with surrounding gliosis in periatrial white matter
n1=en:retardation | n2=en:prominent perivascular spaces with surrounding gliosis in periatrial white matter | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:prominent sulci
n1=en:retardation | n2=en:prominent sulci | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:prominent trigone and occipital horns
n1=en:retardation | n2=en:prominent trigone and occipital horns | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:prominent ventricles (in some patients)
n1=en:retardation | n2=en:prominent ventricles (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:prosoposchisis
n1=en:retardation | n2=en:prosoposchisis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:prostatitis/seminal vesiculitis
n1=en:retardation | n2=en:prostatitis/seminal vesiculitis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:proximal amyotrophy
n1=en:retardation | n2=en:proximal amyotrophy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:proximal limb muscle stiffness
n1=en:retardation | n2=en:proximal limb muscle stiffness | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:proximal muscle weakness
n1=en:retardation | n2=en:proximal muscle weakness | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:proximal muscle weakness in lower limbs
n1=en:retardation | n2=en:proximal muscle weakness in lower limbs | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:proximal weakness occurs first
n1=en:retardation | n2=en:proximal weakness occurs first | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:proximal weakness occurs later
n1=en:retardation | n2=en:proximal weakness occurs later | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:proximal weakness of the lower extremities
n1=en:retardation | n2=en:proximal weakness of the lower extremities | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:prp immunoreactivity limited to cerebellum and putamen
n1=en:retardation | n2=en:prp immunoreactivity limited to cerebellum and putamen | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pseudo-hurler polydystrophy
n1=en:retardation | n2=en:pseudo-hurler polydystrophy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pseudobulbar palsy
n1=en:retardation | n2=en:pseudobulbar palsy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pseudobulbar palsy (e.g. involuntary weeping or laughter)
n1=en:retardation | n2=en:pseudobulbar palsy (e.g. involuntary weeping or laughter) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pseudobulbar signs
n1=en:retardation | n2=en:pseudobulbar signs | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pseudobulbar symptoms (uncontrolled laughter, weeping)
n1=en:retardation | n2=en:pseudobulbar symptoms (uncontrolled laughter, weeping) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pseudohypoparathyroidism type 1c
n1=en:retardation | n2=en:pseudohypoparathyroidism type 1c | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pseudolaminar spongiform changes
n1=en:retardation | n2=en:pseudolaminar spongiform changes | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pseudotumor
n1=en:retardation | n2=en:pseudotumor | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pseudotumor cerebri
n1=en:retardation | n2=en:pseudotumor cerebri | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:psoriasis
n1=en:retardation | n2=en:psoriasis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:psychiatric and behavioural symptoms nec
n1=en:retardation | n2=en:psychiatric and behavioural symptoms nec | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:psychiatric behavioral disability
n1=en:retardation | n2=en:psychiatric behavioral disability | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:psychiatric disorder
n1=en:retardation | n2=en:psychiatric disorder | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:psychiatric disorders nec
n1=en:retardation | n2=en:psychiatric disorders nec | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:psychiatric problem
n1=en:retardation | n2=en:psychiatric problem | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:psychiatric symptoms (delusions, hallucinations)
n1=en:retardation | n2=en:psychiatric symptoms (delusions, hallucinations) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:psychic disease
n1=en:retardation | n2=en:psychic disease | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:psychic factors associated with diseases classified elsewhere
n1=en:retardation | n2=en:psychic factors associated with diseases classified elsewhere | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:psychomotor agitation
n1=en:retardation | n2=en:psychomotor agitation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:psychomotor arrest and regression
n1=en:retardation | n2=en:psychomotor arrest and regression | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:psychomotor delay (evident at 3 months)
n1=en:retardation | n2=en:psychomotor delay (evident at 3 months) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:psychomotor delay (in one family)
n1=en:retardation | n2=en:psychomotor delay (in one family) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:psychomotor delay (rare)
n1=en:retardation | n2=en:psychomotor delay (rare) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:psychomotor delay after second year
n1=en:retardation | n2=en:psychomotor delay after second year | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:psychomotor delay, mild to moderate
n1=en:retardation | n2=en:psychomotor delay, mild to moderate | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:psychomotor delay, severe
n1=en:retardation | n2=en:psychomotor delay, severe | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:psychomotor deterioration
n1=en:retardation | n2=en:psychomotor deterioration | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:psychomotor deterioration (classical form)
n1=en:retardation | n2=en:psychomotor deterioration (classical form) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:psychomotor disorders
n1=en:retardation | n2=en:psychomotor disorders | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:psychomotor impairments
n1=en:retardation | n2=en:psychomotor impairments | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:psychomotor regression
n1=en:retardation | n2=en:psychomotor regression | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:psychomotor regression (in milder cases)
n1=en:retardation | n2=en:psychomotor regression (in milder cases) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:psychomotor regression (in some patients)
n1=en:retardation | n2=en:psychomotor regression (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:psychomotor regression (in some)
n1=en:retardation | n2=en:psychomotor regression (in some) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:psychomotor regression (onset within first year of life)
n1=en:retardation | n2=en:psychomotor regression (onset within first year of life) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:psychomotor regression beginning in infancy
n1=en:retardation | n2=en:psychomotor regression beginning in infancy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:psychomotor regression in infants
n1=en:retardation | n2=en:psychomotor regression in infants | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:psychomotor regression may occur
n1=en:retardation | n2=en:psychomotor regression may occur | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:psychomotor regression, episodic, often associated with common childhood infections
n1=en:retardation | n2=en:psychomotor regression, episodic, often associated with common childhood infections | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:psychomotor regression, progressive
n1=en:retardation | n2=en:psychomotor regression, progressive | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:psychomotor regression, severe
n1=en:retardation | n2=en:psychomotor regression, severe | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:psychomotor retardation (2/4 patients)
n1=en:retardation | n2=en:psychomotor retardation (2/4 patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:psychomotor retardation (in 1 patient)
n1=en:retardation | n2=en:psychomotor retardation (in 1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:psychomotor retardation (in some patients)
n1=en:retardation | n2=en:psychomotor retardation (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:psychomotor retardation in those that survive
n1=en:retardation | n2=en:psychomotor retardation in those that survive | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:psychomotor retardation, mild
n1=en:retardation | n2=en:psychomotor retardation, mild | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:psychomotor retardation, mild to moderate
n1=en:retardation | n2=en:psychomotor retardation, mild to moderate | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:psychomotor retardation, moderate
n1=en:retardation | n2=en:psychomotor retardation, moderate | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:psychomotor retardation, profound
n1=en:retardation | n2=en:psychomotor retardation, profound | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:psychomotor retardation, profound, in those who survive
n1=en:retardation | n2=en:psychomotor retardation, profound, in those who survive | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:psychomotor retardation, severe to profound
n1=en:retardation | n2=en:psychomotor retardation, severe to profound | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:psychomotor retardation, variable
n1=en:retardation | n2=en:psychomotor retardation, variable | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:psychoneuropathy nos
n1=en:retardation | n2=en:psychoneuropathy nos | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:psychopathology
n1=en:retardation | n2=en:psychopathology | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:psychophysiologic disorders
n1=en:retardation | n2=en:psychophysiologic disorders | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:psychosexual disorders
n1=en:retardation | n2=en:psychosexual disorders | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:psychosis
n1=en:retardation | n2=en:psychosis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:psychosis (rare)
n1=en:retardation | n2=en:psychosis (rare) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:psychosis with origin in childhood
n1=en:retardation | n2=en:psychosis with origin in childhood | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:psychotic episodes
n1=en:retardation | n2=en:psychotic episodes | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pterygium colli
n1=en:retardation | n2=en:pterygium colli | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:puerperal infection/sepsis
n1=en:retardation | n2=en:puerperal infection/sepsis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pulmonary embolism
n1=en:retardation | n2=en:pulmonary embolism | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pulmonary emphysema
n1=en:retardation | n2=en:pulmonary emphysema | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pulmonary tuberculosis
n1=en:retardation | n2=en:pulmonary tuberculosis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pulsating quality
n1=en:retardation | n2=en:pulsating quality | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:purposeless movements (if left untreated)
n1=en:retardation | n2=en:purposeless movements (if left untreated) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:purpura/coagulation defects/abnormal platelets
n1=en:retardation | n2=en:purpura/coagulation defects/abnormal platelets | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:putamen atrophy
n1=en:retardation | n2=en:putamen atrophy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pyelonephritis/pyelitis acute
n1=en:retardation | n2=en:pyelonephritis/pyelitis acute | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pyloric stenosis
n1=en:retardation | n2=en:pyloric stenosis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pyramidal features (rare)
n1=en:retardation | n2=en:pyramidal features (rare) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pyramidal hypertonia
n1=en:retardation | n2=en:pyramidal hypertonia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pyramidal sign
n1=en:retardation | n2=en:pyramidal sign | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pyramidal signs (1 family)
n1=en:retardation | n2=en:pyramidal signs (1 family) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pyramidal signs (1 patient)
n1=en:retardation | n2=en:pyramidal signs (1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pyramidal signs (21% of patients)
n1=en:retardation | n2=en:pyramidal signs (21% of patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pyramidal signs (in some patients)
n1=en:retardation | n2=en:pyramidal signs (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pyramidal signs (in some)
n1=en:retardation | n2=en:pyramidal signs (in some) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pyramidal signs (less common)
n1=en:retardation | n2=en:pyramidal signs (less common) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pyramidal signs, mild
n1=en:retardation | n2=en:pyramidal signs, mild | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pyramidal signs, mild (uncommon)
n1=en:retardation | n2=en:pyramidal signs, mild (uncommon) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pyramidal symptoms
n1=en:retardation | n2=en:pyramidal symptoms | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pyramidal syndrome
n1=en:retardation | n2=en:pyramidal syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pyramidal syndrome of the lower limbs
n1=en:retardation | n2=en:pyramidal syndrome of the lower limbs | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pyramidal system
n1=en:retardation | n2=en:pyramidal system | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pyramidal tetraparesis
n1=en:retardation | n2=en:pyramidal tetraparesis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pyramidal tract dysfunction (juvenile-onset, less common)
n1=en:retardation | n2=en:pyramidal tract dysfunction (juvenile-onset, less common) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pyramidal tract involvement
n1=en:retardation | n2=en:pyramidal tract involvement | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pyramidal tract signs (in some patients)
n1=en:retardation | n2=en:pyramidal tract signs (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pyruvate carboxylase deficiency
n1=en:retardation | n2=en:pyruvate carboxylase deficiency | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pyruvate dehydrogenase e3-binding protein deficiency
n1=en:retardation | n2=en:pyruvate dehydrogenase e3-binding protein deficiency | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:pyruvate dehydrogenase phosphatase deficiency
n1=en:retardation | n2=en:pyruvate dehydrogenase phosphatase deficiency | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:quadriparesis
n1=en:retardation | n2=en:quadriparesis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:quadriplegia
n1=en:retardation | n2=en:quadriplegia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:quadriplegia, episodic
n1=en:retardation | n2=en:quadriplegia, episodic | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:quadriplegia, flaccid
n1=en:retardation | n2=en:quadriplegia, flaccid | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:quadriplegic dyskinesia
n1=en:retardation | n2=en:quadriplegic dyskinesia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:quadrupedal gait
n1=en:retardation | n2=en:quadrupedal gait | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:quadrupedal gait (in some)
n1=en:retardation | n2=en:quadrupedal gait (in some) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:quadrupedal gait (palm of hands, legs straight) with diagonal walking
n1=en:retardation | n2=en:quadrupedal gait (palm of hands, legs straight) with diagonal walking | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:quadrupedal locomotion (in some patients)
n1=en:retardation | n2=en:quadrupedal locomotion (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ramon syndrome
n1=en:retardation | n2=en:ramon syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ramos arroyo clark syndrome
n1=en:retardation | n2=en:ramos arroyo clark syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:rapid complete resolution of symptoms
n1=en:retardation | n2=en:rapid complete resolution of symptoms | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:rapid initial onset of symptoms (hours to weeks)
n1=en:retardation | n2=en:rapid initial onset of symptoms (hours to weeks) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:rapid onset
n1=en:retardation | n2=en:rapid onset | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:rapid regression
n1=en:retardation | n2=en:rapid regression | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:rapid, instantaneous neurologic decline may occur after fright
n1=en:retardation | n2=en:rapid, instantaneous neurologic decline may occur after fright | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:rapid, jerky movements
n1=en:retardation | n2=en:rapid, jerky movements | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:rapidly progressive brainstem degeneration
n1=en:retardation | n2=en:rapidly progressive brainstem degeneration | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:rare dementia
n1=en:retardation | n2=en:rare dementia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:rare secondary generalization
n1=en:retardation | n2=en:rare secondary generalization | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:reactive attachment disorder of infancy or early childhood
n1=en:retardation | n2=en:reactive attachment disorder of infancy or early childhood | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:reactive gliosis
n1=en:retardation | n2=en:reactive gliosis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:recurrent bacterial meningitis
n1=en:retardation | n2=en:recurrent bacterial meningitis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:recurrent encephalopathy
n1=en:retardation | n2=en:recurrent encephalopathy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:recurrent meningitis
n1=en:retardation | n2=en:recurrent meningitis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:recurrent muscle twitches (symptom)
n1=en:retardation | n2=en:recurrent muscle twitches (symptom) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:recurrent seizures nos
n1=en:retardation | n2=en:recurrent seizures nos | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:recurrent subcortical infarcts (strokes)
n1=en:retardation | n2=en:recurrent subcortical infarcts (strokes) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:reduced brain gyri
n1=en:retardation | n2=en:reduced brain gyri | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:reduced brain size
n1=en:retardation | n2=en:reduced brain size | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:reduced cerebral white matter
n1=en:retardation | n2=en:reduced cerebral white matter | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:reduced concentration span
n1=en:retardation | n2=en:reduced concentration span | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:reduced consciousness
n1=en:retardation | n2=en:reduced consciousness | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:reduced consciousness, hypoglycemia-related
n1=en:retardation | n2=en:reduced consciousness, hypoglycemia-related | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:reduced numbers of neurons
n1=en:retardation | n2=en:reduced numbers of neurons | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:reduced posterior white matter volume (in some patients)
n1=en:retardation | n2=en:reduced posterior white matter volume (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:reduced size of the pituitary gland
n1=en:retardation | n2=en:reduced size of the pituitary gland | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:reduced sleep latency
n1=en:retardation | n2=en:reduced sleep latency | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:reduced tendon reflexes
n1=en:retardation | n2=en:reduced tendon reflexes | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:reduced white matter
n1=en:retardation | n2=en:reduced white matter | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:reduced white matter volume
n1=en:retardation | n2=en:reduced white matter volume | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:reduction of white matter, generalized
n1=en:retardation | n2=en:reduction of white matter, generalized | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:reduction or loss of acquired skills (e.g., purposeful hand use, speech)
n1=en:retardation | n2=en:reduction or loss of acquired skills (e.g., purposeful hand use, speech) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:redundant prepuce and phimosis
n1=en:retardation | n2=en:redundant prepuce and phimosis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:reflex epilepsy, photosensitive
n1=en:retardation | n2=en:reflex epilepsy, photosensitive | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:reflex, deep tendon, absent
n1=en:retardation | n2=en:reflex, deep tendon, absent | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:refractive error
n1=en:retardation | n2=en:refractive error | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:registered disabled
n1=en:retardation | n2=en:registered disabled | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:regression of development
n1=en:retardation | n2=en:regression of development | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:regression of early motor skills
n1=en:retardation | n2=en:regression of early motor skills | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:regression of motor development
n1=en:retardation | n2=en:regression of motor development | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:relative preservation of purkinje cells, but they are deformed and disaligned
n1=en:retardation | n2=en:relative preservation of purkinje cells, but they are deformed and disaligned | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:relative preservation of the cerebellar folia
n1=en:retardation | n2=en:relative preservation of the cerebellar folia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:relative preservation of the cerebellum
n1=en:retardation | n2=en:relative preservation of the cerebellum | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:relative sparing of language
n1=en:retardation | n2=en:relative sparing of language | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:relief with motor activation
n1=en:retardation | n2=en:relief with motor activation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:rem sleep behavior disorder
n1=en:retardation | n2=en:rem sleep behavior disorder | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:renal tubular acidosis, proximal, with ocular abnormalities and mental retardation
n1=en:retardation | n2=en:renal tubular acidosis, proximal, with ocular abnormalities and mental retardation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:renpenning syndrome 1
n1=en:retardation | n2=en:renpenning syndrome 1 | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:residual ataxia
n1=en:retardation | n2=en:residual ataxia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:response to pyridoxal phosphate
n1=en:retardation | n2=en:response to pyridoxal phosphate | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:resting myoclonus
n1=en:retardation | n2=en:resting myoclonus | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:resting tremor (in some patients)
n1=en:retardation | n2=en:resting tremor (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:resting tremors
n1=en:retardation | n2=en:resting tremors | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:restlessness at birth
n1=en:retardation | n2=en:restlessness at birth | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:restrictive behavior, interests, and activities
n1=en:retardation | n2=en:restrictive behavior, interests, and activities | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:results in nocturnal insomnia and chronic sleep deprivation
n1=en:retardation | n2=en:results in nocturnal insomnia and chronic sleep deprivation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:retardations, psychosocial mental
n1=en:retardation | n2=en:retardations, psychosocial mental | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:retinal detachment
n1=en:retardation | n2=en:retinal detachment | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:retinitis pigmentosa, deafness, mental retardation, and hypogonadism
n1=en:retardation | n2=en:retinitis pigmentosa, deafness, mental retardation, and hypogonadism | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:retinopathy
n1=en:retardation | n2=en:retinopathy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:retrocerebellar cyst
n1=en:retardation | n2=en:retrocerebellar cyst | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:retrocerebellar cyst (in some patients)
n1=en:retardation | n2=en:retrocerebellar cyst (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:retrocerebellar cyst (rare)
n1=en:retardation | n2=en:retrocerebellar cyst (rare) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:retrocollis
n1=en:retardation | n2=en:retrocollis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:retroflexion of the neck
n1=en:retardation | n2=en:retroflexion of the neck | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:rett syndrome
n1=en:retardation | n2=en:rett syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:reye syndrome
n1=en:retardation | n2=en:reye syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:rheumatic heart disease
n1=en:retardation | n2=en:rheumatic heart disease | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:rhinitis seasonal
n1=en:retardation | n2=en:rhinitis seasonal | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:rhinocephaly
n1=en:retardation | n2=en:rhinocephaly | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:rhizomelic chondrodysplasia punctata, type 1
n1=en:retardation | n2=en:rhizomelic chondrodysplasia punctata, type 1 | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:rhizomelic chondrodysplasia punctata, type 2
n1=en:retardation | n2=en:rhizomelic chondrodysplasia punctata, type 2 | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:rhombencephalosynapsis
n1=en:retardation | n2=en:rhombencephalosynapsis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:richards-rundle syndrome
n1=en:retardation | n2=en:richards-rundle syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:rigidity (juvenile form)
n1=en:retardation | n2=en:rigidity (juvenile form) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:rigidity (later)
n1=en:retardation | n2=en:rigidity (later) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:rigidity during seizures
n1=en:retardation | n2=en:rigidity during seizures | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:rigidity of limbs
n1=en:retardation | n2=en:rigidity of limbs | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:rigidity, axial and limb
n1=en:retardation | n2=en:rigidity, axial and limb | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:roberts syndrome
n1=en:retardation | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:robin sequence with distinctive facial appearance and brachydactyly
n1=en:retardation | n2=en:robin sequence with distinctive facial appearance and brachydactyly | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:romberg's sign positive
n1=en:retardation | n2=en:romberg's sign positive | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:rotary head movements ('rolling,' 'tremor')
n1=en:retardation | n2=en:rotary head movements ('rolling,' 'tremor') | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:roving eye movements (infancy)
n1=en:retardation | n2=en:roving eye movements (infancy) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:rubella infection
n1=en:retardation | n2=en:rubella infection | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:rubinstein-taybi syndrome
n1=en:retardation | n2=en:rubinstein-taybi syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:rudimentary white matter
n1=en:retardation | n2=en:rudimentary white matter | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ruvalcaba syndrome
n1=en:retardation | n2=en:ruvalcaba syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:sabinas brittle hair syndrome
n1=en:retardation | n2=en:sabinas brittle hair syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:sacral dimple
n1=en:retardation | n2=en:sacral dimple | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:sagittal sinus thrombosis
n1=en:retardation | n2=en:sagittal sinus thrombosis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:salaam seizures
n1=en:retardation | n2=en:salaam seizures | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:say meyer syndrome
n1=en:retardation | n2=en:say meyer syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:scabies and other acariases
n1=en:retardation | n2=en:scabies and other acariases | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:scanning speech
n1=en:retardation | n2=en:scanning speech | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:scant iron deposition in the brain (1 family)
n1=en:retardation | n2=en:scant iron deposition in the brain (1 family) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:scattered cns demyelination
n1=en:retardation | n2=en:scattered cns demyelination | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:schinzel-giedion midface-retraction syndrome
n1=en:retardation | n2=en:schinzel-giedion midface-retraction syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:schizencephaly
n1=en:retardation | n2=en:schizencephaly | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:schizophrenia
n1=en:retardation | n2=en:schizophrenia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:schizophrenia and other psychotic disorders
n1=en:retardation | n2=en:schizophrenia and other psychotic disorders | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:schizophrenia mental retardation deafness retinitis
n1=en:retardation | n2=en:schizophrenia mental retardation deafness retinitis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:schizophrenia spectrum and other psychotic disorders
n1=en:retardation | n2=en:schizophrenia spectrum and other psychotic disorders | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:schizophrenia, schizotypal and delusional disorders
n1=en:retardation | n2=en:schizophrenia, schizotypal and delusional disorders | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:schizophrenic reaction
n1=en:retardation | n2=en:schizophrenic reaction | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:school problem (finding)
n1=en:retardation | n2=en:school problem (finding) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:scissoring
n1=en:retardation | n2=en:scissoring | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:scissors gait
n1=en:retardation | n2=en:scissors gait | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:scott bryant graham syndrome
n1=en:retardation | n2=en:scott bryant graham syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:screening and history of mental health and substance abuse codes
n1=en:retardation | n2=en:screening and history of mental health and substance abuse codes | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:sebaceous cyst
n1=en:retardation | n2=en:sebaceous cyst | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seborrheic dermatitis
n1=en:retardation | n2=en:seborrheic dermatitis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seckel syndrome
n1=en:retardation | n2=en:seckel syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:secondary generalization
n1=en:retardation | n2=en:secondary generalization | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:secondary generalization may occur
n1=en:retardation | n2=en:secondary generalization may occur | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:secondary generalization occurs in about 33% of patients
n1=en:retardation | n2=en:secondary generalization occurs in about 33% of patients | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:secondary generalized tonic-clonic seizures may occur
n1=en:retardation | n2=en:secondary generalized tonic-clonic seizures may occur | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:secondary hand muscle weakness predominating at the wrist and finger extensor muscles
n1=en:retardation | n2=en:secondary hand muscle weakness predominating at the wrist and finger extensor muscles | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:secondary hypertonia
n1=en:retardation | n2=en:secondary hypertonia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:secondary involvement of proximal and trunk muscles
n1=en:retardation | n2=en:secondary involvement of proximal and trunk muscles | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:secondary motor complications develop in 50% of those on levodopa therapy
n1=en:retardation | n2=en:secondary motor complications develop in 50% of those on levodopa therapy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:secondary seizures (in some patients)
n1=en:retardation | n2=en:secondary seizures (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:secondary spinal cord compression may occur
n1=en:retardation | n2=en:secondary spinal cord compression may occur | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:secretory otitis media
n1=en:retardation | n2=en:secretory otitis media | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:see juvenile myoclonic epilepsy (606904)
n1=en:retardation | n2=en:see juvenile myoclonic epilepsy (606904) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:see spg5a (270800)
n1=en:retardation | n2=en:see spg5a (270800) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:segmental callosal hypoplasia, mild
n1=en:retardation | n2=en:segmental callosal hypoplasia, mild | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:segmental odontomaxillary dysplasia
n1=en:retardation | n2=en:segmental odontomaxillary dysplasia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:segmental sensory loss, especially of pain and temperature
n1=en:retardation | n2=en:segmental sensory loss, especially of pain and temperature | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizure
n1=en:retardation | n2=en:seizure | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizure (in a subset of patients in infancy)
n1=en:retardation | n2=en:seizure (in a subset of patients in infancy) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizure disorder
n1=en:retardation | n2=en:seizure disorder | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizure disorder (homozygote)
n1=en:retardation | n2=en:seizure disorder (homozygote) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizure including seizure-like activity in utero starting around 18 weeks gestation
n1=en:retardation | n2=en:seizure including seizure-like activity in utero starting around 18 weeks gestation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizure, febrile (2/3 children)
n1=en:retardation | n2=en:seizure, febrile (2/3 children) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizure, focal or multifocal onset
n1=en:retardation | n2=en:seizure, focal or multifocal onset | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizures (> 90%)
n1=en:retardation | n2=en:seizures (> 90%) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizures (1 family)
n1=en:retardation | n2=en:seizures (1 family) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizures (1 patient)
n1=en:retardation | n2=en:seizures (1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizures (2-10% of patients)
n1=en:retardation | n2=en:seizures (2-10% of patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizures (3 patients)
n1=en:retardation | n2=en:seizures (3 patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizures (40%)
n1=en:retardation | n2=en:seizures (40%) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizures (50% of patients)
n1=en:retardation | n2=en:seizures (50% of patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizures (50%)
n1=en:retardation | n2=en:seizures (50%) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizures (about 50% of patients)
n1=en:retardation | n2=en:seizures (about 50% of patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizures (adult)
n1=en:retardation | n2=en:seizures (adult) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizures (cvs+)
n1=en:retardation | n2=en:seizures (cvs+) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizures (eclampsia)
n1=en:retardation | n2=en:seizures (eclampsia) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizures (if left untreated)
n1=en:retardation | n2=en:seizures (if left untreated) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizures (in 1 of 2 sibs)
n1=en:retardation | n2=en:seizures (in 1 of 2 sibs) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizures (in 1 of 3 patients)
n1=en:retardation | n2=en:seizures (in 1 of 3 patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizures (in 2 of 6 patients)
n1=en:retardation | n2=en:seizures (in 2 of 6 patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizures (in 2 of 9 patients)
n1=en:retardation | n2=en:seizures (in 2 of 9 patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizures (in 35%)
n1=en:retardation | n2=en:seizures (in 35%) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizures (in one patient)
n1=en:retardation | n2=en:seizures (in one patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizures (in some patients)
n1=en:retardation | n2=en:seizures (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizures (in some)
n1=en:retardation | n2=en:seizures (in some) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizures (juvenile form)
n1=en:retardation | n2=en:seizures (juvenile form) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizures (less common)
n1=en:retardation | n2=en:seizures (less common) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizures (may be difficult to control)
n1=en:retardation | n2=en:seizures (may be difficult to control) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizures (mean onset 4-5 months)
n1=en:retardation | n2=en:seizures (mean onset 4-5 months) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizures (meb)
n1=en:retardation | n2=en:seizures (meb) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizures (onset <2 years)
n1=en:retardation | n2=en:seizures (onset <2 years) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizures (rare, in males)
n1=en:retardation | n2=en:seizures (rare, in males) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizures (rare)
n1=en:retardation | n2=en:seizures (rare) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizures (reported in 1 family)
n1=en:retardation | n2=en:seizures (reported in 1 family) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizures (reported in 2 patients)
n1=en:retardation | n2=en:seizures (reported in 2 patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizures (tetany)
n1=en:retardation | n2=en:seizures (tetany) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizures (type i and type ii, juvenile)
n1=en:retardation | n2=en:seizures (type i and type ii, juvenile) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizures (uncommon)
n1=en:retardation | n2=en:seizures (uncommon) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizures (variable)
n1=en:retardation | n2=en:seizures (variable) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizures affect the vocal cords, lips, mouth, and face
n1=en:retardation | n2=en:seizures affect the vocal cords, lips, mouth, and face | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizures are poorly controlled
n1=en:retardation | n2=en:seizures are poorly controlled | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizures in 15-30%
n1=en:retardation | n2=en:seizures in 15-30% | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizures in the newborn, refractory
n1=en:retardation | n2=en:seizures in the newborn, refractory | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizures may occur during hypotensive episodes
n1=en:retardation | n2=en:seizures may occur during hypotensive episodes | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizures occur in absence of intracranial infection or defined pathologic or traumatic cause
n1=en:retardation | n2=en:seizures occur in absence of intracranial infection or defined pathologic or traumatic cause | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizures occur in clusters
n1=en:retardation | n2=en:seizures occur in clusters | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizures occur in clusters over 1 or several days
n1=en:retardation | n2=en:seizures occur in clusters over 1 or several days | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizures occur multiple times per day
n1=en:retardation | n2=en:seizures occur multiple times per day | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizures often associated with infections
n1=en:retardation | n2=en:seizures often associated with infections | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizures often begin focally with head and eye deviation
n1=en:retardation | n2=en:seizures often begin focally with head and eye deviation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizures often begin with head and eye deviation
n1=en:retardation | n2=en:seizures often begin with head and eye deviation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizures provoked by tactile stimulation or extreme emotion
n1=en:retardation | n2=en:seizures provoked by tactile stimulation or extreme emotion | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizures recur in 33% of patients
n1=en:retardation | n2=en:seizures recur in 33% of patients | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizures usually last 1 to 5 minutes (less commonly up to 10 minutes)
n1=en:retardation | n2=en:seizures usually last 1 to 5 minutes (less commonly up to 10 minutes) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizures usually last less than 15 minutes
n1=en:retardation | n2=en:seizures usually last less than 15 minutes | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizures usually occur less than 3 times
n1=en:retardation | n2=en:seizures usually occur less than 3 times | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizures, complex partial, episodic
n1=en:retardation | n2=en:seizures, complex partial, episodic | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizures, complex, myoclonic
n1=en:retardation | n2=en:seizures, complex, myoclonic | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizures, continuous, refractory
n1=en:retardation | n2=en:seizures, continuous, refractory | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizures, diurnal partial, rare (in some patients)
n1=en:retardation | n2=en:seizures, diurnal partial, rare (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizures, early onset
n1=en:retardation | n2=en:seizures, early onset | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizures, early-onset (1 family)
n1=en:retardation | n2=en:seizures, early-onset (1 family) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizures, febrile (1 family)
n1=en:retardation | n2=en:seizures, febrile (1 family) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizures, focal, partial, motor
n1=en:retardation | n2=en:seizures, focal, partial, motor | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizures, generalized tonic/clonic, myoclonic, atonic, or atypical absence, aggravated by fatigue and fasting with frequency ranges from daily to monthly (in some patients)
n1=en:retardation | n2=en:seizures, generalized tonic/clonic, myoclonic, atonic, or atypical absence, aggravated by fatigue and fasting with frequency ranges from daily to monthly (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizures, generalized, afebrile
n1=en:retardation | n2=en:seizures, generalized, afebrile | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizures, generalized, may occur
n1=en:retardation | n2=en:seizures, generalized, may occur | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizures, hypoglycemic (in some patients)
n1=en:retardation | n2=en:seizures, hypoglycemic (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizures, infantile-onset
n1=en:retardation | n2=en:seizures, infantile-onset | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizures, intractable
n1=en:retardation | n2=en:seizures, intractable | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizures, intractable (in 1 family)
n1=en:retardation | n2=en:seizures, intractable (in 1 family) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizures, juvenile myoclonic
n1=en:retardation | n2=en:seizures, juvenile myoclonic | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizures, mild
n1=en:retardation | n2=en:seizures, mild | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizures, multiple types
n1=en:retardation | n2=en:seizures, multiple types | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizures, neonatal (2p21del)
n1=en:retardation | n2=en:seizures, neonatal (2p21del) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizures, nocturnal, usually occur in daily clusters
n1=en:retardation | n2=en:seizures, nocturnal, usually occur in daily clusters | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizures, onset age 5 to 10 years
n1=en:retardation | n2=en:seizures, onset age 5 to 10 years | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizures, partial complex (rare)
n1=en:retardation | n2=en:seizures, partial complex (rare) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizures, partial with secondary generalization, focal at onset, usually motor
n1=en:retardation | n2=en:seizures, partial with secondary generalization, focal at onset, usually motor | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizures, partial, often hemifacial
n1=en:retardation | n2=en:seizures, partial, often hemifacial | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizures, partial, unilateral
n1=en:retardation | n2=en:seizures, partial, unilateral | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizures, particularly absence (in some patients)
n1=en:retardation | n2=en:seizures, particularly absence (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizures, poorly controlled
n1=en:retardation | n2=en:seizures, poorly controlled | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizures, recurrent, refractory
n1=en:retardation | n2=en:seizures, recurrent, refractory | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizures, refractory
n1=en:retardation | n2=en:seizures, refractory | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizures, refractory to treatment
n1=en:retardation | n2=en:seizures, refractory to treatment | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizures, refractory, infantile-onset
n1=en:retardation | n2=en:seizures, refractory, infantile-onset | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizures, severe, drug-resistant, intractable
n1=en:retardation | n2=en:seizures, severe, drug-resistant, intractable | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizures, severe, intractable
n1=en:retardation | n2=en:seizures, severe, intractable | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizures, sudden-onset, drug-resistant
n1=en:retardation | n2=en:seizures, sudden-onset, drug-resistant | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizures, tonic-clonic (1 patient)
n1=en:retardation | n2=en:seizures, tonic-clonic (1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizures, tonic-clonic (rare)
n1=en:retardation | n2=en:seizures, tonic-clonic (rare) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizures, tonic-clonic or absence (in some patients)
n1=en:retardation | n2=en:seizures, tonic-clonic or absence (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizures, tonic, clonic, focal
n1=en:retardation | n2=en:seizures, tonic, clonic, focal | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seizures, tonic, hyperekplectic
n1=en:retardation | n2=en:seizures, tonic, hyperekplectic | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:selective loss of cerebellar purkinje cells
n1=en:retardation | n2=en:selective loss of cerebellar purkinje cells | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:self mutilation
n1=en:retardation | n2=en:self mutilation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:self-injurious behavior, median onset age 2 years
n1=en:retardation | n2=en:self-injurious behavior, median onset age 2 years | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:semilobar holoprosencephalies
n1=en:retardation | n2=en:semilobar holoprosencephalies | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:semilobar hpe shows posterior interhemispheric fissure with rudimentary cerebral hemispheres and single ventricle
n1=en:retardation | n2=en:semilobar hpe shows posterior interhemispheric fissure with rudimentary cerebral hemispheres and single ventricle | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:sensitivity to neuroleptic medication
n1=en:retardation | n2=en:sensitivity to neuroleptic medication | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:sensorineural hearing loss
n1=en:retardation | n2=en:sensorineural hearing loss | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:sensory ataxia (less common)
n1=en:retardation | n2=en:sensory ataxia (less common) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:sensory aura may occur
n1=en:retardation | n2=en:sensory aura may occur | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:sensory disability
n1=en:retardation | n2=en:sensory disability | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:septum pellucidum deficient or cavum
n1=en:retardation | n2=en:septum pellucidum deficient or cavum | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:seropositive rheumatoid arthritis
n1=en:retardation | n2=en:seropositive rheumatoid arthritis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:sesame syndrome
n1=en:retardation | n2=en:sesame syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:severe behavioral problems at age 3-4
n1=en:retardation | n2=en:severe behavioral problems at age 3-4 | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:severe brain damage
n1=en:retardation | n2=en:severe brain damage | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:severe cognitive deficits (develop later)
n1=en:retardation | n2=en:severe cognitive deficits (develop later) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:severe cognitive impairment
n1=en:retardation | n2=en:severe cognitive impairment | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:severe delay in myelination
n1=en:retardation | n2=en:severe delay in myelination | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:severe demyelination of the white matter
n1=en:retardation | n2=en:severe demyelination of the white matter | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:severe developmental delay in survivors
n1=en:retardation | n2=en:severe developmental delay in survivors | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:severe expressive language delay
n1=en:retardation | n2=en:severe expressive language delay | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:severe expressive speech delay
n1=en:retardation | n2=en:severe expressive speech delay | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:severe form may never achieve sitting or walking
n1=en:retardation | n2=en:severe form may never achieve sitting or walking | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:severe global developmental delay
n1=en:retardation | n2=en:severe global developmental delay | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:severe hydrocephalus
n1=en:retardation | n2=en:severe hydrocephalus | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:severe involvement of globus pallidus
n1=en:retardation | n2=en:severe involvement of globus pallidus | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:severe mental retardation (congenital form)
n1=en:retardation | n2=en:severe mental retardation (congenital form) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:severe mental retardation (i.q. 20-34)
n1=en:retardation | n2=en:severe mental retardation (i.q. 20-34) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:severe mental retardation (iq 10-40)
n1=en:retardation | n2=en:severe mental retardation (iq 10-40) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:severe muscular hypotonia
n1=en:retardation | n2=en:severe muscular hypotonia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:severe neonatal hypotonia improving with age
n1=en:retardation | n2=en:severe neonatal hypotonia improving with age | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:severe prenatal onset hydrocephalus
n1=en:retardation | n2=en:severe prenatal onset hydrocephalus | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:severe psychomotor retardation
n1=en:retardation | n2=en:severe psychomotor retardation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:severe psychomotor retardation (iq 35-65)
n1=en:retardation | n2=en:severe psychomotor retardation (iq 35-65) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:severe psychomotor retardation from birth
n1=en:retardation | n2=en:severe psychomotor retardation from birth | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:severe speech delay
n1=en:retardation | n2=en:severe speech delay | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:severe speech impairment
n1=en:retardation | n2=en:severe speech impairment | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:severely delayed psychomotor development
n1=en:retardation | n2=en:severely delayed psychomotor development | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:severely impaired or absent speech
n1=en:retardation | n2=en:severely impaired or absent speech | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:severity of symptoms peak in the second decade and do not progress
n1=en:retardation | n2=en:severity of symptoms peak in the second decade and do not progress | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:sex behavior disorder
n1=en:retardation | n2=en:sex behavior disorder | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:sex maturation female accelerated
n1=en:retardation | n2=en:sex maturation female accelerated | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:sex maturation male accelerated
n1=en:retardation | n2=en:sex maturation male accelerated | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:sexual and gender identity disorders
n1=en:retardation | n2=en:sexual and gender identity disorders | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:sexual dysfunctions, disturbances and gender identity disorders
n1=en:retardation | n2=en:sexual dysfunctions, disturbances and gender identity disorders | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:shaheen syndrome
n1=en:retardation | n2=en:shaheen syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:shivering sensation
n1=en:retardation | n2=en:shivering sensation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:short pons
n1=en:retardation | n2=en:short pons | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:short-rib thoracic dysplasia 10 with or without polydactyly
n1=en:retardation | n2=en:short-rib thoracic dysplasia 10 with or without polydactyly | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:shorter daily total sleep times compared to age-matched controls
n1=en:retardation | n2=en:shorter daily total sleep times compared to age-matched controls | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:shoulder syndrome
n1=en:retardation | n2=en:shoulder syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:shprintzen-goldberg craniosynostosis syndrome
n1=en:retardation | n2=en:shprintzen-goldberg craniosynostosis syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:shrunken inferior olivary nuclei
n1=en:retardation | n2=en:shrunken inferior olivary nuclei | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:shuffling gaits
n1=en:retardation | n2=en:shuffling gaits | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:sialic acid storage disease, finnish type (disorder)
n1=en:retardation | n2=en:sialic acid storage disease, finnish type (disorder) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:signal abnormalities in the posterior limbs of the internal capsules, middle cerebral peduncles, pyramidal tracts in the pons, and middle cerebellar peduncles seen on mri
n1=en:retardation | n2=en:signal abnormalities in the posterior limbs of the internal capsules, middle cerebral peduncles, pyramidal tracts in the pons, and middle cerebellar peduncles seen on mri | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:signal changes in the caudate and putamen
n1=en:retardation | n2=en:signal changes in the caudate and putamen | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:simple partial seizures
n1=en:retardation | n2=en:simple partial seizures | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:simple partial seizures with secondary generalization
n1=en:retardation | n2=en:simple partial seizures with secondary generalization | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:simplified cortical gyral pattern
n1=en:retardation | n2=en:simplified cortical gyral pattern | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:simplified cortical gyration pattern
n1=en:retardation | n2=en:simplified cortical gyration pattern | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:simplified gyral pattern (1 patient)
n1=en:retardation | n2=en:simplified gyral pattern (1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:simplified gyral pattern (in 1 of 2 sibs)
n1=en:retardation | n2=en:simplified gyral pattern (in 1 of 2 sibs) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:simplified gyral pattern (in one patient)
n1=en:retardation | n2=en:simplified gyral pattern (in one patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:simplified gyral pattern (in some patients)
n1=en:retardation | n2=en:simplified gyral pattern (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:simplified gyration in the frontal cortex (less common)
n1=en:retardation | n2=en:simplified gyration in the frontal cortex (less common) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:simplified gyration pattern
n1=en:retardation | n2=en:simplified gyration pattern | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:single congenital anomaly
n1=en:retardation | n2=en:single congenital anomaly | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:sinus pericranii (rare)
n1=en:retardation | n2=en:sinus pericranii (rare) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:sinusitis acute/chronic
n1=en:retardation | n2=en:sinusitis acute/chronic | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:sirenomelia
n1=en:retardation | n2=en:sirenomelia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:situs inversus
n1=en:retardation | n2=en:situs inversus | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:sjogren-larsson syndrome
n1=en:retardation | n2=en:sjogren-larsson syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:skeletal defects, genital hypoplasia, and mental retardation
n1=en:retardation | n2=en:skeletal defects, genital hypoplasia, and mental retardation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:skin photosensitivity
n1=en:retardation | n2=en:skin photosensitivity | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:sleep abnormalities
n1=en:retardation | n2=en:sleep abnormalities | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:sleep apnea
n1=en:retardation | n2=en:sleep apnea | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:sleep apnea (in 1/4 patients)
n1=en:retardation | n2=en:sleep apnea (in 1/4 patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:sleep benefit (31%)
n1=en:retardation | n2=en:sleep benefit (31%) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:sleep disorder
n1=en:retardation | n2=en:sleep disorder | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:sleep disorder (rare)
n1=en:retardation | n2=en:sleep disorder (rare) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:sleep disorder with severe insomnia (in adulthood)
n1=en:retardation | n2=en:sleep disorder with severe insomnia (in adulthood) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:sleep disturbances
n1=en:retardation | n2=en:sleep disturbances | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:sleep disturbances (in some patients)
n1=en:retardation | n2=en:sleep disturbances (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:sleep disturbances common
n1=en:retardation | n2=en:sleep disturbances common | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:sleep impairment, progressive
n1=en:retardation | n2=en:sleep impairment, progressive | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:sleep paralysis at beginning or end of sleep period (in 60% of patients)
n1=en:retardation | n2=en:sleep paralysis at beginning or end of sleep period (in 60% of patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:sleep pattern disturbance
n1=en:retardation | n2=en:sleep pattern disturbance | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:sleep talking
n1=en:retardation | n2=en:sleep talking | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:sleep wake disorders
n1=en:retardation | n2=en:sleep wake disorders | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:sleep-onset rem
n1=en:retardation | n2=en:sleep-onset rem | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:sleep-wake cycle disturbance
n1=en:retardation | n2=en:sleep-wake cycle disturbance | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:sleepiness
n1=en:retardation | n2=en:sleepiness | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:slow gait
n1=en:retardation | n2=en:slow gait | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:slow gross motor activity
n1=en:retardation | n2=en:slow gross motor activity | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:slow paraparetic gait
n1=en:retardation | n2=en:slow paraparetic gait | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:slow reactions
n1=en:retardation | n2=en:slow reactions | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:slow speech
n1=en:retardation | n2=en:slow speech | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:slow spike-wave discharges
n1=en:retardation | n2=en:slow spike-wave discharges | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:slow, broad-based gait
n1=en:retardation | n2=en:slow, broad-based gait | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:slowed background activity
n1=en:retardation | n2=en:slowed background activity | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:slowing mental development by 1.5 to 3 years
n1=en:retardation | n2=en:slowing mental development by 1.5 to 3 years | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:slowing mental development by 1.5 to 3 years of age
n1=en:retardation | n2=en:slowing mental development by 1.5 to 3 years of age | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:slowly progressive neurologic deterioration
n1=en:retardation | n2=en:slowly progressive neurologic deterioration | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:slurred speech
n1=en:retardation | n2=en:slurred speech | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:slurred speech, episodic
n1=en:retardation | n2=en:slurred speech, episodic | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:sly syndrome
n1=en:retardation | n2=en:sly syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:small and medium-sized leptomeningeal arteries show luminal narrowing or obliteration
n1=en:retardation | n2=en:small and medium-sized leptomeningeal arteries show luminal narrowing or obliteration | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:small anterior commissure
n1=en:retardation | n2=en:small anterior commissure | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:small brain
n1=en:retardation | n2=en:small brain | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:small brain size (some patients)
n1=en:retardation | n2=en:small brain size (some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:small brain with no other malformation see on mri
n1=en:retardation | n2=en:small brain with no other malformation see on mri | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:small but structurally normal cerebral cortex
n1=en:retardation | n2=en:small but structurally normal cerebral cortex | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:small caudate
n1=en:retardation | n2=en:small caudate | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:small cavum septum
n1=en:retardation | n2=en:small cavum septum | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:small cerebellum
n1=en:retardation | n2=en:small cerebellum | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:small cerebellum (especially vermis)
n1=en:retardation | n2=en:small cerebellum (especially vermis) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:small cerebral cortex
n1=en:retardation | n2=en:small cerebral cortex | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:small frontal lobes (in one patient)
n1=en:retardation | n2=en:small frontal lobes (in one patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:small hippocampi (1 patient)
n1=en:retardation | n2=en:small hippocampi (1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:small midbrain
n1=en:retardation | n2=en:small midbrain | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:small pituitary gland (in some patients)
n1=en:retardation | n2=en:small pituitary gland (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:small rotary component may be present
n1=en:retardation | n2=en:small rotary component may be present | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:small sella
n1=en:retardation | n2=en:small sella | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:small shrunken brain
n1=en:retardation | n2=en:small shrunken brain | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:small size of the left hippocampus gyri
n1=en:retardation | n2=en:small size of the left hippocampus gyri | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:small thalami
n1=en:retardation | n2=en:small thalami | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:small, smooth cerebellum
n1=en:retardation | n2=en:small, smooth cerebellum | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:small, thin cerebellum
n1=en:retardation | n2=en:small, thin cerebellum | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:smith-lemli-opitz syndrome
n1=en:retardation | n2=en:smith-lemli-opitz syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:smith-magenis syndrome
n1=en:retardation | n2=en:smith-magenis syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:smooth brain surface
n1=en:retardation | n2=en:smooth brain surface | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:smooth, thin cortical mantle (wws)
n1=en:retardation | n2=en:smooth, thin cortical mantle (wws) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:social and occupational deterioration
n1=en:retardation | n2=en:social and occupational deterioration | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:social communication disorder
n1=en:retardation | n2=en:social communication disorder | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:socialized conduct disorder
n1=en:retardation | n2=en:socialized conduct disorder | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:somatic symptom and related disorders
n1=en:retardation | n2=en:somatic symptom and related disorders | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:somatoform disorder
n1=en:retardation | n2=en:somatoform disorder | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:somatosensory evoked potentials show prolonged latency
n1=en:retardation | n2=en:somatosensory evoked potentials show prolonged latency | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:some may not achieve ambulation
n1=en:retardation | n2=en:some may not achieve ambulation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:some patients do not achieve ability to walk
n1=en:retardation | n2=en:some patients do not achieve ability to walk | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:some patients have neurologic involvement
n1=en:retardation | n2=en:some patients have neurologic involvement | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:some patients have no structural brain abnormalities
n1=en:retardation | n2=en:some patients have no structural brain abnormalities | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:some patients have periodic wave complexes on eeg
n1=en:retardation | n2=en:some patients have periodic wave complexes on eeg | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:some patients may develop afebrile seizures later in life
n1=en:retardation | n2=en:some patients may develop afebrile seizures later in life | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:some patients may show normal early development
n1=en:retardation | n2=en:some patients may show normal early development | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:some patients never achieve independent ambulation
n1=en:retardation | n2=en:some patients never achieve independent ambulation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:some patients only achieve sitting
n1=en:retardation | n2=en:some patients only achieve sitting | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:somnolence
n1=en:retardation | n2=en:somnolence | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:sparing of central white matter structures
n1=en:retardation | n2=en:sparing of central white matter structures | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:sparing of optic tracts
n1=en:retardation | n2=en:sparing of optic tracts | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:sparing of the inferior olives
n1=en:retardation | n2=en:sparing of the inferior olives | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spasmodic dysphonia
n1=en:retardation | n2=en:spasmodic dysphonia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spasmodic torticollis
n1=en:retardation | n2=en:spasmodic torticollis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spastic ataxia
n1=en:retardation | n2=en:spastic ataxia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spastic cerebral palsy
n1=en:retardation | n2=en:spastic cerebral palsy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spastic diplegia
n1=en:retardation | n2=en:spastic diplegia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spastic diplegia (1 patient)
n1=en:retardation | n2=en:spastic diplegia (1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spastic diplegia (in some patients)
n1=en:retardation | n2=en:spastic diplegia (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spastic diplegia, progressive
n1=en:retardation | n2=en:spastic diplegia, progressive | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spastic diplegia, symmetric
n1=en:retardation | n2=en:spastic diplegia, symmetric | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spastic dystonia
n1=en:retardation | n2=en:spastic dystonia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spastic gait
n1=en:retardation | n2=en:spastic gait | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spastic paralysis
n1=en:retardation | n2=en:spastic paralysis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spastic paraparesis (1 patient)
n1=en:retardation | n2=en:spastic paraparesis (1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spastic paraparesis (rare)
n1=en:retardation | n2=en:spastic paraparesis (rare) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spastic paraplegia
n1=en:retardation | n2=en:spastic paraplegia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spastic paraplegia (in some patients)
n1=en:retardation | n2=en:spastic paraplegia (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spastic paraplegia 15, autosomal recessive
n1=en:retardation | n2=en:spastic paraplegia 15, autosomal recessive | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spastic paraplegia 16, x-linked (disorder)
n1=en:retardation | n2=en:spastic paraplegia 16, x-linked (disorder) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spastic paraplegia 2, x-linked (disorder)
n1=en:retardation | n2=en:spastic paraplegia 2, x-linked (disorder) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spastic paraplegia 54, autosomal recessive
n1=en:retardation | n2=en:spastic paraplegia 54, autosomal recessive | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spastic paraplegia, ataxia, and mental retardation
n1=en:retardation | n2=en:spastic paraplegia, ataxia, and mental retardation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spastic paraplegia, later onset (in one patient)
n1=en:retardation | n2=en:spastic paraplegia, later onset (in one patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spastic paraplegia, pure
n1=en:retardation | n2=en:spastic paraplegia, pure | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spastic paraplegia, severe
n1=en:retardation | n2=en:spastic paraplegia, severe | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spastic paraplegia, slowly progressive
n1=en:retardation | n2=en:spastic paraplegia, slowly progressive | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spastic quadriplegia
n1=en:retardation | n2=en:spastic quadriplegia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spastic quadriplegia (in one patient)
n1=en:retardation | n2=en:spastic quadriplegia (in one patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spastic quadriplegia, residual mild-to-severe (in some patients)
n1=en:retardation | n2=en:spastic quadriplegia, residual mild-to-severe (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spastic quadriplegia, severe
n1=en:retardation | n2=en:spastic quadriplegia, severe | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spastic tetraparesis
n1=en:retardation | n2=en:spastic tetraparesis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spastic tetraparesis (in severe cases)
n1=en:retardation | n2=en:spastic tetraparesis (in severe cases) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spastic tetraplegia (in some patients)
n1=en:retardation | n2=en:spastic tetraplegia (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spastic tetraplegia (onset in the second decade)
n1=en:retardation | n2=en:spastic tetraplegia (onset in the second decade) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spastic-ataxic gait
n1=en:retardation | n2=en:spastic-ataxic gait | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spastic-ataxic tetraparesis
n1=en:retardation | n2=en:spastic-ataxic tetraparesis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spasticity
n1=en:retardation | n2=en:spasticity | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spasticity (1 family)
n1=en:retardation | n2=en:spasticity (1 family) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spasticity (1 of 4 patients)
n1=en:retardation | n2=en:spasticity (1 of 4 patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spasticity (in some patients)
n1=en:retardation | n2=en:spasticity (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spasticity (in some)
n1=en:retardation | n2=en:spasticity (in some) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spasticity (later onset)
n1=en:retardation | n2=en:spasticity (later onset) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spasticity (later)
n1=en:retardation | n2=en:spasticity (later) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spasticity (less common)
n1=en:retardation | n2=en:spasticity (less common) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spasticity (patient a)
n1=en:retardation | n2=en:spasticity (patient a) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spasticity (rare)
n1=en:retardation | n2=en:spasticity (rare) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spasticity (reported in 1 patient)
n1=en:retardation | n2=en:spasticity (reported in 1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spasticity (type ii)
n1=en:retardation | n2=en:spasticity (type ii) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spasticity in infancy (1 patient)
n1=en:retardation | n2=en:spasticity in infancy (1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spasticity may be present
n1=en:retardation | n2=en:spasticity may be present | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spasticity may occur
n1=en:retardation | n2=en:spasticity may occur | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spasticity of facial muscles
n1=en:retardation | n2=en:spasticity of facial muscles | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spasticity of lower and upper limbs
n1=en:retardation | n2=en:spasticity of lower and upper limbs | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spasticity of pharyngeal muscles
n1=en:retardation | n2=en:spasticity of pharyngeal muscles | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spasticity, distal
n1=en:retardation | n2=en:spasticity, distal | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spasticity, hyperreflexia
n1=en:retardation | n2=en:spasticity, hyperreflexia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spasticity, lower limbs greater than upper limbs
n1=en:retardation | n2=en:spasticity, lower limbs greater than upper limbs | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spasticity, mainly in the lower limbs
n1=en:retardation | n2=en:spasticity, mainly in the lower limbs | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spasticity, mild (in some patients)
n1=en:retardation | n2=en:spasticity, mild (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spasticity, more apparent in the lower limbs
n1=en:retardation | n2=en:spasticity, more apparent in the lower limbs | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spasticity, primarily lower limbs, but upper limbs may be involved
n1=en:retardation | n2=en:spasticity, primarily lower limbs, but upper limbs may be involved | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spasticity, progressive, develops in childhood
n1=en:retardation | n2=en:spasticity, progressive, develops in childhood | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spasticity, severe
n1=en:retardation | n2=en:spasticity, severe | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spasticity, severe, affecting lower limbs
n1=en:retardation | n2=en:spasticity, severe, affecting lower limbs | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spasticity, usually of the lower limbs
n1=en:retardation | n2=en:spasticity, usually of the lower limbs | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spasticity/paresis (rare)
n1=en:retardation | n2=en:spasticity/paresis (rare) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:special symptoms or syndromes, nec in mdr18_1
n1=en:retardation | n2=en:special symptoms or syndromes, nec in mdr18_1 | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:specific developmental disorder
n1=en:retardation | n2=en:specific developmental disorder | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:specific developmental disorders of scholastic skills
n1=en:retardation | n2=en:specific developmental disorders of scholastic skills | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:specific learning problems
n1=en:retardation | n2=en:specific learning problems | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:specific nonpsychotic mental disorders following organic brain damage
n1=en:retardation | n2=en:specific nonpsychotic mental disorders following organic brain damage | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:specific visual spatial processing defect
n1=en:retardation | n2=en:specific visual spatial processing defect | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spect scan may show hypermetabolism of the temporal lobe
n1=en:retardation | n2=en:spect scan may show hypermetabolism of the temporal lobe | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:speech abnormalities (palilalia)
n1=en:retardation | n2=en:speech abnormalities (palilalia) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:speech absent or delayed
n1=en:retardation | n2=en:speech absent or delayed | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:speech and language delay (rare)
n1=en:retardation | n2=en:speech and language delay (rare) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:speech and language delay, severe
n1=en:retardation | n2=en:speech and language delay, severe | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:speech and language disorder
n1=en:retardation | n2=en:speech and language disorder | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:speech and language regression
n1=en:retardation | n2=en:speech and language regression | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:speech articulation defects
n1=en:retardation | n2=en:speech articulation defects | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:speech articulation problems
n1=en:retardation | n2=en:speech articulation problems | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:speech deficits
n1=en:retardation | n2=en:speech deficits | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:speech delay
n1=en:retardation | n2=en:speech delay | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:speech delay (1 patient)
n1=en:retardation | n2=en:speech delay (1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:speech delay (10%)
n1=en:retardation | n2=en:speech delay (10%) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:speech delay (59%)
n1=en:retardation | n2=en:speech delay (59%) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:speech delay (in all patients)
n1=en:retardation | n2=en:speech delay (in all patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:speech delay (in some patients)
n1=en:retardation | n2=en:speech delay (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:speech deterioration
n1=en:retardation | n2=en:speech deterioration | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:speech development delayed (in some patients)
n1=en:retardation | n2=en:speech development delayed (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:speech difficulties (48%)
n1=en:retardation | n2=en:speech difficulties (48%) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:speech difficulties due to hypoglossia
n1=en:retardation | n2=en:speech difficulties due to hypoglossia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:speech disability
n1=en:retardation | n2=en:speech disability | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:speech disorder
n1=en:retardation | n2=en:speech disorder | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:speech disorder (in 1 of 6 patients)
n1=en:retardation | n2=en:speech disorder (in 1 of 6 patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:speech disorders (rare)
n1=en:retardation | n2=en:speech disorders (rare) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:speech hesitancy
n1=en:retardation | n2=en:speech hesitancy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:speech impairment
n1=en:retardation | n2=en:speech impairment | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:speech limited
n1=en:retardation | n2=en:speech limited | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:speech limited to single word or no words
n1=en:retardation | n2=en:speech limited to single word or no words | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:speech never acquired
n1=en:retardation | n2=en:speech never acquired | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:speech severely limited or absent
n1=en:retardation | n2=en:speech severely limited or absent | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:speech, limited or nonverbal
n1=en:retardation | n2=en:speech, limited or nonverbal | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spheroids contain neurofilaments
n1=en:retardation | n2=en:spheroids contain neurofilaments | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spina bifida
n1=en:retardation | n2=en:spina bifida | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spina bifida (less common)
n1=en:retardation | n2=en:spina bifida (less common) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spina bifida occulta
n1=en:retardation | n2=en:spina bifida occulta | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spinal arteriovenous malformation
n1=en:retardation | n2=en:spinal arteriovenous malformation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spinal cord atrophy (1 family)
n1=en:retardation | n2=en:spinal cord atrophy (1 family) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spinal cord atrophy (rare)
n1=en:retardation | n2=en:spinal cord atrophy (rare) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spinal cord compression
n1=en:retardation | n2=en:spinal cord compression | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spinal cord compression by tumor infiltration
n1=en:retardation | n2=en:spinal cord compression by tumor infiltration | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spinal cord disorder
n1=en:retardation | n2=en:spinal cord disorder | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spinal cord glial hyperplasia
n1=en:retardation | n2=en:spinal cord glial hyperplasia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spinal cord paresis
n1=en:retardation | n2=en:spinal cord paresis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spinal cord syrinx (in 2 patients)
n1=en:retardation | n2=en:spinal cord syrinx (in 2 patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spinal cysts (in some patients)
n1=en:retardation | n2=en:spinal cysts (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spinal muscular atrophy
n1=en:retardation | n2=en:spinal muscular atrophy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spinal neurofibromas (64%)
n1=en:retardation | n2=en:spinal neurofibromas (64%) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spinal neuropathy
n1=en:retardation | n2=en:spinal neuropathy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spinal stenosis
n1=en:retardation | n2=en:spinal stenosis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spinal tract degeneration
n1=en:retardation | n2=en:spinal tract degeneration | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spinocerebellar ataxia
n1=en:retardation | n2=en:spinocerebellar ataxia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spinocerebellar ataxia (in some patients)
n1=en:retardation | n2=en:spinocerebellar ataxia (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spinocerebellar ataxia (upper and lower limb involvement)
n1=en:retardation | n2=en:spinocerebellar ataxia (upper and lower limb involvement) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spinocerebellar ataxia 21
n1=en:retardation | n2=en:spinocerebellar ataxia 21 | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spinocerebellar ataxia, autosomal recessive 12
n1=en:retardation | n2=en:spinocerebellar ataxia, autosomal recessive 12 | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spinocerebellar degeneration
n1=en:retardation | n2=en:spinocerebellar degeneration | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spinocerebellar tract degeneration
n1=en:retardation | n2=en:spinocerebellar tract degeneration | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spinocerebellar tract disease in lower limbs (in adulthood)
n1=en:retardation | n2=en:spinocerebellar tract disease in lower limbs (in adulthood) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:splenic rupture
n1=en:retardation | n2=en:splenic rupture | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:splenomegaly
n1=en:retardation | n2=en:splenomegaly | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spondyloepimetaphyseal dysplasia, genevieve type
n1=en:retardation | n2=en:spondyloepimetaphyseal dysplasia, genevieve type | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spongiform changes are mild or may not be present
n1=en:retardation | n2=en:spongiform changes are mild or may not be present | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spongiform degeneration
n1=en:retardation | n2=en:spongiform degeneration | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spongiform encephalomyelopathy
n1=en:retardation | n2=en:spongiform encephalomyelopathy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spongiosis, mild
n1=en:retardation | n2=en:spongiosis, mild | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spongy degeneration
n1=en:retardation | n2=en:spongy degeneration | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spongy gliosis
n1=en:retardation | n2=en:spongy gliosis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:spontaneous abortion
n1=en:retardation | n2=en:spontaneous abortion | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:sprain and strain of ankle
n1=en:retardation | n2=en:sprain and strain of ankle | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:stammering/stuttering/tics
n1=en:retardation | n2=en:stammering/stuttering/tics | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:stance ataxia
n1=en:retardation | n2=en:stance ataxia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:stargardt macular degeneration absent or hypoplastic corpus callosum mental retardation and dysmorphic features
n1=en:retardation | n2=en:stargardt macular degeneration absent or hypoplastic corpus callosum mental retardation and dysmorphic features | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:staring
n1=en:retardation | n2=en:staring | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:staring episodes during seizures
n1=en:retardation | n2=en:staring episodes during seizures | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:staring spells
n1=en:retardation | n2=en:staring spells | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:start with tonic posturing
n1=en:retardation | n2=en:start with tonic posturing | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:startle myoclonus
n1=en:retardation | n2=en:startle myoclonus | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:status dystonicus
n1=en:retardation | n2=en:status dystonicus | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:status epilepticus
n1=en:retardation | n2=en:status epilepticus | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:status epilepticus (in 1 of 6 patients)
n1=en:retardation | n2=en:status epilepticus (in 1 of 6 patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:status epilepticus (in some patients)
n1=en:retardation | n2=en:status epilepticus (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:status epilepticus (in some)
n1=en:retardation | n2=en:status epilepticus (in some) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:status epilepticus may occur
n1=en:retardation | n2=en:status epilepticus may occur | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:status epilepticus rarely occurs
n1=en:retardation | n2=en:status epilepticus rarely occurs | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:stenosis of the aqueduct of sylvius (rare)
n1=en:retardation | n2=en:stenosis of the aqueduct of sylvius (rare) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:stenosis of the jugular foramen
n1=en:retardation | n2=en:stenosis of the jugular foramen | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:stereotypic movements
n1=en:retardation | n2=en:stereotypic movements | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:stevenson-carey syndrome
n1=en:retardation | n2=en:stevenson-carey syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:stiff gait
n1=en:retardation | n2=en:stiff gait | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:stiff limbs
n1=en:retardation | n2=en:stiff limbs | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:stiffness
n1=en:retardation | n2=en:stiffness | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:stiffness of the lower limbs
n1=en:retardation | n2=en:stiffness of the lower limbs | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:stiffness while walking
n1=en:retardation | n2=en:stiffness while walking | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:stimulation sensitive generalized myoclonus (stage 3)
n1=en:retardation | n2=en:stimulation sensitive generalized myoclonus (stage 3) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:stimulation sensitive segmental myoclonus (stage 2)
n1=en:retardation | n2=en:stimulation sensitive segmental myoclonus (stage 2) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:stoke-like lesions
n1=en:retardation | n2=en:stoke-like lesions | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:stomach function disorder
n1=en:retardation | n2=en:stomach function disorder | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:stomatognathic system abnormalities
n1=en:retardation | n2=en:stomatognathic system abnormalities | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:strabismus
n1=en:retardation | n2=en:strabismus | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:strep throat/scarlet fever
n1=en:retardation | n2=en:strep throat/scarlet fever | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:stretched cerebellar peduncles
n1=en:retardation | n2=en:stretched cerebellar peduncles | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:striatal atrophy
n1=en:retardation | n2=en:striatal atrophy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:striatal lesions
n1=en:retardation | n2=en:striatal lesions | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:striatal necrosis
n1=en:retardation | n2=en:striatal necrosis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:striatonigral degeneration, infantile (disorder)
n1=en:retardation | n2=en:striatonigral degeneration, infantile (disorder) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:stroke (in some patients)
n1=en:retardation | n2=en:stroke (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:stroke (rare)
n1=en:retardation | n2=en:stroke (rare) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:stroke (uncommon)
n1=en:retardation | n2=en:stroke (uncommon) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:stroke-like episodes
n1=en:retardation | n2=en:stroke-like episodes | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:stroke-like episodes (in some patients)
n1=en:retardation | n2=en:stroke-like episodes (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:stroke-like symptoms
n1=en:retardation | n2=en:stroke-like symptoms | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:strokes due to coagulopathy
n1=en:retardation | n2=en:strokes due to coagulopathy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:structural abnormalities in the basal ganglia (especially caudate)
n1=en:retardation | n2=en:structural abnormalities in the basal ganglia (especially caudate) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:structural abnormalities of cerebellum
n1=en:retardation | n2=en:structural abnormalities of cerebellum | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:structural brain abnormalities
n1=en:retardation | n2=en:structural brain abnormalities | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:structural brain anomalies
n1=en:retardation | n2=en:structural brain anomalies | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:structural changes in the temporal lobe
n1=en:retardation | n2=en:structural changes in the temporal lobe | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:structure of central auditory system
n1=en:retardation | n2=en:structure of central auditory system | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:structure of central sensory visual system
n1=en:retardation | n2=en:structure of central sensory visual system | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:structure of decussation of superior cerebellar peduncles
n1=en:retardation | n2=en:structure of decussation of superior cerebellar peduncles | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:stt3a-cdg and stt3b-cdg
n1=en:retardation | n2=en:stt3a-cdg and stt3b-cdg | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:sturge-weber syndrome
n1=en:retardation | n2=en:sturge-weber syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:subacute neurologic deterioration
n1=en:retardation | n2=en:subacute neurologic deterioration | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:subarachnoid cyst
n1=en:retardation | n2=en:subarachnoid cyst | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:subarachnoid hemorrhage
n1=en:retardation | n2=en:subarachnoid hemorrhage | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:subarachnoid hemorrhage (rare)
n1=en:retardation | n2=en:subarachnoid hemorrhage (rare) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:subclinical absence seizures
n1=en:retardation | n2=en:subclinical absence seizures | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:subcortical and periventricular white matter abnormalities seen on mri (in some patients)
n1=en:retardation | n2=en:subcortical and periventricular white matter abnormalities seen on mri (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:subcortical atrophy (in some patients)
n1=en:retardation | n2=en:subcortical atrophy (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:subcortical band or laminar heterotopia (in female carriers)
n1=en:retardation | n2=en:subcortical band or laminar heterotopia (in female carriers) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:subcortical cysts in frontal and temporal lobes
n1=en:retardation | n2=en:subcortical cysts in frontal and temporal lobes | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:subcortical cysts may occur elsewhere
n1=en:retardation | n2=en:subcortical cysts may occur elsewhere | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:subcortical cysts temporal lobe
n1=en:retardation | n2=en:subcortical cysts temporal lobe | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:subcortical dementia, progressive (6% of patients)
n1=en:retardation | n2=en:subcortical dementia, progressive (6% of patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:subcortical focal lacunae
n1=en:retardation | n2=en:subcortical focal lacunae | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:subcortical gliosis
n1=en:retardation | n2=en:subcortical gliosis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:subcortical heterotopia
n1=en:retardation | n2=en:subcortical heterotopia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:subcortical hypomyelination
n1=en:retardation | n2=en:subcortical hypomyelination | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:subcortical lacunar lesions seen early in disease
n1=en:retardation | n2=en:subcortical lacunar lesions seen early in disease | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:subcortical lesions
n1=en:retardation | n2=en:subcortical lesions | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:subcortical lesions with edema
n1=en:retardation | n2=en:subcortical lesions with edema | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:subcortical leukodystrophy
n1=en:retardation | n2=en:subcortical leukodystrophy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:subcortical nodular grey matter heterotopia
n1=en:retardation | n2=en:subcortical nodular grey matter heterotopia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:subcortical nodular lesions in perivascular white matter
n1=en:retardation | n2=en:subcortical nodular lesions in perivascular white matter | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:subcortical origin of the myoclonus based on neurophysiologic studies
n1=en:retardation | n2=en:subcortical origin of the myoclonus based on neurophysiologic studies | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:subcortical temporal white matter disease, moderate
n1=en:retardation | n2=en:subcortical temporal white matter disease, moderate | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:subcortical white matter abnormalities (rare)
n1=en:retardation | n2=en:subcortical white matter abnormalities (rare) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:subcortical white matter abnormalities seen on mri
n1=en:retardation | n2=en:subcortical white matter abnormalities seen on mri | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:subcortical white matter calcifications
n1=en:retardation | n2=en:subcortical white matter calcifications | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:subcortical white matter lesions in the temporal lobes seen on brain mri
n1=en:retardation | n2=en:subcortical white matter lesions in the temporal lobes seen on brain mri | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:subependymal calcifications
n1=en:retardation | n2=en:subependymal calcifications | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:subependymal hemorrhage
n1=en:retardation | n2=en:subependymal hemorrhage | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:subependymal heterotopias
n1=en:retardation | n2=en:subependymal heterotopias | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:subependymal heterotopic nodules
n1=en:retardation | n2=en:subependymal heterotopic nodules | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:subependymal nodules
n1=en:retardation | n2=en:subependymal nodules | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:subependymal pseudocyst
n1=en:retardation | n2=en:subependymal pseudocyst | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:subnormal cognition
n1=en:retardation | n2=en:subnormal cognition | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:subnormal intelligence (62%)
n1=en:retardation | n2=en:subnormal intelligence (62%) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:substance abuse related disorder
n1=en:retardation | n2=en:substance abuse related disorder | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:substance withdrawal syndrome
n1=en:retardation | n2=en:substance withdrawal syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:substance-related disorder
n1=en:retardation | n2=en:substance-related disorder | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:substantia nigra gliosis
n1=en:retardation | n2=en:substantia nigra gliosis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:succinic semialdehyde dehydrogenase deficiency
n1=en:retardation | n2=en:succinic semialdehyde dehydrogenase deficiency | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:sudden arousal from slow-wave sleep with screaming, autonomic, and behavioral manifestations of intense fear (sleep terrors)
n1=en:retardation | n2=en:sudden arousal from slow-wave sleep with screaming, autonomic, and behavioral manifestations of intense fear (sleep terrors) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:sudden awakening
n1=en:retardation | n2=en:sudden awakening | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:sudden onset of neuropsychiatric symptoms
n1=en:retardation | n2=en:sudden onset of neuropsychiatric symptoms | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:suicidal and self-injurious behaviours nec
n1=en:retardation | n2=en:suicidal and self-injurious behaviours nec | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:suicide and intentional self-inflicted injury
n1=en:retardation | n2=en:suicide and intentional self-inflicted injury | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:suicide attempt
n1=en:retardation | n2=en:suicide attempt | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:superficial injury of ear
n1=en:retardation | n2=en:superficial injury of ear | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:superficial laminar spongiosis
n1=en:retardation | n2=en:superficial laminar spongiosis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:supernumerary structure
n1=en:retardation | n2=en:supernumerary structure | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:suppression-burst pattern
n1=en:retardation | n2=en:suppression-burst pattern | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:suppression-burst pattern see on eeg
n1=en:retardation | n2=en:suppression-burst pattern see on eeg | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:supranuclear gaze palsy
n1=en:retardation | n2=en:supranuclear gaze palsy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:supratentorial structures unformed or regressed
n1=en:retardation | n2=en:supratentorial structures unformed or regressed | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:swallowed foreign body in digestive system
n1=en:retardation | n2=en:swallowed foreign body in digestive system | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:sweating problem
n1=en:retardation | n2=en:sweating problem | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:swelling of the cerebral white matter
n1=en:retardation | n2=en:swelling of the cerebral white matter | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:swelling of the deep white matter seen on mri
n1=en:retardation | n2=en:swelling of the deep white matter seen on mri | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:swollen achromatic cells (pick cells)
n1=en:retardation | n2=en:swollen achromatic cells (pick cells) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:symmetric lesions in the basal ganglia consistent with leigh syndrome (256000), in a subset of patients
n1=en:retardation | n2=en:symmetric lesions in the basal ganglia consistent with leigh syndrome (256000), in a subset of patients | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:symmetric spinal nerve root neurofibromas
n1=en:retardation | n2=en:symmetric spinal nerve root neurofibromas | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:symmetric ventriculomegaly
n1=en:retardation | n2=en:symmetric ventriculomegaly | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:symmetrical progressive demyelination
n1=en:retardation | n2=en:symmetrical progressive demyelination | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:symptoms are exacerbated during pregnancy
n1=en:retardation | n2=en:symptoms are exacerbated during pregnancy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:symptoms occur at rest
n1=en:retardation | n2=en:symptoms occur at rest | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:symptoms of hypothalamic disturbances (in some patients)
n1=en:retardation | n2=en:symptoms of hypothalamic disturbances (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:symptoms stabilize within 4 weeks
n1=en:retardation | n2=en:symptoms stabilize within 4 weeks | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:syncope
n1=en:retardation | n2=en:syncope | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:syndactyly
n1=en:retardation | n2=en:syndactyly | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:syndrome screaming
n1=en:retardation | n2=en:syndrome screaming | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:syndromes of cervical spine
n1=en:retardation | n2=en:syndromes of cervical spine | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:synkinesia (rare)
n1=en:retardation | n2=en:synkinesia (rare) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:synkinesis
n1=en:retardation | n2=en:synkinesis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:syphilis female
n1=en:retardation | n2=en:syphilis female | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:syphilis male
n1=en:retardation | n2=en:syphilis male | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:syringomyelia
n1=en:retardation | n2=en:syringomyelia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:syringomyelia (in some patients)
n1=en:retardation | n2=en:syringomyelia (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:syringomyelia, noncommunicating (80% of cases)
n1=en:retardation | n2=en:syringomyelia, noncommunicating (80% of cases) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:t1-weighted hyperintensity surrounding a central band of hypointensity in the substantia nigra
n1=en:retardation | n2=en:t1-weighted hyperintensity surrounding a central band of hypointensity in the substantia nigra | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:t2-weighted hyperintense lesions in the thalamus, basal ganglia, and brainstem
n1=en:retardation | n2=en:t2-weighted hyperintense lesions in the thalamus, basal ganglia, and brainstem | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:t2-weighted hyperintensities in deep brain regions
n1=en:retardation | n2=en:t2-weighted hyperintensities in deep brain regions | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:t2-weighted hyperintensities in deep cerebral white matter, brainstem, and cerebellar white matter with sparing of the periventricular rim
n1=en:retardation | n2=en:t2-weighted hyperintensities in deep cerebral white matter, brainstem, and cerebellar white matter with sparing of the periventricular rim | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:t2-weighted hyperintensities in subcortical brain regions seen on mri
n1=en:retardation | n2=en:t2-weighted hyperintensities in subcortical brain regions seen on mri | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:t2-weighted hyperintensities in the basal ganglia
n1=en:retardation | n2=en:t2-weighted hyperintensities in the basal ganglia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:t2-weighted hyperintensities in the basal ganglia, corpus callosum, and brainstem seen on mri
n1=en:retardation | n2=en:t2-weighted hyperintensities in the basal ganglia, corpus callosum, and brainstem seen on mri | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:t2-weighted hyperintensities in the corticospinal tracts and posterior arms of the internal capsule in older patients seen on mri
n1=en:retardation | n2=en:t2-weighted hyperintensities in the corticospinal tracts and posterior arms of the internal capsule in older patients seen on mri | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:t2-weighted hyperintensities in the periventricular and deep subcortical white matter
n1=en:retardation | n2=en:t2-weighted hyperintensities in the periventricular and deep subcortical white matter | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:t2-weighted hyperintensities in the putamen and caudate nuclei
n1=en:retardation | n2=en:t2-weighted hyperintensities in the putamen and caudate nuclei | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:t2-weighted hyperintensities in the supratentorial white matter seen on brain mri
n1=en:retardation | n2=en:t2-weighted hyperintensities in the supratentorial white matter seen on brain mri | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:t2-weighted hypodensities in the basal ganglia
n1=en:retardation | n2=en:t2-weighted hypodensities in the basal ganglia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:t2-weighted mri shows hyperintensities in the thalamus, basal ganglia, and brainstem during acute illness (may later resolve)
n1=en:retardation | n2=en:t2-weighted mri shows hyperintensities in the thalamus, basal ganglia, and brainstem during acute illness (may later resolve) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:t2-weighted signal abnormalities in the deep white matter
n1=en:retardation | n2=en:t2-weighted signal abnormalities in the deep white matter | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:tachycardia, paroxysmal
n1=en:retardation | n2=en:tachycardia, paroxysmal | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:tardive dyskinesia
n1=en:retardation | n2=en:tardive dyskinesia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:tau immunreactivity
n1=en:retardation | n2=en:tau immunreactivity | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:tau inclusions are 'flame-shaped' or 'tuft-like'
n1=en:retardation | n2=en:tau inclusions are 'flame-shaped' or 'tuft-like' | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:tau-containing inclusions
n1=en:retardation | n2=en:tau-containing inclusions | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:tau-immunoreactive inclusions in neurons and astrocytes
n1=en:retardation | n2=en:tau-immunoreactive inclusions in neurons and astrocytes | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:tau-positive inclusions may be found
n1=en:retardation | n2=en:tau-positive inclusions may be found | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:tbp- and 1c2-immunoreactive neuronal inclusions
n1=en:retardation | n2=en:tbp- and 1c2-immunoreactive neuronal inclusions | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:tdp43-positive inclusions
n1=en:retardation | n2=en:tdp43-positive inclusions | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:tdp43-positive neuronal and glial cytoplasmic inclusions
n1=en:retardation | n2=en:tdp43-positive neuronal and glial cytoplasmic inclusions | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:tdp43-positive neuronal inclusions
n1=en:retardation | n2=en:tdp43-positive neuronal inclusions | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:tectal enlargement
n1=en:retardation | n2=en:tectal enlargement | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:temporal epileptiform discharges seen on eeg
n1=en:retardation | n2=en:temporal epileptiform discharges seen on eeg | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:temporal lobe
n1=en:retardation | n2=en:temporal lobe | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:temporal lobe epilepsy (1 patient)
n1=en:retardation | n2=en:temporal lobe epilepsy (1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:temporal lobe heterotopias
n1=en:retardation | n2=en:temporal lobe heterotopias | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:temporal lobe infarct (rare)
n1=en:retardation | n2=en:temporal lobe infarct (rare) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:temporal lobe seizures (in 1 patient)
n1=en:retardation | n2=en:temporal lobe seizures (in 1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:temtamy syndrome
n1=en:retardation | n2=en:temtamy syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:tendency to walk on toes
n1=en:retardation | n2=en:tendency to walk on toes | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:testicular hydrocele
n1=en:retardation | n2=en:testicular hydrocele | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:tetanus
n1=en:retardation | n2=en:tetanus | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:tetany
n1=en:retardation | n2=en:tetany | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:tetany, hypocalcemic (in some patients)
n1=en:retardation | n2=en:tetany, hypocalcemic (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:tetany, hypocalcemic, episodic
n1=en:retardation | n2=en:tetany, hypocalcemic, episodic | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:tethered cord (rare)
n1=en:retardation | n2=en:tethered cord (rare) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:tethered cord (uncommon)
n1=en:retardation | n2=en:tethered cord (uncommon) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:tethered spinal cord
n1=en:retardation | n2=en:tethered spinal cord | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:tethered spinal cord syndrome
n1=en:retardation | n2=en:tethered spinal cord syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:tetralogy of fallot
n1=en:retardation | n2=en:tetralogy of fallot | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:tetraplegic spasticity
n1=en:retardation | n2=en:tetraplegic spasticity | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:tfg- and tdp43-positive intraneuronal inclusions in some sensory and motor spinal cord neurons
n1=en:retardation | n2=en:tfg- and tdp43-positive intraneuronal inclusions in some sensory and motor spinal cord neurons | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:thalamic hypoplasia
n1=en:retardation | n2=en:thalamic hypoplasia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:thalamic lesions
n1=en:retardation | n2=en:thalamic lesions | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:thalamic neuronal loss, especially in the medial dorsal nucleus
n1=en:retardation | n2=en:thalamic neuronal loss, especially in the medial dorsal nucleus | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:thenar muscle atrophy
n1=en:retardation | n2=en:thenar muscle atrophy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:thenar muscle weakness
n1=en:retardation | n2=en:thenar muscle weakness | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:thick and elongated superior cerebellar peduncles
n1=en:retardation | n2=en:thick and elongated superior cerebellar peduncles | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:thick corpus callosum
n1=en:retardation | n2=en:thick corpus callosum | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:thick cortex
n1=en:retardation | n2=en:thick cortex | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:thick, maloriented superior cerebellar peduncles
n1=en:retardation | n2=en:thick, maloriented superior cerebellar peduncles | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:thick, short corpus callosum
n1=en:retardation | n2=en:thick, short corpus callosum | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:thickened cortices
n1=en:retardation | n2=en:thickened cortices | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:thickened frontal cortex
n1=en:retardation | n2=en:thickened frontal cortex | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:thickened optic nerve sheath
n1=en:retardation | n2=en:thickened optic nerve sheath | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:thickening of the skull (less common)
n1=en:retardation | n2=en:thickening of the skull (less common) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:thin bony cortex
n1=en:retardation | n2=en:thin bony cortex | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:thin brainstem
n1=en:retardation | n2=en:thin brainstem | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:thin cerebral cortex
n1=en:retardation | n2=en:thin cerebral cortex | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:thin corpus callosum (1 family)
n1=en:retardation | n2=en:thin corpus callosum (1 family) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:thin corpus callosum (1 patient)
n1=en:retardation | n2=en:thin corpus callosum (1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:thin corpus callosum (1/4 patients)
n1=en:retardation | n2=en:thin corpus callosum (1/4 patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:thin corpus callosum (in some patients)
n1=en:retardation | n2=en:thin corpus callosum (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:thin corpus callosum enlarged ventricles
n1=en:retardation | n2=en:thin corpus callosum enlarged ventricles | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:thin cortical mantle (wws)
n1=en:retardation | n2=en:thin cortical mantle (wws) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:thin optic chiasm
n1=en:retardation | n2=en:thin optic chiasm | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:thin pituitary stalk
n1=en:retardation | n2=en:thin pituitary stalk | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:thinning of the cerebellopontine tracts
n1=en:retardation | n2=en:thinning of the cerebellopontine tracts | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:third ventricle subependymal focal gliosis
n1=en:retardation | n2=en:third ventricle subependymal focal gliosis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:thoracogastroschisis
n1=en:retardation | n2=en:thoracogastroschisis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:thoracoschisis
n1=en:retardation | n2=en:thoracoschisis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:thrombosis of cerebral veins
n1=en:retardation | n2=en:thrombosis of cerebral veins | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:thumb in palm deformity
n1=en:retardation | n2=en:thumb in palm deformity | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:thyroglossal duct cyst
n1=en:retardation | n2=en:thyroglossal duct cyst | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:thyroid dysgenesis
n1=en:retardation | n2=en:thyroid dysgenesis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:thyroid gland malformation
n1=en:retardation | n2=en:thyroid gland malformation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:thyrotoxicosis [hyperthyroidism]
n1=en:retardation | n2=en:thyrotoxicosis [hyperthyroidism] | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:tip-toe gait
n1=en:retardation | n2=en:tip-toe gait | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:tobacco use disorder
n1=en:retardation | n2=en:tobacco use disorder | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:toe-walking gait
n1=en:retardation | n2=en:toe-walking gait | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:toe-walking in early childhood
n1=en:retardation | n2=en:toe-walking in early childhood | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:tongue movements, protrusions
n1=en:retardation | n2=en:tongue movements, protrusions | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:tonic clonic seizures, infrequent (in one patient)
n1=en:retardation | n2=en:tonic clonic seizures, infrequent (in one patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:tonic convulsion
n1=en:retardation | n2=en:tonic convulsion | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:tonic head extension
n1=en:retardation | n2=en:tonic head extension | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:tonic posturing
n1=en:retardation | n2=en:tonic posturing | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:tonic seizures, refractory
n1=en:retardation | n2=en:tonic seizures, refractory | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:tonic spasms
n1=en:retardation | n2=en:tonic spasms | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:tonic-clonic seizures (less common)
n1=en:retardation | n2=en:tonic-clonic seizures (less common) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:tonus dysregulation
n1=en:retardation | n2=en:tonus dysregulation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:tooth development and eruption disorder
n1=en:retardation | n2=en:tooth development and eruption disorder | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:torsion dystonia (involuntary sustained muscle contractions, twisting and repetitive movements, abnormal posturing)
n1=en:retardation | n2=en:torsion dystonia (involuntary sustained muscle contractions, twisting and repetitive movements, abnormal posturing) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:torticollis
n1=en:retardation | n2=en:torticollis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:total body paralysis, paroxysmal
n1=en:retardation | n2=en:total body paralysis, paroxysmal | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:touch, vibration, and limb position may or may not be affected
n1=en:retardation | n2=en:touch, vibration, and limb position may or may not be affected | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:tow-walking
n1=en:retardation | n2=en:tow-walking | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:toxemia of pregnancy
n1=en:retardation | n2=en:toxemia of pregnancy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:toxic effect of other and unspecified substances
n1=en:retardation | n2=en:toxic effect of other and unspecified substances | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:toxic nodular goiter
n1=en:retardation | n2=en:toxic nodular goiter | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:toxoplasmosis
n1=en:retardation | n2=en:toxoplasmosis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:trachoma
n1=en:retardation | n2=en:trachoma | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:transient ataxia
n1=en:retardation | n2=en:transient ataxia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:transient cerebral ischemia
n1=en:retardation | n2=en:transient cerebral ischemia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:transient ischemic attack
n1=en:retardation | n2=en:transient ischemic attack | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:transient mild dystonia may precede abrupt onset of disorder by several years
n1=en:retardation | n2=en:transient mild dystonia may precede abrupt onset of disorder by several years | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:transient, reversible neurologic deficits
n1=en:retardation | n2=en:transient, reversible neurologic deficits | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:transitional facial palsy (15%)
n1=en:retardation | n2=en:transitional facial palsy (15%) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:transposition of great vessels
n1=en:retardation | n2=en:transposition of great vessels | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:trauma and stressor related disorders
n1=en:retardation | n2=en:trauma and stressor related disorders | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:trauma/injury problem
n1=en:retardation | n2=en:trauma/injury problem | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:tremor
n1=en:retardation | n2=en:tremor | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:tremor (1 patient)
n1=en:retardation | n2=en:tremor (1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:tremor (3 patients)
n1=en:retardation | n2=en:tremor (3 patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:tremor (30%)
n1=en:retardation | n2=en:tremor (30%) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:tremor (57% of patients)
n1=en:retardation | n2=en:tremor (57% of patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:tremor (in some patients)
n1=en:retardation | n2=en:tremor (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:tremor (later-onset)
n1=en:retardation | n2=en:tremor (later-onset) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:tremor (less common)
n1=en:retardation | n2=en:tremor (less common) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:tremor (rare)
n1=en:retardation | n2=en:tremor (rare) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:tremor adverse event
n1=en:retardation | n2=en:tremor adverse event | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:tremor due to hyperthyroidism
n1=en:retardation | n2=en:tremor due to hyperthyroidism | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:tremor is exacerbated by stress and exercise
n1=en:retardation | n2=en:tremor is exacerbated by stress and exercise | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:tremor of hands
n1=en:retardation | n2=en:tremor of hands | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:tremor of palate
n1=en:retardation | n2=en:tremor of palate | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:tremor of the upper limb
n1=en:retardation | n2=en:tremor of the upper limb | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:tremor with febrile episodes (rare)
n1=en:retardation | n2=en:tremor with febrile episodes (rare) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:tremor, action (arms, tongue, head, legs and trunk)
n1=en:retardation | n2=en:tremor, action (arms, tongue, head, legs and trunk) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:tremor, action, progressive
n1=en:retardation | n2=en:tremor, action, progressive | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:tremor, mild
n1=en:retardation | n2=en:tremor, mild | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:tremor, postural (arms, tongue, head, legs and trunk)
n1=en:retardation | n2=en:tremor, postural (arms, tongue, head, legs and trunk) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:tremor, postural, upper limb, onset in fourth decade (reported in 1 family)
n1=en:retardation | n2=en:tremor, postural, upper limb, onset in fourth decade (reported in 1 family) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:tremor, small-amplitude, high-frequency, restricted to the hands
n1=en:retardation | n2=en:tremor, small-amplitude, high-frequency, restricted to the hands | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:tremor, static
n1=en:retardation | n2=en:tremor, static | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:tremor, variable
n1=en:retardation | n2=en:tremor, variable | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:tremors, action
n1=en:retardation | n2=en:tremors, action | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:tremors, limb
n1=en:retardation | n2=en:tremors, limb | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:trichorhinophalangeal syndrome type ii
n1=en:retardation | n2=en:trichorhinophalangeal syndrome type ii | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:trigeminal anesthesia
n1=en:retardation | n2=en:trigeminal anesthesia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:trigeminal neuralgia
n1=en:retardation | n2=en:trigeminal neuralgia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:triglyceride storage disease with ichthyosis
n1=en:retardation | n2=en:triglyceride storage disease with ichthyosis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:trismus
n1=en:retardation | n2=en:trismus | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:trismus (rare)
n1=en:retardation | n2=en:trismus (rare) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:trisomy 14
n1=en:retardation | n2=en:trisomy 14 | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:trisomy 17
n1=en:retardation | n2=en:trisomy 17 | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:trisomy 22
n1=en:retardation | n2=en:trisomy 22 | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:truncal arching
n1=en:retardation | n2=en:truncal arching | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:truncal ataxia, mild
n1=en:retardation | n2=en:truncal ataxia, mild | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:truncal ataxia, severe
n1=en:retardation | n2=en:truncal ataxia, severe | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:truncal instability
n1=en:retardation | n2=en:truncal instability | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:truncal titubation
n1=en:retardation | n2=en:truncal titubation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:tuberous sclerosis
n1=en:retardation | n2=en:tuberous sclerosis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:tussive syncopes
n1=en:retardation | n2=en:tussive syncopes | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:twin-twin transfusion syndrome
n1=en:retardation | n2=en:twin-twin transfusion syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:twitching of the fingers and toes
n1=en:retardation | n2=en:twitching of the fingers and toes | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:tympanic membrane perforation
n1=en:retardation | n2=en:tympanic membrane perforation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:type i arnold chiari malformation
n1=en:retardation | n2=en:type i arnold chiari malformation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:type i eeg response is occipital spikes
n1=en:retardation | n2=en:type i eeg response is occipital spikes | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:type ii acrocephalopolysyndactyly
n1=en:retardation | n2=en:type ii acrocephalopolysyndactyly | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:type ii eeg response is parietooccipital spikes followed by biphasic slow waves
n1=en:retardation | n2=en:type ii eeg response is parietooccipital spikes followed by biphasic slow waves | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:type iii eeg response is parietooccipital spikes followed by biphasic slow waves and spreading to the frontal region
n1=en:retardation | n2=en:type iii eeg response is parietooccipital spikes followed by biphasic slow waves and spreading to the frontal region | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:type iv eeg response is generalized spike-wave discharges
n1=en:retardation | n2=en:type iv eeg response is generalized spike-wave discharges | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ubiquitin-positive cytoplasmic and intranuclear neuronal inclusions
n1=en:retardation | n2=en:ubiquitin-positive cytoplasmic and intranuclear neuronal inclusions | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ubiquitin-positive inclusions
n1=en:retardation | n2=en:ubiquitin-positive inclusions | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ubiquitin-positive intranuclear neuronal inclusions
n1=en:retardation | n2=en:ubiquitin-positive intranuclear neuronal inclusions | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ubqln2- and tdp43-immunopositive inclusions in spinal motor, brainstem, and hippocampal neurons
n1=en:retardation | n2=en:ubqln2- and tdp43-immunopositive inclusions in spinal motor, brainstem, and hippocampal neurons | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:udpglucose 4-epimerase deficiency disease
n1=en:retardation | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:unable to grasp objects
n1=en:retardation | n2=en:unable to grasp objects | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:unable to sit unsupported
n1=en:retardation | n2=en:unable to sit unsupported | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:unable to stand
n1=en:retardation | n2=en:unable to stand | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:unable to talk
n1=en:retardation | n2=en:unable to talk | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:unable to walk
n1=en:retardation | n2=en:unable to walk | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:uncomplicated hypertension
n1=en:retardation | n2=en:uncomplicated hypertension | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:uncoordinated movements
n1=en:retardation | n2=en:uncoordinated movements | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:underdeveloped corpus callosum (3 patients)
n1=en:retardation | n2=en:underdeveloped corpus callosum (3 patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:undersulcation of the frontal lobes
n1=en:retardation | n2=en:undersulcation of the frontal lobes | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:undescended testes
n1=en:retardation | n2=en:undescended testes | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:unexplained abnormal blood test
n1=en:retardation | n2=en:unexplained abnormal blood test | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:unidentified bright objects on brain mri
n1=en:retardation | n2=en:unidentified bright objects on brain mri | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:unilateral cerebellar hypoplasia
n1=en:retardation | n2=en:unilateral cerebellar hypoplasia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:unilateral headache location
n1=en:retardation | n2=en:unilateral headache location | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:unintelligible speech, vocalizations, grunting
n1=en:retardation | n2=en:unintelligible speech, vocalizations, grunting | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:unresponsive to stimuli
n1=en:retardation | n2=en:unresponsive to stimuli | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:unresponsiveness
n1=en:retardation | n2=en:unresponsiveness | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:unspecified behavioural and emotional disorders with onset usually occurring in childhood and adolescence
n1=en:retardation | n2=en:unspecified behavioural and emotional disorders with onset usually occurring in childhood and adolescence | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:unspecified disorder of adult personality and behaviour
n1=en:retardation | n2=en:unspecified disorder of adult personality and behaviour | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:unspecified drug-induced mental disorder
n1=en:retardation | n2=en:unspecified drug-induced mental disorder | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:unspecified intellectual disabilities
n1=en:retardation | n2=en:unspecified intellectual disabilities | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:unspecified mental retardation; other impairments of behaviour
n1=en:retardation | n2=en:unspecified mental retardation; other impairments of behaviour | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:unspecified mental retardation; significant impairment of behaviour requiring attention or treatment
n1=en:retardation | n2=en:unspecified mental retardation; significant impairment of behaviour requiring attention or treatment | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:unspecified mental retardation; with the statement of no, or minimal, impairment of behaviour
n1=en:retardation | n2=en:unspecified mental retardation; with the statement of no, or minimal, impairment of behaviour | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:unspecified mental retardation; without mention of impairment of behaviour
n1=en:retardation | n2=en:unspecified mental retardation; without mention of impairment of behaviour | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:unspecified neoplasms
n1=en:retardation | n2=en:unspecified neoplasms | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:unspecified psychophysiological malfunction
n1=en:retardation | n2=en:unspecified psychophysiological malfunction | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:unstable, ataxic gait
n1=en:retardation | n2=en:unstable, ataxic gait | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:unsteadiness, episodic
n1=en:retardation | n2=en:unsteadiness, episodic | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:unsteady gait due to muscle weakness
n1=en:retardation | n2=en:unsteady gait due to muscle weakness | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:unsteady standing
n1=en:retardation | n2=en:unsteady standing | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:unusual aura symptoms include alien limb phenomenon, diplopia, apraxia, dysarthria, impaired hearing, vertigo
n1=en:retardation | n2=en:unusual aura symptoms include alien limb phenomenon, diplopia, apraxia, dysarthria, impaired hearing, vertigo | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:unwanted pregnancy confirmed
n1=en:retardation | n2=en:unwanted pregnancy confirmed | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:upbeat central vestibular nystagmus
n1=en:retardation | n2=en:upbeat central vestibular nystagmus | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:upper and lower motor neuron degeneration
n1=en:retardation | n2=en:upper and lower motor neuron degeneration | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:upper and lower motor neuron disease
n1=en:retardation | n2=en:upper and lower motor neuron disease | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:upper and lower neuron manifestations
n1=en:retardation | n2=en:upper and lower neuron manifestations | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:upper body involvement
n1=en:retardation | n2=en:upper body involvement | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:upper extremities may be involved
n1=en:retardation | n2=en:upper extremities may be involved | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:upper extremity action tremor
n1=en:retardation | n2=en:upper extremity action tremor | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:upper limb ataxia
n1=en:retardation | n2=en:upper limb ataxia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:upper limb dysmetria
n1=en:retardation | n2=en:upper limb dysmetria | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:upper limb dystonia
n1=en:retardation | n2=en:upper limb dystonia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:upper limb hyperreflexia (in some patients)
n1=en:retardation | n2=en:upper limb hyperreflexia (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:upper limb hyperreflexia (some)
n1=en:retardation | n2=en:upper limb hyperreflexia (some) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:upper limb involvement
n1=en:retardation | n2=en:upper limb involvement | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:upper limb involvement (in some patients)
n1=en:retardation | n2=en:upper limb involvement (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:upper limb involvement (onset in the first decade)
n1=en:retardation | n2=en:upper limb involvement (onset in the first decade) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:upper limb involvement may occur
n1=en:retardation | n2=en:upper limb involvement may occur | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:upper limb spasticity
n1=en:retardation | n2=en:upper limb spasticity | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:upper limb spasticity (in some patients)
n1=en:retardation | n2=en:upper limb spasticity (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:upper limb spasticity (some)
n1=en:retardation | n2=en:upper limb spasticity (some) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:upper limb spasticity, mild
n1=en:retardation | n2=en:upper limb spasticity, mild | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:upper limb weakness
n1=en:retardation | n2=en:upper limb weakness | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:upper limb weakness may occur later
n1=en:retardation | n2=en:upper limb weakness may occur later | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:upper limbs affected
n1=en:retardation | n2=en:upper limbs affected | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:upper limbs may be affected
n1=en:retardation | n2=en:upper limbs may be affected | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:upper limbs may show hyperreflexia
n1=en:retardation | n2=en:upper limbs may show hyperreflexia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:upper limbs may show mild involvement
n1=en:retardation | n2=en:upper limbs may show mild involvement | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:upper limbs more often affected than lower limbs
n1=en:retardation | n2=en:upper limbs more often affected than lower limbs | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:upper motor involvement (some patient)
n1=en:retardation | n2=en:upper motor involvement (some patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:upper motor neuron degeneration
n1=en:retardation | n2=en:upper motor neuron degeneration | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:upper motor neuron dysfunction
n1=en:retardation | n2=en:upper motor neuron dysfunction | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:upper motor neuron signs
n1=en:retardation | n2=en:upper motor neuron signs | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:upper motor neuron signs (in some patients)
n1=en:retardation | n2=en:upper motor neuron signs (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:upper motor neuron signs, early
n1=en:retardation | n2=en:upper motor neuron signs, early | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:upper motor signs
n1=en:retardation | n2=en:upper motor signs | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:upper motor signs (in some patients)
n1=en:retardation | n2=en:upper motor signs (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:uremic coma
n1=en:retardation | n2=en:uremic coma | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ureterocele
n1=en:retardation | n2=en:ureterocele | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:urinary stone
n1=en:retardation | n2=en:urinary stone | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:urinary system neoplasm
n1=en:retardation | n2=en:urinary system neoplasm | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:urocanase deficiency
n1=en:retardation | n2=en:urocanase deficiency | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:urogenital trichomoniasis proven
n1=en:retardation | n2=en:urogenital trichomoniasis proven | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:urologic injuries
n1=en:retardation | n2=en:urologic injuries | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:urticaria
n1=en:retardation | n2=en:urticaria | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:usually occurs at night
n1=en:retardation | n2=en:usually occurs at night | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:uterine anomalies
n1=en:retardation | n2=en:uterine anomalies | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:uterovaginal prolapse
n1=en:retardation | n2=en:uterovaginal prolapse | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:vacuolated neurons
n1=en:retardation | n2=en:vacuolated neurons | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:vacuolization (patient a)
n1=en:retardation | n2=en:vacuolization (patient a) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:vacuolizing myelinopathy
n1=en:retardation | n2=en:vacuolizing myelinopathy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:vaginitis/vulvitis nos
n1=en:retardation | n2=en:vaginitis/vulvitis nos | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:van maldergem syndrome 2
n1=en:retardation | n2=en:van maldergem syndrome 2 | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:van maldergem wetzburger verloes syndrome
n1=en:retardation | n2=en:van maldergem wetzburger verloes syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:variable delay (iq range 52-104)
n1=en:retardation | n2=en:variable delay (iq range 52-104) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:variable intracranial abnormalities
n1=en:retardation | n2=en:variable intracranial abnormalities | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:variable mental retardation
n1=en:retardation | n2=en:variable mental retardation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:variable mental retardation (40%)
n1=en:retardation | n2=en:variable mental retardation (40%) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:variable mental retardation ranging from severe neurodegeneration to mild mental retardation
n1=en:retardation | n2=en:variable mental retardation ranging from severe neurodegeneration to mild mental retardation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:variable neurologic deterioration (likely result of hemophagocytic syndrome)
n1=en:retardation | n2=en:variable neurologic deterioration (likely result of hemophagocytic syndrome) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:variable outcome after acute illness
n1=en:retardation | n2=en:variable outcome after acute illness | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:varicose vein of lower extremities
n1=en:retardation | n2=en:varicose vein of lower extremities | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:varying degree of mental retardation
n1=en:retardation | n2=en:varying degree of mental retardation | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:vasculopathy of the small arteries penetrating the white matter
n1=en:retardation | n2=en:vasculopathy of the small arteries penetrating the white matter | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:vasovagal syncope
n1=en:retardation | n2=en:vasovagal syncope | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:vcp-positive inclusions
n1=en:retardation | n2=en:vcp-positive inclusions | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ventricles slightly enlarged
n1=en:retardation | n2=en:ventricles slightly enlarged | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ventricular anomalies
n1=en:retardation | n2=en:ventricular anomalies | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ventricular asymmetry
n1=en:retardation | n2=en:ventricular asymmetry | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ventricular dilatation (29%)
n1=en:retardation | n2=en:ventricular dilatation (29%) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ventricular dilatation (in some patients)
n1=en:retardation | n2=en:ventricular dilatation (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ventricular dilatation (rare)
n1=en:retardation | n2=en:ventricular dilatation (rare) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ventricular enlargement
n1=en:retardation | n2=en:ventricular enlargement | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ventricular enlargement, mild
n1=en:retardation | n2=en:ventricular enlargement, mild | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ventricular septal defect
n1=en:retardation | n2=en:ventricular septal defect | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ventriculomegaly (38%)
n1=en:retardation | n2=en:ventriculomegaly (38%) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ventriculomegaly (in some patients)
n1=en:retardation | n2=en:ventriculomegaly (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ventriculomegaly (variable)
n1=en:retardation | n2=en:ventriculomegaly (variable) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ventriculomegaly, mild (rare)
n1=en:retardation | n2=en:ventriculomegaly, mild (rare) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:ventriculomeglia
n1=en:retardation | n2=en:ventriculomeglia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:verbal delay (in some patients)
n1=en:retardation | n2=en:verbal delay (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:vermian hypoplasia
n1=en:retardation | n2=en:vermian hypoplasia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:vertical orientation of hippocampus
n1=en:retardation | n2=en:vertical orientation of hippocampus | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:vertiginous syndrome
n1=en:retardation | n2=en:vertiginous syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:vertigo
n1=en:retardation | n2=en:vertigo | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:vertigo, episodic (onset in second or third decade)
n1=en:retardation | n2=en:vertigo, episodic (onset in second or third decade) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:vertigo, mild
n1=en:retardation | n2=en:vertigo, mild | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:very poor expressive speech
n1=en:retardation | n2=en:very poor expressive speech | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:vestibular anomalies (less common)
n1=en:retardation | n2=en:vestibular anomalies (less common) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:vestibular diseases
n1=en:retardation | n2=en:vestibular diseases | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:vestibular dysfunction
n1=en:retardation | n2=en:vestibular dysfunction | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:vestibular dysfunction, mild
n1=en:retardation | n2=en:vestibular dysfunction, mild | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:vestibulopathy, bilateral, progressive (onset in fourth or fifth decade)
n1=en:retardation | n2=en:vestibulopathy, bilateral, progressive (onset in fourth or fifth decade) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:viral hepatitis
n1=en:retardation | n2=en:viral hepatitis | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:virtual absence of pyramidal tracts (wws)
n1=en:retardation | n2=en:virtual absence of pyramidal tracts (wws) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:visceroautonomic dysfunction
n1=en:retardation | n2=en:visceroautonomic dysfunction | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:visual acuity is normal
n1=en:retardation | n2=en:visual acuity is normal | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:visual auras
n1=en:retardation | n2=en:visual auras | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:visual blackouts (stage 1)
n1=en:retardation | n2=en:visual blackouts (stage 1) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:visual changes
n1=en:retardation | n2=en:visual changes | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:visual hallucination
n1=en:retardation | n2=en:visual hallucination | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:visual hallucinations may occur
n1=en:retardation | n2=en:visual hallucinations may occur | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:visual impairment
n1=en:retardation | n2=en:visual impairment | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:visual inattention
n1=en:retardation | n2=en:visual inattention | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:visual symptoms (in 60% of patients)
n1=en:retardation | n2=en:visual symptoms (in 60% of patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:visuospatial agnosia (in a subset of patients)
n1=en:retardation | n2=en:visuospatial agnosia (in a subset of patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:vitamin deficiency/other nutritional/disease
n1=en:retardation | n2=en:vitamin deficiency/other nutritional/disease | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:vocalization (finding)
n1=en:retardation | n2=en:vocalization (finding) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:waardenburg syndrome, type iie
n1=en:retardation | n2=en:waardenburg syndrome, type iie | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:waddling gait
n1=en:retardation | n2=en:waddling gait | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:waisman syndrome
n1=en:retardation | n2=en:waisman syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:walking delay
n1=en:retardation | n2=en:walking delay | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:walking disability
n1=en:retardation | n2=en:walking disability | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:walking during slow-wave sleep (sleepwalking)
n1=en:retardation | n2=en:walking during slow-wave sleep (sleepwalking) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:walking impairment due to myoclonus late in disease
n1=en:retardation | n2=en:walking impairment due to myoclonus late in disease | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:walking independently at 2.5 years to 4 years of age
n1=en:retardation | n2=en:walking independently at 2.5 years to 4 years of age | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:warburg sjo fledelius syndrome
n1=en:retardation | n2=en:warburg sjo fledelius syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:warsaw breakage syndrome
n1=en:retardation | n2=en:warsaw breakage syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:weak or absent tendon reflexes of knees and ankles (in some patients)
n1=en:retardation | n2=en:weak or absent tendon reflexes of knees and ankles (in some patients) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:weakness
n1=en:retardation | n2=en:weakness | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:weakness of hip and ankle flexion
n1=en:retardation | n2=en:weakness of hip and ankle flexion | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:weaver syndrome
n1=en:retardation | n2=en:weaver syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:west syndrome
n1=en:retardation | n2=en:west syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:white blood cell abnormality
n1=en:retardation | n2=en:white blood cell abnormality | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:white mater abnormalities in the posterior periventricular region
n1=en:retardation | n2=en:white mater abnormalities in the posterior periventricular region | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:white matter
n1=en:retardation | n2=en:white matter | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:white matter abnormalities (1 patient)
n1=en:retardation | n2=en:white matter abnormalities (1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:white matter abnormalities (in some)
n1=en:retardation | n2=en:white matter abnormalities (in some) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:white matter abnormalities (rare)
n1=en:retardation | n2=en:white matter abnormalities (rare) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:white matter abnormalities (uncommon)
n1=en:retardation | n2=en:white matter abnormalities (uncommon) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:white matter abnormalities in the periventricular regions (1 patient)
n1=en:retardation | n2=en:white matter abnormalities in the periventricular regions (1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:white matter abnormalities on mri
n1=en:retardation | n2=en:white matter abnormalities on mri | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:white matter abnormalities seen on mri
n1=en:retardation | n2=en:white matter abnormalities seen on mri | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:white matter abnormalities seen on mri which resolve over time
n1=en:retardation | n2=en:white matter abnormalities seen on mri which resolve over time | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:white matter alterations (in one family)
n1=en:retardation | n2=en:white matter alterations (in one family) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:white matter changes
n1=en:retardation | n2=en:white matter changes | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:white matter changes may occur (in adulthood)
n1=en:retardation | n2=en:white matter changes may occur (in adulthood) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:white matter changes on brain imaging (less common)
n1=en:retardation | n2=en:white matter changes on brain imaging (less common) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:white matter degeneration
n1=en:retardation | n2=en:white matter degeneration | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:white matter dysmyelination/demyelination (71%)
n1=en:retardation | n2=en:white matter dysmyelination/demyelination (71%) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:white matter hyperintensities
n1=en:retardation | n2=en:white matter hyperintensities | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:white matter hyperintensities (mri, t2 images) suggestive of old infarcts
n1=en:retardation | n2=en:white matter hyperintensities (mri, t2 images) suggestive of old infarcts | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:white matter hyperintensities in t2 imaging
n1=en:retardation | n2=en:white matter hyperintensities in t2 imaging | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:white matter hyperintensities in various brain regions
n1=en:retardation | n2=en:white matter hyperintensities in various brain regions | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:white matter hypodensities on brain imaging
n1=en:retardation | n2=en:white matter hypodensities on brain imaging | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:white matter hypodensities seen on mri
n1=en:retardation | n2=en:white matter hypodensities seen on mri | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:white matter immaturity
n1=en:retardation | n2=en:white matter immaturity | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:white matter lacks axons and myelin
n1=en:retardation | n2=en:white matter lacks axons and myelin | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:white matter lesion
n1=en:retardation | n2=en:white matter lesion | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:white matter lesions (1 patient)
n1=en:retardation | n2=en:white matter lesions (1 patient) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:white matter lesions in the basal ganglia
n1=en:retardation | n2=en:white matter lesions in the basal ganglia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:white matter lesions in the brainstem may occur
n1=en:retardation | n2=en:white matter lesions in the brainstem may occur | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:white matter lesions in the supratentorial white matter, brainstem, cerebellum, and spinal cord
n1=en:retardation | n2=en:white matter lesions in the supratentorial white matter, brainstem, cerebellum, and spinal cord | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:white matter lesions may occur in the thalami, basal ganglia, and periventricular white matter (see leigh syndrome, 256000)
n1=en:retardation | n2=en:white matter lesions may occur in the thalami, basal ganglia, and periventricular white matter (see leigh syndrome, 256000) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:white matter lesions seen on brain imaging
n1=en:retardation | n2=en:white matter lesions seen on brain imaging | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:white matter neuronal heterotopia
n1=en:retardation | n2=en:white matter neuronal heterotopia | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:white matter rarefaction and cystic degeneration
n1=en:retardation | n2=en:white matter rarefaction and cystic degeneration | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:white matter signal abnormalities in the deep white matter and periventricular regions
n1=en:retardation | n2=en:white matter signal abnormalities in the deep white matter and periventricular regions | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:white matter signal abnormalities in various brain regions
n1=en:retardation | n2=en:white matter signal abnormalities in various brain regions | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:white matter streaks
n1=en:retardation | n2=en:white matter streaks | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:white matter vacuolization
n1=en:retardation | n2=en:white matter vacuolization | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:whooping cough due to unspecified organism
n1=en:retardation | n2=en:whooping cough due to unspecified organism | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:wide subarachnoid spaces
n1=en:retardation | n2=en:wide subarachnoid spaces | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:wide sylvian fissures
n1=en:retardation | n2=en:wide sylvian fissures | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:wide sylvian fissures with incomplete opercularization
n1=en:retardation | n2=en:wide sylvian fissures with incomplete opercularization | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:widened lateral ventricles
n1=en:retardation | n2=en:widened lateral ventricles | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:widened subarachnoid spaces
n1=en:retardation | n2=en:widened subarachnoid spaces | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:widening of cortical sulci
n1=en:retardation | n2=en:widening of cortical sulci | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:widening of the operculum
n1=en:retardation | n2=en:widening of the operculum | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:widening of the spinal canal
n1=en:retardation | n2=en:widening of the spinal canal | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:widening of the ventricles
n1=en:retardation | n2=en:widening of the ventricles | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:widespread brain atrophy
n1=en:retardation | n2=en:widespread brain atrophy | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:widespread brain calcifications
n1=en:retardation | n2=en:widespread brain calcifications | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:widespread neuronal loss
n1=en:retardation | n2=en:widespread neuronal loss | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:widespread tau (mapt)-positive glial and neuronal inclusions
n1=en:retardation | n2=en:widespread tau (mapt)-positive glial and neuronal inclusions | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:wieacker-wolff syndrome
n1=en:retardation | n2=en:wieacker-wolff syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:williams syndrome
n1=en:retardation | n2=en:williams syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:wilms tumor-aniridia-genitourinary anomalies-mental retardation syndrome
n1=en:retardation | n2=en:wilms tumor-aniridia-genitourinary anomalies-mental retardation syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:wolf-hirschhorn syndrome
n1=en:retardation | n2=en:wolf-hirschhorn syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:woodhouse sakati syndrome
n1=en:retardation | n2=en:woodhouse sakati syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:word finding difficulty (disorder)
n1=en:retardation | n2=en:word finding difficulty (disorder) | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:writing fatigability
n1=en:retardation | n2=en:writing fatigability | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:x-linked creatine transporter deficiency
n1=en:retardation | n2=en:x-linked creatine transporter deficiency | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:x-linked hydrocephalus syndrome
n1=en:retardation | n2=en:x-linked hydrocephalus syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:x-linked lissencephaly
n1=en:retardation | n2=en:x-linked lissencephaly | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:xeroderma pigmentosum, complementation group b
n1=en:retardation | n2=en:xeroderma pigmentosum, complementation group b | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:xia-gibbs syndrome
n1=en:retardation | n2=en:xia-gibbs syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:zechi-ceide syndrome
n1=en:retardation | n2=en:zechi-ceide syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
en:zunich neuroectodermal syndrome
n1=en:retardation | n2=en:zunich neuroectodermal syndrome | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
enfance
n1=en:retardation | n2=enfance | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
faible développement mental
n1=en:retardation | n2=faible développement mental | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
faiblesse
n1=en:retardation | n2=faiblesse | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
handicap
n1=en:retardation | n2=handicap | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
handicap mental
n1=en:retardation | n2=handicap mental | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
handicap psychique
n1=en:retardation | n2=handicap psychique | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
handicaps moteurs
n1=en:retardation | n2=handicaps moteurs | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
hyperphénylalaninémie
n1=en:retardation | n2=hyperphénylalaninémie | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
incapacité intellectuelle
n1=en:retardation | n2=incapacité intellectuelle | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
infirmité
n1=en:retardation | n2=infirmité | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
intellectuelle
n1=en:retardation | n2=intellectuelle | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
mutisme électif
n1=en:retardation | n2=mutisme électif | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
Retard
n1=en:retardation | n2=Retard | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
retard de l'acquisition du langage secondaire à une perte de l'audition
n1=en:retardation | n2=retard de l'acquisition du langage secondaire à une perte de l'audition | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
retard mental avec atrophie optique, surdité et épilepsie
n1=en:retardation | n2=retard mental avec atrophie optique, surdité et épilepsie | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
retard mental de Jugberg-Marsidi
n1=en:retardation | n2=retard mental de Jugberg-Marsidi | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
retard mental de type Mietens-Weber
n1=en:retardation | n2=retard mental de type Mietens-Weber | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
retard mental lié à l'X
n1=en:retardation | n2=retard mental lié à l'X | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
retard mental lié au chromosome X fragile
n1=en:retardation | n2=retard mental lié au chromosome X fragile | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
retard mental psychosocial
n1=en:retardation | n2=retard mental psychosocial | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
retard mental-psychosocial
n1=en:retardation | n2=retard mental-psychosocial | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
retard mental, pouce et gros orteil larges
n1=en:retardation | n2=retard mental, pouce et gros orteil larges | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
retard mental, sévérité non spécifiée
n1=en:retardation | n2=retard mental, sévérité non spécifiée | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
retardation mentale
n1=en:retardation | n2=retardation mentale | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
retardation mentale non précisée
n1=en:retardation | n2=retardation mentale non précisée | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
retards mentaux psychosociaux
n1=en:retardation | n2=retards mentaux psychosociaux | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
surdité verbale
n1=en:retardation | n2=surdité verbale | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
trouble
n1=en:retardation | n2=trouble | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
trouble mental
n1=en:retardation | n2=trouble mental | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
trouble réceptif auditif congénital
n1=en:retardation | n2=trouble réceptif auditif congénital | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 30 / 0.462 ->
visuels
n1=en:retardation | n2=visuels | rel=r_associated | relid=0 | w=30
- en:retardation --
r_associated #0: 29 / 0.446 ->
anomalie mentale
n1=en:retardation | n2=anomalie mentale | rel=r_associated | relid=0 | w=29
- en:retardation --
r_associated #0: 29 / 0.446 ->
trouble psychiatrique
n1=en:retardation | n2=trouble psychiatrique | rel=r_associated | relid=0 | w=29
- en:retardation --
r_associated #0: 29 / 0.446 ->
trouble psychique
n1=en:retardation | n2=trouble psychique | rel=r_associated | relid=0 | w=29
- en:retardation --
r_associated #0: 28 / 0.431 ->
déficit
n1=en:retardation | n2=déficit | rel=r_associated | relid=0 | w=28
- en:retardation --
r_associated #0: 28 / 0.431 ->
déficit mental
n1=en:retardation | n2=déficit mental | rel=r_associated | relid=0 | w=28
- en:retardation --
r_associated #0: 28 / 0.431 ->
en:oligopsychia
n1=en:retardation | n2=en:oligopsychia | rel=r_associated | relid=0 | w=28
- en:retardation --
r_associated #0: 28 / 0.431 ->
endocriniens
n1=en:retardation | n2=endocriniens | rel=r_associated | relid=0 | w=28
- en:retardation --
r_associated #0: 28 / 0.431 ->
intellectuel
n1=en:retardation | n2=intellectuel | rel=r_associated | relid=0 | w=28
- en:retardation --
r_associated #0: 28 / 0.431 ->
nymphomanie
n1=en:retardation | n2=nymphomanie | rel=r_associated | relid=0 | w=28
- en:retardation --
r_associated #0: 28 / 0.431 ->
troubles endocriniens
n1=en:retardation | n2=troubles endocriniens | rel=r_associated | relid=0 | w=28
- en:retardation --
r_associated #0: 27 / 0.415 ->
en:developmental mental disorder
n1=en:retardation | n2=en:developmental mental disorder | rel=r_associated | relid=0 | w=27
- en:retardation --
r_associated #0: 27 / 0.415 ->
en:feeble-mindedness
n1=en:retardation | n2=en:feeble-mindedness | rel=r_associated | relid=0 | w=27
- en:retardation --
r_associated #0: 27 / 0.415 ->
être bouché
n1=en:retardation | n2=être bouché | rel=r_associated | relid=0 | w=27
- en:retardation --
r_associated #0: 27 / 0.415 ->
maladie
n1=en:retardation | n2=maladie | rel=r_associated | relid=0 | w=27
- en:retardation --
r_associated #0: 26 / 0.4 ->
arriéré
n1=en:retardation | n2=arriéré | rel=r_associated | relid=0 | w=26
- en:retardation --
r_associated #0: 26 / 0.4 ->
con
n1=en:retardation | n2=con | rel=r_associated | relid=0 | w=26
- en:retardation --
r_associated #0: 26 / 0.4 ->
en:developmental dysphasia or aphasia, expressive type
n1=en:retardation | n2=en:developmental dysphasia or aphasia, expressive type | rel=r_associated | relid=0 | w=26
- en:retardation --
r_associated #0: 26 / 0.4 ->
en:epilepsy
n1=en:retardation | n2=en:epilepsy | rel=r_associated | relid=0 | w=26
- en:retardation --
r_associated #0: 26 / 0.4 ->
état mental altéré
n1=en:retardation | n2=état mental altéré | rel=r_associated | relid=0 | w=26
- en:retardation --
r_associated #0: 26 / 0.4 ->
imbécilité
n1=en:retardation | n2=imbécilité | rel=r_associated | relid=0 | w=26
- en:retardation --
r_associated #0: 26 / 0.4 ->
intelligence
n1=en:retardation | n2=intelligence | rel=r_associated | relid=0 | w=26
- en:retardation --
r_associated #0: 26 / 0.4 ->
profonde
n1=en:retardation | n2=profonde | rel=r_associated | relid=0 | w=26
- en:retardation --
r_associated #0: 26 / 0.4 ->
retardé
n1=en:retardation | n2=retardé | rel=r_associated | relid=0 | w=26
- en:retardation --
r_associated #0: 25 / 0.385 ->
en:medicine
n1=en:retardation | n2=en:medicine | rel=r_associated | relid=0 | w=25
- en:retardation --
r_associated #0: 25 / 0.385 ->
mentale
n1=en:retardation | n2=mentale | rel=r_associated | relid=0 | w=25
- en:retardation --
r_associated #0: 25 / 0.385 ->
spécialités médicales
n1=en:retardation | n2=spécialités médicales | rel=r_associated | relid=0 | w=25
- en:retardation --
r_associated #0: 25 / 0.385 ->
stupide
(idiot)
n1=en:retardation | n2=stupide (idiot) | rel=r_associated | relid=0 | w=25
- en:retardation --
r_associated #0: 24 / 0.369 ->
en:endocrine disorder
n1=en:retardation | n2=en:endocrine disorder | rel=r_associated | relid=0 | w=24
- en:retardation --
r_associated #0: 24 / 0.369 ->
en:mental impairment (excl dementia and memory loss)
n1=en:retardation | n2=en:mental impairment (excl dementia and memory loss) | rel=r_associated | relid=0 | w=24
- en:retardation --
r_associated #0: 24 / 0.369 ->
etat mental anormal
n1=en:retardation | n2=etat mental anormal | rel=r_associated | relid=0 | w=24
- en:retardation --
r_associated #0: 24 / 0.369 ->
handicap
(infirmité)
n1=en:retardation | n2=handicap (infirmité) | rel=r_associated | relid=0 | w=24
- en:retardation --
r_associated #0: 24 / 0.369 ->
troubles endocriniens, épilepsie et déficience mentale
n1=en:retardation | n2=troubles endocriniens, épilepsie et déficience mentale | rel=r_associated | relid=0 | w=24
- en:retardation --
r_associated #0: 23 / 0.354 ->
Börjeson-Forssman-Lehmann syndrome
n1=en:retardation | n2=Börjeson-Forssman-Lehmann syndrome | rel=r_associated | relid=0 | w=23
- en:retardation --
r_associated #0: 23 / 0.354 ->
en:failure of the mind
n1=en:retardation | n2=en:failure of the mind | rel=r_associated | relid=0 | w=23
- en:retardation --
r_associated #0: 23 / 0.354 ->
en:feeblemindedness
n1=en:retardation | n2=en:feeblemindedness | rel=r_associated | relid=0 | w=23
- en:retardation --
r_associated #0: 23 / 0.354 ->
état mental anormal
n1=en:retardation | n2=état mental anormal | rel=r_associated | relid=0 | w=23
- en:retardation --
r_associated #0: 23 / 0.354 ->
test de QI
n1=en:retardation | n2=test de QI | rel=r_associated | relid=0 | w=23
- en:retardation --
r_associated #0: 23 / 0.354 ->
vieilli
n1=en:retardation | n2=vieilli | rel=r_associated | relid=0 | w=23
- en:retardation --
r_associated #0: 22 / 0.338 ->
en:mental debility
n1=en:retardation | n2=en:mental debility | rel=r_associated | relid=0 | w=22
- en:retardation --
r_associated #0: 22 / 0.338 ->
ne rien comprendre
n1=en:retardation | n2=ne rien comprendre | rel=r_associated | relid=0 | w=22
- en:retardation --
r_associated #0: 22 / 0.338 ->
retard mental par mutation du gène de la "double cortine"
n1=en:retardation | n2=retard mental par mutation du gène de la "double cortine" | rel=r_associated | relid=0 | w=22
- en:retardation --
r_associated #0: 22 / 0.338 ->
troubles
n1=en:retardation | n2=troubles | rel=r_associated | relid=0 | w=22
- en:retardation --
r_associated #0: 21 / 0.323 ->
arriération mentale de sévérité non précisée
n1=en:retardation | n2=arriération mentale de sévérité non précisée | rel=r_associated | relid=0 | w=21
- en:retardation --
r_associated #0: 21 / 0.323 ->
en:developmental dysphasia or aphasia, receptive type
n1=en:retardation | n2=en:developmental dysphasia or aphasia, receptive type | rel=r_associated | relid=0 | w=21
- en:retardation --
r_associated #0: 21 / 0.323 ->
en:mental dullness
n1=en:retardation | n2=en:mental dullness | rel=r_associated | relid=0 | w=21
- en:retardation --
r_associated #0: 21 / 0.323 ->
en:morosis
n1=en:retardation | n2=en:morosis | rel=r_associated | relid=0 | w=21
- en:retardation --
r_associated #0: 21 / 0.323 ->
épilepsie
n1=en:retardation | n2=épilepsie | rel=r_associated | relid=0 | w=21
- en:retardation --
r_associated #0: 15 / 0.231 ->
Arrhenius (loi d')
n1=en:retardation | n2=Arrhenius (loi d') | rel=r_associated | relid=0 | w=15
- en:retardation --
r_associated #0: 15 / 0.231 ->
en:subnormality
n1=en:retardation | n2=en:subnormality | rel=r_associated | relid=0 | w=15
- en:retardation --
r_associated #0: 15 / 0.231 ->
médecine spécialisée
n1=en:retardation | n2=médecine spécialisée | rel=r_associated | relid=0 | w=15
- en:retardation --
r_associated #0: 15 / 0.231 ->
retard mental, maladie cardiaque congénitale, blépharophimosis, blépharoptosis et dents hypoplasiques
n1=en:retardation | n2=retard mental, maladie cardiaque congénitale, blépharophimosis, blépharoptosis et dents hypoplasiques | rel=r_associated | relid=0 | w=15
- en:retardation --
r_associated #0: 10 / 0.154 ->
a-95 surdités et perceptions auditives
n1=en:retardation | n2=a-95 surdités et perceptions auditives | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
a-950-955 surdités
n1=en:retardation | n2=a-950-955 surdités | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
AAH
n1=en:retardation | n2=AAH | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
abasourdir
n1=en:retardation | n2=abasourdir | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
abasourdissant
n1=en:retardation | n2=abasourdissant | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
abcès cérébral
n1=en:retardation | n2=abcès cérébral | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
accident cérébro-vasculaire
n1=en:retardation | n2=accident cérébro-vasculaire | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
accident cérébrovasculaire
n1=en:retardation | n2=accident cérébrovasculaire | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
accident ischémique cérébral
n1=en:retardation | n2=accident ischémique cérébral | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
accident vasculaire cérébral
n1=en:retardation | n2=accident vasculaire cérébral | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
accidents vasculaires cérébraux
n1=en:retardation | n2=accidents vasculaires cérébraux | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
ACV
n1=en:retardation | n2=ACV | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
adaptation
n1=en:retardation | n2=adaptation | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
adulte handicapé
n1=en:retardation | n2=adulte handicapé | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
aggression
n1=en:retardation | n2=aggression | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
agnosie auditive
n1=en:retardation | n2=agnosie auditive | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
agression
n1=en:retardation | n2=agression | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
altération mentale
n1=en:retardation | n2=altération mentale | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
amusie
n1=en:retardation | n2=amusie | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
anencéphalie
n1=en:retardation | n2=anencéphalie | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
anomalie chromosomique
n1=en:retardation | n2=anomalie chromosomique | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
anomalies
n1=en:retardation | n2=anomalies | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
aphasie
n1=en:retardation | n2=aphasie | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
apoplexie
n1=en:retardation | n2=apoplexie | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
aréflexie
n1=en:retardation | n2=aréflexie | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
arriérations
n1=en:retardation | n2=arriérations | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
arriéré
(Adj)
n1=en:retardation | n2=arriéré (Adj) | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
arriérer
n1=en:retardation | n2=arriérer | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
assourdir
n1=en:retardation | n2=assourdir | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
assourdissant
n1=en:retardation | n2=assourdissant | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
assourdissement
n1=en:retardation | n2=assourdissement | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
asthénie neuro-circulatoire
n1=en:retardation | n2=asthénie neuro-circulatoire | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
asthénie neurocirculatoire
n1=en:retardation | n2=asthénie neurocirculatoire | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
astrocyte
n1=en:retardation | n2=astrocyte | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
ataxie cérébelleuse cataracte, surdité et démence ou psychose
n1=en:retardation | n2=ataxie cérébelleuse cataracte, surdité et démence ou psychose | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
atrophie
n1=en:retardation | n2=atrophie | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
atrophie optique
n1=en:retardation | n2=atrophie optique | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
atrophie optique liée au sexe
n1=en:retardation | n2=atrophie optique liée au sexe | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
atrophie optique liée au sexe de Völker-Dieben
n1=en:retardation | n2=atrophie optique liée au sexe de Völker-Dieben | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
atrophie optique tardive liée au sexe
n1=en:retardation | n2=atrophie optique tardive liée au sexe | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
atrophie optique, surdité, épilepsie, spasticité et décès précoce
n1=en:retardation | n2=atrophie optique, surdité, épilepsie, spasticité et décès précoce | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
atrophie optique, surdité, ophtalmoplégie et myopathie
n1=en:retardation | n2=atrophie optique, surdité, ophtalmoplégie et myopathie | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
attaque apoplectique
n1=en:retardation | n2=attaque apoplectique | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
attaque d'apoplexie
n1=en:retardation | n2=attaque d'apoplexie | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
audiophone
n1=en:retardation | n2=audiophone | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
audition diminuée
n1=en:retardation | n2=audition diminuée | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
audition réduite
n1=en:retardation | n2=audition réduite | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
autisme
n1=en:retardation | n2=autisme | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
auxiliaire de vie sociale
n1=en:retardation | n2=auxiliaire de vie sociale | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
AVC
n1=en:retardation | n2=AVC | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
baisse de l'acuité auditive
n1=en:retardation | n2=baisse de l'acuité auditive | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
blépharophimosis-déficience intellectuelle type Ohdo (syndrome)
n1=en:retardation | n2=blépharophimosis-déficience intellectuelle type Ohdo (syndrome) | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
brain
n1=en:retardation | n2=brain | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
caryotype
n1=en:retardation | n2=caryotype | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
cataplexie
n1=en:retardation | n2=cataplexie | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
cataracte
n1=en:retardation | n2=cataracte | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
cataracte juvénile, atrophie cérébelleuse, retard mental et myopathie
n1=en:retardation | n2=cataracte juvénile, atrophie cérébelleuse, retard mental et myopathie | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
cataracte liée au sexe avec dent de Hutchinson
n1=en:retardation | n2=cataracte liée au sexe avec dent de Hutchinson | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
cataracte-ataxie-surdité et retard mental (syndrome)
n1=en:retardation | n2=cataracte-ataxie-surdité et retard mental (syndrome) | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
cataracte-atrophie du cervelet-myopathie
n1=en:retardation | n2=cataracte-atrophie du cervelet-myopathie | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
cécité
n1=en:retardation | n2=cécité | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
chirologie
n1=en:retardation | n2=chirologie | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
choc cardiogénique
n1=en:retardation | n2=choc cardiogénique | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
colpocéphalie
n1=en:retardation | n2=colpocéphalie | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
coma hépatique
n1=en:retardation | n2=coma hépatique | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
cophochirurgie
n1=en:retardation | n2=cophochirurgie | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
cophose
n1=en:retardation | n2=cophose | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
croissance
n1=en:retardation | n2=croissance | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
débile
n1=en:retardation | n2=débile | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
débile mental
n1=en:retardation | n2=débile mental | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
débile
(débile mental)
n1=en:retardation | n2=débile (débile mental) | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
déficience auditive sévère
n1=en:retardation | n2=déficience auditive sévère | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
déficience auditive totale
n1=en:retardation | n2=déficience auditive totale | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
déficiences mentales
n1=en:retardation | n2=déficiences mentales | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
déficit auditif
n1=en:retardation | n2=déficit auditif | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
dégénérescence granulovacuolaire
n1=en:retardation | n2=dégénérescence granulovacuolaire | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
dégénérescence spongieuse
n1=en:retardation | n2=dégénérescence spongieuse | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
délire
n1=en:retardation | n2=délire | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
demence
n1=en:retardation | n2=demence | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
démence fronto-temporale
n1=en:retardation | n2=démence fronto-temporale | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
démence frontotemporale
n1=en:retardation | n2=démence frontotemporale | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
demi-sourd
n1=en:retardation | n2=demi-sourd | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
détérioration intellectuelle
n1=en:retardation | n2=détérioration intellectuelle | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
détérioration mentale
n1=en:retardation | n2=détérioration mentale | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
développement déficitaire du cerveau
n1=en:retardation | n2=développement déficitaire du cerveau | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
diabète, photomyoclonies, surdité, néphropathie et dysfonction cérébrale
n1=en:retardation | n2=diabète, photomyoclonies, surdité, néphropathie et dysfonction cérébrale | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
diminution auditive
n1=en:retardation | n2=diminution auditive | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
diminution de l'audition
n1=en:retardation | n2=diminution de l'audition | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
diminution de l'ouie
n1=en:retardation | n2=diminution de l'ouie | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
douleur de la face
n1=en:retardation | n2=douleur de la face | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
dur d'oreille
n1=en:retardation | n2=dur d'oreille | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
dystrophie des cônes liée au sexe
n1=en:retardation | n2=dystrophie des cônes liée au sexe | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
dystrophie des cônes liée au sexe avec reflet rétinien jaune-vert
n1=en:retardation | n2=dystrophie des cônes liée au sexe avec reflet rétinien jaune-vert | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
en:a mental disability
n1=en:retardation | n2=en:a mental disability | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
en:absent moro response
n1=en:retardation | n2=en:absent moro response | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
en:acquired deafness
n1=en:retardation | n2=en:acquired deafness | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
en:alport syndrome
n1=en:retardation | n2=en:alport syndrome | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
en:and growth retardation
n1=en:retardation | n2=en:and growth retardation | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
en:and microgenitalism
n1=en:retardation | n2=en:and microgenitalism | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
en:and myopathy
n1=en:retardation | n2=en:and myopathy | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
en:angiomatous meningioma
n1=en:retardation | n2=en:angiomatous meningioma | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
en:aspects of mortality statistics
n1=en:retardation | n2=en:aspects of mortality statistics | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
en:aspects of radionuclide imaging
n1=en:retardation | n2=en:aspects of radionuclide imaging | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
en:auditory hypoacuity
n1=en:retardation | n2=en:auditory hypoacuity | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
en:axial hypertonia
n1=en:retardation | n2=en:axial hypertonia | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
en:bifrontal subdural hygroma
n1=en:retardation | n2=en:bifrontal subdural hygroma | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
en:bilateral deafness
n1=en:retardation | n2=en:bilateral deafness | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
en:blackout - symptom
n1=en:retardation | n2=en:blackout - symptom | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
en:cardiogenic shock
n1=en:retardation | n2=en:cardiogenic shock | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
en:cerebral abscess
n1=en:retardation | n2=en:cerebral abscess | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
en:cerebral ventriculomegaly
n1=en:retardation | n2=en:cerebral ventriculomegaly | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
en:chemically induced
n1=en:retardation | n2=en:chemically induced | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
en:cognitive and attention disorders and disturbances nec
n1=en:retardation | n2=en:cognitive and attention disorders and disturbances nec | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
en:complete deafness
n1=en:retardation | n2=en:complete deafness | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
en:complication aspects
n1=en:retardation | n2=en:complication aspects | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
en:conductive and sensorineural hearing loss
n1=en:retardation | n2=en:conductive and sensorineural hearing loss | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
en:congenital deafness
n1=en:retardation | n2=en:congenital deafness | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
en:deaf, nonspeaking, not elsewhere classifiable
n1=en:retardation | n2=en:deaf, nonspeaking, not elsewhere classifiable | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
en:deafness, prelingual
n1=en:retardation | n2=en:deafness, prelingual | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
en:decreased distal strength (in some patients)
n1=en:retardation | n2=en:decreased distal strength (in some patients) | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
en:delayed myelination (patient c)
n1=en:retardation | n2=en:delayed myelination (patient c) | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
en:delayed myelination (patients a and c)
n1=en:retardation | n2=en:delayed myelination (patients a and c) | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
en:diffuse slow background activity seen on eeg
n1=en:retardation | n2=en:diffuse slow background activity seen on eeg | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
en:dystonic movements (in some patients)
n1=en:retardation | n2=en:dystonic movements (in some patients) | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
en:ear
n1=en:retardation | n2=en:ear | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
en:enzymology
n1=en:retardation | n2=en:enzymology | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
en:epidemiologic
n1=en:retardation | n2=en:epidemiologic | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
en:ethnologic
n1=en:retardation | n2=en:ethnologic | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
en:etiology aspects
n1=en:retardation | n2=en:etiology aspects | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
en:exposure as collected domain
n1=en:retardation | n2=en:exposure as collected domain | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
en:extreme hearing loss
n1=en:retardation | n2=en:extreme hearing loss | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
en:eye abnormality
n1=en:retardation | n2=en:eye abnormality | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
en:hand-arm vibration syndrome
n1=en:retardation | n2=en:hand-arm vibration syndrome | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
en:hearing disorder
n1=en:retardation | n2=en:hearing disorder | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
en:hearing disorders nec in cst95
n1=en:retardation | n2=en:hearing disorders nec in cst95 | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
en:hearing impaired persons
n1=en:retardation | n2=en:hearing impaired persons | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
en:hearing impairment
n1=en:retardation | n2=en:hearing impairment | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
en:hearing loss
n1=en:retardation | n2=en:hearing loss | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
en:hearing loss, bilateral
n1=en:retardation | n2=en:hearing loss, bilateral | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
en:hearing loss, sudden
n1=en:retardation | n2=en:hearing loss, sudden | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
en:hearing loss, unilateral
n1=en:retardation | n2=en:hearing loss, unilateral | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
en:high frequency hearing loss
n1=en:retardation | n2=en:high frequency hearing loss | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
en:immunology aspects
n1=en:retardation | n2=en:immunology aspects | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
en:increased white matter signal
n1=en:retardation | n2=en:increased white matter signal | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
en:juvenile cataract
n1=en:retardation | n2=en:juvenile cataract | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
en:melnick-fraser syndrome
n1=en:retardation | n2=en:melnick-fraser syndrome | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
en:mental
n1=en:retardation | n2=en:mental | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
en:mental disability
n1=en:retardation | n2=en:mental disability | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
en:microbiological
n1=en:retardation | n2=en:microbiological | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
en:mixed hearing loss
n1=en:retardation | n2=en:mixed hearing loss | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
en:mohr-tranebjaerg syndrome
n1=en:retardation | n2=en:mohr-tranebjaerg syndrome | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
en:molar tooth sign seen on brain imaging
n1=en:retardation | n2=en:molar tooth sign seen on brain imaging | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
en:muffled hearing in both ears
n1=en:retardation | n2=en:muffled hearing in both ears | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
en:neurosensory hypoacusis
n1=en:retardation | n2=en:neurosensory hypoacusis | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
en:occupational deafness
n1=en:retardation | n2=en:occupational deafness | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
en:oligergasia
n1=en:retardation | n2=en:oligergasia | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
en:ophthalmoplegia
n1=en:retardation | n2=en:ophthalmoplegia | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
en:optic atrophy
n1=en:retardation | n2=en:optic atrophy | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
en:other and unspecified hearing loss
n1=en:retardation | n2=en:other and unspecified hearing loss | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
en:other specified forms of deafness
n1=en:retardation | n2=en:other specified forms of deafness | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
en:other specified hearing loss
n1=en:retardation | n2=en:other specified hearing loss | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
en:parasitology
n1=en:retardation | n2=en:parasitology | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
en:paresis
n1=en:retardation | n2=en:paresis | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
en:periventricular calcifications (patient c)
n1=en:retardation | n2=en:periventricular calcifications (patient c) | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
en:pharmacotherapeutic
n1=en:retardation | n2=en:pharmacotherapeutic | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
en:psychology qualifier
n1=en:retardation | n2=en:psychology qualifier | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
en:retinitis pigmentosa
n1=en:retardation | n2=en:retinitis pigmentosa | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
en:roentgenographic
n1=en:retardation | n2=en:roentgenographic | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
en:spike-wave discharges
n1=en:retardation | n2=en:spike-wave discharges | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
en:spinal cord
n1=en:retardation | n2=en:spinal cord | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
en:st Avidus' disease
n1=en:retardation | n2=en:st Avidus' disease | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
en:superficial siderosis of central nervous system
n1=en:retardation | n2=en:superficial siderosis of central nervous system | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
en:surditas
n1=en:retardation | n2=en:surditas | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
en:surdity
n1=en:retardation | n2=en:surdity | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
en:therapeutic aspects
n1=en:retardation | n2=en:therapeutic aspects | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
en:traumatic deafness
n1=en:retardation | n2=en:traumatic deafness | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
en:unspecified hearing loss, left ear
n1=en:retardation | n2=en:unspecified hearing loss, left ear | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
en:unspecified hearing loss, unspecified ear
n1=en:retardation | n2=en:unspecified hearing loss, unspecified ear | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
en:unusual facies
n1=en:retardation | n2=en:unusual facies | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
en:usher syndrome
n1=en:retardation | n2=en:usher syndrome | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
en:weakmindedness
n1=en:retardation | n2=en:weakmindedness | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
en:white matter rarefaction
n1=en:retardation | n2=en:white matter rarefaction | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
en:wildervanck's syndrome
n1=en:retardation | n2=en:wildervanck's syndrome | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
en:with growth retardation
n1=en:retardation | n2=en:with growth retardation | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
en:worsening of auditory acuity
n1=en:retardation | n2=en:worsening of auditory acuity | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
en:X-linked
n1=en:retardation | n2=en:X-linked | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
en:x-linked dyskeratosis congenita
n1=en:retardation | n2=en:x-linked dyskeratosis congenita | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
encéphalite
n1=en:retardation | n2=encéphalite | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
encéphalopathie
n1=en:retardation | n2=encéphalopathie | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
encéphalopathie hépatique
n1=en:retardation | n2=encéphalopathie hépatique | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
encéphalopathie hépato-cérébrale
n1=en:retardation | n2=encéphalopathie hépato-cérébrale | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
encéphalopathie porto-cave
n1=en:retardation | n2=encéphalopathie porto-cave | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
enfant handicapé
n1=en:retardation | n2=enfant handicapé | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
entendre
n1=en:retardation | n2=entendre | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
ergothérapie
n1=en:retardation | n2=ergothérapie | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
étourdissement
n1=en:retardation | n2=étourdissement | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
eye
n1=en:retardation | n2=eye | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
faciale (paralysie du nouveau-né)
n1=en:retardation | n2=faciale (paralysie du nouveau-né) | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
faciès anormal, retard de croissance et retard mental
n1=en:retardation | n2=faciès anormal, retard de croissance et retard mental | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
faiblesse d'esprit
n1=en:retardation | n2=faiblesse d'esprit | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
faiblesse de muscle
n1=en:retardation | n2=faiblesse de muscle | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
faiblesse du muscle
n1=en:retardation | n2=faiblesse du muscle | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
faiblesse musculaire
n1=en:retardation | n2=faiblesse musculaire | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
fauteuil roulant
n1=en:retardation | n2=fauteuil roulant | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
fibrillation
n1=en:retardation | n2=fibrillation | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
folie
n1=en:retardation | n2=folie | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
Fothergill
n1=en:retardation | n2=Fothergill | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
gêne
n1=en:retardation | n2=gêne | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
Hand-Schüller-Christian (maladie de)
n1=en:retardation | n2=Hand-Schüller-Christian (maladie de) | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
handicap moteur
n1=en:retardation | n2=handicap moteur | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
handicapé moteur
n1=en:retardation | n2=handicapé moteur | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
handicapé physique
n1=en:retardation | n2=handicapé physique | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
handicapés
n1=en:retardation | n2=handicapés | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
hæmorrhagie
n1=en:retardation | n2=hæmorrhagie | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
hémimégalencéphalie
n1=en:retardation | n2=hémimégalencéphalie | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
hémorragie
n1=en:retardation | n2=hémorragie | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
hemorragie
n1=en:retardation | n2=hemorragie | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
hémorrhagie
n1=en:retardation | n2=hémorrhagie | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
holoprosencéphalie
n1=en:retardation | n2=holoprosencéphalie | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
hydrocéphalie
n1=en:retardation | n2=hydrocéphalie | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
hydrocéphalies
n1=en:retardation | n2=hydrocéphalies | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
hyperthermie
n1=en:retardation | n2=hyperthermie | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
hypo-acousie
n1=en:retardation | n2=hypo-acousie | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
hypoacousie
n1=en:retardation | n2=hypoacousie | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
hypoacousies
n1=en:retardation | n2=hypoacousies | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
hypoplasie du nerf optique
n1=en:retardation | n2=hypoplasie du nerf optique | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
hypotension orthostatique
n1=en:retardation | n2=hypotension orthostatique | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
hypothalamus
n1=en:retardation | n2=hypothalamus | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
ictus apoplectique
n1=en:retardation | n2=ictus apoplectique | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
idiotie
(arriération mentale)
n1=en:retardation | n2=idiotie (arriération mentale) | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
impotence
n1=en:retardation | n2=impotence | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
incapacité
n1=en:retardation | n2=incapacité | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
incapacité mentale
n1=en:retardation | n2=incapacité mentale | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
infarctus
n1=en:retardation | n2=infarctus | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
infirme
n1=en:retardation | n2=infirme | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
infirmité mentale
n1=en:retardation | n2=infirmité mentale | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
insensibilité
n1=en:retardation | n2=insensibilité | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
insuffisance
n1=en:retardation | n2=insuffisance | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
insuffisance hépatique transitoire
n1=en:retardation | n2=insuffisance hépatique transitoire | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
intellect
n1=en:retardation | n2=intellect | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
Jugberg-Marsidi (retard mental de)
n1=en:retardation | n2=Jugberg-Marsidi (retard mental de) | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
langage des signes
n1=en:retardation | n2=langage des signes | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
leuco-encéphalopathie
n1=en:retardation | n2=leuco-encéphalopathie | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
leucoencéphalopathie
n1=en:retardation | n2=leucoencéphalopathie | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
lissencéphalie
n1=en:retardation | n2=lissencéphalie | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
mal-entendant
n1=en:retardation | n2=mal-entendant | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
malade mental
n1=en:retardation | n2=malade mental | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
maladie cérébrovasculaire aiguë mal définie
n1=en:retardation | n2=maladie cérébrovasculaire aiguë mal définie | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
maladie de trousseau
n1=en:retardation | n2=maladie de trousseau | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
maladie mentale
n1=en:retardation | n2=maladie mentale | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
maladie
(médecine)
n1=en:retardation | n2=maladie (médecine) | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
maladies
n1=en:retardation | n2=maladies | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
malentendant
n1=en:retardation | n2=malentendant | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
Marinesco-Sjögren-like (syndrome de)
n1=en:retardation | n2=Marinesco-Sjögren-like (syndrome de) | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
MDPH
n1=en:retardation | n2=MDPH | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
Médecine
n1=en:retardation | n2=Médecine | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
médecine
(science)
n1=en:retardation | n2=médecine (science) | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
méninges
n1=en:retardation | n2=méninges | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
méningiome
n1=en:retardation | n2=méningiome | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
méningiome angiomateux
n1=en:retardation | n2=méningiome angiomateux | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
méningiomes
n1=en:retardation | n2=méningiomes | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
méningite
n1=en:retardation | n2=méningite | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
mevalonic aciduria
n1=en:retardation | n2=mevalonic aciduria | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
migraine avec aura
n1=en:retardation | n2=migraine avec aura | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
moelle épinière
n1=en:retardation | n2=moelle épinière | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
Mollica (syndrome de)
n1=en:retardation | n2=Mollica (syndrome de) | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
Mollica Pavone Antener (syndrome)
n1=en:retardation | n2=Mollica Pavone Antener (syndrome) | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
mongolien
n1=en:retardation | n2=mongolien | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
mongolien
(mongolisme)
n1=en:retardation | n2=mongolien (mongolisme) | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
mongolisme
n1=en:retardation | n2=mongolisme | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
muet
n1=en:retardation | n2=muet | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
mutisme
n1=en:retardation | n2=mutisme | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
myringoplastie
n1=en:retardation | n2=myringoplastie | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
nanisme
n1=en:retardation | n2=nanisme | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
nanisme, retard mental, anomalies oculaires
n1=en:retardation | n2=nanisme, retard mental, anomalies oculaires | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
neuralgie trigéminale
n1=en:retardation | n2=neuralgie trigéminale | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
névralgie du nerf trijumeau
n1=en:retardation | n2=névralgie du nerf trijumeau | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
névralgie du trijumeau
n1=en:retardation | n2=névralgie du trijumeau | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
névralgie essentielle du trijumeau
n1=en:retardation | n2=névralgie essentielle du trijumeau | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
névralgie faciale
n1=en:retardation | n2=névralgie faciale | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
névralgie trigéminale
n1=en:retardation | n2=névralgie trigéminale | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
nosologie
n1=en:retardation | n2=nosologie | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
nystagmus lié au sexe
n1=en:retardation | n2=nystagmus lié au sexe | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
oculaires
n1=en:retardation | n2=oculaires | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
oligopsychie
n1=en:retardation | n2=oligopsychie | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
oreille
n1=en:retardation | n2=oreille | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
otalgie
n1=en:retardation | n2=otalgie | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
otorrhée
n1=en:retardation | n2=otorrhée | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
otospongiose
n1=en:retardation | n2=otospongiose | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
paralysie générale
n1=en:retardation | n2=paralysie générale | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
paralysis
n1=en:retardation | n2=paralysis | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
paraplégie
n1=en:retardation | n2=paraplégie | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
paraplégie spasmodique
n1=en:retardation | n2=paraplégie spasmodique | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
paraplégie spastique
n1=en:retardation | n2=paraplégie spastique | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
paraplégies
n1=en:retardation | n2=paraplégies | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
paraplégique
n1=en:retardation | n2=paraplégique | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
parésie
n1=en:retardation | n2=parésie | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
parésié
n1=en:retardation | n2=parésié | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
parésie musculaire
n1=en:retardation | n2=parésie musculaire | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
parkinsonisme
n1=en:retardation | n2=parkinsonisme | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
partie centrale du système nerveux
n1=en:retardation | n2=partie centrale du système nerveux | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
pas d'audition
n1=en:retardation | n2=pas d'audition | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
pathologie
n1=en:retardation | n2=pathologie | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
perte auditive
n1=en:retardation | n2=perte auditive | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
perte auditive non précisée
n1=en:retardation | n2=perte auditive non précisée | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
perte auditive sévère
n1=en:retardation | n2=perte auditive sévère | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
perte auditive totale
n1=en:retardation | n2=perte auditive totale | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
perte d'audition
n1=en:retardation | n2=perte d'audition | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
perte d'audition sensorineurale
n1=en:retardation | n2=perte d'audition sensorineurale | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
perte d'audition sévère
n1=en:retardation | n2=perte d'audition sévère | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
perte d'audition totale
n1=en:retardation | n2=perte d'audition totale | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
perte de connaissance
n1=en:retardation | n2=perte de connaissance | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
perte de conscience
n1=en:retardation | n2=perte de conscience | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
perte de l'audition due au bruit
n1=en:retardation | n2=perte de l'audition due au bruit | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
perte de l'audition par ototoxicité
n1=en:retardation | n2=perte de l'audition par ototoxicité | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
pertes auditives
n1=en:retardation | n2=pertes auditives | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
Pitt-Rogers-Danks (syndrome de)[O1]Édit. 2017
n1=en:retardation | n2=Pitt-Rogers-Danks (syndrome de)[O1]Édit. 2017 | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
poliomyélite aiguë
n1=en:retardation | n2=poliomyélite aiguë | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
poliomyélite aigüe
n1=en:retardation | n2=poliomyélite aigüe | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
presbyacousie
n1=en:retardation | n2=presbyacousie | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
psychiatre
n1=en:retardation | n2=psychiatre | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
psychologie
n1=en:retardation | n2=psychologie | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
reduction de l'ouie
n1=en:retardation | n2=reduction de l'ouie | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
retard psychomoteur
n1=en:retardation | n2=retard psychomoteur | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
rétinite pigmentaire, surdité, retard mental, et hypogonadisme
n1=en:retardation | n2=rétinite pigmentaire, surdité, retard mental, et hypogonadisme | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
schizophrénie
n1=en:retardation | n2=schizophrénie | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
schizophrénie greffée
n1=en:retardation | n2=schizophrénie greffée | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
sensation de rotation
n1=en:retardation | n2=sensation de rotation | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
sensation de tournoiement
n1=en:retardation | n2=sensation de tournoiement | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
sensation rotatoire
n1=en:retardation | n2=sensation rotatoire | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
sensation vertigineuse
n1=en:retardation | n2=sensation vertigineuse | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
somnolence
n1=en:retardation | n2=somnolence | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
sonotone
n1=en:retardation | n2=sonotone | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
sourd
n1=en:retardation | n2=sourd | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
sourd-muet
n1=en:retardation | n2=sourd-muet | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
sourdaud
n1=en:retardation | n2=sourdaud | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
sourde
n1=en:retardation | n2=sourde | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
sourdement
n1=en:retardation | n2=sourdement | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
sourdingue
n1=en:retardation | n2=sourdingue | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
substance grise
n1=en:retardation | n2=substance grise | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
subsurdité
n1=en:retardation | n2=subsurdité | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
surdi-mutité
n1=en:retardation | n2=surdi-mutité | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
surdimutité
n1=en:retardation | n2=surdimutité | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
surdité
n1=en:retardation | n2=surdité | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
surdité acquise
n1=en:retardation | n2=surdité acquise | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
surdité auto-immune
n1=en:retardation | n2=surdité auto-immune | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
surdité bilatérale
n1=en:retardation | n2=surdité bilatérale | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
surdité bilatérale totale
n1=en:retardation | n2=surdité bilatérale totale | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
surdité centrale
n1=en:retardation | n2=surdité centrale | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
surdité cochléaire avec myopie et retard intellectuel
n1=en:retardation | n2=surdité cochléaire avec myopie et retard intellectuel | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
surdité complète
n1=en:retardation | n2=surdité complète | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
surdité congénitale
n1=en:retardation | n2=surdité congénitale | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
surdité corticale
n1=en:retardation | n2=surdité corticale | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
surdité de transmission et neurosensorielle
n1=en:retardation | n2=surdité de transmission et neurosensorielle | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
surdité des deux oreilles
n1=en:retardation | n2=surdité des deux oreilles | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
surdité et cataracte progressive
n1=en:retardation | n2=surdité et cataracte progressive | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
surdité fluctuante
n1=en:retardation | n2=surdité fluctuante | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
surdité fonctionnelle
n1=en:retardation | n2=surdité fonctionnelle | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
surdité mélodique et tonale
n1=en:retardation | n2=surdité mélodique et tonale | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
surdité mixte
n1=en:retardation | n2=surdité mixte | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
surdité musicale
n1=en:retardation | n2=surdité musicale | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
surdité non précisée
n1=en:retardation | n2=surdité non précisée | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
surdité pour fréquences basses
n1=en:retardation | n2=surdité pour fréquences basses | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
surdité pour fréquences hautes
n1=en:retardation | n2=surdité pour fréquences hautes | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
surdité profonde
n1=en:retardation | n2=surdité profonde | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
surdité progressive
n1=en:retardation | n2=surdité progressive | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
surdité psychogénique
n1=en:retardation | n2=surdité psychogénique | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
surdité totale
n1=en:retardation | n2=surdité totale | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
surdité toxique
n1=en:retardation | n2=surdité toxique | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
surdité verbale congénitale
n1=en:retardation | n2=surdité verbale congénitale | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
surdités
n1=en:retardation | n2=surdités | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
syncope due à la chaleur
n1=en:retardation | n2=syncope due à la chaleur | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
syncope et collapsus
n1=en:retardation | n2=syncope et collapsus | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
syncope psychogène
n1=en:retardation | n2=syncope psychogène | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
syndrome
n1=en:retardation | n2=syndrome | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
syndrome cataracte-ataxie-surdité et retard mental
n1=en:retardation | n2=syndrome cataracte-ataxie-surdité et retard mental | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
syndrome COACH
n1=en:retardation | n2=syndrome COACH | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
syndrome de Down
n1=en:retardation | n2=syndrome de Down | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
syndrome de Rett
n1=en:retardation | n2=syndrome de Rett | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
syndrome de Treft-Sanborn-Carey
n1=en:retardation | n2=syndrome de Treft-Sanborn-Carey | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
syndrome du sinus carotidien
n1=en:retardation | n2=syndrome du sinus carotidien | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
système nerveux central
n1=en:retardation | n2=système nerveux central | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
thrombose d'un sinus sagittal
n1=en:retardation | n2=thrombose d'un sinus sagittal | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
thrombose de sinus sagittaux
n1=en:retardation | n2=thrombose de sinus sagittaux | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
thrombose des sinus sagittaux
n1=en:retardation | n2=thrombose des sinus sagittaux | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
thrombose du sinus sagittal
n1=en:retardation | n2=thrombose du sinus sagittal | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
tic douloureux
n1=en:retardation | n2=tic douloureux | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
tic douloureux de la face
n1=en:retardation | n2=tic douloureux de la face | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
tics douloureux de la face
n1=en:retardation | n2=tics douloureux de la face | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
tremor
n1=en:retardation | n2=tremor | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
trémor
n1=en:retardation | n2=trémor | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
trisomie
n1=en:retardation | n2=trisomie | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
trisomie 21
n1=en:retardation | n2=trisomie 21 | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
trisomique
n1=en:retardation | n2=trisomique | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
trompe
n1=en:retardation | n2=trompe | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
tronc cérébral
n1=en:retardation | n2=tronc cérébral | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
trouble cognitif
n1=en:retardation | n2=trouble cognitif | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
trouble de la communication
n1=en:retardation | n2=trouble de la communication | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
trouble neurologique du développement
n1=en:retardation | n2=trouble neurologique du développement | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
tumeur du système nerveux central
n1=en:retardation | n2=tumeur du système nerveux central | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
tympanoplastie
n1=en:retardation | n2=tympanoplastie | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
tympanosclérose
n1=en:retardation | n2=tympanosclérose | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
urticaire-surdité-amylose rénale
n1=en:retardation | n2=urticaire-surdité-amylose rénale | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
ventriculomégalie cérébrale
n1=en:retardation | n2=ventriculomégalie cérébrale | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
vertige
n1=en:retardation | n2=vertige | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
vertigo
n1=en:retardation | n2=vertigo | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
voile noir
n1=en:retardation | n2=voile noir | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
Völker-Dieben (atrophie optique liée au sexe de)
n1=en:retardation | n2=Völker-Dieben (atrophie optique liée au sexe de) | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 10 / 0.154 ->
Went (atrophie optique liée au sexe de)
n1=en:retardation | n2=Went (atrophie optique liée au sexe de) | rel=r_associated | relid=0 | w=10
- en:retardation --
r_associated #0: 5 / 0.077 ->
en:backwardness
n1=en:retardation | n2=en:backwardness | rel=r_associated | relid=0 | w=5
- en:retardation --
r_associated #0: 5 / 0.077 ->
en:deceleration
n1=en:retardation | n2=en:deceleration | rel=r_associated | relid=0 | w=5
- en:retardation --
r_associated #0: 5 / 0.077 ->
en:lag
n1=en:retardation | n2=en:lag | rel=r_associated | relid=0 | w=5
- en:retardation --
r_associated #0: 5 / 0.077 ->
en:slowdown
n1=en:retardation | n2=en:slowdown | rel=r_associated | relid=0 | w=5
- en:retardation --
r_associated #0: 5 / 0.077 ->
en:slowness
n1=en:retardation | n2=en:slowness | rel=r_associated | relid=0 | w=5
- en:retardation --
r_associated #0: 1 / 0.015 ->
en:wait
n1=en:retardation | n2=en:wait | rel=r_associated | relid=0 | w=1
| ≈ 6177 relations entrantes
- hyposomnie ---
r_associated #0: 45 -->
en:retardation
n1=hyposomnie | n2=en:retardation | rel=r_associated | relid=0 | w=45
- trouble insomniaque ---
r_associated #0: 45 -->
en:retardation
n1=trouble insomniaque | n2=en:retardation | rel=r_associated | relid=0 | w=45
- arriération mentale ---
r_associated #0: 42 -->
en:retardation
n1=arriération mentale | n2=en:retardation | rel=r_associated | relid=0 | w=42
- arriération ---
r_associated #0: 40 -->
en:retardation
n1=arriération | n2=en:retardation | rel=r_associated | relid=0 | w=40
- débilité mentale ---
r_associated #0: 40 -->
en:retardation
n1=débilité mentale | n2=en:retardation | rel=r_associated | relid=0 | w=40
- en:insomnia ---
r_associated #0: 40 -->
en:retardation
n1=en:insomnia | n2=en:retardation | rel=r_associated | relid=0 | w=40
- en:learning disability ---
r_associated #0: 40 -->
en:retardation
n1=en:learning disability | n2=en:retardation | rel=r_associated | relid=0 | w=40
- en:mental handicap ---
r_associated #0: 40 -->
en:retardation
n1=en:mental handicap | n2=en:retardation | rel=r_associated | relid=0 | w=40
- en:mental retardation ---
r_associated #0: 40 -->
en:retardation
n1=en:mental retardation | n2=en:retardation | rel=r_associated | relid=0 | w=40
- nanisme, retard mental, anomalies oculaires ---
r_associated #0: 40 -->
en:retardation
n1=nanisme, retard mental, anomalies oculaires | n2=en:retardation | rel=r_associated | relid=0 | w=40
- retard mental, retard de croissance, surdité, microgénitalisme lié au sexe ---
r_associated #0: 40 -->
en:retardation
n1=retard mental, retard de croissance, surdité, microgénitalisme lié au sexe | n2=en:retardation | rel=r_associated | relid=0 | w=40
- trouble endormissement et maintien du sommeil ---
r_associated #0: 40 -->
en:retardation
n1=trouble endormissement et maintien du sommeil | n2=en:retardation | rel=r_associated | relid=0 | w=40
- faciès anormal, retard de croissance et retard mental ---
r_associated #0: 38 -->
en:retardation
n1=faciès anormal, retard de croissance et retard mental | n2=en:retardation | rel=r_associated | relid=0 | w=38
- retardation mentale ---
r_associated #0: 35 -->
en:retardation
n1=retardation mentale | n2=en:retardation | rel=r_associated | relid=0 | w=35
- troubles endormissement et maintien du sommeil ---
r_associated #0: 35 -->
en:retardation
n1=troubles endormissement et maintien du sommeil | n2=en:retardation | rel=r_associated | relid=0 | w=35
- retardement ---
r_associated #0: 34 -->
en:retardation
n1=retardement | n2=en:retardation | rel=r_associated | relid=0 | w=34
- en:feeble-mindedness ---
r_associated #0: 33 -->
en:retardation
n1=en:feeble-mindedness | n2=en:retardation | rel=r_associated | relid=0 | w=33
- en:mental dullness ---
r_associated #0: 33 -->
en:retardation
n1=en:mental dullness | n2=en:retardation | rel=r_associated | relid=0 | w=33
- en:failure of the mind ---
r_associated #0: 31 -->
en:retardation
n1=en:failure of the mind | n2=en:retardation | rel=r_associated | relid=0 | w=31
- en:mental deficiency ---
r_associated #0: 31 -->
en:retardation
n1=en:mental deficiency | n2=en:retardation | rel=r_associated | relid=0 | w=31
- oligophrénie ---
r_associated #0: 31 -->
en:retardation
n1=oligophrénie | n2=en:retardation | rel=r_associated | relid=0 | w=31
- retard ---
r_associated #0: 31 -->
en:retardation
n1=retard | n2=en:retardation | rel=r_associated | relid=0 | w=31
- cataracte juvénile, atrophie cérébelleuse, retard mental et myopathie ---
r_associated #0: 30 -->
en:retardation
n1=cataracte juvénile, atrophie cérébelleuse, retard mental et myopathie | n2=en:retardation | rel=r_associated | relid=0 | w=30
- en:juvenile cataract ---
r_associated #0: 30 -->
en:retardation
n1=en:juvenile cataract | n2=en:retardation | rel=r_associated | relid=0 | w=30
- en:deafness ---
r_associated #0: 29 -->
en:retardation
n1=en:deafness | n2=en:retardation | rel=r_associated | relid=0 | w=29
- en:morosis ---
r_associated #0: 29 -->
en:retardation
n1=en:morosis | n2=en:retardation | rel=r_associated | relid=0 | w=29
- cataracte-atrophie du cervelet-myopathie ---
r_associated #0: 28 -->
en:retardation
n1=cataracte-atrophie du cervelet-myopathie | n2=en:retardation | rel=r_associated | relid=0 | w=28
- en:with growth retardation ---
r_associated #0: 28 -->
en:retardation
n1=en:with growth retardation | n2=en:retardation | rel=r_associated | relid=0 | w=28
- troubles endocriniens, épilepsie et déficience mentale ---
r_associated #0: 28 -->
en:retardation
n1=troubles endocriniens, épilepsie et déficience mentale | n2=en:retardation | rel=r_associated | relid=0 | w=28
- déficience mentale ---
r_associated #0: 27 -->
en:retardation
n1=déficience mentale | n2=en:retardation | rel=r_associated | relid=0 | w=27
- en:oligopsychia ---
r_associated #0: 26 -->
en:retardation
n1=en:oligopsychia | n2=en:retardation | rel=r_associated | relid=0 | w=26
- déficience intellectuelle ---
r_associated #0: 25 -->
en:retardation
n1=déficience intellectuelle | n2=en:retardation | rel=r_associated | relid=0 | w=25
- en:and microgenitalism ---
r_associated #0: 25 -->
en:retardation
n1=en:and microgenitalism | n2=en:retardation | rel=r_associated | relid=0 | w=25
- en:oligergasia ---
r_associated #0: 25 -->
en:retardation
n1=en:oligergasia | n2=en:retardation | rel=r_associated | relid=0 | w=25
- en:oligophrenia ---
r_associated #0: 25 -->
en:retardation
n1=en:oligophrenia | n2=en:retardation | rel=r_associated | relid=0 | w=25
- handicap mental ---
r_associated #0: 25 -->
en:retardation
n1=handicap mental | n2=en:retardation | rel=r_associated | relid=0 | w=25
- leucinose ---
r_associated #0: 25 -->
en:retardation
n1=leucinose | n2=en:retardation | rel=r_associated | relid=0 | w=25
- maladie de trousseau ---
r_associated #0: 25 -->
en:retardation
n1=maladie de trousseau | n2=en:retardation | rel=r_associated | relid=0 | w=25
- méningiomes ---
r_associated #0: 25 -->
en:retardation
n1=méningiomes | n2=en:retardation | rel=r_associated | relid=0 | w=25
- neuralgie trigéminale ---
r_associated #0: 25 -->
en:retardation
n1=neuralgie trigéminale | n2=en:retardation | rel=r_associated | relid=0 | w=25
- tics douloureux de la face ---
r_associated #0: 25 -->
en:retardation
n1=tics douloureux de la face | n2=en:retardation | rel=r_associated | relid=0 | w=25
- trouble de conduite en société ---
r_associated #0: 25 -->
en:retardation
n1=trouble de conduite en société | n2=en:retardation | rel=r_associated | relid=0 | w=25
- trouble du comportement socialisé ---
r_associated #0: 25 -->
en:retardation
n1=trouble du comportement socialisé | n2=en:retardation | rel=r_associated | relid=0 | w=25
- en:X-linked ---
r_associated #0: 24 -->
en:retardation
n1=en:X-linked | n2=en:retardation | rel=r_associated | relid=0 | w=24
- en:cerebellar atrophy ---
r_associated #0: 24 -->
en:retardation
n1=en:cerebellar atrophy | n2=en:retardation | rel=r_associated | relid=0 | w=24
- en:intellectual disability ---
r_associated #0: 24 -->
en:retardation
n1=en:intellectual disability | n2=en:retardation | rel=r_associated | relid=0 | w=24
- Déficience intellectuelle ---
r_associated #0: 23 -->
en:retardation
n1=Déficience intellectuelle | n2=en:retardation | rel=r_associated | relid=0 | w=23
- en:dwarfism ---
r_associated #0: 22 -->
en:retardation
n1=en:dwarfism | n2=en:retardation | rel=r_associated | relid=0 | w=22
- sous-développement ---
r_associated #0: 21 -->
en:retardation
n1=sous-développement | n2=en:retardation | rel=r_associated | relid=0 | w=21
- Retard ---
r_associated #0: 20 -->
en:retardation
n1=Retard | n2=en:retardation | rel=r_associated | relid=0 | w=20
- action ---
r_associated #0: 20 -->
en:retardation
n1=action | n2=en:retardation | rel=r_associated | relid=0 | w=20
- aliénation ---
r_associated #0: 20 -->
en:retardation
n1=aliénation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- anomalie mentale ---
r_associated #0: 20 -->
en:retardation
n1=anomalie mentale | n2=en:retardation | rel=r_associated | relid=0 | w=20
- arriérations mentales ---
r_associated #0: 20 -->
en:retardation
n1=arriérations mentales | n2=en:retardation | rel=r_associated | relid=0 | w=20
- arriéré ---
r_associated #0: 20 -->
en:retardation
n1=arriéré | n2=en:retardation | rel=r_associated | relid=0 | w=20
- arriéré
(retard mental) ---
r_associated #0: 20 -->
en:retardation
n1=arriéré (retard mental) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- auditifs ---
r_associated #0: 20 -->
en:retardation
n1=auditifs | n2=en:retardation | rel=r_associated | relid=0 | w=20
- cognition ---
r_associated #0: 20 -->
en:retardation
n1=cognition | n2=en:retardation | rel=r_associated | relid=0 | w=20
- con ---
r_associated #0: 20 -->
en:retardation
n1=con | n2=en:retardation | rel=r_associated | relid=0 | w=20
- crétinisme ---
r_associated #0: 20 -->
en:retardation
n1=crétinisme | n2=en:retardation | rel=r_associated | relid=0 | w=20
- dysphasie et aphasie ---
r_associated #0: 20 -->
en:retardation
n1=dysphasie et aphasie | n2=en:retardation | rel=r_associated | relid=0 | w=20
- débilité ---
r_associated #0: 20 -->
en:retardation
n1=débilité | n2=en:retardation | rel=r_associated | relid=0 | w=20
- débilité
(Nom) ---
r_associated #0: 20 -->
en:retardation
n1=débilité (Nom) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- déficience ---
r_associated #0: 20 -->
en:retardation
n1=déficience | n2=en:retardation | rel=r_associated | relid=0 | w=20
- déficit ---
r_associated #0: 20 -->
en:retardation
n1=déficit | n2=en:retardation | rel=r_associated | relid=0 | w=20
- déficit mental ---
r_associated #0: 20 -->
en:retardation
n1=déficit mental | n2=en:retardation | rel=r_associated | relid=0 | w=20
- développement mental tardif ---
r_associated #0: 20 -->
en:retardation
n1=développement mental tardif | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:'ballooned' neurons with autofluorescent fine granular material ---
r_associated #0: 20 -->
en:retardation
n1=en:'ballooned' neurons with autofluorescent fine granular material | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:'double contour' convolutional calcification on ct scan ---
r_associated #0: 20 -->
en:retardation
n1=en:'double contour' convolutional calcification on ct scan | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:'dragonfly' pattern on imaging ---
r_associated #0: 20 -->
en:retardation
n1=en:'dragonfly' pattern on imaging | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:'dragonfly-like' pattern ---
r_associated #0: 20 -->
en:retardation
n1=en:'dragonfly-like' pattern | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:'eye of the tiger' sign on mri ---
r_associated #0: 20 -->
en:retardation
n1=en:'eye of the tiger' sign on mri | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:'globoid multinucleated cells' in brain tissue ---
r_associated #0: 20 -->
en:retardation
n1=en:'globoid multinucleated cells' in brain tissue | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:'spheroid' inclusions in axons ---
r_associated #0: 20 -->
en:retardation
n1=en:'spheroid' inclusions in axons | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:1p36 deletion syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:1p36 deletion syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:3-4 hz slow sharp waves seen on eeg ---
r_associated #0: 20 -->
en:retardation
n1=en:3-4 hz slow sharp waves seen on eeg | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:3-6 hz polyspike eeg ---
r_associated #0: 20 -->
en:retardation
n1=en:3-6 hz polyspike eeg | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:3-methylglutaconic aciduria with deafness, encephalopathy, and leigh-like syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:3-methylglutaconic aciduria with deafness, encephalopathy, and leigh-like syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:6-pyruvoyl-tetrahydropterin synthase deficiency ---
r_associated #0: 20 -->
en:retardation
n1=en:6-pyruvoyl-tetrahydropterin synthase deficiency | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:a subset of patients develop frontotemporal dementia ---
r_associated #0: 20 -->
en:retardation
n1=en:a subset of patients develop frontotemporal dementia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:a subset of patients have neurologic abnormalities ---
r_associated #0: 20 -->
en:retardation
n1=en:a subset of patients have neurologic abnormalities | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:abducens nerve palsy (cn vi) ---
r_associated #0: 20 -->
en:retardation
n1=en:abducens nerve palsy (cn vi) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:abnormal 'cap' on the dorsal pons extending into the fourth ventricle ---
r_associated #0: 20 -->
en:retardation
n1=en:abnormal 'cap' on the dorsal pons extending into the fourth ventricle | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:abnormal 'hobby horse' ataxic gait ---
r_associated #0: 20 -->
en:retardation
n1=en:abnormal 'hobby horse' ataxic gait | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:abnormal behavior ---
r_associated #0: 20 -->
en:retardation
n1=en:abnormal behavior | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:abnormal brain myelination ---
r_associated #0: 20 -->
en:retardation
n1=en:abnormal brain myelination | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:abnormal cell orientation ---
r_associated #0: 20 -->
en:retardation
n1=en:abnormal cell orientation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:abnormal coordination ---
r_associated #0: 20 -->
en:retardation
n1=en:abnormal coordination | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:abnormal cortical eeg discharges triggered by intermittent light ---
r_associated #0: 20 -->
en:retardation
n1=en:abnormal cortical eeg discharges triggered by intermittent light | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:abnormal cortical gyration ---
r_associated #0: 20 -->
en:retardation
n1=en:abnormal cortical gyration | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:abnormal cortical lamination ---
r_associated #0: 20 -->
en:retardation
n1=en:abnormal cortical lamination | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:abnormal cortical layering ---
r_associated #0: 20 -->
en:retardation
n1=en:abnormal cortical layering | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:abnormal corticospinal tract decussation ---
r_associated #0: 20 -->
en:retardation
n1=en:abnormal corticospinal tract decussation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:abnormal eeg (abnormal slowing of background activity) ---
r_associated #0: 20 -->
en:retardation
n1=en:abnormal eeg (abnormal slowing of background activity) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:abnormal eeg (poor alpha rhythms) ---
r_associated #0: 20 -->
en:retardation
n1=en:abnormal eeg (poor alpha rhythms) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:abnormal eeg activity during sleep ---
r_associated #0: 20 -->
en:retardation
n1=en:abnormal eeg activity during sleep | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:abnormal eeg with epileptiform changes ---
r_associated #0: 20 -->
en:retardation
n1=en:abnormal eeg with epileptiform changes | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:abnormal fetal duplication ---
r_associated #0: 20 -->
en:retardation
n1=en:abnormal fetal duplication | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:abnormal gait (67%) ---
r_associated #0: 20 -->
en:retardation
n1=en:abnormal gait (67%) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:abnormal gait due to muscle weakness ---
r_associated #0: 20 -->
en:retardation
n1=en:abnormal gait due to muscle weakness | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:abnormal gray and white matter differentiation in frontal, occipital, and cerebellar regions on ct scan ---
r_associated #0: 20 -->
en:retardation
n1=en:abnormal gray and white matter differentiation in frontal, occipital, and cerebellar regions on ct scan | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:abnormal gyral pattern ---
r_associated #0: 20 -->
en:retardation
n1=en:abnormal gyral pattern | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:abnormal gyri ---
r_associated #0: 20 -->
en:retardation
n1=en:abnormal gyri | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:abnormal gyri (in 1 of 2 patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:abnormal gyri (in 1 of 2 patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:abnormal hippocampus ---
r_associated #0: 20 -->
en:retardation
n1=en:abnormal hippocampus | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:abnormal hypothalamo-pituitary axis ---
r_associated #0: 20 -->
en:retardation
n1=en:abnormal hypothalamo-pituitary axis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:abnormal interictal eeg (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:abnormal interictal eeg (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:abnormal involuntary movement ---
r_associated #0: 20 -->
en:retardation
n1=en:abnormal involuntary movement | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:abnormal lipid peak on brain mrs ---
r_associated #0: 20 -->
en:retardation
n1=en:abnormal lipid peak on brain mrs | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:abnormal lower motor neuron morphology ---
r_associated #0: 20 -->
en:retardation
n1=en:abnormal lower motor neuron morphology | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:abnormal movement ---
r_associated #0: 20 -->
en:retardation
n1=en:abnormal movement | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:abnormal myelination ---
r_associated #0: 20 -->
en:retardation
n1=en:abnormal myelination | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:abnormal ocular motility ---
r_associated #0: 20 -->
en:retardation
n1=en:abnormal ocular motility | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:abnormal pap smear ---
r_associated #0: 20 -->
en:retardation
n1=en:abnormal pap smear | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:abnormal posture ---
r_associated #0: 20 -->
en:retardation
n1=en:abnormal posture | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:abnormal primitive reflexes ---
r_associated #0: 20 -->
en:retardation
n1=en:abnormal primitive reflexes | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:abnormal purkinje cells ---
r_associated #0: 20 -->
en:retardation
n1=en:abnormal purkinje cells | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:abnormal rapid eye movement sleep ---
r_associated #0: 20 -->
en:retardation
n1=en:abnormal rapid eye movement sleep | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:abnormal results investigation nos ---
r_associated #0: 20 -->
en:retardation
n1=en:abnormal results investigation nos | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:abnormal septum pellucidum ---
r_associated #0: 20 -->
en:retardation
n1=en:abnormal septum pellucidum | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:abnormal signals in the thalami seen on mri ---
r_associated #0: 20 -->
en:retardation
n1=en:abnormal signals in the thalami seen on mri | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:abnormal sleep pattern ---
r_associated #0: 20 -->
en:retardation
n1=en:abnormal sleep pattern | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:abnormal sleep-wake cycles ---
r_associated #0: 20 -->
en:retardation
n1=en:abnormal sleep-wake cycles | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:abnormal spike waves ---
r_associated #0: 20 -->
en:retardation
n1=en:abnormal spike waves | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:abnormal sulci ---
r_associated #0: 20 -->
en:retardation
n1=en:abnormal sulci | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:abnormal t2-weighted signals in the occipital white and gray matter ---
r_associated #0: 20 -->
en:retardation
n1=en:abnormal t2-weighted signals in the occipital white and gray matter | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:abnormal urine test result ---
r_associated #0: 20 -->
en:retardation
n1=en:abnormal urine test result | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:abnormal visual evoked potential ---
r_associated #0: 20 -->
en:retardation
n1=en:abnormal visual evoked potential | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:abnormal visual evoked potential (vep) ---
r_associated #0: 20 -->
en:retardation
n1=en:abnormal visual evoked potential (vep) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:abnormal visual sensitivity of the brain in reaction to intermittent photic stimulation ---
r_associated #0: 20 -->
en:retardation
n1=en:abnormal visual sensitivity of the brain in reaction to intermittent photic stimulation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:abnormal white matter signals, in the basal ganglia or cerebellum seen on brain mri ---
r_associated #0: 20 -->
en:retardation
n1=en:abnormal white matter signals, in the basal ganglia or cerebellum seen on brain mri | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:abnormalities, drug-induced ---
r_associated #0: 20 -->
en:retardation
n1=en:abnormalities, drug-induced | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:abnormality of brainstem morphology ---
r_associated #0: 20 -->
en:retardation
n1=en:abnormality of brainstem morphology | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:abnormality of ocular smooth pursuit ---
r_associated #0: 20 -->
en:retardation
n1=en:abnormality of ocular smooth pursuit | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:abnormality of the cerebellum ---
r_associated #0: 20 -->
en:retardation
n1=en:abnormality of the cerebellum | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:abnormality of the corpus callosum ---
r_associated #0: 20 -->
en:retardation
n1=en:abnormality of the corpus callosum | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:abnormality of the posterior cranial fossa ---
r_associated #0: 20 -->
en:retardation
n1=en:abnormality of the posterior cranial fossa | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:abnormality, severe teratoid ---
r_associated #0: 20 -->
en:retardation
n1=en:abnormality, severe teratoid | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:abnormally marked pontobulbar sulcus ---
r_associated #0: 20 -->
en:retardation
n1=en:abnormally marked pontobulbar sulcus | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:absence of anterior pituitary ---
r_associated #0: 20 -->
en:retardation
n1=en:absence of anterior pituitary | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:absence of balloon cells (in type iia) ---
r_associated #0: 20 -->
en:retardation
n1=en:absence of balloon cells (in type iia) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:absence of cerebral aneurysms ---
r_associated #0: 20 -->
en:retardation
n1=en:absence of cerebral aneurysms | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:absence of language development ---
r_associated #0: 20 -->
en:retardation
n1=en:absence of language development | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:absence of lower motor neuron involvement ---
r_associated #0: 20 -->
en:retardation
n1=en:absence of lower motor neuron involvement | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:absence of myelin in the posterior column of the spinal cord (1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:absence of myelin in the posterior column of the spinal cord (1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:absence of neurologic manifestations ---
r_associated #0: 20 -->
en:retardation
n1=en:absence of neurologic manifestations | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:absence of neuropathologic findings in the brainstem and anterior horn cells ---
r_associated #0: 20 -->
en:retardation
n1=en:absence of neuropathologic findings in the brainstem and anterior horn cells | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:absence of olfactory bulbs ---
r_associated #0: 20 -->
en:retardation
n1=en:absence of olfactory bulbs | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:absence of primitive reflexes ---
r_associated #0: 20 -->
en:retardation
n1=en:absence of primitive reflexes | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:absence of septum pellucidum ---
r_associated #0: 20 -->
en:retardation
n1=en:absence of septum pellucidum | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:absence of spontaneous movements ---
r_associated #0: 20 -->
en:retardation
n1=en:absence of spontaneous movements | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:absence of the basal ganglia ---
r_associated #0: 20 -->
en:retardation
n1=en:absence of the basal ganglia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:absence of the cerebellar vermis ---
r_associated #0: 20 -->
en:retardation
n1=en:absence of the cerebellar vermis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:absence of the inferior olives ---
r_associated #0: 20 -->
en:retardation
n1=en:absence of the inferior olives | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:absence of the olfactory bulbs and tracts ---
r_associated #0: 20 -->
en:retardation
n1=en:absence of the olfactory bulbs and tracts | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:absence of transverse pontine fibers ---
r_associated #0: 20 -->
en:retardation
n1=en:absence of transverse pontine fibers | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:absence of vestibular schwannomas at age greater than 18 years ---
r_associated #0: 20 -->
en:retardation
n1=en:absence of vestibular schwannomas at age greater than 18 years | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:absence or atrophy of the putamen ---
r_associated #0: 20 -->
en:retardation
n1=en:absence or atrophy of the putamen | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:absence or hypoplasia of the anterior limb of the internal capsule ---
r_associated #0: 20 -->
en:retardation
n1=en:absence or hypoplasia of the anterior limb of the internal capsule | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:absence seizures (in some) ---
r_associated #0: 20 -->
en:retardation
n1=en:absence seizures (in some) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:absence seizures (stage 2 and 3) ---
r_associated #0: 20 -->
en:retardation
n1=en:absence seizures (stage 2 and 3) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:absence seizures may occur ---
r_associated #0: 20 -->
en:retardation
n1=en:absence seizures may occur | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:absent cisterna magna ---
r_associated #0: 20 -->
en:retardation
n1=en:absent cisterna magna | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:absent corpus callosum (variable) ---
r_associated #0: 20 -->
en:retardation
n1=en:absent corpus callosum (variable) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:absent cortical responses of somatosensory evoked potentials ---
r_associated #0: 20 -->
en:retardation
n1=en:absent cortical responses of somatosensory evoked potentials | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:absent development ---
r_associated #0: 20 -->
en:retardation
n1=en:absent development | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:absent myelination of the brain (severe connatal form) ---
r_associated #0: 20 -->
en:retardation
n1=en:absent myelination of the brain (severe connatal form) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:absent olfactory bulbs ---
r_associated #0: 20 -->
en:retardation
n1=en:absent olfactory bulbs | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:absent olfactory tract or bulbs ---
r_associated #0: 20 -->
en:retardation
n1=en:absent olfactory tract or bulbs | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:absent olfactory tracts and bulbs ---
r_associated #0: 20 -->
en:retardation
n1=en:absent olfactory tracts and bulbs | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:absent optic nerves, chiasm, and tracts ---
r_associated #0: 20 -->
en:retardation
n1=en:absent optic nerves, chiasm, and tracts | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:absent or delayed psychomotor development, severe ---
r_associated #0: 20 -->
en:retardation
n1=en:absent or delayed psychomotor development, severe | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:absent or delayed speech development ---
r_associated #0: 20 -->
en:retardation
n1=en:absent or delayed speech development | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:absent or immature dentate nuclei ---
r_associated #0: 20 -->
en:retardation
n1=en:absent or immature dentate nuclei | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:absent or limited speech development ---
r_associated #0: 20 -->
en:retardation
n1=en:absent or limited speech development | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:absent or poor expressive speech ---
r_associated #0: 20 -->
en:retardation
n1=en:absent or poor expressive speech | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:absent pituitary ---
r_associated #0: 20 -->
en:retardation
n1=en:absent pituitary | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:absent posterior pituitary bright spot ---
r_associated #0: 20 -->
en:retardation
n1=en:absent posterior pituitary bright spot | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:absent primitive reflexes ---
r_associated #0: 20 -->
en:retardation
n1=en:absent primitive reflexes | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:absent rem sleep ---
r_associated #0: 20 -->
en:retardation
n1=en:absent rem sleep | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:absent speech ---
r_associated #0: 20 -->
en:retardation
n1=en:absent speech | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:absent superior division of oculomotor nerve and corresponding alpha motor neurons ---
r_associated #0: 20 -->
en:retardation
n1=en:absent superior division of oculomotor nerve and corresponding alpha motor neurons | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:academic disorders, developmental ---
r_associated #0: 20 -->
en:retardation
n1=en:academic disorders, developmental | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:accumulation of autofluorescent material in neurons ---
r_associated #0: 20 -->
en:retardation
n1=en:accumulation of autofluorescent material in neurons | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:accumulation of pas-positive diastase-resistant neuronal inclusion bodies in the cerebral cortex (collins bodies) ---
r_associated #0: 20 -->
en:retardation
n1=en:accumulation of pas-positive diastase-resistant neuronal inclusion bodies in the cerebral cortex (collins bodies) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:acephalostomia ---
r_associated #0: 20 -->
en:retardation
n1=en:acephalostomia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:acne ---
r_associated #0: 20 -->
en:retardation
n1=en:acne | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:acoustic trauma ---
r_associated #0: 20 -->
en:retardation
n1=en:acoustic trauma | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:acquired deformity of limb ---
r_associated #0: 20 -->
en:retardation
n1=en:acquired deformity of limb | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:acquired deformity of spine ---
r_associated #0: 20 -->
en:retardation
n1=en:acquired deformity of spine | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:acranias ---
r_associated #0: 20 -->
en:retardation
n1=en:acranias | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:acromelic frontonasal dysostosis ---
r_associated #0: 20 -->
en:retardation
n1=en:acromelic frontonasal dysostosis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:actin depolymerizing factor/cofilin-immunoreactive eosinophilic rod-like cytoplasmic inclusions in neocortical and thalamic neurons ---
r_associated #0: 20 -->
en:retardation
n1=en:actin depolymerizing factor/cofilin-immunoreactive eosinophilic rod-like cytoplasmic inclusions in neocortical and thalamic neurons | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:actin- and actin depolymerizing factor/cofilin-immunoreactive eosinophilic spherical structures in the striatum ---
r_associated #0: 20 -->
en:retardation
n1=en:actin- and actin depolymerizing factor/cofilin-immunoreactive eosinophilic spherical structures in the striatum | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:action and postural tremor ---
r_associated #0: 20 -->
en:retardation
n1=en:action and postural tremor | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:action dystonia ---
r_associated #0: 20 -->
en:retardation
n1=en:action dystonia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:action myoclonus ---
r_associated #0: 20 -->
en:retardation
n1=en:action myoclonus | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:action myoclonus (triggered by voluntary movements) ---
r_associated #0: 20 -->
en:retardation
n1=en:action myoclonus (triggered by voluntary movements) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:actual effective cognition ---
r_associated #0: 20 -->
en:retardation
n1=en:actual effective cognition | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:acute alcohol abuse ---
r_associated #0: 20 -->
en:retardation
n1=en:acute alcohol abuse | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:acute bronchitis and bronchiolitis ---
r_associated #0: 20 -->
en:retardation
n1=en:acute bronchitis and bronchiolitis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:acute cerebrovascular accidents ---
r_associated #0: 20 -->
en:retardation
n1=en:acute cerebrovascular accidents | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:acute damage meniscus knee ---
r_associated #0: 20 -->
en:retardation
n1=en:acute damage meniscus knee | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:acute encephalopathy ---
r_associated #0: 20 -->
en:retardation
n1=en:acute encephalopathy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:acute episodes of neuropathic symptoms ---
r_associated #0: 20 -->
en:retardation
n1=en:acute episodes of neuropathic symptoms | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:acute episodes of neuropathic symptoms (hcp) ---
r_associated #0: 20 -->
en:retardation
n1=en:acute episodes of neuropathic symptoms (hcp) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:acute laryngitis and/or tracheitis ---
r_associated #0: 20 -->
en:retardation
n1=en:acute laryngitis and/or tracheitis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:acute lymphadenitis ---
r_associated #0: 20 -->
en:retardation
n1=en:acute lymphadenitis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:acute miliary tuberculosis ---
r_associated #0: 20 -->
en:retardation
n1=en:acute miliary tuberculosis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:acute myocardial infarction ---
r_associated #0: 20 -->
en:retardation
n1=en:acute myocardial infarction | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:acute nasopharyngitis ---
r_associated #0: 20 -->
en:retardation
n1=en:acute nasopharyngitis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:acute necrotizing encephalopathy ---
r_associated #0: 20 -->
en:retardation
n1=en:acute necrotizing encephalopathy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:acute neurologic decompensation (in later-onset cases) ---
r_associated #0: 20 -->
en:retardation
n1=en:acute neurologic decompensation (in later-onset cases) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:acute neurologic deficits due to cerebrovascular disease ---
r_associated #0: 20 -->
en:retardation
n1=en:acute neurologic deficits due to cerebrovascular disease | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:acute otitis media/myringitis ---
r_associated #0: 20 -->
en:retardation
n1=en:acute otitis media/myringitis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:acute poliomyelitis ---
r_associated #0: 20 -->
en:retardation
n1=en:acute poliomyelitis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:acute stress/transient/situational disturbance ---
r_associated #0: 20 -->
en:retardation
n1=en:acute stress/transient/situational disturbance | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:acute tonsillitis ---
r_associated #0: 20 -->
en:retardation
n1=en:acute tonsillitis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:addiction ---
r_associated #0: 20 -->
en:retardation
n1=en:addiction | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:additional sex chromosome ---
r_associated #0: 20 -->
en:retardation
n1=en:additional sex chromosome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:adenylosuccinate lyase deficiency (disorder) ---
r_associated #0: 20 -->
en:retardation
n1=en:adenylosuccinate lyase deficiency (disorder) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:adipose tissue in subarachnoid space ---
r_associated #0: 20 -->
en:retardation
n1=en:adipose tissue in subarachnoid space | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:adjustment disorder ---
r_associated #0: 20 -->
en:retardation
n1=en:adjustment disorder | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:adjustment disorders (incl subtypes) ---
r_associated #0: 20 -->
en:retardation
n1=en:adjustment disorders (incl subtypes) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:adjustment stress reaction syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:adjustment stress reaction syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:adult attention deficit hyperactivity disorder ---
r_associated #0: 20 -->
en:retardation
n1=en:adult attention deficit hyperactivity disorder | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:adverse effect medical agent proper dose ---
r_associated #0: 20 -->
en:retardation
n1=en:adverse effect medical agent proper dose | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:adverse effect of physical agent ---
r_associated #0: 20 -->
en:retardation
n1=en:adverse effect of physical agent | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:afebrile seizure ---
r_associated #0: 20 -->
en:retardation
n1=en:afebrile seizure | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:affected arteries have electron-dense granular material close to vascular smooth muscle cell membranes ---
r_associated #0: 20 -->
en:retardation
n1=en:affected arteries have electron-dense granular material close to vascular smooth muscle cell membranes | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:affected arteries show loss of smooth muscle cells ---
r_associated #0: 20 -->
en:retardation
n1=en:affected arteries show loss of smooth muscle cells | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:affected children are unable to sit without support ---
r_associated #0: 20 -->
en:retardation
n1=en:affected children are unable to sit without support | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:affective psychosis ---
r_associated #0: 20 -->
en:retardation
n1=en:affective psychosis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:agenesis ---
r_associated #0: 20 -->
en:retardation
n1=en:agenesis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:agenesis of corpus callosum, partial or complete (rare) ---
r_associated #0: 20 -->
en:retardation
n1=en:agenesis of corpus callosum, partial or complete (rare) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:agenesis of pineal gland ---
r_associated #0: 20 -->
en:retardation
n1=en:agenesis of pineal gland | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:agenesis of the anterior commissure ---
r_associated #0: 20 -->
en:retardation
n1=en:agenesis of the anterior commissure | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:agenesis of the corpus callosum (1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:agenesis of the corpus callosum (1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:agenesis of the corpus callosum (in 1 of 2 patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:agenesis of the corpus callosum (in 1 of 2 patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:agenesis of the corpus callosum (in 2 patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:agenesis of the corpus callosum (in 2 patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:agenesis of the corpus callosum (less common) ---
r_associated #0: 20 -->
en:retardation
n1=en:agenesis of the corpus callosum (less common) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:agenesis of the corpus callosum (patient a) ---
r_associated #0: 20 -->
en:retardation
n1=en:agenesis of the corpus callosum (patient a) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:agenesis of the corpus callosum (rare) ---
r_associated #0: 20 -->
en:retardation
n1=en:agenesis of the corpus callosum (rare) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:agenesis of the corpus callosum (variable) ---
r_associated #0: 20 -->
en:retardation
n1=en:agenesis of the corpus callosum (variable) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:agenesis of the occipital lobes (1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:agenesis of the occipital lobes (1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:agenesis of the rostrum of corpus callosum ---
r_associated #0: 20 -->
en:retardation
n1=en:agenesis of the rostrum of corpus callosum | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:agenesis or hypogenesis of the cerebellar vermis ---
r_associated #0: 20 -->
en:retardation
n1=en:agenesis or hypogenesis of the cerebellar vermis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:agenesis or hypoplasia of the corpus callosum ---
r_associated #0: 20 -->
en:retardation
n1=en:agenesis or hypoplasia of the corpus callosum | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:agenesis or severe hypoplasia of cerebellar vermis ---
r_associated #0: 20 -->
en:retardation
n1=en:agenesis or severe hypoplasia of cerebellar vermis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:aggregation of snca-immunopositive inclusions ---
r_associated #0: 20 -->
en:retardation
n1=en:aggregation of snca-immunopositive inclusions | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:aggression ---
r_associated #0: 20 -->
en:retardation
n1=en:aggression | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:agnosia ---
r_associated #0: 20 -->
en:retardation
n1=en:agnosia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:agraphia ---
r_associated #0: 20 -->
en:retardation
n1=en:agraphia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:agyria (1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:agyria (1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:agyria (posterior-to-anterior gradient) ---
r_associated #0: 20 -->
en:retardation
n1=en:agyria (posterior-to-anterior gradient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:agyria (wws) ---
r_associated #0: 20 -->
en:retardation
n1=en:agyria (wws) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:aicardi syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:aicardi syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:aicardi-goutieres syndrome 7 ---
r_associated #0: 20 -->
en:retardation
n1=en:aicardi-goutieres syndrome 7 | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:akathisia ---
r_associated #0: 20 -->
en:retardation
n1=en:akathisia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:akinesia ---
r_associated #0: 20 -->
en:retardation
n1=en:akinesia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:akinetic mutism (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:akinetic mutism (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:albinism ---
r_associated #0: 20 -->
en:retardation
n1=en:albinism | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:albright's hereditary osteodystrophy ---
r_associated #0: 20 -->
en:retardation
n1=en:albright's hereditary osteodystrophy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:alcohol dependence ---
r_associated #0: 20 -->
en:retardation
n1=en:alcohol dependence | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:alcohol-related disorders ---
r_associated #0: 20 -->
en:retardation
n1=en:alcohol-related disorders | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:alcohol-related intrauterine disorder ---
r_associated #0: 20 -->
en:retardation
n1=en:alcohol-related intrauterine disorder | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:all other perinatal morbidity ---
r_associated #0: 20 -->
en:retardation
n1=en:all other perinatal morbidity | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:allgrove syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:allgrove syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:alobar holoprosencephaly (rare) ---
r_associated #0: 20 -->
en:retardation
n1=en:alobar holoprosencephaly (rare) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:alobar hpe shows absence of interhemispheric cleavage and single ventricle ---
r_associated #0: 20 -->
en:retardation
n1=en:alobar hpe shows absence of interhemispheric cleavage and single ventricle | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:alpha thalassemia x-linked mental retardation syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:alpha thalassemia x-linked mental retardation syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:alpha-b-crystallin expression in oligodendrocytes ---
r_associated #0: 20 -->
en:retardation
n1=en:alpha-b-crystallin expression in oligodendrocytes | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:alpha-synuclein immunoreactive neuronal and glial inclusions ---
r_associated #0: 20 -->
en:retardation
n1=en:alpha-synuclein immunoreactive neuronal and glial inclusions | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:alpha-synuclein-containing inclusions ---
r_associated #0: 20 -->
en:retardation
n1=en:alpha-synuclein-containing inclusions | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:alpha-synuclein-immunoreactive lewy neurites ---
r_associated #0: 20 -->
en:retardation
n1=en:alpha-synuclein-immunoreactive lewy neurites | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:alpha-synuclein-immunreactive lewy bodies ---
r_associated #0: 20 -->
en:retardation
n1=en:alpha-synuclein-immunreactive lewy bodies | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:altered breathing patterns ---
r_associated #0: 20 -->
en:retardation
n1=en:altered breathing patterns | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:altered mental status ---
r_associated #0: 20 -->
en:retardation
n1=en:altered mental status | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:alternating hemiplegia of childhood 1 ---
r_associated #0: 20 -->
en:retardation
n1=en:alternating hemiplegia of childhood 1 | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:alzheimer disease, early onset ---
r_associated #0: 20 -->
en:retardation
n1=en:alzheimer disease, early onset | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:alzheimer's disease ---
r_associated #0: 20 -->
en:retardation
n1=en:alzheimer's disease | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:amastia ---
r_associated #0: 20 -->
en:retardation
n1=en:amastia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:amaurosis congenita of leber, type 1 ---
r_associated #0: 20 -->
en:retardation
n1=en:amaurosis congenita of leber, type 1 | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:amaurotic familial idiocy ---
r_associated #0: 20 -->
en:retardation
n1=en:amaurotic familial idiocy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ambulation difficulty ---
r_associated #0: 20 -->
en:retardation
n1=en:ambulation difficulty | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:amegakaryocytic thrombocytopenia with congenital malformation ---
r_associated #0: 20 -->
en:retardation
n1=en:amegakaryocytic thrombocytopenia with congenital malformation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:amnesia ---
r_associated #0: 20 -->
en:retardation
n1=en:amnesia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:amniotic band syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:amniotic band syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:amyloid deposition in the leptomeningeal vessels, brainstem, spinal cord ---
r_associated #0: 20 -->
en:retardation
n1=en:amyloid deposition in the leptomeningeal vessels, brainstem, spinal cord | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:amyloid plaques may be present ---
r_associated #0: 20 -->
en:retardation
n1=en:amyloid plaques may be present | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:amyloid-like plaques are not immunoreactive to app (104760) ---
r_associated #0: 20 -->
en:retardation
n1=en:amyloid-like plaques are not immunoreactive to app (104760) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:amyloid-like plaques, immunoreactive to prp, predominantly in the cerebellum ---
r_associated #0: 20 -->
en:retardation
n1=en:amyloid-like plaques, immunoreactive to prp, predominantly in the cerebellum | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:amyotrophic lateral sclerosis ---
r_associated #0: 20 -->
en:retardation
n1=en:amyotrophic lateral sclerosis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:amyotrophy, distal, severe ---
r_associated #0: 20 -->
en:retardation
n1=en:amyotrophy, distal, severe | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:anal fissure/perianal abscess ---
r_associated #0: 20 -->
en:retardation
n1=en:anal fissure/perianal abscess | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:anarthria speech disorder ---
r_associated #0: 20 -->
en:retardation
n1=en:anarthria speech disorder | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:anauxetic dysplasia ---
r_associated #0: 20 -->
en:retardation
n1=en:anauxetic dysplasia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:anencephalus and similar anomalies ---
r_associated #0: 20 -->
en:retardation
n1=en:anencephalus and similar anomalies | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:anencephaly ---
r_associated #0: 20 -->
en:retardation
n1=en:anencephaly | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:anencephaly (1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:anencephaly (1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:angelman syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:angelman syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:angiitis, cerebral ---
r_associated #0: 20 -->
en:retardation
n1=en:angiitis, cerebral | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:angina ---
r_associated #0: 20 -->
en:retardation
n1=en:angina | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:angiographically 'silent' ---
r_associated #0: 20 -->
en:retardation
n1=en:angiographically 'silent' | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:angiomatous meningioma ---
r_associated #0: 20 -->
en:retardation
n1=en:angiomatous meningioma | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:angulation of the frontal horns ---
r_associated #0: 20 -->
en:retardation
n1=en:angulation of the frontal horns | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:anisocoria ---
r_associated #0: 20 -->
en:retardation
n1=en:anisocoria | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ankle clonus ---
r_associated #0: 20 -->
en:retardation
n1=en:ankle clonus | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ankle clonus (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:ankle clonus (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ankle clonus (in some) ---
r_associated #0: 20 -->
en:retardation
n1=en:ankle clonus (in some) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ankle or knee clonus ---
r_associated #0: 20 -->
en:retardation
n1=en:ankle or knee clonus | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ankle reflex absent ---
r_associated #0: 20 -->
en:retardation
n1=en:ankle reflex absent | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ankyloglossia ---
r_associated #0: 20 -->
en:retardation
n1=en:ankyloglossia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:anomalies of the folding of the right sylvian area ---
r_associated #0: 20 -->
en:retardation
n1=en:anomalies of the folding of the right sylvian area | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:anomalies of the temporal area ---
r_associated #0: 20 -->
en:retardation
n1=en:anomalies of the temporal area | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:anomaly congenital special senses ---
r_associated #0: 20 -->
en:retardation
n1=en:anomaly congenital special senses | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:anomia ---
r_associated #0: 20 -->
en:retardation
n1=en:anomia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:anosmia ---
r_associated #0: 20 -->
en:retardation
n1=en:anosmia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:anosmia (1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:anosmia (1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:anosmia (in contiguous gene syndrome patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:anosmia (in contiguous gene syndrome patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:anosmia (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:anosmia (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:antenatal intracerebral hemorrhage ---
r_associated #0: 20 -->
en:retardation
n1=en:antenatal intracerebral hemorrhage | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:anterior basal encephalocele ---
r_associated #0: 20 -->
en:retardation
n1=en:anterior basal encephalocele | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:anterior commissure not evident ---
r_associated #0: 20 -->
en:retardation
n1=en:anterior commissure not evident | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:anterior horn atrophy ---
r_associated #0: 20 -->
en:retardation
n1=en:anterior horn atrophy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:anterior horn cell impairment ---
r_associated #0: 20 -->
en:retardation
n1=en:anterior horn cell impairment | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:anterior pachygyria and posterior agyria ---
r_associated #0: 20 -->
en:retardation
n1=en:anterior pachygyria and posterior agyria | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:anterior pituitary adenoma ---
r_associated #0: 20 -->
en:retardation
n1=en:anterior pituitary adenoma | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:anterior pituitary hypoplasia ---
r_associated #0: 20 -->
en:retardation
n1=en:anterior pituitary hypoplasia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:anterior sacral meningocele ---
r_associated #0: 20 -->
en:retardation
n1=en:anterior sacral meningocele | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:anterior temporal lobe subcortical cysts ---
r_associated #0: 20 -->
en:retardation
n1=en:anterior temporal lobe subcortical cysts | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:antisocial behavior ---
r_associated #0: 20 -->
en:retardation
n1=en:antisocial behavior | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:anxiety ---
r_associated #0: 20 -->
en:retardation
n1=en:anxiety | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:anxiety adverse event ---
r_associated #0: 20 -->
en:retardation
n1=en:anxiety adverse event | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:anxiety disorder ---
r_associated #0: 20 -->
en:retardation
n1=en:anxiety disorder | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:anxiety disorder/anxiety state ---
r_associated #0: 20 -->
en:retardation
n1=en:anxiety disorder/anxiety state | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:anxiety disorders and symptoms ---
r_associated #0: 20 -->
en:retardation
n1=en:anxiety disorders and symptoms | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:apathy ---
r_associated #0: 20 -->
en:retardation
n1=en:apathy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:aphasia ---
r_associated #0: 20 -->
en:retardation
n1=en:aphasia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:aplasia of corpus callosum ---
r_associated #0: 20 -->
en:retardation
n1=en:aplasia of corpus callosum | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:aplasia of olfactory bulbs, bilateral ---
r_associated #0: 20 -->
en:retardation
n1=en:aplasia of olfactory bulbs, bilateral | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:aplasia of the corpus callosum (wws) encephalocele (1 patient, meb) ---
r_associated #0: 20 -->
en:retardation
n1=en:aplasia of the corpus callosum (wws) encephalocele (1 patient, meb) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:aplasia of the inferior half of the cerebellar vermis ---
r_associated #0: 20 -->
en:retardation
n1=en:aplasia of the inferior half of the cerebellar vermis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:aplasia of the vermis ---
r_associated #0: 20 -->
en:retardation
n1=en:aplasia of the vermis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:aplasia, nos ---
r_associated #0: 20 -->
en:retardation
n1=en:aplasia, nos | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:aplasia/hypoplasia of the cerebellar vermis ---
r_associated #0: 20 -->
en:retardation
n1=en:aplasia/hypoplasia of the cerebellar vermis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:aplasia/hypoplasia of the cerebellum ---
r_associated #0: 20 -->
en:retardation
n1=en:aplasia/hypoplasia of the cerebellum | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:aplasia/hypoplasia of the corpus callosum ---
r_associated #0: 20 -->
en:retardation
n1=en:aplasia/hypoplasia of the corpus callosum | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:apoptotic neurons ---
r_associated #0: 20 -->
en:retardation
n1=en:apoptotic neurons | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:appendicitis ---
r_associated #0: 20 -->
en:retardation
n1=en:appendicitis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:appendicular hypertonia ---
r_associated #0: 20 -->
en:retardation
n1=en:appendicular hypertonia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:approximately 30% of patients show normal early development ---
r_associated #0: 20 -->
en:retardation
n1=en:approximately 30% of patients show normal early development | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:apraxia (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:apraxia (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:apraxia, verbal ---
r_associated #0: 20 -->
en:retardation
n1=en:apraxia, verbal | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:apraxias ---
r_associated #0: 20 -->
en:retardation
n1=en:apraxias | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:aqueductal stenosis ---
r_associated #0: 20 -->
en:retardation
n1=en:aqueductal stenosis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:arachnoid cyst ---
r_associated #0: 20 -->
en:retardation
n1=en:arachnoid cyst | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:arachnoid cyst (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:arachnoid cyst (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:arachnoid cysts (1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:arachnoid cysts (1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:arachnoid cysts (in one family) ---
r_associated #0: 20 -->
en:retardation
n1=en:arachnoid cysts (in one family) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:arachnoid cysts of the cerebellopontine angle (reported in 1 family) ---
r_associated #0: 20 -->
en:retardation
n1=en:arachnoid cysts of the cerebellopontine angle (reported in 1 family) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:arachnoid hemangiomata ---
r_associated #0: 20 -->
en:retardation
n1=en:arachnoid hemangiomata | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:arachnoidal cysts ---
r_associated #0: 20 -->
en:retardation
n1=en:arachnoidal cysts | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:areflexia ---
r_associated #0: 20 -->
en:retardation
n1=en:areflexia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:areflexia (30%) ---
r_associated #0: 20 -->
en:retardation
n1=en:areflexia (30%) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:areflexia of lower limbs ---
r_associated #0: 20 -->
en:retardation
n1=en:areflexia of lower limbs | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:areflexia of upper limbs ---
r_associated #0: 20 -->
en:retardation
n1=en:areflexia of upper limbs | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:argininemia ---
r_associated #0: 20 -->
en:retardation
n1=en:argininemia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:argininosuccinic aciduria ---
r_associated #0: 20 -->
en:retardation
n1=en:argininosuccinic aciduria | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:argyrophilic hyperphosphorylated tau-positive inclusions (pick bodies) ---
r_associated #0: 20 -->
en:retardation
n1=en:argyrophilic hyperphosphorylated tau-positive inclusions (pick bodies) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:arhinencephaly ---
r_associated #0: 20 -->
en:retardation
n1=en:arhinencephaly | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:arhinencephaly (1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:arhinencephaly (1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:arithmetic disorder ---
r_associated #0: 20 -->
en:retardation
n1=en:arithmetic disorder | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:arm flexion ---
r_associated #0: 20 -->
en:retardation
n1=en:arm flexion | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:arm pain ---
r_associated #0: 20 -->
en:retardation
n1=en:arm pain | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:arnold-chiari i malformation ---
r_associated #0: 20 -->
en:retardation
n1=en:arnold-chiari i malformation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:arnold-chiari malformation ---
r_associated #0: 20 -->
en:retardation
n1=en:arnold-chiari malformation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:arrest of psychomotor development after seizure onset ---
r_associated #0: 20 -->
en:retardation
n1=en:arrest of psychomotor development after seizure onset | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:arrested hydrocephalus (rare) ---
r_associated #0: 20 -->
en:retardation
n1=en:arrested hydrocephalus (rare) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:arrhythmia ---
r_associated #0: 20 -->
en:retardation
n1=en:arrhythmia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:arthrogryposis, mental retardation, and seizures ---
r_associated #0: 20 -->
en:retardation
n1=en:arthrogryposis, mental retardation, and seizures | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:articulation difficulties ---
r_associated #0: 20 -->
en:retardation
n1=en:articulation difficulties | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:articulation, unintelligible ---
r_associated #0: 20 -->
en:retardation
n1=en:articulation, unintelligible | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:articulatory defect ---
r_associated #0: 20 -->
en:retardation
n1=en:articulatory defect | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:aspartylglycosaminuria ---
r_associated #0: 20 -->
en:retardation
n1=en:aspartylglycosaminuria | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:asperger syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:asperger syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:asperger syndrome (rare) ---
r_associated #0: 20 -->
en:retardation
n1=en:asperger syndrome (rare) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:associated with paresthesias and dysesthesias ---
r_associated #0: 20 -->
en:retardation
n1=en:associated with paresthesias and dysesthesias | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:associated with syringomyelia (186700) ---
r_associated #0: 20 -->
en:retardation
n1=en:associated with syringomyelia (186700) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:association between poor metabolizers (pm) and parkinson disease ---
r_associated #0: 20 -->
en:retardation
n1=en:association between poor metabolizers (pm) and parkinson disease | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:asthma ---
r_associated #0: 20 -->
en:retardation
n1=en:asthma | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:astrocyte ---
r_associated #0: 20 -->
en:retardation
n1=en:astrocyte | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:astrocytes show reactive changes ---
r_associated #0: 20 -->
en:retardation
n1=en:astrocytes show reactive changes | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:astrocytic gliosis ---
r_associated #0: 20 -->
en:retardation
n1=en:astrocytic gliosis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:astrocytosis ---
r_associated #0: 20 -->
en:retardation
n1=en:astrocytosis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:astrogliosis (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:astrogliosis (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:asymmetric brain development ---
r_associated #0: 20 -->
en:retardation
n1=en:asymmetric brain development | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:asymmetry at onset (74%) ---
r_associated #0: 20 -->
en:retardation
n1=en:asymmetry at onset (74%) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:asymmetry of symptoms ---
r_associated #0: 20 -->
en:retardation
n1=en:asymmetry of symptoms | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ataxia ---
r_associated #0: 20 -->
en:retardation
n1=en:ataxia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ataxia (1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:ataxia (1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ataxia (cvs+) ---
r_associated #0: 20 -->
en:retardation
n1=en:ataxia (cvs+) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ataxia (deletion patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:ataxia (deletion patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ataxia (early-onset form) ---
r_associated #0: 20 -->
en:retardation
n1=en:ataxia (early-onset form) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ataxia (if untreated) ---
r_associated #0: 20 -->
en:retardation
n1=en:ataxia (if untreated) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ataxia (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:ataxia (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ataxia (less common) ---
r_associated #0: 20 -->
en:retardation
n1=en:ataxia (less common) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ataxia (type i and type ii, infantile and juvenile) ---
r_associated #0: 20 -->
en:retardation
n1=en:ataxia (type i and type ii, infantile and juvenile) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ataxia (uncommon) ---
r_associated #0: 20 -->
en:retardation
n1=en:ataxia (uncommon) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ataxia in those who survive ---
r_associated #0: 20 -->
en:retardation
n1=en:ataxia in those who survive | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ataxia may develop in middle age (less common) ---
r_associated #0: 20 -->
en:retardation
n1=en:ataxia may develop in middle age (less common) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ataxia with febrile episodes (rare) ---
r_associated #0: 20 -->
en:retardation
n1=en:ataxia with febrile episodes (rare) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ataxia with jerky arm movements ---
r_associated #0: 20 -->
en:retardation
n1=en:ataxia with jerky arm movements | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ataxia worsens in the dark ---
r_associated #0: 20 -->
en:retardation
n1=en:ataxia worsens in the dark | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ataxia, (1 family) ---
r_associated #0: 20 -->
en:retardation
n1=en:ataxia, (1 family) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ataxia, cerebellar (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:ataxia, cerebellar (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ataxia, cerebellar (upper and lower limbs affected) ---
r_associated #0: 20 -->
en:retardation
n1=en:ataxia, cerebellar (upper and lower limbs affected) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ataxia, cerebellar, limb and gait ---
r_associated #0: 20 -->
en:retardation
n1=en:ataxia, cerebellar, limb and gait | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ataxia, episodic (episodes last from hours to days) ---
r_associated #0: 20 -->
en:retardation
n1=en:ataxia, episodic (episodes last from hours to days) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ataxia, episodic, occurring after febrile illness or stress ---
r_associated #0: 20 -->
en:retardation
n1=en:ataxia, episodic, occurring after febrile illness or stress | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ataxia, fatal x-linked, with deafness and loss of vision ---
r_associated #0: 20 -->
en:retardation
n1=en:ataxia, fatal x-linked, with deafness and loss of vision | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ataxia, gait and appendicular ---
r_associated #0: 20 -->
en:retardation
n1=en:ataxia, gait and appendicular | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ataxia, mild ---
r_associated #0: 20 -->
en:retardation
n1=en:ataxia, mild | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ataxia, spastic, childhood-onset, autosomal recessive, with optic atrophy and mental retardation ---
r_associated #0: 20 -->
en:retardation
n1=en:ataxia, spastic, childhood-onset, autosomal recessive, with optic atrophy and mental retardation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ataxias, appendicular ---
r_associated #0: 20 -->
en:retardation
n1=en:ataxias, appendicular | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ataxias, sensory ---
r_associated #0: 20 -->
en:retardation
n1=en:ataxias, sensory | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ataxias, truncal ---
r_associated #0: 20 -->
en:retardation
n1=en:ataxias, truncal | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ataxic gait ---
r_associated #0: 20 -->
en:retardation
n1=en:ataxic gait | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ataxic gait (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:ataxic gait (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ataxic gait (juvenile form) ---
r_associated #0: 20 -->
en:retardation
n1=en:ataxic gait (juvenile form) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ataxic movements ---
r_associated #0: 20 -->
en:retardation
n1=en:ataxic movements | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:atelencephaly ---
r_associated #0: 20 -->
en:retardation
n1=en:atelencephaly | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:atherosclerosis excluding heart/brain ---
r_associated #0: 20 -->
en:retardation
n1=en:atherosclerosis excluding heart/brain | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:athetoid and dystonic hand movements (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:athetoid and dystonic hand movements (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:athetosis ---
r_associated #0: 20 -->
en:retardation
n1=en:athetosis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:athetosis (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:athetosis (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:athetosis (later) ---
r_associated #0: 20 -->
en:retardation
n1=en:athetosis (later) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:athetosis, mild (in one patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:athetosis, mild (in one patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:atlantoaxial instability ---
r_associated #0: 20 -->
en:retardation
n1=en:atlantoaxial instability | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:atopic conjunctivitis ---
r_associated #0: 20 -->
en:retardation
n1=en:atopic conjunctivitis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:atopic dermatitis/eczema ---
r_associated #0: 20 -->
en:retardation
n1=en:atopic dermatitis/eczema | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:atresia ---
r_associated #0: 20 -->
en:retardation
n1=en:atresia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:atretic occipital cephalocele ---
r_associated #0: 20 -->
en:retardation
n1=en:atretic occipital cephalocele | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:atrial fibrillation and flutter ---
r_associated #0: 20 -->
en:retardation
n1=en:atrial fibrillation and flutter | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:atrial septal defect ---
r_associated #0: 20 -->
en:retardation
n1=en:atrial septal defect | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:atrophic pons (in some) ---
r_associated #0: 20 -->
en:retardation
n1=en:atrophic pons (in some) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:atrophy and weakness of limb musculature ---
r_associated #0: 20 -->
en:retardation
n1=en:atrophy and weakness of limb musculature | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:atrophy and weakness of the tongue, jaw, and throat muscles ---
r_associated #0: 20 -->
en:retardation
n1=en:atrophy and weakness of the tongue, jaw, and throat muscles | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:atrophy may be more severe in the left hemisphere ---
r_associated #0: 20 -->
en:retardation
n1=en:atrophy may be more severe in the left hemisphere | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:atrophy of cerebellum, brainstem, cervical spinal cord ---
r_associated #0: 20 -->
en:retardation
n1=en:atrophy of cerebellum, brainstem, cervical spinal cord | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:atrophy of corpus callosum ---
r_associated #0: 20 -->
en:retardation
n1=en:atrophy of corpus callosum | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:atrophy of hippocampal dentate gyrus ---
r_associated #0: 20 -->
en:retardation
n1=en:atrophy of hippocampal dentate gyrus | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:atrophy of pyramids ---
r_associated #0: 20 -->
en:retardation
n1=en:atrophy of pyramids | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:atrophy of the cerebellar vermis seen on mri ---
r_associated #0: 20 -->
en:retardation
n1=en:atrophy of the cerebellar vermis seen on mri | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:atrophy of the dentate nucleus ---
r_associated #0: 20 -->
en:retardation
n1=en:atrophy of the dentate nucleus | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:atrophy of the frontal and parietal cortex ---
r_associated #0: 20 -->
en:retardation
n1=en:atrophy of the frontal and parietal cortex | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:atrophy of the granular cell layer of the cerebellum ---
r_associated #0: 20 -->
en:retardation
n1=en:atrophy of the granular cell layer of the cerebellum | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:atrophy of the motor cortex in older patients seen on mri ---
r_associated #0: 20 -->
en:retardation
n1=en:atrophy of the motor cortex in older patients seen on mri | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:atrophy of the pituitary (1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:atrophy of the pituitary (1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:atrophy of the pons (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:atrophy of the pons (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:atrophy of the posterior columns and spinocerebellar tracts ---
r_associated #0: 20 -->
en:retardation
n1=en:atrophy of the posterior columns and spinocerebellar tracts | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:atrophy of the spinal cord ---
r_associated #0: 20 -->
en:retardation
n1=en:atrophy of the spinal cord | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:atrophy of the spinal cord and cerebellar tracts ---
r_associated #0: 20 -->
en:retardation
n1=en:atrophy of the spinal cord and cerebellar tracts | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:atrophy, thin hemisphere ---
r_associated #0: 20 -->
en:retardation
n1=en:atrophy, thin hemisphere | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:atrophy/degeneration involving the spinal cord ---
r_associated #0: 20 -->
en:retardation
n1=en:atrophy/degeneration involving the spinal cord | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:attacks characterized by lethargy, incoordination, loss of motor skills ---
r_associated #0: 20 -->
en:retardation
n1=en:attacks characterized by lethargy, incoordination, loss of motor skills | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:attacks of disabling daytime drowsiness and low alertness ---
r_associated #0: 20 -->
en:retardation
n1=en:attacks of disabling daytime drowsiness and low alertness | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:attention deficit conduct and disruptive behavior disorders ---
r_associated #0: 20 -->
en:retardation
n1=en:attention deficit conduct and disruptive behavior disorders | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:attention deficit disorder ---
r_associated #0: 20 -->
en:retardation
n1=en:attention deficit disorder | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:attention deficit hyperactivity disorder ---
r_associated #0: 20 -->
en:retardation
n1=en:attention deficit hyperactivity disorder | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:attenuated gyri ---
r_associated #0: 20 -->
en:retardation
n1=en:attenuated gyri | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:atypical absence seizure ---
r_associated #0: 20 -->
en:retardation
n1=en:atypical absence seizure | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:atypical absence, atonic/tonic, or tonic-clonic seizures ---
r_associated #0: 20 -->
en:retardation
n1=en:atypical absence, atonic/tonic, or tonic-clonic seizures | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:auditory auras ---
r_associated #0: 20 -->
en:retardation
n1=en:auditory auras | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:auditory, olfactory, and visual auras ---
r_associated #0: 20 -->
en:retardation
n1=en:auditory, olfactory, and visual auras | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:aura ---
r_associated #0: 20 -->
en:retardation
n1=en:aura | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:aura (in some instances) ---
r_associated #0: 20 -->
en:retardation
n1=en:aura (in some instances) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:aura may occur ---
r_associated #0: 20 -->
en:retardation
n1=en:aura may occur | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:autism ---
r_associated #0: 20 -->
en:retardation
n1=en:autism | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:autism (rare) ---
r_associated #0: 20 -->
en:retardation
n1=en:autism (rare) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:autism or autistic features ---
r_associated #0: 20 -->
en:retardation
n1=en:autism or autistic features | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:autofluorescent lipopigment in neurons ---
r_associated #0: 20 -->
en:retardation
n1=en:autofluorescent lipopigment in neurons | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:autofluorescent pigment in microglia and macrophages ---
r_associated #0: 20 -->
en:retardation
n1=en:autofluorescent pigment in microglia and macrophages | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:automatism ---
r_associated #0: 20 -->
en:retardation
n1=en:automatism | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:autonomic abnormalities ---
r_associated #0: 20 -->
en:retardation
n1=en:autonomic abnormalities | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:autonomic disturbances ---
r_associated #0: 20 -->
en:retardation
n1=en:autonomic disturbances | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:autonomic dysfunction (in patients with hsan2d) ---
r_associated #0: 20 -->
en:retardation
n1=en:autonomic dysfunction (in patients with hsan2d) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:autonomic dysfunction may occur ---
r_associated #0: 20 -->
en:retardation
n1=en:autonomic dysfunction may occur | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:autonomic dysregulation ---
r_associated #0: 20 -->
en:retardation
n1=en:autonomic dysregulation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:autonomic features may occur ---
r_associated #0: 20 -->
en:retardation
n1=en:autonomic features may occur | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:autonomic features may occur (diaphoresis, tachycardia, hyperthermia, hypertension) ---
r_associated #0: 20 -->
en:retardation
n1=en:autonomic features may occur (diaphoresis, tachycardia, hyperthermia, hypertension) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:autonomic instability (22%) ---
r_associated #0: 20 -->
en:retardation
n1=en:autonomic instability (22%) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:autonomic involvement ---
r_associated #0: 20 -->
en:retardation
n1=en:autonomic involvement | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:autonomic involvement affecting limbs during episodes ---
r_associated #0: 20 -->
en:retardation
n1=en:autonomic involvement affecting limbs during episodes | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:autonomic involvement may occur ---
r_associated #0: 20 -->
en:retardation
n1=en:autonomic involvement may occur | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:autonomic manifestations ---
r_associated #0: 20 -->
en:retardation
n1=en:autonomic manifestations | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:autonomic nervous system disorders ---
r_associated #0: 20 -->
en:retardation
n1=en:autonomic nervous system disorders | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:autonomic signs ---
r_associated #0: 20 -->
en:retardation
n1=en:autonomic signs | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:autonomic symptoms ---
r_associated #0: 20 -->
en:retardation
n1=en:autonomic symptoms | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:average intellect ---
r_associated #0: 20 -->
en:retardation
n1=en:average intellect | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:axenfeld-rieger anomaly with partially absent eye muscles, distinctive face, hydrocephaly, and skeletal abnormalities ---
r_associated #0: 20 -->
en:retardation
n1=en:axenfeld-rieger anomaly with partially absent eye muscles, distinctive face, hydrocephaly, and skeletal abnormalities | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:axial dystonia ---
r_associated #0: 20 -->
en:retardation
n1=en:axial dystonia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:axial hypotonia (1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:axial hypotonia (1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:axial hypotonia (rare) ---
r_associated #0: 20 -->
en:retardation
n1=en:axial hypotonia (rare) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:axial imbalance (34%) ---
r_associated #0: 20 -->
en:retardation
n1=en:axial imbalance (34%) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:axial muscle stiffness, symmetric ---
r_associated #0: 20 -->
en:retardation
n1=en:axial muscle stiffness, symmetric | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:axial rigidity ---
r_associated #0: 20 -->
en:retardation
n1=en:axial rigidity | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:axis i diagnosis ---
r_associated #0: 20 -->
en:retardation
n1=en:axis i diagnosis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:axis ii diagnosis ---
r_associated #0: 20 -->
en:retardation
n1=en:axis ii diagnosis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:axis iii diagnosis ---
r_associated #0: 20 -->
en:retardation
n1=en:axis iii diagnosis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:axis iv diagnosis ---
r_associated #0: 20 -->
en:retardation
n1=en:axis iv diagnosis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:axis v diagnosis ---
r_associated #0: 20 -->
en:retardation
n1=en:axis v diagnosis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:axonal 'spheroid' inclusions ---
r_associated #0: 20 -->
en:retardation
n1=en:axonal 'spheroid' inclusions | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:axonal 'spheroid' inclusions in the cns ---
r_associated #0: 20 -->
en:retardation
n1=en:axonal 'spheroid' inclusions in the cns | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:axonal dystrophy ---
r_associated #0: 20 -->
en:retardation
n1=en:axonal dystrophy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:axonal dystrophy (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:axonal dystrophy (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:axonal loss ---
r_associated #0: 20 -->
en:retardation
n1=en:axonal loss | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:axonal loss and gliosis in the corticospinal tracts ---
r_associated #0: 20 -->
en:retardation
n1=en:axonal loss and gliosis in the corticospinal tracts | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:axonal spheroids ---
r_associated #0: 20 -->
en:retardation
n1=en:axonal spheroids | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:axonal spheroids in the dorsal column ---
r_associated #0: 20 -->
en:retardation
n1=en:axonal spheroids in the dorsal column | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:axonal swelling of spinal nerve roots and cranial nerves ---
r_associated #0: 20 -->
en:retardation
n1=en:axonal swelling of spinal nerve roots and cranial nerves | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:axonal swelling or thickening ---
r_associated #0: 20 -->
en:retardation
n1=en:axonal swelling or thickening | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:axonal swelling or thickening in the cns ---
r_associated #0: 20 -->
en:retardation
n1=en:axonal swelling or thickening in the cns | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:axonal swellings or spheroids ---
r_associated #0: 20 -->
en:retardation
n1=en:axonal swellings or spheroids | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:babinski sign ---
r_associated #0: 20 -->
en:retardation
n1=en:babinski sign | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:back pain ---
r_associated #0: 20 -->
en:retardation
n1=en:back pain | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:background slowing ---
r_associated #0: 20 -->
en:retardation
n1=en:background slowing | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:balanitis ---
r_associated #0: 20 -->
en:retardation
n1=en:balanitis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:baller-gerold syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:baller-gerold syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:balloon cells (in type iib) ---
r_associated #0: 20 -->
en:retardation
n1=en:balloon cells (in type iib) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ballooned neurons ---
r_associated #0: 20 -->
en:retardation
n1=en:ballooned neurons | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:band heterotopia (1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:band heterotopia (1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:bardet-biedl syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:bardet-biedl syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:bardet-biedl syndrome 1 (disorder) ---
r_associated #0: 20 -->
en:retardation
n1=en:bardet-biedl syndrome 1 (disorder) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:bardet-biedl syndrome 13 ---
r_associated #0: 20 -->
en:retardation
n1=en:bardet-biedl syndrome 13 | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:bardet-biedl syndrome 14 (disorder) ---
r_associated #0: 20 -->
en:retardation
n1=en:bardet-biedl syndrome 14 (disorder) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:bardet-biedl syndrome 16 ---
r_associated #0: 20 -->
en:retardation
n1=en:bardet-biedl syndrome 16 | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:bardet-biedl syndrome 2 (disorder) ---
r_associated #0: 20 -->
en:retardation
n1=en:bardet-biedl syndrome 2 (disorder) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:bardet-biedl syndrome 6 ---
r_associated #0: 20 -->
en:retardation
n1=en:bardet-biedl syndrome 6 | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:bardet-biedl syndrome 7 ---
r_associated #0: 20 -->
en:retardation
n1=en:bardet-biedl syndrome 7 | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:bardet-biedl syndrome 8 ---
r_associated #0: 20 -->
en:retardation
n1=en:bardet-biedl syndrome 8 | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:bardet-biedl syndrome 9 ---
r_associated #0: 20 -->
en:retardation
n1=en:bardet-biedl syndrome 9 | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:bartter syndrome, antenatal type 1 ---
r_associated #0: 20 -->
en:retardation
n1=en:bartter syndrome, antenatal type 1 | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:bartter syndrome, antenatal, type 2 ---
r_associated #0: 20 -->
en:retardation
n1=en:bartter syndrome, antenatal, type 2 | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:bartter syndrome, type 4a ---
r_associated #0: 20 -->
en:retardation
n1=en:bartter syndrome, type 4a | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:bartter syndrome, type 4b ---
r_associated #0: 20 -->
en:retardation
n1=en:bartter syndrome, type 4b | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:basal ganglia atrophy ---
r_associated #0: 20 -->
en:retardation
n1=en:basal ganglia atrophy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:basal ganglia atrophy, progressive ---
r_associated #0: 20 -->
en:retardation
n1=en:basal ganglia atrophy, progressive | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:basal ganglia calcification ---
r_associated #0: 20 -->
en:retardation
n1=en:basal ganglia calcification | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:basal ganglia calcifications (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:basal ganglia calcifications (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:basal ganglia calcifications (rare) ---
r_associated #0: 20 -->
en:retardation
n1=en:basal ganglia calcifications (rare) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:basal ganglia cysts ---
r_associated #0: 20 -->
en:retardation
n1=en:basal ganglia cysts | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:basal ganglia dysfunction ---
r_associated #0: 20 -->
en:retardation
n1=en:basal ganglia dysfunction | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:basal ganglia gliosis ---
r_associated #0: 20 -->
en:retardation
n1=en:basal ganglia gliosis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:basal ganglia lesions may be present before onset of clinical symptoms ---
r_associated #0: 20 -->
en:retardation
n1=en:basal ganglia lesions may be present before onset of clinical symptoms | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:basal ganglia lesions seen on mri ---
r_associated #0: 20 -->
en:retardation
n1=en:basal ganglia lesions seen on mri | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:basal ganglia lucencies ---
r_associated #0: 20 -->
en:retardation
n1=en:basal ganglia lucencies | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:basal ganglion degeneration ---
r_associated #0: 20 -->
en:retardation
n1=en:basal ganglion degeneration | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:bathing disability ---
r_associated #0: 20 -->
en:retardation
n1=en:bathing disability | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:beaulieu-boycott-innes syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:beaulieu-boycott-innes syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:begins in limbs, later generalized (childhood onset) ---
r_associated #0: 20 -->
en:retardation
n1=en:begins in limbs, later generalized (childhood onset) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:behavior disorders ---
r_associated #0: 20 -->
en:retardation
n1=en:behavior disorders | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:behavioral and emotional disorder with onset in childhood ---
r_associated #0: 20 -->
en:retardation
n1=en:behavioral and emotional disorder with onset in childhood | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:behavioral disability ---
r_associated #0: 20 -->
en:retardation
n1=en:behavioral disability | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:behavioral syndrome associated with physiological disturbance and physical factors ---
r_associated #0: 20 -->
en:retardation
n1=en:behavioral syndrome associated with physiological disturbance and physical factors | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:behavioral variant of frontotemporal dementia ---
r_associated #0: 20 -->
en:retardation
n1=en:behavioral variant of frontotemporal dementia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:behaviors, adaptive ---
r_associated #0: 20 -->
en:retardation
n1=en:behaviors, adaptive | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:behr syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:behr syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:benign digestive system neoplasm ---
r_associated #0: 20 -->
en:retardation
n1=en:benign digestive system neoplasm | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:benign female breast neoplasm ---
r_associated #0: 20 -->
en:retardation
n1=en:benign female breast neoplasm | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:benign neoplasm of male genital organ ---
r_associated #0: 20 -->
en:retardation
n1=en:benign neoplasm of male genital organ | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:benign nervous system neoplasm ---
r_associated #0: 20 -->
en:retardation
n1=en:benign nervous system neoplasm | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:benign obstetric neoplasm ---
r_associated #0: 20 -->
en:retardation
n1=en:benign obstetric neoplasm | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:benign prostatic hyperplasia ---
r_associated #0: 20 -->
en:retardation
n1=en:benign prostatic hyperplasia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:benign respiratory neoplasm ---
r_associated #0: 20 -->
en:retardation
n1=en:benign respiratory neoplasm | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:benign thyroid gland neoplasm ---
r_associated #0: 20 -->
en:retardation
n1=en:benign thyroid gland neoplasm | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:benign urinary system neoplasm ---
r_associated #0: 20 -->
en:retardation
n1=en:benign urinary system neoplasm | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:benign/unspecified neoplasms ---
r_associated #0: 20 -->
en:retardation
n1=en:benign/unspecified neoplasms | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:beta-amyloid-positive senile plaques ---
r_associated #0: 20 -->
en:retardation
n1=en:beta-amyloid-positive senile plaques | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:beta-mannosidosis ---
r_associated #0: 20 -->
en:retardation
n1=en:beta-mannosidosis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:between 2 and 7% of children will develop afebrile seizure disorders later in life ---
r_associated #0: 20 -->
en:retardation
n1=en:between 2 and 7% of children will develop afebrile seizure disorders later in life | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:biemond syndrome ii ---
r_associated #0: 20 -->
en:retardation
n1=en:biemond syndrome ii | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:bilateral calcification of basal ganglia and cerebellum ---
r_associated #0: 20 -->
en:retardation
n1=en:bilateral calcification of basal ganglia and cerebellum | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:bilateral convulsive seizures ---
r_associated #0: 20 -->
en:retardation
n1=en:bilateral convulsive seizures | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:bilateral perisylvian cortical malformations on mri ---
r_associated #0: 20 -->
en:retardation
n1=en:bilateral perisylvian cortical malformations on mri | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:bilateral schizencephaly ---
r_associated #0: 20 -->
en:retardation
n1=en:bilateral schizencephaly | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:bilateral signals in the basal ganglia ---
r_associated #0: 20 -->
en:retardation
n1=en:bilateral signals in the basal ganglia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:bilateral striatal lucencies on imaging ---
r_associated #0: 20 -->
en:retardation
n1=en:bilateral striatal lucencies on imaging | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:bilateral striatal necrosis ---
r_associated #0: 20 -->
en:retardation
n1=en:bilateral striatal necrosis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:bilateral thalamic lesions on mri ---
r_associated #0: 20 -->
en:retardation
n1=en:bilateral thalamic lesions on mri | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:bilateral, symmetric intracerebral calcifications, especially in the basal ganglia and periventricular areas ---
r_associated #0: 20 -->
en:retardation
n1=en:bilateral, symmetric intracerebral calcifications, especially in the basal ganglia and periventricular areas | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:biliary atresia ---
r_associated #0: 20 -->
en:retardation
n1=en:biliary atresia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:biopsy in both types shows neuronal cytomegaly (large, bizarre, maloriented neurons) in the laminar cortex ---
r_associated #0: 20 -->
en:retardation
n1=en:biopsy in both types shows neuronal cytomegaly (large, bizarre, maloriented neurons) in the laminar cortex | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:biopsy shows foamy lipid-laden macrophages ---
r_associated #0: 20 -->
en:retardation
n1=en:biopsy shows foamy lipid-laden macrophages | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:biopsy shows white matter hypomyelination, demyelination, gliosis ---
r_associated #0: 20 -->
en:retardation
n1=en:biopsy shows white matter hypomyelination, demyelination, gliosis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:bipolar and related disorders ---
r_associated #0: 20 -->
en:retardation
n1=en:bipolar and related disorders | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:bipolar disorder ---
r_associated #0: 20 -->
en:retardation
n1=en:bipolar disorder | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:blake's pouch (rare) ---
r_associated #0: 20 -->
en:retardation
n1=en:blake's pouch (rare) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:blepharitis/stye/chalazion ---
r_associated #0: 20 -->
en:retardation
n1=en:blepharitis/stye/chalazion | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:blepharophimosis syndrome ohdo type ---
r_associated #0: 20 -->
en:retardation
n1=en:blepharophimosis syndrome ohdo type | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:blepharophimosis with facial and genital anomalies and mental retardation ---
r_associated #0: 20 -->
en:retardation
n1=en:blepharophimosis with facial and genital anomalies and mental retardation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:blindness ---
r_associated #0: 20 -->
en:retardation
n1=en:blindness | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:blindness all degrees/types ---
r_associated #0: 20 -->
en:retardation
n1=en:blindness all degrees/types | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:blocked lacrimal duct of infant ---
r_associated #0: 20 -->
en:retardation
n1=en:blocked lacrimal duct of infant | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:blood-brain barrier ---
r_associated #0: 20 -->
en:retardation
n1=en:blood-brain barrier | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:blurring of the gray-white junction (in type iib) ---
r_associated #0: 20 -->
en:retardation
n1=en:blurring of the gray-white junction (in type iib) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:blurry cortical-white matter junction due to spillover of abnormal neurons (in type iib) ---
r_associated #0: 20 -->
en:retardation
n1=en:blurry cortical-white matter junction due to spillover of abnormal neurons (in type iib) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:board and poorly defined gyri ---
r_associated #0: 20 -->
en:retardation
n1=en:board and poorly defined gyri | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:body mass index 30+ - obesity ---
r_associated #0: 20 -->
en:retardation
n1=en:body mass index 30+ - obesity | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:boil/abscess nose ---
r_associated #0: 20 -->
en:retardation
n1=en:boil/abscess nose | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:borderline intelligence ---
r_associated #0: 20 -->
en:retardation
n1=en:borderline intelligence | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:borderline mental retardation (i.q. 70-85) ---
r_associated #0: 20 -->
en:retardation
n1=en:borderline mental retardation (i.q. 70-85) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:bowen-conradi syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:bowen-conradi syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:brachydactyly, type a1, with short stature, scoliosis, microcephaly, ptosis, hearing loss, and mental retardation ---
r_associated #0: 20 -->
en:retardation
n1=en:brachydactyly, type a1, with short stature, scoliosis, microcephaly, ptosis, hearing loss, and mental retardation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:bradykinesia ---
r_associated #0: 20 -->
en:retardation
n1=en:bradykinesia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:bradykinesia (in severe cases) ---
r_associated #0: 20 -->
en:retardation
n1=en:bradykinesia (in severe cases) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:brain ---
r_associated #0: 20 -->
en:retardation
n1=en:brain | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:brain abscess ---
r_associated #0: 20 -->
en:retardation
n1=en:brain abscess | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:brain and spinal cord structure ---
r_associated #0: 20 -->
en:retardation
n1=en:brain and spinal cord structure | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:brain atrophy (1 family) ---
r_associated #0: 20 -->
en:retardation
n1=en:brain atrophy (1 family) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:brain atrophy (1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:brain atrophy (1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:brain atrophy (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:brain atrophy (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:brain atrophy seen on mri ---
r_associated #0: 20 -->
en:retardation
n1=en:brain atrophy seen on mri | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:brain atrophy, particularly of the frontal and temporal lobes ---
r_associated #0: 20 -->
en:retardation
n1=en:brain atrophy, particularly of the frontal and temporal lobes | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:brain calcification (if left untreated) ---
r_associated #0: 20 -->
en:retardation
n1=en:brain calcification (if left untreated) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:brain cell ---
r_associated #0: 20 -->
en:retardation
n1=en:brain cell | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:brain cerebrospinal fluid pathway ---
r_associated #0: 20 -->
en:retardation
n1=en:brain cerebrospinal fluid pathway | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:brain circuit ---
r_associated #0: 20 -->
en:retardation
n1=en:brain circuit | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:brain commissure ---
r_associated #0: 20 -->
en:retardation
n1=en:brain commissure | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:brain edema ---
r_associated #0: 20 -->
en:retardation
n1=en:brain edema | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:brain edema following head injury (less common) ---
r_associated #0: 20 -->
en:retardation
n1=en:brain edema following head injury (less common) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:brain imaging shows calcification of the dentate nucleus ---
r_associated #0: 20 -->
en:retardation
n1=en:brain imaging shows calcification of the dentate nucleus | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:brain imaging shows cortical atrophy ---
r_associated #0: 20 -->
en:retardation
n1=en:brain imaging shows cortical atrophy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:brain imaging shows decreased white matter density ---
r_associated #0: 20 -->
en:retardation
n1=en:brain imaging shows decreased white matter density | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:brain imaging shows diffuse white matter abnormalities ---
r_associated #0: 20 -->
en:retardation
n1=en:brain imaging shows diffuse white matter abnormalities | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:brain imaging shows functional defects in the cortical and subcortical motor-related areas of the frontal lobe ---
r_associated #0: 20 -->
en:retardation
n1=en:brain imaging shows functional defects in the cortical and subcortical motor-related areas of the frontal lobe | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:brain imaging shows generalized atrophy ---
r_associated #0: 20 -->
en:retardation
n1=en:brain imaging shows generalized atrophy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:brain imaging shows hypomyelination ---
r_associated #0: 20 -->
en:retardation
n1=en:brain imaging shows hypomyelination | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:brain imaging shows lesions in the thalami, brainstem, and cerebellum ---
r_associated #0: 20 -->
en:retardation
n1=en:brain imaging shows lesions in the thalami, brainstem, and cerebellum | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:brain imaging shows white-matter hypodensities and demyelination ---
r_associated #0: 20 -->
en:retardation
n1=en:brain imaging shows white-matter hypodensities and demyelination | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:brain injury ---
r_associated #0: 20 -->
en:retardation
n1=en:brain injury | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:brain iron accumulation (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:brain iron accumulation (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:brain iron accumulation in the basal ganglia (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:brain iron accumulation in the basal ganglia (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:brain morphology ---
r_associated #0: 20 -->
en:retardation
n1=en:brain morphology | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:brain mri shows abnormal cortical thickening in the anteromesial frontal areas (1 family) ---
r_associated #0: 20 -->
en:retardation
n1=en:brain mri shows abnormal cortical thickening in the anteromesial frontal areas (1 family) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:brain mri shows abnormal gyral pattern in frontal lobes ---
r_associated #0: 20 -->
en:retardation
n1=en:brain mri shows abnormal gyral pattern in frontal lobes | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:brain mri shows arrest in myelination ---
r_associated #0: 20 -->
en:retardation
n1=en:brain mri shows arrest in myelination | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:brain mri shows cerebellar atrophy ---
r_associated #0: 20 -->
en:retardation
n1=en:brain mri shows cerebellar atrophy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:brain mri shows cerebellar atrophy (1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:brain mri shows cerebellar atrophy (1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:brain mri shows cerebellar hypoplasia ---
r_associated #0: 20 -->
en:retardation
n1=en:brain mri shows cerebellar hypoplasia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:brain mri shows cortical atrophy ---
r_associated #0: 20 -->
en:retardation
n1=en:brain mri shows cortical atrophy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:brain mri shows diffusion abnormalities ---
r_associated #0: 20 -->
en:retardation
n1=en:brain mri shows diffusion abnormalities | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:brain mri shows flattening of the ventral pons ---
r_associated #0: 20 -->
en:retardation
n1=en:brain mri shows flattening of the ventral pons | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:brain mri shows hyperintensities in the basal ganglia ---
r_associated #0: 20 -->
en:retardation
n1=en:brain mri shows hyperintensities in the basal ganglia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:brain mri shows hypoplasia of the corpus callosum ---
r_associated #0: 20 -->
en:retardation
n1=en:brain mri shows hypoplasia of the corpus callosum | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:brain mri shows hypoplastic pituitary ---
r_associated #0: 20 -->
en:retardation
n1=en:brain mri shows hypoplastic pituitary | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:brain mri shows lesions consistent with epileptic episodes ---
r_associated #0: 20 -->
en:retardation
n1=en:brain mri shows lesions consistent with epileptic episodes | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:brain mri shows lesions in the basal ganglia ---
r_associated #0: 20 -->
en:retardation
n1=en:brain mri shows lesions in the basal ganglia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:brain mri shows molar tooth sign ---
r_associated #0: 20 -->
en:retardation
n1=en:brain mri shows molar tooth sign | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:brain mri shows proportionate pontocerebellar hypoplasia ---
r_associated #0: 20 -->
en:retardation
n1=en:brain mri shows proportionate pontocerebellar hypoplasia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:brain mri shows signal abnormalities in the basal ganglia ---
r_associated #0: 20 -->
en:retardation
n1=en:brain mri shows signal abnormalities in the basal ganglia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:brain mri shows t2-weighted hyperintensities (17%) ---
r_associated #0: 20 -->
en:retardation
n1=en:brain mri shows t2-weighted hyperintensities (17%) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:brain mrs shows decreased creatine content ---
r_associated #0: 20 -->
en:retardation
n1=en:brain mrs shows decreased creatine content | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:brain mrs shows reduced choline and inositol peaks in the parieto-occipital white matter ---
r_associated #0: 20 -->
en:retardation
n1=en:brain mrs shows reduced choline and inositol peaks in the parieto-occipital white matter | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:brain part ---
r_associated #0: 20 -->
en:retardation
n1=en:brain part | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:brain pathway ---
r_associated #0: 20 -->
en:retardation
n1=en:brain pathway | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:brain prp-immunoreactive amyloid plaques (in 10% if patients with sporadic cjd and in variant cjd) ---
r_associated #0: 20 -->
en:retardation
n1=en:brain prp-immunoreactive amyloid plaques (in 10% if patients with sporadic cjd and in variant cjd) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:brain region ---
r_associated #0: 20 -->
en:retardation
n1=en:brain region | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:brain regulatory center ---
r_associated #0: 20 -->
en:retardation
n1=en:brain regulatory center | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:brain small vessel disease with hemorrhage ---
r_associated #0: 20 -->
en:retardation
n1=en:brain small vessel disease with hemorrhage | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:brain stem ---
r_associated #0: 20 -->
en:retardation
n1=en:brain stem | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:brain stem atrophy ---
r_associated #0: 20 -->
en:retardation
n1=en:brain stem atrophy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:brain stem atrophy, progressive ---
r_associated #0: 20 -->
en:retardation
n1=en:brain stem atrophy, progressive | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:brain stem disorder ---
r_associated #0: 20 -->
en:retardation
n1=en:brain stem disorder | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:brain subcortex ---
r_associated #0: 20 -->
en:retardation
n1=en:brain subcortex | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:brain tissue shows abnormal spherical aggregates of iron and ferritin in the basal ganglia, forebrain, and cerebellum ---
r_associated #0: 20 -->
en:retardation
n1=en:brain tissue shows abnormal spherical aggregates of iron and ferritin in the basal ganglia, forebrain, and cerebellum | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:brain tissue shows cavitation of the basal ganglia ---
r_associated #0: 20 -->
en:retardation
n1=en:brain tissue shows cavitation of the basal ganglia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:brain vascular anomalies (rare) ---
r_associated #0: 20 -->
en:retardation
n1=en:brain vascular anomalies (rare) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:brain ventricle ---
r_associated #0: 20 -->
en:retardation
n1=en:brain ventricle | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:brain white matter hyperintensities on mri ---
r_associated #0: 20 -->
en:retardation
n1=en:brain white matter hyperintensities on mri | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:brainstem atrophy ---
r_associated #0: 20 -->
en:retardation
n1=en:brainstem atrophy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:brainstem concavity ---
r_associated #0: 20 -->
en:retardation
n1=en:brainstem concavity | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:brainstem damage ---
r_associated #0: 20 -->
en:retardation
n1=en:brainstem damage | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:brainstem dysplasia ---
r_associated #0: 20 -->
en:retardation
n1=en:brainstem dysplasia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:brainstem hypoplasia (1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:brainstem hypoplasia (1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:brainstem hypoplasia (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:brainstem hypoplasia (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:brainstem lesions, hyperintense on t2-weighted imaging ---
r_associated #0: 20 -->
en:retardation
n1=en:brainstem lesions, hyperintense on t2-weighted imaging | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:brainstem may show neuronal loss ---
r_associated #0: 20 -->
en:retardation
n1=en:brainstem may show neuronal loss | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:brainstem white matter lesions ---
r_associated #0: 20 -->
en:retardation
n1=en:brainstem white matter lesions | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:branchial cleft remnant ---
r_associated #0: 20 -->
en:retardation
n1=en:branchial cleft remnant | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:breast disorder in pregnancy/puerperium other ---
r_associated #0: 20 -->
en:retardation
n1=en:breast disorder in pregnancy/puerperium other | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:breathing difficulty due to vocal cord paralysis ---
r_associated #0: 20 -->
en:retardation
n1=en:breathing difficulty due to vocal cord paralysis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:brief involuntary movements of upper extremities ---
r_associated #0: 20 -->
en:retardation
n1=en:brief involuntary movements of upper extremities | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:brisk knee reflexes (early-on) ---
r_associated #0: 20 -->
en:retardation
n1=en:brisk knee reflexes (early-on) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:brisk lower limb reflexes (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:brisk lower limb reflexes (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:brisk reflexes ---
r_associated #0: 20 -->
en:retardation
n1=en:brisk reflexes | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:brisk reflexes (1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:brisk reflexes (1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:brisk tendon reflex ---
r_associated #0: 20 -->
en:retardation
n1=en:brisk tendon reflex | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:broad gait ---
r_associated #0: 20 -->
en:retardation
n1=en:broad gait | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:broad-based gait ---
r_associated #0: 20 -->
en:retardation
n1=en:broad-based gait | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:broad-based gait (1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:broad-based gait (1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:broca's aphasia ---
r_associated #0: 20 -->
en:retardation
n1=en:broca's aphasia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:bruxism ---
r_associated #0: 20 -->
en:retardation
n1=en:bruxism | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:buccolingofacial dyspraxia ---
r_associated #0: 20 -->
en:retardation
n1=en:buccolingofacial dyspraxia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:bulbar and upper limb symptoms more severe than lower limb symptoms ---
r_associated #0: 20 -->
en:retardation
n1=en:bulbar and upper limb symptoms more severe than lower limb symptoms | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:bulbar dysfunction ---
r_associated #0: 20 -->
en:retardation
n1=en:bulbar dysfunction | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:bulbar dysfunction (e.g. dysarthria and dysphagia) ---
r_associated #0: 20 -->
en:retardation
n1=en:bulbar dysfunction (e.g. dysarthria and dysphagia) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:bulbar dysfunction (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:bulbar dysfunction (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:bulbar dysfunction (juvenile-onset, less common) ---
r_associated #0: 20 -->
en:retardation
n1=en:bulbar dysfunction (juvenile-onset, less common) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:bulbar involvement ---
r_associated #0: 20 -->
en:retardation
n1=en:bulbar involvement | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:bulbar paresis ---
r_associated #0: 20 -->
en:retardation
n1=en:bulbar paresis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:bulbar signs ---
r_associated #0: 20 -->
en:retardation
n1=en:bulbar signs | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:bulbar spasticity ---
r_associated #0: 20 -->
en:retardation
n1=en:bulbar spasticity | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:bulbar symptoms may occur (less common) ---
r_associated #0: 20 -->
en:retardation
n1=en:bulbar symptoms may occur (less common) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:bulbar weakness ---
r_associated #0: 20 -->
en:retardation
n1=en:bulbar weakness | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:bulbus cordis anomalies and anomalies of cardiac septal closure ---
r_associated #0: 20 -->
en:retardation
n1=en:bulbus cordis anomalies and anomalies of cardiac septal closure | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:bulging of the caudate nuclei ---
r_associated #0: 20 -->
en:retardation
n1=en:bulging of the caudate nuclei | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:burning or tingling of plantar surface of foot (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:burning or tingling of plantar surface of foot (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:burning pain in the limbs ---
r_associated #0: 20 -->
en:retardation
n1=en:burning pain in the limbs | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:burst suppression pattern on neonatal eeg ---
r_associated #0: 20 -->
en:retardation
n1=en:burst suppression pattern on neonatal eeg | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:burst suppression pattern seen on eeg ---
r_associated #0: 20 -->
en:retardation
n1=en:burst suppression pattern seen on eeg | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:by 10-15 years after onset, postural dystonia spreads to all limbs ---
r_associated #0: 20 -->
en:retardation
n1=en:by 10-15 years after onset, postural dystonia spreads to all limbs | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:c3hex, decreased ability to smell ---
r_associated #0: 20 -->
en:retardation
n1=en:c3hex, decreased ability to smell | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:calcification in the pons and cerebellum ---
r_associated #0: 20 -->
en:retardation
n1=en:calcification in the pons and cerebellum | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:calcification may occur in other brain regions, including cerebellum, thalamus, white matter ---
r_associated #0: 20 -->
en:retardation
n1=en:calcification may occur in other brain regions, including cerebellum, thalamus, white matter | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:calcification of the amygdala and the amygdala-hippocampal transition area ---
r_associated #0: 20 -->
en:retardation
n1=en:calcification of the amygdala and the amygdala-hippocampal transition area | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:calcification of the falx ---
r_associated #0: 20 -->
en:retardation
n1=en:calcification of the falx | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:calcifications in white matter, basal ganglia, brainstem, cerebellum, and spinal cord ---
r_associated #0: 20 -->
en:retardation
n1=en:calcifications in white matter, basal ganglia, brainstem, cerebellum, and spinal cord | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:calcifications may be seen in the thalamus, hippocampus, subcortical white matter, and cortex ---
r_associated #0: 20 -->
en:retardation
n1=en:calcifications may be seen in the thalamus, hippocampus, subcortical white matter, and cortex | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:calcifications of cerebral ventricles ---
r_associated #0: 20 -->
en:retardation
n1=en:calcifications of cerebral ventricles | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:calicification of the falx cerebri ---
r_associated #0: 20 -->
en:retardation
n1=en:calicification of the falx cerebri | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:camptodactyly syndrome, guadalajara type i ---
r_associated #0: 20 -->
en:retardation
n1=en:camptodactyly syndrome, guadalajara type i | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:candidal meningitis (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:candidal meningitis (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:carbamoyl-phosphate synthetase i deficiency ---
r_associated #0: 20 -->
en:retardation
n1=en:carbamoyl-phosphate synthetase i deficiency | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:carcinomatosis (unknown primary site) ---
r_associated #0: 20 -->
en:retardation
n1=en:carcinomatosis (unknown primary site) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cardiac and circulatory congenital anomalies ---
r_associated #0: 20 -->
en:retardation
n1=en:cardiac and circulatory congenital anomalies | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cardiovascular abnormalities ---
r_associated #0: 20 -->
en:retardation
n1=en:cardiovascular abnormalities | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cardiovascular neoplasm ---
r_associated #0: 20 -->
en:retardation
n1=en:cardiovascular neoplasm | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:caroli disease ---
r_associated #0: 20 -->
en:retardation
n1=en:caroli disease | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:carpal tunnel syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:carpal tunnel syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cataplexy ---
r_associated #0: 20 -->
en:retardation
n1=en:cataplexy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cataplexy often triggered by strong emotions ---
r_associated #0: 20 -->
en:retardation
n1=en:cataplexy often triggered by strong emotions | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cataplexy, paroxysmal weakness or paralysis ---
r_associated #0: 20 -->
en:retardation
n1=en:cataplexy, paroxysmal weakness or paralysis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cataract ---
r_associated #0: 20 -->
en:retardation
n1=en:cataract | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:catatonia ---
r_associated #0: 20 -->
en:retardation
n1=en:catatonia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:catatonic behavior ---
r_associated #0: 20 -->
en:retardation
n1=en:catatonic behavior | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cauda equina syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:cauda equina syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:caudal dysplasia ---
r_associated #0: 20 -->
en:retardation
n1=en:caudal dysplasia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:caudate atrophy ---
r_associated #0: 20 -->
en:retardation
n1=en:caudate atrophy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:caudate nuclei atrophy ---
r_associated #0: 20 -->
en:retardation
n1=en:caudate nuclei atrophy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cavitating leukoencephalopathy ---
r_associated #0: 20 -->
en:retardation
n1=en:cavitating leukoencephalopathy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cavitating white matter degeneration ---
r_associated #0: 20 -->
en:retardation
n1=en:cavitating white matter degeneration | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cavum septum pellucidum atrophy ---
r_associated #0: 20 -->
en:retardation
n1=en:cavum septum pellucidum atrophy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cavum vergae ---
r_associated #0: 20 -->
en:retardation
n1=en:cavum vergae | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ccerebellar ataxia ---
r_associated #0: 20 -->
en:retardation
n1=en:ccerebellar ataxia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cdgiw ---
r_associated #0: 20 -->
en:retardation
n1=en:cdgiw | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cebocephaly ---
r_associated #0: 20 -->
en:retardation
n1=en:cebocephaly | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cell loss and gliosis in the basal ganglia ---
r_associated #0: 20 -->
en:retardation
n1=en:cell loss and gliosis in the basal ganglia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:celosomy ---
r_associated #0: 20 -->
en:retardation
n1=en:celosomy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:central canal malformation ---
r_associated #0: 20 -->
en:retardation
n1=en:central canal malformation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:central facial nerve paralysis (rare) ---
r_associated #0: 20 -->
en:retardation
n1=en:central facial nerve paralysis (rare) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:central facial palsy (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:central facial palsy (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:central hypotonia ---
r_associated #0: 20 -->
en:retardation
n1=en:central hypotonia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:central nervous system ---
r_associated #0: 20 -->
en:retardation
n1=en:central nervous system | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:central nervous system degeneration ---
r_associated #0: 20 -->
en:retardation
n1=en:central nervous system degeneration | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:central nervous system demyelination ---
r_associated #0: 20 -->
en:retardation
n1=en:central nervous system demyelination | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:central nervous system depression (disorder) ---
r_associated #0: 20 -->
en:retardation
n1=en:central nervous system depression (disorder) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:central nervous system involvement (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:central nervous system involvement (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:central nervous system involvement in approximately 50% of patients ---
r_associated #0: 20 -->
en:retardation
n1=en:central nervous system involvement in approximately 50% of patients | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:central nervous system malformations (40%) ---
r_associated #0: 20 -->
en:retardation
n1=en:central nervous system malformations (40%) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:central nervous system neoplasm ---
r_associated #0: 20 -->
en:retardation
n1=en:central nervous system neoplasm | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:central nervous system part ---
r_associated #0: 20 -->
en:retardation
n1=en:central nervous system part | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:central nervous system space ---
r_associated #0: 20 -->
en:retardation
n1=en:central nervous system space | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:central neural pathway/tract ---
r_associated #0: 20 -->
en:retardation
n1=en:central neural pathway/tract | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellar and brainstem atrophy, mild (1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellar and brainstem atrophy, mild (1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellar ataxia ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellar ataxia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellar ataxia (1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellar ataxia (1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellar ataxia (in 1 of 3 families) ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellar ataxia (in 1 of 3 families) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellar ataxia (may be permanent in 50% of patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellar ataxia (may be permanent in 50% of patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellar ataxia (rare) ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellar ataxia (rare) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellar ataxia (seen in hhs variant) ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellar ataxia (seen in hhs variant) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellar ataxia during episodes ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellar ataxia during episodes | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellar ataxia, adult-onset (in 1 family) ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellar ataxia, adult-onset (in 1 family) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellar ataxia, gait and stance ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellar ataxia, gait and stance | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellar ataxia, limb and trunk ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellar ataxia, limb and trunk | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellar ataxia, mental retardation, and dysequilibrium syndrome 4 ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellar ataxia, mental retardation, and dysequilibrium syndrome 4 | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellar ataxia, mild, late-onset ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellar ataxia, mild, late-onset | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellar ataxia, severe ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellar ataxia, severe | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellar ataxia, slowly progressive ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellar ataxia, slowly progressive | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellar atrophy (1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellar atrophy (1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellar atrophy (96% of patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellar atrophy (96% of patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellar atrophy (especially in the superior cerebellar vermis) ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellar atrophy (especially in the superior cerebellar vermis) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellar atrophy (especially of the vermis) ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellar atrophy (especially of the vermis) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellar atrophy (in 1 family) ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellar atrophy (in 1 family) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellar atrophy (in adulthood) ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellar atrophy (in adulthood) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellar atrophy (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellar atrophy (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellar atrophy (juvenile form) ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellar atrophy (juvenile form) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellar atrophy (reported in 1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellar atrophy (reported in 1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellar atrophy in most cases ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellar atrophy in most cases | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellar atrophy in older patients ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellar atrophy in older patients | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellar atrophy seen on mri ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellar atrophy seen on mri | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellar atrophy with signal hyperintensity in the cerebellar cortex seen on t2-weighted mri ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellar atrophy with signal hyperintensity in the cerebellar cortex seen on t2-weighted mri | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellar atrophy, diffuse, severe ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellar atrophy, diffuse, severe | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellar atrophy, mild ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellar atrophy, mild | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellar atrophy, mild (1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellar atrophy, mild (1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellar atrophy, mild (in 1 of 3 families) ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellar atrophy, mild (in 1 of 3 families) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellar atrophy, particularly of the hemispheres ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellar atrophy, particularly of the hemispheres | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellar atrophy, progressive ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellar atrophy, progressive | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellar atrophy, progressive (1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellar atrophy, progressive (1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellar atrophy, progressive (cerebellar vermal atrophy before cerebral atrophy) ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellar atrophy, progressive (cerebellar vermal atrophy before cerebral atrophy) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellar atrophy, progressive (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellar atrophy, progressive (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellar atrophy, severe ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellar atrophy, severe | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellar calcifications ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellar calcifications | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellar cell paucity, more marked in vermis than hemispheres ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellar cell paucity, more marked in vermis than hemispheres | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellar cortex shows normal layers ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellar cortex shows normal layers | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellar cortical degeneration ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellar cortical degeneration | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellar cyst ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellar cyst | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellar cyst (rare) ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellar cyst (rare) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellar cysts (meb) ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellar cysts (meb) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellar degeneration ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellar degeneration | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellar diseases ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellar diseases | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellar dysarthria ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellar dysarthria | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellar dysfunction, progressive ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellar dysfunction, progressive | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellar dysplasia ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellar dysplasia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellar enlargement ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellar enlargement | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellar gangliocytoma manifesting as seizure and tremor ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellar gangliocytoma manifesting as seizure and tremor | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellar hemangioblastoma ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellar hemangioblastoma | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellar hemorrhage (rare) ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellar hemorrhage (rare) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellar herniation (rare) ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellar herniation (rare) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellar heterotopias ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellar heterotopias | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellar hypoplasia (1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellar hypoplasia (1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellar hypoplasia (in 1 of 2 patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellar hypoplasia (in 1 of 2 patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellar hypoplasia (in 1 of 2 sibs) ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellar hypoplasia (in 1 of 2 sibs) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellar hypoplasia (in most patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellar hypoplasia (in most patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellar hypoplasia (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellar hypoplasia (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellar hypoplasia (in some) ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellar hypoplasia (in some) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellar hypoplasia (male) ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellar hypoplasia (male) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellar hypoplasia (reported in 1 family) ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellar hypoplasia (reported in 1 family) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellar hypoplasia (seen in hhs variant) ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellar hypoplasia (seen in hhs variant) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellar hypoplasia (seen in recessive form) ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellar hypoplasia (seen in recessive form) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellar hypoplasia (variable) ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellar hypoplasia (variable) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellar hypoplasia due to enlarged foramen magnum ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellar hypoplasia due to enlarged foramen magnum | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellar hypoplasia or agenesis ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellar hypoplasia or agenesis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellar hypoplasia predominantly affecting the vermis ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellar hypoplasia predominantly affecting the vermis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellar hypoplasia, mild (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellar hypoplasia, mild (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellar hypoplasia, mild asymmetric (rare) ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellar hypoplasia, mild asymmetric (rare) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellar hypoplasia, particularly of the hemispheres ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellar hypoplasia, particularly of the hemispheres | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellar hypoplasia, severe (wws) ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellar hypoplasia, severe (wws) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellar hypoplasia/atrophy (27%) ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellar hypoplasia/atrophy (27%) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellar lesion nos ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellar lesion nos | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellar medulloblastoma (rare) ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellar medulloblastoma (rare) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellar neuronal loss ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellar neuronal loss | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellar origin most likely ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellar origin most likely | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellar signs ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellar signs | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellar signs (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellar signs (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellar signs (less common) ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellar signs (less common) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellar signs (may be permanent in 50% of patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellar signs (may be permanent in 50% of patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellar signs (more common in variant cjd) ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellar signs (more common in variant cjd) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellar signs during episodes ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellar signs during episodes | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellar signs may develop ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellar signs may develop | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellar signs, mild (in 1 of 3 families) ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellar signs, mild (in 1 of 3 families) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellar stroke ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellar stroke | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellar tonsil herniation ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellar tonsil herniation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellar tonsillar herniation ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellar tonsillar herniation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellar vermis aplasia or hypoplasia ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellar vermis aplasia or hypoplasia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellar vermis atrophy ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellar vermis atrophy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellar vermis hypoplasia ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellar vermis hypoplasia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellar vermis hypoplasia (in 1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellar vermis hypoplasia (in 1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellar vermis hypoplasia (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellar vermis hypoplasia (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellar white matter lesions on mri ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellar white matter lesions on mri | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebellum ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebellum | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebral and cerebellar atrophy ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebral and cerebellar atrophy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebral arterial hemorrhage ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebral arterial hemorrhage | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebral arterial thrombosis ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebral arterial thrombosis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebral atrophy ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebral atrophy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebral atrophy (1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebral atrophy (1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebral atrophy (in 1 family) ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebral atrophy (in 1 family) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebral atrophy (in severe cases) ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebral atrophy (in severe cases) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebral atrophy (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebral atrophy (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebral atrophy (rare) ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebral atrophy (rare) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebral atrophy (reported in 1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebral atrophy (reported in 1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebral atrophy diffuse ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebral atrophy diffuse | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebral atrophy, diffuse, severe ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebral atrophy, diffuse, severe | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebral atrophy, frontotemporal, progressive ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebral atrophy, frontotemporal, progressive | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebral atrophy, generalized mild ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebral atrophy, generalized mild | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebral atrophy, mild ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebral atrophy, mild | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebral atrophy, mild, diffuse ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebral atrophy, mild, diffuse | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebral atrophy, progressive ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebral atrophy, progressive | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebral atrophy, progressive, from anterior to posterior ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebral atrophy, progressive, from anterior to posterior | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebral atrophy, severe ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebral atrophy, severe | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebral calcification ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebral calcification | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebral cavernous malformation ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebral cavernous malformation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebral cortex myoclonus ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebral cortex myoclonus | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebral cortex with spongiform changes ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebral cortex with spongiform changes | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebral cortical and cerebellar atrophy (patient a) ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebral cortical and cerebellar atrophy (patient a) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebral cortical atrophy, diffuse ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebral cortical atrophy, diffuse | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebral cortical atrophy, especially frontal lobes ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebral cortical atrophy, especially frontal lobes | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebral cortical neurodegeneration ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebral cortical neurodegeneration | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebral cyst ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebral cyst | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebral degeneration ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebral degeneration | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebral demyelination and inflammation ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebral demyelination and inflammation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebral dysmyelination ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebral dysmyelination | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebral edema ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebral edema | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebral hemorrhage ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebral hemorrhage | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebral hypomyelination ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebral hypomyelination | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebral hypoplasia ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebral hypoplasia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebral infarction ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebral infarction | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebral infarction dandy-walker malformation ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebral infarction dandy-walker malformation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebral malformations ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebral malformations | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebral oligogyria ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebral oligogyria | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebral palsy ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebral palsy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebral palsy, spastic quadriplegic, 1 ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebral palsy, spastic quadriplegic, 1 | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebral spongiosis ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebral spongiosis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebral thrombosis ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebral thrombosis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebral thrombosis (e.g. 612283.0014 protein c deficiency) ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebral thrombosis (e.g. 612283.0014 protein c deficiency) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebral vasculitis or vasculopathy (rare) ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebral vasculitis or vasculopathy (rare) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebral white matter atrophy, progressive ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebral white matter atrophy, progressive | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebral white matter lesion ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebral white matter lesion | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebral white matter lesions (1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebral white matter lesions (1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebrofaciothoracic dysplasia ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebrofaciothoracic dysplasia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebrooculonasal syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebrooculonasal syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebrospinal fluid ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebrospinal fluid | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebrospinal fluid glucose decreased ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebrospinal fluid glucose decreased | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebrospinal fluid may show decreased levels of homovanillic acid (hva) ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebrospinal fluid may show decreased levels of homovanillic acid (hva) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebrotendinous xanthomatosis ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebrotendinous xanthomatosis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebrovascular accident ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebrovascular accident | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebrovascular accident (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebrovascular accident (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebrovascular disorder ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebrovascular disorder | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebrovascular ischemia ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebrovascular ischemia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebrovascular ischemic attacks, transient (proceed secondary neurologic findings) ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebrovascular ischemic attacks, transient (proceed secondary neurologic findings) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cerebrum ---
r_associated #0: 20 -->
en:retardation
n1=en:cerebrum | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ceroid lipofuscinosis, neuronal, 1 ---
r_associated #0: 20 -->
en:retardation
n1=en:ceroid lipofuscinosis, neuronal, 1 | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ceroid lipofuscinosis, neuronal, 5 ---
r_associated #0: 20 -->
en:retardation
n1=en:ceroid lipofuscinosis, neuronal, 5 | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ceroid lipofuscinosis, neuronal, 9 (disorder) ---
r_associated #0: 20 -->
en:retardation
n1=en:ceroid lipofuscinosis, neuronal, 9 (disorder) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:certain congenital musculoskeletal deformities ---
r_associated #0: 20 -->
en:retardation
n1=en:certain congenital musculoskeletal deformities | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cervical cord compression ---
r_associated #0: 20 -->
en:retardation
n1=en:cervical cord compression | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cervical disorder ---
r_associated #0: 20 -->
en:retardation
n1=en:cervical disorder | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cervical myelopathy ---
r_associated #0: 20 -->
en:retardation
n1=en:cervical myelopathy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:changes in physical activity ---
r_associated #0: 20 -->
en:retardation
n1=en:changes in physical activity | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:characteristic arm position with wrist and elbow flexion ---
r_associated #0: 20 -->
en:retardation
n1=en:characteristic arm position with wrist and elbow flexion | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:characteristic electroencephalogram (eeg) discharges ---
r_associated #0: 20 -->
en:retardation
n1=en:characteristic electroencephalogram (eeg) discharges | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:characteristic findings on mri ---
r_associated #0: 20 -->
en:retardation
n1=en:characteristic findings on mri | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:characteristic periodic eeg complexes (only in sporadic and familial cjd, not in variant cjd) ---
r_associated #0: 20 -->
en:retardation
n1=en:characteristic periodic eeg complexes (only in sporadic and familial cjd, not in variant cjd) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:charge syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:charge syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cheilognathopalatoschisis ---
r_associated #0: 20 -->
en:retardation
n1=en:cheilognathopalatoschisis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cheilognathoschisis ---
r_associated #0: 20 -->
en:retardation
n1=en:cheilognathoschisis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:chiari i malformation of the cerebellum (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:chiari i malformation of the cerebellum (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:chiari i malformation on mri ---
r_associated #0: 20 -->
en:retardation
n1=en:chiari i malformation on mri | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:chiari i malformation on mri (some) ---
r_associated #0: 20 -->
en:retardation
n1=en:chiari i malformation on mri (some) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:chiari malformation (uncommon) ---
r_associated #0: 20 -->
en:retardation
n1=en:chiari malformation (uncommon) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:chiari malformation type ii ---
r_associated #0: 20 -->
en:retardation
n1=en:chiari malformation type ii | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:chiari type i ---
r_associated #0: 20 -->
en:retardation
n1=en:chiari type i | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:chiari type i malformation (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:chiari type i malformation (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:chicken pox ---
r_associated #0: 20 -->
en:retardation
n1=en:chicken pox | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:childhood emotional disorder ---
r_associated #0: 20 -->
en:retardation
n1=en:childhood emotional disorder | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:childhood or adolescent disorder of social functioning ---
r_associated #0: 20 -->
en:retardation
n1=en:childhood or adolescent disorder of social functioning | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:childhood polyphagia ---
r_associated #0: 20 -->
en:retardation
n1=en:childhood polyphagia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cholecystitis with cholelithiasis ---
r_associated #0: 20 -->
en:retardation
n1=en:cholecystitis with cholelithiasis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:chorea ---
r_associated #0: 20 -->
en:retardation
n1=en:chorea | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:chorea (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:chorea (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:chorea of all limbs ---
r_associated #0: 20 -->
en:retardation
n1=en:chorea of all limbs | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:chorea of hands ---
r_associated #0: 20 -->
en:retardation
n1=en:chorea of hands | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:chorea, mild (in some) ---
r_associated #0: 20 -->
en:retardation
n1=en:chorea, mild (in some) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:chorea, prominent (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:chorea, prominent (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:chorea-ballism ---
r_associated #0: 20 -->
en:retardation
n1=en:chorea-ballism | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:choreic movements (10 to 22% of patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:choreic movements (10 to 22% of patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:choreic movements, episodic ---
r_associated #0: 20 -->
en:retardation
n1=en:choreic movements, episodic | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:choreoathetoid movements ---
r_associated #0: 20 -->
en:retardation
n1=en:choreoathetoid movements | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:choreoathetosis ---
r_associated #0: 20 -->
en:retardation
n1=en:choreoathetosis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:choreoathetosis (2 patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:choreoathetosis (2 patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:choreoathetosis (described in 1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:choreoathetosis (described in 1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:choreoathetosis (in 79%), more frequent at disease onset ---
r_associated #0: 20 -->
en:retardation
n1=en:choreoathetosis (in 79%), more frequent at disease onset | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:choreoathetosis (in a subset of patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:choreoathetosis (in a subset of patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:choreoathetosis (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:choreoathetosis (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:choreoathetosis of the face, trunk, extremities ---
r_associated #0: 20 -->
en:retardation
n1=en:choreoathetosis of the face, trunk, extremities | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:choreodystonia of the upper limbs ---
r_associated #0: 20 -->
en:retardation
n1=en:choreodystonia of the upper limbs | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:choristoma ---
r_associated #0: 20 -->
en:retardation
n1=en:choristoma | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:choroid plexus calcification ---
r_associated #0: 20 -->
en:retardation
n1=en:choroid plexus calcification | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:choroid plexus cyst ---
r_associated #0: 20 -->
en:retardation
n1=en:choroid plexus cyst | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:choroid plexus papilloma (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:choroid plexus papilloma (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:choroideremia, deafness, and mental retardation ---
r_associated #0: 20 -->
en:retardation
n1=en:choroideremia, deafness, and mental retardation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:chromosome 10q26 deletion syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:chromosome 10q26 deletion syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:chromosome 13q14 deletion syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:chromosome 13q14 deletion syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:chromosome 15q24 deletion syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:chromosome 15q24 deletion syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:chromosome 15q26-qter deletion syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:chromosome 15q26-qter deletion syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:chromosome 16p12.2-p11.2 deletion syndrome, 7.1- to 8.7-mb ---
r_associated #0: 20 -->
en:retardation
n1=en:chromosome 16p12.2-p11.2 deletion syndrome, 7.1- to 8.7-mb | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:chromosome 17q12 duplication syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:chromosome 17q12 duplication syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:chromosome 19q13.11 deletion syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:chromosome 19q13.11 deletion syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:chromosome 1p32-p31 deletion syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:chromosome 1p32-p31 deletion syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:chromosome 22q11.2 microduplication syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:chromosome 22q11.2 microduplication syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:chromosome 2p16.1-p15 deletion syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:chromosome 2p16.1-p15 deletion syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:chromosome 2q32-q33 deletion syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:chromosome 2q32-q33 deletion syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:chromosome 2q37 deletion syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:chromosome 2q37 deletion syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:chromosome 5p13 duplication syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:chromosome 5p13 duplication syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:chromosome 6pter-p24 deletion syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:chromosome 6pter-p24 deletion syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:chromosome 9p deletion syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:chromosome 9p deletion syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:chromosome disorder ---
r_associated #0: 20 -->
en:retardation
n1=en:chromosome disorder | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:chronic bronchitis/bronchiectasis ---
r_associated #0: 20 -->
en:retardation
n1=en:chronic bronchitis/bronchiectasis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:chronic cystic disease breast ---
r_associated #0: 20 -->
en:retardation
n1=en:chronic cystic disease breast | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:chronic encephalopathy ---
r_associated #0: 20 -->
en:retardation
n1=en:chronic encephalopathy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:chronic enteritis/ulcerative colitis ---
r_associated #0: 20 -->
en:retardation
n1=en:chronic enteritis/ulcerative colitis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:chronic headaches ---
r_associated #0: 20 -->
en:retardation
n1=en:chronic headaches | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:chronic internal knee derangement ---
r_associated #0: 20 -->
en:retardation
n1=en:chronic internal knee derangement | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:chronic lymphocytic meningitis ---
r_associated #0: 20 -->
en:retardation
n1=en:chronic lymphocytic meningitis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:chronic mental disorder ---
r_associated #0: 20 -->
en:retardation
n1=en:chronic mental disorder | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:chronic otitis other infection ear ---
r_associated #0: 20 -->
en:retardation
n1=en:chronic otitis other infection ear | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:chronic pain ---
r_associated #0: 20 -->
en:retardation
n1=en:chronic pain | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:chronic physical disability ---
r_associated #0: 20 -->
en:retardation
n1=en:chronic physical disability | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:chronic skin ulcer ---
r_associated #0: 20 -->
en:retardation
n1=en:chronic skin ulcer | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:chronic subtype, headaches occur without remission for 1 year ---
r_associated #0: 20 -->
en:retardation
n1=en:chronic subtype, headaches occur without remission for 1 year | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:chronic-progressive course with episodes of rapid deterioration following fever or head trauma ---
r_associated #0: 20 -->
en:retardation
n1=en:chronic-progressive course with episodes of rapid deterioration following fever or head trauma | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:chronic/non specific lymphadenitis ---
r_associated #0: 20 -->
en:retardation
n1=en:chronic/non specific lymphadenitis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cirrhosis/other liver disease ---
r_associated #0: 20 -->
en:retardation
n1=en:cirrhosis/other liver disease | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:citrullinemia ---
r_associated #0: 20 -->
en:retardation
n1=en:citrullinemia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ck syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:ck syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:classical lissencephaly ---
r_associated #0: 20 -->
en:retardation
n1=en:classical lissencephaly | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:classical maple syrup urine disease ---
r_associated #0: 20 -->
en:retardation
n1=en:classical maple syrup urine disease | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:classical phenylketonuria ---
r_associated #0: 20 -->
en:retardation
n1=en:classical phenylketonuria | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cleft jaw ---
r_associated #0: 20 -->
en:retardation
n1=en:cleft jaw | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cleft lip ---
r_associated #0: 20 -->
en:retardation
n1=en:cleft lip | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cleft maxilla ---
r_associated #0: 20 -->
en:retardation
n1=en:cleft maxilla | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cleft palate ---
r_associated #0: 20 -->
en:retardation
n1=en:cleft palate | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cleft palate with cleft lip ---
r_associated #0: 20 -->
en:retardation
n1=en:cleft palate with cleft lip | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cleft palate, cardiac defect, genital anomalies, and ectrodactyly ---
r_associated #0: 20 -->
en:retardation
n1=en:cleft palate, cardiac defect, genital anomalies, and ectrodactyly | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:clinical anxiety ---
r_associated #0: 20 -->
en:retardation
n1=en:clinical anxiety | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:clonic convulsion ---
r_associated #0: 20 -->
en:retardation
n1=en:clonic convulsion | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:clonus ---
r_associated #0: 20 -->
en:retardation
n1=en:clonus | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:clonus may occur ---
r_associated #0: 20 -->
en:retardation
n1=en:clonus may occur | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:closed-lip schizencephaly ---
r_associated #0: 20 -->
en:retardation
n1=en:closed-lip schizencephaly | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:clubfoot ---
r_associated #0: 20 -->
en:retardation
n1=en:clubfoot | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:clumsiness ---
r_associated #0: 20 -->
en:retardation
n1=en:clumsiness | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:clumsiness (82%) ---
r_associated #0: 20 -->
en:retardation
n1=en:clumsiness (82%) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:clumsiness (mild) ---
r_associated #0: 20 -->
en:retardation
n1=en:clumsiness (mild) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:clumsiness in childhood ---
r_associated #0: 20 -->
en:retardation
n1=en:clumsiness in childhood | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:clumsiness, unsteadiness ---
r_associated #0: 20 -->
en:retardation
n1=en:clumsiness, unsteadiness | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:clumsy gait ---
r_associated #0: 20 -->
en:retardation
n1=en:clumsy gait | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cluster headache ---
r_associated #0: 20 -->
en:retardation
n1=en:cluster headache | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cns component ---
r_associated #0: 20 -->
en:retardation
n1=en:cns component | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cns infarctions ---
r_associated #0: 20 -->
en:retardation
n1=en:cns infarctions | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cns stimulation (finding) ---
r_associated #0: 20 -->
en:retardation
n1=en:cns stimulation (finding) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cns venous malformations ---
r_associated #0: 20 -->
en:retardation
n1=en:cns venous malformations | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:coach syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:coach syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:coarctation ---
r_associated #0: 20 -->
en:retardation
n1=en:coarctation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:coarse tremors ---
r_associated #0: 20 -->
en:retardation
n1=en:coarse tremors | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:coarsened pattern of sulci and gyri ---
r_associated #0: 20 -->
en:retardation
n1=en:coarsened pattern of sulci and gyri | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cobblestone lissencephaly ---
r_associated #0: 20 -->
en:retardation
n1=en:cobblestone lissencephaly | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cobblestone lissencephaly (1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:cobblestone lissencephaly (1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cobblestone lissencephaly (posterior brain regions more affected than anterior regions) ---
r_associated #0: 20 -->
en:retardation
n1=en:cobblestone lissencephaly (posterior brain regions more affected than anterior regions) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cobblestone lissencephaly, posterior frontal and parietal regions ---
r_associated #0: 20 -->
en:retardation
n1=en:cobblestone lissencephaly, posterior frontal and parietal regions | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cobblestone lissencephaly, type ii ---
r_associated #0: 20 -->
en:retardation
n1=en:cobblestone lissencephaly, type ii | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cobblestone lissencephaly, type ii (wws) ---
r_associated #0: 20 -->
en:retardation
n1=en:cobblestone lissencephaly, type ii (wws) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cockayne syndrome, type i ---
r_associated #0: 20 -->
en:retardation
n1=en:cockayne syndrome, type i | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cockayne syndrome, type ii ---
r_associated #0: 20 -->
en:retardation
n1=en:cockayne syndrome, type ii | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:coenzyme q10 deficiency, primary, 1 ---
r_associated #0: 20 -->
en:retardation
n1=en:coenzyme q10 deficiency, primary, 1 | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:coffin-lowry syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:coffin-lowry syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:coffin-siris syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:coffin-siris syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cognition is preserved ---
r_associated #0: 20 -->
en:retardation
n1=en:cognition is preserved | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cognition is spared ---
r_associated #0: 20 -->
en:retardation
n1=en:cognition is spared | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cognitive and attention disorders and disturbances ---
r_associated #0: 20 -->
en:retardation
n1=en:cognitive and attention disorders and disturbances | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cognitive decline (1 family) ---
r_associated #0: 20 -->
en:retardation
n1=en:cognitive decline (1 family) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cognitive decline (1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:cognitive decline (1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cognitive decline (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:cognitive decline (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cognitive decline (later in life) ---
r_associated #0: 20 -->
en:retardation
n1=en:cognitive decline (later in life) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cognitive decline (rare) ---
r_associated #0: 20 -->
en:retardation
n1=en:cognitive decline (rare) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cognitive decline in adulthood ---
r_associated #0: 20 -->
en:retardation
n1=en:cognitive decline in adulthood | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cognitive decline in older patients ---
r_associated #0: 20 -->
en:retardation
n1=en:cognitive decline in older patients | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cognitive decline, rapid ---
r_associated #0: 20 -->
en:retardation
n1=en:cognitive decline, rapid | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cognitive defects (rare) ---
r_associated #0: 20 -->
en:retardation
n1=en:cognitive defects (rare) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cognitive defects (variable from mild to severe) ---
r_associated #0: 20 -->
en:retardation
n1=en:cognitive defects (variable from mild to severe) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cognitive defects develop later in the disease ---
r_associated #0: 20 -->
en:retardation
n1=en:cognitive defects develop later in the disease | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cognitive defects in executive function and attention ---
r_associated #0: 20 -->
en:retardation
n1=en:cognitive defects in executive function and attention | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cognitive deficits (less common) ---
r_associated #0: 20 -->
en:retardation
n1=en:cognitive deficits (less common) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cognitive deficits may occur ---
r_associated #0: 20 -->
en:retardation
n1=en:cognitive deficits may occur | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cognitive deficits, mild (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:cognitive deficits, mild (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cognitive delay ---
r_associated #0: 20 -->
en:retardation
n1=en:cognitive delay | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cognitive delay, mild (1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:cognitive delay, mild (1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cognitive delay, mild to severe ---
r_associated #0: 20 -->
en:retardation
n1=en:cognitive delay, mild to severe | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cognitive deterioration ---
r_associated #0: 20 -->
en:retardation
n1=en:cognitive deterioration | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cognitive disorder ---
r_associated #0: 20 -->
en:retardation
n1=en:cognitive disorder | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cognitive dysfunction ---
r_associated #0: 20 -->
en:retardation
n1=en:cognitive dysfunction | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cognitive dysfunction (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:cognitive dysfunction (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cognitive dysfunction (rare) ---
r_associated #0: 20 -->
en:retardation
n1=en:cognitive dysfunction (rare) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cognitive function, variable ---
r_associated #0: 20 -->
en:retardation
n1=en:cognitive function, variable | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cognitive impairment ---
r_associated #0: 20 -->
en:retardation
n1=en:cognitive impairment | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cognitive impairment (1 family) ---
r_associated #0: 20 -->
en:retardation
n1=en:cognitive impairment (1 family) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cognitive impairment (1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:cognitive impairment (1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cognitive impairment (3 patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:cognitive impairment (3 patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cognitive impairment (cvs+) ---
r_associated #0: 20 -->
en:retardation
n1=en:cognitive impairment (cvs+) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cognitive impairment (in 1 of 3 patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:cognitive impairment (in 1 of 3 patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cognitive impairment (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:cognitive impairment (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cognitive impairment (rare) ---
r_associated #0: 20 -->
en:retardation
n1=en:cognitive impairment (rare) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cognitive impairment, gradual onset ---
r_associated #0: 20 -->
en:retardation
n1=en:cognitive impairment, gradual onset | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cognitive impairment, mild (1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:cognitive impairment, mild (1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cognitive impairment, mild (44%) ---
r_associated #0: 20 -->
en:retardation
n1=en:cognitive impairment, mild (44%) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cognitive impairment, mild (in 2 of 3 patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:cognitive impairment, mild (in 2 of 3 patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cognitive impairment, mild to moderate ---
r_associated #0: 20 -->
en:retardation
n1=en:cognitive impairment, mild to moderate | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cognitive impairment, mild to severe ---
r_associated #0: 20 -->
en:retardation
n1=en:cognitive impairment, mild to severe | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cognitive motor disorder ---
r_associated #0: 20 -->
en:retardation
n1=en:cognitive motor disorder | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cognitive regression ---
r_associated #0: 20 -->
en:retardation
n1=en:cognitive regression | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cognitive regression, mild ---
r_associated #0: 20 -->
en:retardation
n1=en:cognitive regression, mild | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cogwheel rigidities ---
r_associated #0: 20 -->
en:retardation
n1=en:cogwheel rigidities | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cogwheel rigidity (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:cogwheel rigidity (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cohen syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:cohen syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:coloboma, ocular, and ichthyosis, brain malformations, and endocrine abnormalities ---
r_associated #0: 20 -->
en:retardation
n1=en:coloboma, ocular, and ichthyosis, brain malformations, and endocrine abnormalities | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:colpocephaly ---
r_associated #0: 20 -->
en:retardation
n1=en:colpocephaly | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:coma (if untreated) ---
r_associated #0: 20 -->
en:retardation
n1=en:coma (if untreated) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:coma (in up to 33% of patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:coma (in up to 33% of patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:coma (less common) ---
r_associated #0: 20 -->
en:retardation
n1=en:coma (less common) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:coma during episodes (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:coma during episodes (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:coma may occur after force feeding of high protein diet ---
r_associated #0: 20 -->
en:retardation
n1=en:coma may occur after force feeding of high protein diet | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:common atrioventricular orifice in double inlet ventricle ---
r_associated #0: 20 -->
en:retardation
n1=en:common atrioventricular orifice in double inlet ventricle | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:communicating hydrocephalus ---
r_associated #0: 20 -->
en:retardation
n1=en:communicating hydrocephalus | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:communication defects ---
r_associated #0: 20 -->
en:retardation
n1=en:communication defects | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:communication disorder ---
r_associated #0: 20 -->
en:retardation
n1=en:communication disorder | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:complete or partial absence of the corpus callosum ---
r_associated #0: 20 -->
en:retardation
n1=en:complete or partial absence of the corpus callosum | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:complete or partial absence of the corpus callosum (wws) ---
r_associated #0: 20 -->
en:retardation
n1=en:complete or partial absence of the corpus callosum (wws) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:complete trisomy 18 syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:complete trisomy 18 syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:complex motor behavior such as sleep walking ---
r_associated #0: 20 -->
en:retardation
n1=en:complex motor behavior such as sleep walking | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:complex partial seizure with impairment of consciousness ---
r_associated #0: 20 -->
en:retardation
n1=en:complex partial seizure with impairment of consciousness | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:complex partial seizures ---
r_associated #0: 20 -->
en:retardation
n1=en:complex partial seizures | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:complex partial seizures (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:complex partial seizures (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:complex partial seizures, often with secondary generalization, are the most common type ---
r_associated #0: 20 -->
en:retardation
n1=en:complex partial seizures, often with secondary generalization, are the most common type | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:complicated delivery deadborn ---
r_associated #0: 20 -->
en:retardation
n1=en:complicated delivery deadborn | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:complicated delivery liveborn ---
r_associated #0: 20 -->
en:retardation
n1=en:complicated delivery liveborn | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:complication of surgical and medical care, unspecified ---
r_associated #0: 20 -->
en:retardation
n1=en:complication of surgical and medical care, unspecified | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:compromised expressive language development, severe ---
r_associated #0: 20 -->
en:retardation
n1=en:compromised expressive language development, severe | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:concentration impairment ---
r_associated #0: 20 -->
en:retardation
n1=en:concentration impairment | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:concern sexual preference ---
r_associated #0: 20 -->
en:retardation
n1=en:concern sexual preference | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:concussion ---
r_associated #0: 20 -->
en:retardation
n1=en:concussion | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:conduct disorder ---
r_associated #0: 20 -->
en:retardation
n1=en:conduct disorder | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:condylomata acuminata in men ---
r_associated #0: 20 -->
en:retardation
n1=en:condylomata acuminata in men | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:condylomata acuminata in women ---
r_associated #0: 20 -->
en:retardation
n1=en:condylomata acuminata in women | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:confirmation of pregnancy ---
r_associated #0: 20 -->
en:retardation
n1=en:confirmation of pregnancy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:confusion ---
r_associated #0: 20 -->
en:retardation
n1=en:confusion | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:confusion (later-onset) ---
r_associated #0: 20 -->
en:retardation
n1=en:confusion (later-onset) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:confusion adverse event ---
r_associated #0: 20 -->
en:retardation
n1=en:confusion adverse event | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:confusion, paroxysmal ---
r_associated #0: 20 -->
en:retardation
n1=en:confusion, paroxysmal | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:congenital ---
r_associated #0: 20 -->
en:retardation
n1=en:congenital | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:congenital abnormal communication ---
r_associated #0: 20 -->
en:retardation
n1=en:congenital abnormal communication | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:congenital abnormal fusion ---
r_associated #0: 20 -->
en:retardation
n1=en:congenital abnormal fusion | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:congenital abnormality ---
r_associated #0: 20 -->
en:retardation
n1=en:congenital abnormality | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:congenital abnormality of lower limb and/or pelvic girdle ---
r_associated #0: 20 -->
en:retardation
n1=en:congenital abnormality of lower limb and/or pelvic girdle | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:congenital absence of the vermis ---
r_associated #0: 20 -->
en:retardation
n1=en:congenital absence of the vermis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:congenital anomalies of fetus ---
r_associated #0: 20 -->
en:retardation
n1=en:congenital anomalies of fetus | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:congenital anomalies of mother ---
r_associated #0: 20 -->
en:retardation
n1=en:congenital anomalies of mother | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:congenital anomaly of back ---
r_associated #0: 20 -->
en:retardation
n1=en:congenital anomaly of back | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:congenital anomaly of body wall ---
r_associated #0: 20 -->
en:retardation
n1=en:congenital anomaly of body wall | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:congenital anomaly of brain ---
r_associated #0: 20 -->
en:retardation
n1=en:congenital anomaly of brain | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:congenital anomaly of central nervous system ---
r_associated #0: 20 -->
en:retardation
n1=en:congenital anomaly of central nervous system | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:congenital anomaly of endocrine gland ---
r_associated #0: 20 -->
en:retardation
n1=en:congenital anomaly of endocrine gland | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:congenital anomaly of face ---
r_associated #0: 20 -->
en:retardation
n1=en:congenital anomaly of face | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:congenital anomaly of female genital system ---
r_associated #0: 20 -->
en:retardation
n1=en:congenital anomaly of female genital system | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:congenital anomaly of gastrointestinal tract ---
r_associated #0: 20 -->
en:retardation
n1=en:congenital anomaly of gastrointestinal tract | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:congenital anomaly of head ---
r_associated #0: 20 -->
en:retardation
n1=en:congenital anomaly of head | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:congenital anomaly of male genital system ---
r_associated #0: 20 -->
en:retardation
n1=en:congenital anomaly of male genital system | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:congenital anomaly of neck ---
r_associated #0: 20 -->
en:retardation
n1=en:congenital anomaly of neck | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:congenital anomaly of skeletal bone ---
r_associated #0: 20 -->
en:retardation
n1=en:congenital anomaly of skeletal bone | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:congenital anomaly of skull ---
r_associated #0: 20 -->
en:retardation
n1=en:congenital anomaly of skull | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:congenital anomaly of spine ---
r_associated #0: 20 -->
en:retardation
n1=en:congenital anomaly of spine | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:congenital anomaly of the hematopoietic system ---
r_associated #0: 20 -->
en:retardation
n1=en:congenital anomaly of the hematopoietic system | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:congenital anomaly of trunk ---
r_associated #0: 20 -->
en:retardation
n1=en:congenital anomaly of trunk | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:congenital anomaly of visual system ---
r_associated #0: 20 -->
en:retardation
n1=en:congenital anomaly of visual system | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:congenital cardiovascular abnormality ---
r_associated #0: 20 -->
en:retardation
n1=en:congenital cardiovascular abnormality | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:congenital cardiovascular malformation ---
r_associated #0: 20 -->
en:retardation
n1=en:congenital cardiovascular malformation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:congenital cataracts, facial dysmorphism, and neuropathy ---
r_associated #0: 20 -->
en:retardation
n1=en:congenital cataracts, facial dysmorphism, and neuropathy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:congenital cavitation ---
r_associated #0: 20 -->
en:retardation
n1=en:congenital cavitation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:congenital cerebellar hypoplasia ---
r_associated #0: 20 -->
en:retardation
n1=en:congenital cerebellar hypoplasia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:congenital deformity of ankle joint ---
r_associated #0: 20 -->
en:retardation
n1=en:congenital deformity of ankle joint | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:congenital deformity of chest wall ---
r_associated #0: 20 -->
en:retardation
n1=en:congenital deformity of chest wall | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:congenital deformity of clavicle ---
r_associated #0: 20 -->
en:retardation
n1=en:congenital deformity of clavicle | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:congenital deformity of hip ---
r_associated #0: 20 -->
en:retardation
n1=en:congenital deformity of hip | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:congenital deformity of knee joint ---
r_associated #0: 20 -->
en:retardation
n1=en:congenital deformity of knee joint | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:congenital deformity of labyrinth ---
r_associated #0: 20 -->
en:retardation
n1=en:congenital deformity of labyrinth | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:congenital deformity of mitral valve annulus ---
r_associated #0: 20 -->
en:retardation
n1=en:congenital deformity of mitral valve annulus | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:congenital deformity of pharynx ---
r_associated #0: 20 -->
en:retardation
n1=en:congenital deformity of pharynx | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:congenital deformity of pinna ---
r_associated #0: 20 -->
en:retardation
n1=en:congenital deformity of pinna | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:congenital deformity of scapula ---
r_associated #0: 20 -->
en:retardation
n1=en:congenital deformity of scapula | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:congenital diaphragmatic hernia ---
r_associated #0: 20 -->
en:retardation
n1=en:congenital diaphragmatic hernia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:congenital disorder of glycosylation type 1i ---
r_associated #0: 20 -->
en:retardation
n1=en:congenital disorder of glycosylation type 1i | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:congenital disorder of glycosylation type ij ---
r_associated #0: 20 -->
en:retardation
n1=en:congenital disorder of glycosylation type ij | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:congenital disruption ---
r_associated #0: 20 -->
en:retardation
n1=en:congenital disruption | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:congenital dysplasia ---
r_associated #0: 20 -->
en:retardation
n1=en:congenital dysplasia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:congenital ear anomaly nos (disorder) ---
r_associated #0: 20 -->
en:retardation
n1=en:congenital ear anomaly nos (disorder) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:congenital enlargement ---
r_associated #0: 20 -->
en:retardation
n1=en:congenital enlargement | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:congenital extension deformity ---
r_associated #0: 20 -->
en:retardation
n1=en:congenital extension deformity | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:congenital eye disorder ---
r_associated #0: 20 -->
en:retardation
n1=en:congenital eye disorder | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:congenital failure of fusion ---
r_associated #0: 20 -->
en:retardation
n1=en:congenital failure of fusion | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:congenital flat back deformity ---
r_associated #0: 20 -->
en:retardation
n1=en:congenital flat back deformity | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:congenital flexion deformity ---
r_associated #0: 20 -->
en:retardation
n1=en:congenital flexion deformity | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:congenital foot deformity ---
r_associated #0: 20 -->
en:retardation
n1=en:congenital foot deformity | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:congenital functional anomaly ---
r_associated #0: 20 -->
en:retardation
n1=en:congenital functional anomaly | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:congenital genitourinary abnormality ---
r_associated #0: 20 -->
en:retardation
n1=en:congenital genitourinary abnormality | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:congenital growth alteration ---
r_associated #0: 20 -->
en:retardation
n1=en:congenital growth alteration | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:congenital hallux valgus ---
r_associated #0: 20 -->
en:retardation
n1=en:congenital hallux valgus | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:congenital hamartoma ---
r_associated #0: 20 -->
en:retardation
n1=en:congenital hamartoma | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:congenital hand and foot deformity ---
r_associated #0: 20 -->
en:retardation
n1=en:congenital hand and foot deformity | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:congenital hernia ---
r_associated #0: 20 -->
en:retardation
n1=en:congenital hernia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:congenital hyperextension of limb ---
r_associated #0: 20 -->
en:retardation
n1=en:congenital hyperextension of limb | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:congenital hyperflexion of limb ---
r_associated #0: 20 -->
en:retardation
n1=en:congenital hyperflexion of limb | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:congenital hypoplasia of genital tubercle ---
r_associated #0: 20 -->
en:retardation
n1=en:congenital hypoplasia of genital tubercle | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:congenital hypothyroidism ---
r_associated #0: 20 -->
en:retardation
n1=en:congenital hypothyroidism | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:congenital hypotonia, axial or generalized ---
r_associated #0: 20 -->
en:retardation
n1=en:congenital hypotonia, axial or generalized | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:congenital hypotonia, mild ---
r_associated #0: 20 -->
en:retardation
n1=en:congenital hypotonia, mild | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:congenital infundibular stenosis ---
r_associated #0: 20 -->
en:retardation
n1=en:congenital infundibular stenosis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:congenital insensitivity to pain with anhidrosis ---
r_associated #0: 20 -->
en:retardation
n1=en:congenital insensitivity to pain with anhidrosis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:congenital keratoglobus ---
r_associated #0: 20 -->
en:retardation
n1=en:congenital keratoglobus | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:congenital macrocephaly ---
r_associated #0: 20 -->
en:retardation
n1=en:congenital macrocephaly | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:congenital malformation of genital organs ---
r_associated #0: 20 -->
en:retardation
n1=en:congenital malformation of genital organs | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:congenital malformation syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:congenital malformation syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:congenital malformation syndrome related to known exogenous cause ---
r_associated #0: 20 -->
en:retardation
n1=en:congenital malformation syndrome related to known exogenous cause | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:congenital malposition ---
r_associated #0: 20 -->
en:retardation
n1=en:congenital malposition | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:congenital melanosis ---
r_associated #0: 20 -->
en:retardation
n1=en:congenital melanosis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:congenital metabolic disorder ---
r_associated #0: 20 -->
en:retardation
n1=en:congenital metabolic disorder | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:congenital microtia ---
r_associated #0: 20 -->
en:retardation
n1=en:congenital microtia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:congenital morphologic anomaly ---
r_associated #0: 20 -->
en:retardation
n1=en:congenital morphologic anomaly | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:congenital muscular dystrophy-dystroglycanopathy with mental retardation type b2 ---
r_associated #0: 20 -->
en:retardation
n1=en:congenital muscular dystrophy-dystroglycanopathy with mental retardation type b2 | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:congenital musculoskeletal defect ---
r_associated #0: 20 -->
en:retardation
n1=en:congenital musculoskeletal defect | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:congenital nervous system disorder ---
r_associated #0: 20 -->
en:retardation
n1=en:congenital nervous system disorder | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:congenital opacity ---
r_associated #0: 20 -->
en:retardation
n1=en:congenital opacity | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:congenital pigmentation ---
r_associated #0: 20 -->
en:retardation
n1=en:congenital pigmentation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:congenital porencephaly ---
r_associated #0: 20 -->
en:retardation
n1=en:congenital porencephaly | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:congenital red cell hypoplasia ---
r_associated #0: 20 -->
en:retardation
n1=en:congenital red cell hypoplasia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:congenital respiratory system disorder ---
r_associated #0: 20 -->
en:retardation
n1=en:congenital respiratory system disorder | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:congenital septation ---
r_associated #0: 20 -->
en:retardation
n1=en:congenital septation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:congenital sequestration ---
r_associated #0: 20 -->
en:retardation
n1=en:congenital sequestration | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:congenital skin disorder ---
r_associated #0: 20 -->
en:retardation
n1=en:congenital skin disorder | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:congenital stenosis ---
r_associated #0: 20 -->
en:retardation
n1=en:congenital stenosis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:congenital systemic disorder ---
r_associated #0: 20 -->
en:retardation
n1=en:congenital systemic disorder | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:congenital urinary system abnormality ---
r_associated #0: 20 -->
en:retardation
n1=en:congenital urinary system abnormality | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:congenital vascular anomaly ---
r_associated #0: 20 -->
en:retardation
n1=en:congenital vascular anomaly | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:congenital vena cava abnormality ---
r_associated #0: 20 -->
en:retardation
n1=en:congenital vena cava abnormality | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:congenital visceral anomaly ---
r_associated #0: 20 -->
en:retardation
n1=en:congenital visceral anomaly | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:conjoined twins ---
r_associated #0: 20 -->
en:retardation
n1=en:conjoined twins | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:connatal disorder ---
r_associated #0: 20 -->
en:retardation
n1=en:connatal disorder | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:connective and soft tissue injury ---
r_associated #0: 20 -->
en:retardation
n1=en:connective and soft tissue injury | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:consciousness fluctuating ---
r_associated #0: 20 -->
en:retardation
n1=en:consciousness fluctuating | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:constructional apraxia (in a subset of patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:constructional apraxia (in a subset of patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:contact dermatitis and other eczema ---
r_associated #0: 20 -->
en:retardation
n1=en:contact dermatitis and other eczema | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:continuous spike-wave discharges during sleep ---
r_associated #0: 20 -->
en:retardation
n1=en:continuous spike-wave discharges during sleep | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:continuous spike-waves during slow-wave sleep ---
r_associated #0: 20 -->
en:retardation
n1=en:continuous spike-waves during slow-wave sleep | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:contractures (older children and adolescents) ---
r_associated #0: 20 -->
en:retardation
n1=en:contractures (older children and adolescents) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:contralateral hemiparesis, congenital ---
r_associated #0: 20 -->
en:retardation
n1=en:contralateral hemiparesis, congenital | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:contusion/hemorrhage eye ---
r_associated #0: 20 -->
en:retardation
n1=en:contusion/hemorrhage eye | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:convulsions, febrile (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:convulsions, febrile (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:convulsive seizures ---
r_associated #0: 20 -->
en:retardation
n1=en:convulsive seizures | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cor pulmonale ---
r_associated #0: 20 -->
en:retardation
n1=en:cor pulmonale | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:corneal ulcer ---
r_associated #0: 20 -->
en:retardation
n1=en:corneal ulcer | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:corprolalia ---
r_associated #0: 20 -->
en:retardation
n1=en:corprolalia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:corpus callosum abnormalities (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:corpus callosum abnormalities (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:corpus callosum agenesis ---
r_associated #0: 20 -->
en:retardation
n1=en:corpus callosum agenesis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:corpus callosum lipoma ---
r_associated #0: 20 -->
en:retardation
n1=en:corpus callosum lipoma | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:corpus callosum, agenesis of (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:corpus callosum, agenesis of (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:corpus callosum, agenesis of, with mental retardation, ocular coloboma, and micrognathia ---
r_associated #0: 20 -->
en:retardation
n1=en:corpus callosum, agenesis of, with mental retardation, ocular coloboma, and micrognathia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:corpus callosum, thin (rare) ---
r_associated #0: 20 -->
en:retardation
n1=en:corpus callosum, thin (rare) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cortada kousseff matsumoto syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:cortada kousseff matsumoto syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cortical and brainstem neuronal loss ---
r_associated #0: 20 -->
en:retardation
n1=en:cortical and brainstem neuronal loss | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cortical and subcortical atrophy (1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:cortical and subcortical atrophy (1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cortical and subcortical hyperintensities ---
r_associated #0: 20 -->
en:retardation
n1=en:cortical and subcortical hyperintensities | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cortical and subcortical neuronal loss in the frontal and temporal regions ---
r_associated #0: 20 -->
en:retardation
n1=en:cortical and subcortical neuronal loss in the frontal and temporal regions | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cortical and subcortical regions involved ---
r_associated #0: 20 -->
en:retardation
n1=en:cortical and subcortical regions involved | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cortical atrophy (43%) ---
r_associated #0: 20 -->
en:retardation
n1=en:cortical atrophy (43%) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cortical atrophy (frontal area) ---
r_associated #0: 20 -->
en:retardation
n1=en:cortical atrophy (frontal area) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cortical atrophy (in 2 siblings) ---
r_associated #0: 20 -->
en:retardation
n1=en:cortical atrophy (in 2 siblings) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cortical atrophy (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:cortical atrophy (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cortical atrophy (rare) ---
r_associated #0: 20 -->
en:retardation
n1=en:cortical atrophy (rare) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cortical atrophy with loss of pyramidal neurons in the motor cortex ---
r_associated #0: 20 -->
en:retardation
n1=en:cortical atrophy with loss of pyramidal neurons in the motor cortex | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cortical atrophy, progressive ---
r_associated #0: 20 -->
en:retardation
n1=en:cortical atrophy, progressive | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cortical blindness (in 1 moroccan patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:cortical blindness (in 1 moroccan patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cortical cytotoxic edema ---
r_associated #0: 20 -->
en:retardation
n1=en:cortical cytotoxic edema | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cortical degeneration ---
r_associated #0: 20 -->
en:retardation
n1=en:cortical degeneration | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cortical dysgenesis ---
r_associated #0: 20 -->
en:retardation
n1=en:cortical dysgenesis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cortical dysgenesis, complex ---
r_associated #0: 20 -->
en:retardation
n1=en:cortical dysgenesis, complex | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cortical dysplasia ---
r_associated #0: 20 -->
en:retardation
n1=en:cortical dysplasia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cortical dysplasia (1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:cortical dysplasia (1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cortical dysplasia (2 patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:cortical dysplasia (2 patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cortical dysplasia, focal (1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:cortical dysplasia, focal (1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cortical dysplasia, focal (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:cortical dysplasia, focal (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cortical gyral simplification ---
r_associated #0: 20 -->
en:retardation
n1=en:cortical gyral simplification | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cortical hypergyria (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:cortical hypergyria (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cortical malformations ---
r_associated #0: 20 -->
en:retardation
n1=en:cortical malformations | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cortical myoclonic tremors characterized by 8 to 10-hz discharges ---
r_associated #0: 20 -->
en:retardation
n1=en:cortical myoclonic tremors characterized by 8 to 10-hz discharges | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cortical neuronal loss ---
r_associated #0: 20 -->
en:retardation
n1=en:cortical neuronal loss | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cortical origin of the tremor ---
r_associated #0: 20 -->
en:retardation
n1=en:cortical origin of the tremor | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cortical reflex myoclonus ---
r_associated #0: 20 -->
en:retardation
n1=en:cortical reflex myoclonus | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cortical simplification ---
r_associated #0: 20 -->
en:retardation
n1=en:cortical simplification | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cortical thinning ---
r_associated #0: 20 -->
en:retardation
n1=en:cortical thinning | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cortical tubers ---
r_associated #0: 20 -->
en:retardation
n1=en:cortical tubers | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cortical venous thromboses ---
r_associated #0: 20 -->
en:retardation
n1=en:cortical venous thromboses | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:corticobasal degeneration (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:corticobasal degeneration (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:corticospinal signs (87% of patients in 1 report) ---
r_associated #0: 20 -->
en:retardation
n1=en:corticospinal signs (87% of patients in 1 report) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:corticospinal tract atrophy ---
r_associated #0: 20 -->
en:retardation
n1=en:corticospinal tract atrophy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:corticospinal tract disease in lower limbs (in adulthood) ---
r_associated #0: 20 -->
en:retardation
n1=en:corticospinal tract disease in lower limbs (in adulthood) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:corticospinal tract hypoplasia ---
r_associated #0: 20 -->
en:retardation
n1=en:corticospinal tract hypoplasia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:corticospinal tracts with decreased myelin staining ---
r_associated #0: 20 -->
en:retardation
n1=en:corticospinal tracts with decreased myelin staining | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:costello syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:costello syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cranial nerve anomalies ---
r_associated #0: 20 -->
en:retardation
n1=en:cranial nerve anomalies | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cranial nerve dysfunction ---
r_associated #0: 20 -->
en:retardation
n1=en:cranial nerve dysfunction | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cranial nerve palsies can arise with head and neck paragangliomas ---
r_associated #0: 20 -->
en:retardation
n1=en:cranial nerve palsies can arise with head and neck paragangliomas | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cranial nerve palsy ---
r_associated #0: 20 -->
en:retardation
n1=en:cranial nerve palsy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cranial nerve palsy, intermittent, transient ---
r_associated #0: 20 -->
en:retardation
n1=en:cranial nerve palsy, intermittent, transient | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:craniofacial dyssynostosis ---
r_associated #0: 20 -->
en:retardation
n1=en:craniofacial dyssynostosis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:craniofenestria ---
r_associated #0: 20 -->
en:retardation
n1=en:craniofenestria | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cranioschisis ---
r_associated #0: 20 -->
en:retardation
n1=en:cranioschisis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:craniostenosis with congenital heart disease mental retardation ---
r_associated #0: 20 -->
en:retardation
n1=en:craniostenosis with congenital heart disease mental retardation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:craniosynostosis ---
r_associated #0: 20 -->
en:retardation
n1=en:craniosynostosis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:crawling and standing not achieved ---
r_associated #0: 20 -->
en:retardation
n1=en:crawling and standing not achieved | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cri du chat syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:cri du chat syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:crowding of the posterior fossa ---
r_associated #0: 20 -->
en:retardation
n1=en:crowding of the posterior fossa | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cryptophthalmia ---
r_associated #0: 20 -->
en:retardation
n1=en:cryptophthalmia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cryptorchidism arachnodactyly mental retardation ---
r_associated #0: 20 -->
en:retardation
n1=en:cryptorchidism arachnodactyly mental retardation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ct scan shows dense calcifications in the basal ganglia ---
r_associated #0: 20 -->
en:retardation
n1=en:ct scan shows dense calcifications in the basal ganglia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cutaneous mastocytosis, conductive hearing loss and microtia ---
r_associated #0: 20 -->
en:retardation
n1=en:cutaneous mastocytosis, conductive hearing loss and microtia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cutis laxa, autosomal recessive, type iia ---
r_associated #0: 20 -->
en:retardation
n1=en:cutis laxa, autosomal recessive, type iia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cutis verticis gyrata, retinitis pigmentosa, and sensorineural deafness ---
r_associated #0: 20 -->
en:retardation
n1=en:cutis verticis gyrata, retinitis pigmentosa, and sensorineural deafness | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cyclopia ---
r_associated #0: 20 -->
en:retardation
n1=en:cyclopia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cyst of septum pellucidum ---
r_associated #0: 20 -->
en:retardation
n1=en:cyst of septum pellucidum | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cyst of septum pellucidum (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:cyst of septum pellucidum (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cystathionine beta-synthase deficiency disease ---
r_associated #0: 20 -->
en:retardation
n1=en:cystathionine beta-synthase deficiency disease | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cystic cavitation of the white matter ---
r_associated #0: 20 -->
en:retardation
n1=en:cystic cavitation of the white matter | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cystic degeneration of cerebral white matter with preserved cortex ---
r_associated #0: 20 -->
en:retardation
n1=en:cystic degeneration of cerebral white matter with preserved cortex | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cystic degeneration of the white matter ---
r_associated #0: 20 -->
en:retardation
n1=en:cystic degeneration of the white matter | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cystic destruction of brain tissue, including basal ganglia ---
r_associated #0: 20 -->
en:retardation
n1=en:cystic destruction of brain tissue, including basal ganglia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cystic lesions consistent with leigh syndrome (256000) ---
r_associated #0: 20 -->
en:retardation
n1=en:cystic lesions consistent with leigh syndrome (256000) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cystic lesions in the basal ganglia, brainstem, and cerebral hemispheres similar to leigh syndrome (256000) ---
r_associated #0: 20 -->
en:retardation
n1=en:cystic lesions in the basal ganglia, brainstem, and cerebral hemispheres similar to leigh syndrome (256000) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cystic lysis of the deep white matter ---
r_associated #0: 20 -->
en:retardation
n1=en:cystic lysis of the deep white matter | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cystitis/other urinary infection nos ---
r_associated #0: 20 -->
en:retardation
n1=en:cystitis/other urinary infection nos | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cysts tend to enlarge with age ---
r_associated #0: 20 -->
en:retardation
n1=en:cysts tend to enlarge with age | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cytochrome-c oxidase deficiency ---
r_associated #0: 20 -->
en:retardation
n1=en:cytochrome-c oxidase deficiency | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cytogenetic abnormality ---
r_associated #0: 20 -->
en:retardation
n1=en:cytogenetic abnormality | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:cytopathic effect ---
r_associated #0: 20 -->
en:retardation
n1=en:cytopathic effect | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:d-2-hydroxyglutaric aciduria 1 ---
r_associated #0: 20 -->
en:retardation
n1=en:d-2-hydroxyglutaric aciduria 1 | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:d-glyceric aciduria ---
r_associated #0: 20 -->
en:retardation
n1=en:d-glyceric aciduria | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dandy walker variant ---
r_associated #0: 20 -->
en:retardation
n1=en:dandy walker variant | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dandy-walker malformation ---
r_associated #0: 20 -->
en:retardation
n1=en:dandy-walker malformation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dandy-walker malformation (1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:dandy-walker malformation (1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dandy-walker malformation (in 1 of 4 patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:dandy-walker malformation (in 1 of 4 patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dandy-walker malformation (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:dandy-walker malformation (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dandy-walker malformation (rare) ---
r_associated #0: 20 -->
en:retardation
n1=en:dandy-walker malformation (rare) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dandy-walker malformation (variable) ---
r_associated #0: 20 -->
en:retardation
n1=en:dandy-walker malformation (variable) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dandy-walker malformation (wws) ---
r_associated #0: 20 -->
en:retardation
n1=en:dandy-walker malformation (wws) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:death ---
r_associated #0: 20 -->
en:retardation
n1=en:death | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:decerebrate or decorticate posturing late ---
r_associated #0: 20 -->
en:retardation
n1=en:decerebrate or decorticate posturing late | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:decerebrate posturings ---
r_associated #0: 20 -->
en:retardation
n1=en:decerebrate posturings | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:decorticate posture ---
r_associated #0: 20 -->
en:retardation
n1=en:decorticate posture | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:decrease in abstract thinking ---
r_associated #0: 20 -->
en:retardation
n1=en:decrease in abstract thinking | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:decreased active movements ---
r_associated #0: 20 -->
en:retardation
n1=en:decreased active movements | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:decreased amount of myelin-specific lipids ---
r_associated #0: 20 -->
en:retardation
n1=en:decreased amount of myelin-specific lipids | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:decreased amount of myelin-specific proteins ---
r_associated #0: 20 -->
en:retardation
n1=en:decreased amount of myelin-specific proteins | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:decreased brain volume (female) ---
r_associated #0: 20 -->
en:retardation
n1=en:decreased brain volume (female) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:decreased brain weight ---
r_associated #0: 20 -->
en:retardation
n1=en:decreased brain weight | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:decreased cerebellar folia ---
r_associated #0: 20 -->
en:retardation
n1=en:decreased cerebellar folia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:decreased cerebral volume, especially of the frontal lobes ---
r_associated #0: 20 -->
en:retardation
n1=en:decreased cerebral volume, especially of the frontal lobes | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:decreased cognition (later-onset) ---
r_associated #0: 20 -->
en:retardation
n1=en:decreased cognition (later-onset) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:decreased core body temperature ---
r_associated #0: 20 -->
en:retardation
n1=en:decreased core body temperature | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:decreased creatine signal seen on magnetic resonance spectroscopy ---
r_associated #0: 20 -->
en:retardation
n1=en:decreased creatine signal seen on magnetic resonance spectroscopy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:decreased csf volume in posterior fossa ---
r_associated #0: 20 -->
en:retardation
n1=en:decreased csf volume in posterior fossa | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:decreased delineation of the basal ganglia (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:decreased delineation of the basal ganglia (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:decreased fine motor coordination ---
r_associated #0: 20 -->
en:retardation
n1=en:decreased fine motor coordination | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:decreased iq ---
r_associated #0: 20 -->
en:retardation
n1=en:decreased iq | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:decreased iq (1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:decreased iq (1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:decreased iq (some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:decreased iq (some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:decreased iron content in the substantia nigra ---
r_associated #0: 20 -->
en:retardation
n1=en:decreased iron content in the substantia nigra | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:decreased libido ---
r_associated #0: 20 -->
en:retardation
n1=en:decreased libido | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:decreased mental processing speed ---
r_associated #0: 20 -->
en:retardation
n1=en:decreased mental processing speed | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:decreased mitochondrial respiratory chain complex activity ---
r_associated #0: 20 -->
en:retardation
n1=en:decreased mitochondrial respiratory chain complex activity | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:decreased motor nerve conduction velocity ---
r_associated #0: 20 -->
en:retardation
n1=en:decreased motor nerve conduction velocity | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:decreased myelin ---
r_associated #0: 20 -->
en:retardation
n1=en:decreased myelin | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:decreased myelination seen on mri ---
r_associated #0: 20 -->
en:retardation
n1=en:decreased myelination seen on mri | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:decreased n-acetylaspartate ---
r_associated #0: 20 -->
en:retardation
n1=en:decreased n-acetylaspartate | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:decreased need for sleep ---
r_associated #0: 20 -->
en:retardation
n1=en:decreased need for sleep | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:decreased nonverbal iq ---
r_associated #0: 20 -->
en:retardation
n1=en:decreased nonverbal iq | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:decreased numbers of astrocytes ---
r_associated #0: 20 -->
en:retardation
n1=en:decreased numbers of astrocytes | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:decreased or absent gyri (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:decreased or absent gyri (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:decreased or absent motor evoked potentials (mep), indicating dysfunction of the corticospinal tracts ---
r_associated #0: 20 -->
en:retardation
n1=en:decreased or absent motor evoked potentials (mep), indicating dysfunction of the corticospinal tracts | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:decreased pain response ---
r_associated #0: 20 -->
en:retardation
n1=en:decreased pain response | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:decreased pyramidal cells ---
r_associated #0: 20 -->
en:retardation
n1=en:decreased pyramidal cells | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:decreased rapid automatized naming (ran) speed ---
r_associated #0: 20 -->
en:retardation
n1=en:decreased rapid automatized naming (ran) speed | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:decreased reflexes (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:decreased reflexes (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:decreased sleep latency ---
r_associated #0: 20 -->
en:retardation
n1=en:decreased sleep latency | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:decreased somatosensory-evoked potentials ---
r_associated #0: 20 -->
en:retardation
n1=en:decreased somatosensory-evoked potentials | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:decreased speech ---
r_associated #0: 20 -->
en:retardation
n1=en:decreased speech | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:decreased spontaneous movements at birth ---
r_associated #0: 20 -->
en:retardation
n1=en:decreased spontaneous movements at birth | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:decreased supratentorial volume ---
r_associated #0: 20 -->
en:retardation
n1=en:decreased supratentorial volume | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:decreased tendon reflex ---
r_associated #0: 20 -->
en:retardation
n1=en:decreased tendon reflex | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:decreased upper extremity reflexes ---
r_associated #0: 20 -->
en:retardation
n1=en:decreased upper extremity reflexes | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:decreased vibration sense, suggesting posterior column involvement ---
r_associated #0: 20 -->
en:retardation
n1=en:decreased vibration sense, suggesting posterior column involvement | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:decreased vibratory sense ---
r_associated #0: 20 -->
en:retardation
n1=en:decreased vibratory sense | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:decreased volume of the cerebral white matter ---
r_associated #0: 20 -->
en:retardation
n1=en:decreased volume of the cerebral white matter | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:decreased volume of the posterior cranial fossa with normal hindbrain volume ---
r_associated #0: 20 -->
en:retardation
n1=en:decreased volume of the posterior cranial fossa with normal hindbrain volume | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:decreased white matter ---
r_associated #0: 20 -->
en:retardation
n1=en:decreased white matter | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:decreased white matter volume ---
r_associated #0: 20 -->
en:retardation
n1=en:decreased white matter volume | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:decreasing responsiveness ---
r_associated #0: 20 -->
en:retardation
n1=en:decreasing responsiveness | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:deep hypointensities (mri, t2) suggestive of past microbleeds ---
r_associated #0: 20 -->
en:retardation
n1=en:deep hypointensities (mri, t2) suggestive of past microbleeds | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:deep interpeduncular fossa ---
r_associated #0: 20 -->
en:retardation
n1=en:deep interpeduncular fossa | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:deep posterior interpeduncular fossa ---
r_associated #0: 20 -->
en:retardation
n1=en:deep posterior interpeduncular fossa | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:deep white matter changes ---
r_associated #0: 20 -->
en:retardation
n1=en:deep white matter changes | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:deep white matter hypodensities ---
r_associated #0: 20 -->
en:retardation
n1=en:deep white matter hypodensities | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:deep white matter lesions, particularly affecting the frontal and parietal lobes ---
r_associated #0: 20 -->
en:retardation
n1=en:deep white matter lesions, particularly affecting the frontal and parietal lobes | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:defect in axonal guidance ---
r_associated #0: 20 -->
en:retardation
n1=en:defect in axonal guidance | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:defect in morphosyntactic rules ---
r_associated #0: 20 -->
en:retardation
n1=en:defect in morphosyntactic rules | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:defective myelination of the deep white matter ---
r_associated #0: 20 -->
en:retardation
n1=en:defective myelination of the deep white matter | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:defective opercularization ---
r_associated #0: 20 -->
en:retardation
n1=en:defective opercularization | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:defects in auditory cue processing ---
r_associated #0: 20 -->
en:retardation
n1=en:defects in auditory cue processing | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:defects in fine motor skills ---
r_associated #0: 20 -->
en:retardation
n1=en:defects in fine motor skills | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:defects in visual cue processing ---
r_associated #0: 20 -->
en:retardation
n1=en:defects in visual cue processing | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:deficient myelination ---
r_associated #0: 20 -->
en:retardation
n1=en:deficient myelination | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:deficit in basic reading ---
r_associated #0: 20 -->
en:retardation
n1=en:deficit in basic reading | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:deficit in expressive language ---
r_associated #0: 20 -->
en:retardation
n1=en:deficit in expressive language | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:deficit in nonword repetition (nwr) ---
r_associated #0: 20 -->
en:retardation
n1=en:deficit in nonword repetition (nwr) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:deficit in phonologic short-term memory ---
r_associated #0: 20 -->
en:retardation
n1=en:deficit in phonologic short-term memory | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:deficit in reading comprehension ---
r_associated #0: 20 -->
en:retardation
n1=en:deficit in reading comprehension | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:deficit in spelling ---
r_associated #0: 20 -->
en:retardation
n1=en:deficit in spelling | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:deficits in abstraction ---
r_associated #0: 20 -->
en:retardation
n1=en:deficits in abstraction | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:deficits in language expression ---
r_associated #0: 20 -->
en:retardation
n1=en:deficits in language expression | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:deformed temporal lobes ---
r_associated #0: 20 -->
en:retardation
n1=en:deformed temporal lobes | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:degeneration of anterior horn cells ---
r_associated #0: 20 -->
en:retardation
n1=en:degeneration of anterior horn cells | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:degeneration of purkinje cells in the cerebellum ---
r_associated #0: 20 -->
en:retardation
n1=en:degeneration of purkinje cells in the cerebellum | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:degeneration of the dentatorubral and pallidoluysian systems ---
r_associated #0: 20 -->
en:retardation
n1=en:degeneration of the dentatorubral and pallidoluysian systems | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:degeneration of the lateral corticospinal tracts ---
r_associated #0: 20 -->
en:retardation
n1=en:degeneration of the lateral corticospinal tracts | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:deja vu feeling ---
r_associated #0: 20 -->
en:retardation
n1=en:deja vu feeling | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:delay in gross motor development due to weakness ---
r_associated #0: 20 -->
en:retardation
n1=en:delay in gross motor development due to weakness | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:delay of gross motor function ---
r_associated #0: 20 -->
en:retardation
n1=en:delay of gross motor function | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:delayed adaptive hand use ---
r_associated #0: 20 -->
en:retardation
n1=en:delayed adaptive hand use | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:delayed ambulation ---
r_associated #0: 20 -->
en:retardation
n1=en:delayed ambulation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:delayed brainstem development (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:delayed brainstem development (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:delayed cerebellar development (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:delayed cerebellar development (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:delayed cerebral myelination ---
r_associated #0: 20 -->
en:retardation
n1=en:delayed cerebral myelination | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:delayed cognitive development (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:delayed cognitive development (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:delayed cognitive development, mild (reported in 1 family) ---
r_associated #0: 20 -->
en:retardation
n1=en:delayed cognitive development, mild (reported in 1 family) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:delayed cognitive development/learning disabilities (93%) ---
r_associated #0: 20 -->
en:retardation
n1=en:delayed cognitive development/learning disabilities (93%) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:delayed development (1 family) ---
r_associated #0: 20 -->
en:retardation
n1=en:delayed development (1 family) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:delayed development (about 25%) ---
r_associated #0: 20 -->
en:retardation
n1=en:delayed development (about 25%) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:delayed development (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:delayed development (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:delayed development (in some) ---
r_associated #0: 20 -->
en:retardation
n1=en:delayed development (in some) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:delayed development if untreated ---
r_associated #0: 20 -->
en:retardation
n1=en:delayed development if untreated | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:delayed development in early childhood (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:delayed development in early childhood (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:delayed development may occur ---
r_associated #0: 20 -->
en:retardation
n1=en:delayed development may occur | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:delayed development, after 8-15 months ---
r_associated #0: 20 -->
en:retardation
n1=en:delayed development, after 8-15 months | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:delayed development, ranging from mild to severe ---
r_associated #0: 20 -->
en:retardation
n1=en:delayed development, ranging from mild to severe | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:delayed development, severe ---
r_associated #0: 20 -->
en:retardation
n1=en:delayed development, severe | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:delayed development, variable (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:delayed development, variable (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:delayed development, variable severity, from birth in some patients ---
r_associated #0: 20 -->
en:retardation
n1=en:delayed development, variable severity, from birth in some patients | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:delayed developmental milestones ---
r_associated #0: 20 -->
en:retardation
n1=en:delayed developmental milestones | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:delayed epiphyseal fusion ---
r_associated #0: 20 -->
en:retardation
n1=en:delayed epiphyseal fusion | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:delayed gross motor development (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:delayed gross motor development (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:delayed gyration ---
r_associated #0: 20 -->
en:retardation
n1=en:delayed gyration | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:delayed independent walking ---
r_associated #0: 20 -->
en:retardation
n1=en:delayed independent walking | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:delayed intellectual development ---
r_associated #0: 20 -->
en:retardation
n1=en:delayed intellectual development | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:delayed motor and speech development, mild (1 family) ---
r_associated #0: 20 -->
en:retardation
n1=en:delayed motor and speech development, mild (1 family) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:delayed motor development (1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:delayed motor development (1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:delayed motor development (secondary to skeletal abnormalities) ---
r_associated #0: 20 -->
en:retardation
n1=en:delayed motor development (secondary to skeletal abnormalities) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:delayed motor development due to muscle weakness ---
r_associated #0: 20 -->
en:retardation
n1=en:delayed motor development due to muscle weakness | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:delayed motor development, mild, transient ---
r_associated #0: 20 -->
en:retardation
n1=en:delayed motor development, mild, transient | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:delayed motor development, severe ---
r_associated #0: 20 -->
en:retardation
n1=en:delayed motor development, severe | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:delayed motor milestones due to muscle weakness ---
r_associated #0: 20 -->
en:retardation
n1=en:delayed motor milestones due to muscle weakness | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:delayed myelination ---
r_associated #0: 20 -->
en:retardation
n1=en:delayed myelination | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:delayed myelination (1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:delayed myelination (1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:delayed myelination (1/4 patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:delayed myelination (1/4 patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:delayed myelination (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:delayed myelination (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:delayed myelination (reported in 1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:delayed myelination (reported in 1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:delayed myelination on brain mri (reported in 1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:delayed myelination on brain mri (reported in 1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:delayed myelination seen on mri ---
r_associated #0: 20 -->
en:retardation
n1=en:delayed myelination seen on mri | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:delayed myelination, mild ---
r_associated #0: 20 -->
en:retardation
n1=en:delayed myelination, mild | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:delayed myelinization (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:delayed myelinization (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:delayed onset of phrase speech (> 36 months) ---
r_associated #0: 20 -->
en:retardation
n1=en:delayed onset of phrase speech (> 36 months) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:delayed opercularization ---
r_associated #0: 20 -->
en:retardation
n1=en:delayed opercularization | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:delayed or absent independent walking ---
r_associated #0: 20 -->
en:retardation
n1=en:delayed or absent independent walking | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:delayed psychomotor development (1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:delayed psychomotor development (1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:delayed psychomotor development (in 1 family) ---
r_associated #0: 20 -->
en:retardation
n1=en:delayed psychomotor development (in 1 family) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:delayed psychomotor development (in most patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:delayed psychomotor development (in most patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:delayed psychomotor development (in severe cases) ---
r_associated #0: 20 -->
en:retardation
n1=en:delayed psychomotor development (in severe cases) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:delayed psychomotor development (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:delayed psychomotor development (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:delayed psychomotor development (in some) ---
r_associated #0: 20 -->
en:retardation
n1=en:delayed psychomotor development (in some) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:delayed psychomotor development (mild to severe) ---
r_associated #0: 20 -->
en:retardation
n1=en:delayed psychomotor development (mild to severe) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:delayed psychomotor development (stops at development levels of 1-2 years) ---
r_associated #0: 20 -->
en:retardation
n1=en:delayed psychomotor development (stops at development levels of 1-2 years) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:delayed psychomotor development after onset of seizures ---
r_associated #0: 20 -->
en:retardation
n1=en:delayed psychomotor development after onset of seizures | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:delayed psychomotor development, mild ---
r_associated #0: 20 -->
en:retardation
n1=en:delayed psychomotor development, mild | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:delayed psychomotor development, mild (in 3 of 5 patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:delayed psychomotor development, mild (in 3 of 5 patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:delayed psychomotor development, mild (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:delayed psychomotor development, mild (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:delayed psychomotor development, moderate to severe ---
r_associated #0: 20 -->
en:retardation
n1=en:delayed psychomotor development, moderate to severe | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:delayed psychomotor development, profound ---
r_associated #0: 20 -->
en:retardation
n1=en:delayed psychomotor development, profound | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:delayed psychomotor development, profound (1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:delayed psychomotor development, profound (1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:delayed psychomotor development, profound (patient a) ---
r_associated #0: 20 -->
en:retardation
n1=en:delayed psychomotor development, profound (patient a) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:delayed psychomotor development, severe ---
r_associated #0: 20 -->
en:retardation
n1=en:delayed psychomotor development, severe | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:delayed psychomotor development, severe (> 90%) ---
r_associated #0: 20 -->
en:retardation
n1=en:delayed psychomotor development, severe (> 90%) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:delayed psychomotor development, severe (in 2 of 6 patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:delayed psychomotor development, severe (in 2 of 6 patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:delayed psychomotor development, severe to profound ---
r_associated #0: 20 -->
en:retardation
n1=en:delayed psychomotor development, severe to profound | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:delayed psychomotor development, variable ---
r_associated #0: 20 -->
en:retardation
n1=en:delayed psychomotor development, variable | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:delayed puberty ---
r_associated #0: 20 -->
en:retardation
n1=en:delayed puberty | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:delayed speech and language development ---
r_associated #0: 20 -->
en:retardation
n1=en:delayed speech and language development | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:delayed speech development, severe ---
r_associated #0: 20 -->
en:retardation
n1=en:delayed speech development, severe | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:delayed walking (1 family) ---
r_associated #0: 20 -->
en:retardation
n1=en:delayed walking (1 family) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:delayed walking (less common) ---
r_associated #0: 20 -->
en:retardation
n1=en:delayed walking (less common) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:delayed walking (rare) ---
r_associated #0: 20 -->
en:retardation
n1=en:delayed walking (rare) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:delayed walking and running in early childhood ---
r_associated #0: 20 -->
en:retardation
n1=en:delayed walking and running in early childhood | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:delayed walking, mild (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:delayed walking, mild (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:deletion 18p syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:deletion 18p syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:deliria (incl confusion) ---
r_associated #0: 20 -->
en:retardation
n1=en:deliria (incl confusion) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:delirium ---
r_associated #0: 20 -->
en:retardation
n1=en:delirium | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:delirium (later-onset) ---
r_associated #0: 20 -->
en:retardation
n1=en:delirium (later-onset) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:delirium dementia and amnestic and other cognitive disorders ---
r_associated #0: 20 -->
en:retardation
n1=en:delirium dementia and amnestic and other cognitive disorders | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:delusion ---
r_associated #0: 20 -->
en:retardation
n1=en:delusion | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:delusional disorder ---
r_associated #0: 20 -->
en:retardation
n1=en:delusional disorder | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dementia ---
r_associated #0: 20 -->
en:retardation
n1=en:dementia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dementia (1 family) ---
r_associated #0: 20 -->
en:retardation
n1=en:dementia (1 family) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dementia (5%) ---
r_associated #0: 20 -->
en:retardation
n1=en:dementia (5%) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dementia (<20%) ---
r_associated #0: 20 -->
en:retardation
n1=en:dementia (<20%) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dementia (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:dementia (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dementia (later-onset) ---
r_associated #0: 20 -->
en:retardation
n1=en:dementia (later-onset) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dementia (onset in fifth decade) ---
r_associated #0: 20 -->
en:retardation
n1=en:dementia (onset in fifth decade) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dementia (subtype 3a) ---
r_associated #0: 20 -->
en:retardation
n1=en:dementia (subtype 3a) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dementia and amnestic conditions ---
r_associated #0: 20 -->
en:retardation
n1=en:dementia and amnestic conditions | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dementia in a subset of patients ---
r_associated #0: 20 -->
en:retardation
n1=en:dementia in a subset of patients | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dementia may occur ---
r_associated #0: 20 -->
en:retardation
n1=en:dementia may occur | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dementia of frontal lobe type ---
r_associated #0: 20 -->
en:retardation
n1=en:dementia of frontal lobe type | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dementia senile/alzheimer ---
r_associated #0: 20 -->
en:retardation
n1=en:dementia senile/alzheimer | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dementia, presenile, progressive, beginning around age 30 years ---
r_associated #0: 20 -->
en:retardation
n1=en:dementia, presenile, progressive, beginning around age 30 years | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dementia, progressive (more common in males) ---
r_associated #0: 20 -->
en:retardation
n1=en:dementia, progressive (more common in males) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dementia, progressive, with onset of disease ---
r_associated #0: 20 -->
en:retardation
n1=en:dementia, progressive, with onset of disease | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dementia, rapidly progressive ---
r_associated #0: 20 -->
en:retardation
n1=en:dementia, rapidly progressive | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:demyelination ---
r_associated #0: 20 -->
en:retardation
n1=en:demyelination | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:demyelination of the posterior and lateral columns of the spinal cord ---
r_associated #0: 20 -->
en:retardation
n1=en:demyelination of the posterior and lateral columns of the spinal cord | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:demyelination with white matter disease in internal capsule, external capsule, genu of corpus callosum, subcortical white matter, and posterior fossa ---
r_associated #0: 20 -->
en:retardation
n1=en:demyelination with white matter disease in internal capsule, external capsule, genu of corpus callosum, subcortical white matter, and posterior fossa | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:demyelination, symmetric ---
r_associated #0: 20 -->
en:retardation
n1=en:demyelination, symmetric | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:demyelinization ---
r_associated #0: 20 -->
en:retardation
n1=en:demyelinization | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:denervation seen on emg ---
r_associated #0: 20 -->
en:retardation
n1=en:denervation seen on emg | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dense calcifications in the cerebellar dentate nucleus ---
r_associated #0: 20 -->
en:retardation
n1=en:dense calcifications in the cerebellar dentate nucleus | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:depersonalization ---
r_associated #0: 20 -->
en:retardation
n1=en:depersonalization | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:depressed mood disorders and disturbances ---
r_associated #0: 20 -->
en:retardation
n1=en:depressed mood disorders and disturbances | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:depression ---
r_associated #0: 20 -->
en:retardation
n1=en:depression | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:depression, psychotic ---
r_associated #0: 20 -->
en:retardation
n1=en:depression, psychotic | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:depressive disorder ---
r_associated #0: 20 -->
en:retardation
n1=en:depressive disorder | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dermatophytosis ---
r_associated #0: 20 -->
en:retardation
n1=en:dermatophytosis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dermoid cyst ---
r_associated #0: 20 -->
en:retardation
n1=en:dermoid cyst | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:deterioration of motor development ---
r_associated #0: 20 -->
en:retardation
n1=en:deterioration of motor development | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:development varies from normal to retarded ---
r_associated #0: 20 -->
en:retardation
n1=en:development varies from normal to retarded | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:developmental agnosias ---
r_associated #0: 20 -->
en:retardation
n1=en:developmental agnosias | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:developmental arithmetic disorder ---
r_associated #0: 20 -->
en:retardation
n1=en:developmental arithmetic disorder | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:developmental arrest, 2nd year of life ---
r_associated #0: 20 -->
en:retardation
n1=en:developmental arrest, 2nd year of life | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:developmental coordination disorder ---
r_associated #0: 20 -->
en:retardation
n1=en:developmental coordination disorder | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:developmental delay ---
r_associated #0: 20 -->
en:retardation
n1=en:developmental delay | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:developmental delay (1 family) ---
r_associated #0: 20 -->
en:retardation
n1=en:developmental delay (1 family) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:developmental delay (1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:developmental delay (1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:developmental delay (100%) ---
r_associated #0: 20 -->
en:retardation
n1=en:developmental delay (100%) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:developmental delay (20%) ---
r_associated #0: 20 -->
en:retardation
n1=en:developmental delay (20%) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:developmental delay (apparent after the first year of life) ---
r_associated #0: 20 -->
en:retardation
n1=en:developmental delay (apparent after the first year of life) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:developmental delay (female) ---
r_associated #0: 20 -->
en:retardation
n1=en:developmental delay (female) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:developmental delay (homozygote) ---
r_associated #0: 20 -->
en:retardation
n1=en:developmental delay (homozygote) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:developmental delay (in most patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:developmental delay (in most patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:developmental delay (in some patients who survive infancy) ---
r_associated #0: 20 -->
en:retardation
n1=en:developmental delay (in some patients who survive infancy) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:developmental delay (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:developmental delay (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:developmental delay (in some) ---
r_associated #0: 20 -->
en:retardation
n1=en:developmental delay (in some) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:developmental delay (microdeletion patients only) ---
r_associated #0: 20 -->
en:retardation
n1=en:developmental delay (microdeletion patients only) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:developmental delay (mild-severe) ---
r_associated #0: 20 -->
en:retardation
n1=en:developmental delay (mild-severe) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:developmental delay (rare) ---
r_associated #0: 20 -->
en:retardation
n1=en:developmental delay (rare) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:developmental delay (seen in recessive form) ---
r_associated #0: 20 -->
en:retardation
n1=en:developmental delay (seen in recessive form) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:developmental delay (type ii) ---
r_associated #0: 20 -->
en:retardation
n1=en:developmental delay (type ii) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:developmental delay (uncommon) ---
r_associated #0: 20 -->
en:retardation
n1=en:developmental delay (uncommon) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:developmental delay evident by 12-24 months of age ---
r_associated #0: 20 -->
en:retardation
n1=en:developmental delay evident by 12-24 months of age | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:developmental delay if undiagnosed or untreated ---
r_associated #0: 20 -->
en:retardation
n1=en:developmental delay if undiagnosed or untreated | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:developmental delay or regression ---
r_associated #0: 20 -->
en:retardation
n1=en:developmental delay or regression | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:developmental delay, mild ---
r_associated #0: 20 -->
en:retardation
n1=en:developmental delay, mild | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:developmental delay, mild (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:developmental delay, mild (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:developmental delay, mild (in some) ---
r_associated #0: 20 -->
en:retardation
n1=en:developmental delay, mild (in some) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:developmental delay, mild to moderate ---
r_associated #0: 20 -->
en:retardation
n1=en:developmental delay, mild to moderate | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:developmental delay, moderate (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:developmental delay, moderate (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:developmental delay, primarily motor, resolves in childhood ---
r_associated #0: 20 -->
en:retardation
n1=en:developmental delay, primarily motor, resolves in childhood | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:developmental delay, profound ---
r_associated #0: 20 -->
en:retardation
n1=en:developmental delay, profound | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:developmental delay, progressive ---
r_associated #0: 20 -->
en:retardation
n1=en:developmental delay, progressive | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:developmental delay, severe ---
r_associated #0: 20 -->
en:retardation
n1=en:developmental delay, severe | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:developmental delay, severe (2p21del) ---
r_associated #0: 20 -->
en:retardation
n1=en:developmental delay, severe (2p21del) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:developmental delay, significant ---
r_associated #0: 20 -->
en:retardation
n1=en:developmental delay, significant | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:developmental delay, variable ---
r_associated #0: 20 -->
en:retardation
n1=en:developmental delay, variable | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:developmental delay, variable severity ---
r_associated #0: 20 -->
en:retardation
n1=en:developmental delay, variable severity | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:developmental disease/disorder ---
r_associated #0: 20 -->
en:retardation
n1=en:developmental disease/disorder | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:developmental dislocation ---
r_associated #0: 20 -->
en:retardation
n1=en:developmental dislocation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:developmental disorder ---
r_associated #0: 20 -->
en:retardation
n1=en:developmental disorder | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:developmental disorders nec ---
r_associated #0: 20 -->
en:retardation
n1=en:developmental disorders nec | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:developmental dysphasia or aphasia, expressive type ---
r_associated #0: 20 -->
en:retardation
n1=en:developmental dysphasia or aphasia, expressive type | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:developmental expressive writing disorder ---
r_associated #0: 20 -->
en:retardation
n1=en:developmental expressive writing disorder | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:developmental failure of fusion ---
r_associated #0: 20 -->
en:retardation
n1=en:developmental failure of fusion | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:developmental hereditary disorder ---
r_associated #0: 20 -->
en:retardation
n1=en:developmental hereditary disorder | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:developmental immaturity ---
r_associated #0: 20 -->
en:retardation
n1=en:developmental immaturity | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:developmental language impairment ---
r_associated #0: 20 -->
en:retardation
n1=en:developmental language impairment | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:developmental malformation of branchial arch ---
r_associated #0: 20 -->
en:retardation
n1=en:developmental malformation of branchial arch | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:developmental mental disorder ---
r_associated #0: 20 -->
en:retardation
n1=en:developmental mental disorder | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:developmental reading disorder ---
r_associated #0: 20 -->
en:retardation
n1=en:developmental reading disorder | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:developmental regression ---
r_associated #0: 20 -->
en:retardation
n1=en:developmental regression | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:developmental regression (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:developmental regression (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:developmental regression after age 2 years ---
r_associated #0: 20 -->
en:retardation
n1=en:developmental regression after age 2 years | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:developmental regression after onset of seizures ---
r_associated #0: 20 -->
en:retardation
n1=en:developmental regression after onset of seizures | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:developmental regression after the first year ---
r_associated #0: 20 -->
en:retardation
n1=en:developmental regression after the first year | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:developmental regression before age 6 months ---
r_associated #0: 20 -->
en:retardation
n1=en:developmental regression before age 6 months | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:developmental regression in about 50% of patients ---
r_associated #0: 20 -->
en:retardation
n1=en:developmental regression in about 50% of patients | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:developmental regression in affected children ---
r_associated #0: 20 -->
en:retardation
n1=en:developmental regression in affected children | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:developmental regression, after age 2 years (some) ---
r_associated #0: 20 -->
en:retardation
n1=en:developmental regression, after age 2 years (some) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:developmental regression, severe ---
r_associated #0: 20 -->
en:retardation
n1=en:developmental regression, severe | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:developmental retardation (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:developmental retardation (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:developmental retardation, profound ---
r_associated #0: 20 -->
en:retardation
n1=en:developmental retardation, profound | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:developmental retardation, severe ---
r_associated #0: 20 -->
en:retardation
n1=en:developmental retardation, severe | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:developmental stagnation ---
r_associated #0: 20 -->
en:retardation
n1=en:developmental stagnation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:developmental stagnation at onset of seizures ---
r_associated #0: 20 -->
en:retardation
n1=en:developmental stagnation at onset of seizures | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:developmental stricture ---
r_associated #0: 20 -->
en:retardation
n1=en:developmental stricture | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:developmentally disabled (finding) ---
r_associated #0: 20 -->
en:retardation
n1=en:developmentally disabled (finding) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:diabetes mellitus ---
r_associated #0: 20 -->
en:retardation
n1=en:diabetes mellitus | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:diabetes with coma (disorder) ---
r_associated #0: 20 -->
en:retardation
n1=en:diabetes with coma (disorder) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:diagnosis/diseases component ---
r_associated #0: 20 -->
en:retardation
n1=en:diagnosis/diseases component | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:diaper dermatitis ---
r_associated #0: 20 -->
en:retardation
n1=en:diaper dermatitis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:difficulties in fine bimanual activities ---
r_associated #0: 20 -->
en:retardation
n1=en:difficulties in fine bimanual activities | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:difficulties in fine movement of the hands ---
r_associated #0: 20 -->
en:retardation
n1=en:difficulties in fine movement of the hands | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:difficulties with equilibrium ---
r_associated #0: 20 -->
en:retardation
n1=en:difficulties with equilibrium | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:difficulties with fine motor skills and coordination ---
r_associated #0: 20 -->
en:retardation
n1=en:difficulties with fine motor skills and coordination | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:difficulty in phonologic coding ---
r_associated #0: 20 -->
en:retardation
n1=en:difficulty in phonologic coding | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:difficulty in spelling ---
r_associated #0: 20 -->
en:retardation
n1=en:difficulty in spelling | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:difficulty reading ---
r_associated #0: 20 -->
en:retardation
n1=en:difficulty reading | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:difficulty running ---
r_associated #0: 20 -->
en:retardation
n1=en:difficulty running | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:difficulty running and climbing stairs ---
r_associated #0: 20 -->
en:retardation
n1=en:difficulty running and climbing stairs | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:difficulty sleeping ---
r_associated #0: 20 -->
en:retardation
n1=en:difficulty sleeping | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:difficulty speaking during seizures ---
r_associated #0: 20 -->
en:retardation
n1=en:difficulty speaking during seizures | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:difficulty standing ---
r_associated #0: 20 -->
en:retardation
n1=en:difficulty standing | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:difficulty standing alone ---
r_associated #0: 20 -->
en:retardation
n1=en:difficulty standing alone | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:difficulty walking and climbing stairs ---
r_associated #0: 20 -->
en:retardation
n1=en:difficulty walking and climbing stairs | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:difficulty walking in childhood ---
r_associated #0: 20 -->
en:retardation
n1=en:difficulty walking in childhood | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:difficulty walking, running ---
r_associated #0: 20 -->
en:retardation
n1=en:difficulty walking, running | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:difficulty with writing and drawing ---
r_associated #0: 20 -->
en:retardation
n1=en:difficulty with writing and drawing | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:difficulty writing ---
r_associated #0: 20 -->
en:retardation
n1=en:difficulty writing | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:diffuse atrophy of cerebral hemispheres, corpus callosum, and brainstem ---
r_associated #0: 20 -->
en:retardation
n1=en:diffuse atrophy of cerebral hemispheres, corpus callosum, and brainstem | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:diffuse axonal swelling ---
r_associated #0: 20 -->
en:retardation
n1=en:diffuse axonal swelling | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:diffuse brain and spinal cord atrophy on brain ct/mri ---
r_associated #0: 20 -->
en:retardation
n1=en:diffuse brain and spinal cord atrophy on brain ct/mri | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:diffuse brain swelling occurs during coma ---
r_associated #0: 20 -->
en:retardation
n1=en:diffuse brain swelling occurs during coma | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:diffuse cerebellar atrophy ---
r_associated #0: 20 -->
en:retardation
n1=en:diffuse cerebellar atrophy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:diffuse cerebral atrophy on ct and mri ---
r_associated #0: 20 -->
en:retardation
n1=en:diffuse cerebral atrophy on ct and mri | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:diffuse cerebral atrophy seen on mri ---
r_associated #0: 20 -->
en:retardation
n1=en:diffuse cerebral atrophy seen on mri | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:diffuse cerebral gliosis ---
r_associated #0: 20 -->
en:retardation
n1=en:diffuse cerebral gliosis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:diffuse demyelination (increased signal intensity in t2-weighted images, especially frontal lobes) ---
r_associated #0: 20 -->
en:retardation
n1=en:diffuse demyelination (increased signal intensity in t2-weighted images, especially frontal lobes) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:diffuse enlargement of subarachnoid spaces and lateral ventricles (rare) ---
r_associated #0: 20 -->
en:retardation
n1=en:diffuse enlargement of subarachnoid spaces and lateral ventricles (rare) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:diffuse fibrillar astrocytosis (in type iib) ---
r_associated #0: 20 -->
en:retardation
n1=en:diffuse fibrillar astrocytosis (in type iib) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:diffuse hyperintense signal abnormalities in the white matter (in children) ---
r_associated #0: 20 -->
en:retardation
n1=en:diffuse hyperintense signal abnormalities in the white matter (in children) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:diffuse hypomyelination ---
r_associated #0: 20 -->
en:retardation
n1=en:diffuse hypomyelination | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:diffuse hyporeflexia (later) ---
r_associated #0: 20 -->
en:retardation
n1=en:diffuse hyporeflexia (later) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:diffuse hypotonia ---
r_associated #0: 20 -->
en:retardation
n1=en:diffuse hypotonia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:diffuse leptomeningeal enhancement seen on mri ---
r_associated #0: 20 -->
en:retardation
n1=en:diffuse leptomeningeal enhancement seen on mri | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:diffuse leukoencephalopathy ---
r_associated #0: 20 -->
en:retardation
n1=en:diffuse leukoencephalopathy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:diffuse lewy bodies throughout the brain (cortical and subcortical regions) ---
r_associated #0: 20 -->
en:retardation
n1=en:diffuse lewy bodies throughout the brain (cortical and subcortical regions) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:diffuse lewy body pathology ---
r_associated #0: 20 -->
en:retardation
n1=en:diffuse lewy body pathology | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:diffuse paroxysmal discharges ---
r_associated #0: 20 -->
en:retardation
n1=en:diffuse paroxysmal discharges | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:diffuse periventricular leukoencephalopathy ---
r_associated #0: 20 -->
en:retardation
n1=en:diffuse periventricular leukoencephalopathy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:diffuse signal abnormality of central white matter ---
r_associated #0: 20 -->
en:retardation
n1=en:diffuse signal abnormality of central white matter | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:diffuse slowing ---
r_associated #0: 20 -->
en:retardation
n1=en:diffuse slowing | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:diffuse slowing of background ---
r_associated #0: 20 -->
en:retardation
n1=en:diffuse slowing of background | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:diffuse spongiform leukoencephalopathy ---
r_associated #0: 20 -->
en:retardation
n1=en:diffuse spongiform leukoencephalopathy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:diffuse swelling of cerebral white matter ---
r_associated #0: 20 -->
en:retardation
n1=en:diffuse swelling of cerebral white matter | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:diffuse white matter abnormalities on brain mri ---
r_associated #0: 20 -->
en:retardation
n1=en:diffuse white matter abnormalities on brain mri | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:diffuse white matter abnormalities seen on brain mri ---
r_associated #0: 20 -->
en:retardation
n1=en:diffuse white matter abnormalities seen on brain mri | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:diffuse white matter changes (meb) ---
r_associated #0: 20 -->
en:retardation
n1=en:diffuse white matter changes (meb) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:diffuse white matter dysmyelination ---
r_associated #0: 20 -->
en:retardation
n1=en:diffuse white matter dysmyelination | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:diffuse white matter hyperintensities on t2-weighed imaging ---
r_associated #0: 20 -->
en:retardation
n1=en:diffuse white matter hyperintensities on t2-weighed imaging | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:diffuse white matter loss ---
r_associated #0: 20 -->
en:retardation
n1=en:diffuse white matter loss | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:diffuse, severe neuronal loss ---
r_associated #0: 20 -->
en:retardation
n1=en:diffuse, severe neuronal loss | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:digeorge syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:digeorge syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:digitorenocerebral syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:digitorenocerebral syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dihydropyrimidine dehydrogenase deficiency ---
r_associated #0: 20 -->
en:retardation
n1=en:dihydropyrimidine dehydrogenase deficiency | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dilatation of the 3rd ventricle (in one family) ---
r_associated #0: 20 -->
en:retardation
n1=en:dilatation of the 3rd ventricle (in one family) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dilatation of the lateral and third ventricles ---
r_associated #0: 20 -->
en:retardation
n1=en:dilatation of the lateral and third ventricles | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dilatation of the lateral ventricles (in one family) ---
r_associated #0: 20 -->
en:retardation
n1=en:dilatation of the lateral ventricles (in one family) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dilated fourth ventricle ---
r_associated #0: 20 -->
en:retardation
n1=en:dilated fourth ventricle | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dilated lateral ventricles (1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:dilated lateral ventricles (1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dilated perivascular spaces ---
r_associated #0: 20 -->
en:retardation
n1=en:dilated perivascular spaces | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dilated venous sinuses ---
r_associated #0: 20 -->
en:retardation
n1=en:dilated venous sinuses | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dilated ventricles (finding) ---
r_associated #0: 20 -->
en:retardation
n1=en:dilated ventricles (finding) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dilation of cerebral ventricles ---
r_associated #0: 20 -->
en:retardation
n1=en:dilation of cerebral ventricles | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dilation of lateral ventricles ---
r_associated #0: 20 -->
en:retardation
n1=en:dilation of lateral ventricles | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dilation of lateral ventricles (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:dilation of lateral ventricles (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:diminished visual activity ---
r_associated #0: 20 -->
en:retardation
n1=en:diminished visual activity | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:diplegia ---
r_associated #0: 20 -->
en:retardation
n1=en:diplegia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:disability ---
r_associated #0: 20 -->
en:retardation
n1=en:disability | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:disability - moderate ---
r_associated #0: 20 -->
en:retardation
n1=en:disability - moderate | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:disability - severe ---
r_associated #0: 20 -->
en:retardation
n1=en:disability - severe | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:disability - slight ---
r_associated #0: 20 -->
en:retardation
n1=en:disability - slight | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:disability affecting daily living ---
r_associated #0: 20 -->
en:retardation
n1=en:disability affecting daily living | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:disability evaluation, normal, no disability, no impairment ---
r_associated #0: 20 -->
en:retardation
n1=en:disability evaluation, normal, no disability, no impairment | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:disability of lower limb ---
r_associated #0: 20 -->
en:retardation
n1=en:disability of lower limb | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:disability of upper limb ---
r_associated #0: 20 -->
en:retardation
n1=en:disability of upper limb | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:disability percentage ---
r_associated #0: 20 -->
en:retardation
n1=en:disability percentage | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:disabled population ---
r_associated #0: 20 -->
en:retardation
n1=en:disabled population | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:discrepancy between verbal and nonverbal abilities ---
r_associated #0: 20 -->
en:retardation
n1=en:discrepancy between verbal and nonverbal abilities | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:disdiadochokinesia ---
r_associated #0: 20 -->
en:retardation
n1=en:disdiadochokinesia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:disease of mouth/tongue/lips ---
r_associated #0: 20 -->
en:retardation
n1=en:disease of mouth/tongue/lips | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:disease of teeth/gums ---
r_associated #0: 20 -->
en:retardation
n1=en:disease of teeth/gums | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:disease or disorder ---
r_associated #0: 20 -->
en:retardation
n1=en:disease or disorder | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dislocation ---
r_associated #0: 20 -->
en:retardation
n1=en:dislocation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:disorder of branched-chain amino acid metabolism ---
r_associated #0: 20 -->
en:retardation
n1=en:disorder of branched-chain amino acid metabolism | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:disorder of higher mental process ---
r_associated #0: 20 -->
en:retardation
n1=en:disorder of higher mental process | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:disorder of psychological development ---
r_associated #0: 20 -->
en:retardation
n1=en:disorder of psychological development | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:disorder of stature ---
r_associated #0: 20 -->
en:retardation
n1=en:disorder of stature | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:disordered myelination ---
r_associated #0: 20 -->
en:retardation
n1=en:disordered myelination | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:disordered sleep pattern (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:disordered sleep pattern (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:disordered thinking ---
r_associated #0: 20 -->
en:retardation
n1=en:disordered thinking | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:disorders of cutaneous image and perception ---
r_associated #0: 20 -->
en:retardation
n1=en:disorders of cutaneous image and perception | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:disorganised speech ---
r_associated #0: 20 -->
en:retardation
n1=en:disorganised speech | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:disorganization of the anterior cerebellar vermis ---
r_associated #0: 20 -->
en:retardation
n1=en:disorganization of the anterior cerebellar vermis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:disorganized brain cytoarchitecture ---
r_associated #0: 20 -->
en:retardation
n1=en:disorganized brain cytoarchitecture | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:disorganized cortical architecture ---
r_associated #0: 20 -->
en:retardation
n1=en:disorganized cortical architecture | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:disorganized eeg ---
r_associated #0: 20 -->
en:retardation
n1=en:disorganized eeg | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:disorganized slow background activity seen on eeg ---
r_associated #0: 20 -->
en:retardation
n1=en:disorganized slow background activity seen on eeg | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:disorientation ---
r_associated #0: 20 -->
en:retardation
n1=en:disorientation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:disproportionately small cerebral cortex ---
r_associated #0: 20 -->
en:retardation
n1=en:disproportionately small cerebral cortex | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dissociative disorder ---
r_associated #0: 20 -->
en:retardation
n1=en:dissociative disorder | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:distal amyotrophy ---
r_associated #0: 20 -->
en:retardation
n1=en:distal amyotrophy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:distal muscle weakness ---
r_associated #0: 20 -->
en:retardation
n1=en:distal muscle weakness | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:distal muscle weakness and atrophy due to motor neuronopathy ---
r_associated #0: 20 -->
en:retardation
n1=en:distal muscle weakness and atrophy due to motor neuronopathy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:distal muscle weakness, upper and lower limbs ---
r_associated #0: 20 -->
en:retardation
n1=en:distal muscle weakness, upper and lower limbs | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:distal sensory impairment ---
r_associated #0: 20 -->
en:retardation
n1=en:distal sensory impairment | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:distal sensory loss to all modalities, lower limbs more affected than upper limbs ---
r_associated #0: 20 -->
en:retardation
n1=en:distal sensory loss to all modalities, lower limbs more affected than upper limbs | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:distal tapering of the carotid, cerebellar, and meningeal arteries ---
r_associated #0: 20 -->
en:retardation
n1=en:distal tapering of the carotid, cerebellar, and meningeal arteries | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:distal weakness occurs later ---
r_associated #0: 20 -->
en:retardation
n1=en:distal weakness occurs later | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:disturbance of attention ---
r_associated #0: 20 -->
en:retardation
n1=en:disturbance of attention | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:disturbance of consciousness ---
r_associated #0: 20 -->
en:retardation
n1=en:disturbance of consciousness | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:disturbances in thinking and perception ---
r_associated #0: 20 -->
en:retardation
n1=en:disturbances in thinking and perception | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:disturbed equilibrium ---
r_associated #0: 20 -->
en:retardation
n1=en:disturbed equilibrium | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:disturbed gait ---
r_associated #0: 20 -->
en:retardation
n1=en:disturbed gait | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:disturbed myelination affecting the periventricular and subcortical white matter ---
r_associated #0: 20 -->
en:retardation
n1=en:disturbed myelination affecting the periventricular and subcortical white matter | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:disturbed sleep-wake cycle ---
r_associated #0: 20 -->
en:retardation
n1=en:disturbed sleep-wake cycle | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:diurnal fluctuations of symptoms (in a subset of patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:diurnal fluctuations of symptoms (in a subset of patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:diverticulosis ---
r_associated #0: 20 -->
en:retardation
n1=en:diverticulosis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dizziness ---
r_associated #0: 20 -->
en:retardation
n1=en:dizziness | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dizziness adverse event ---
r_associated #0: 20 -->
en:retardation
n1=en:dizziness adverse event | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dizziness may occur ---
r_associated #0: 20 -->
en:retardation
n1=en:dizziness may occur | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dizziness, episodic ---
r_associated #0: 20 -->
en:retardation
n1=en:dizziness, episodic | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dopamine-responsive parkinsonism ---
r_associated #0: 20 -->
en:retardation
n1=en:dopamine-responsive parkinsonism | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dopaminergic fiber systems in the brain ---
r_associated #0: 20 -->
en:retardation
n1=en:dopaminergic fiber systems in the brain | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:double cortex syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:double cortex syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:down syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:down syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dream disorder ---
r_associated #0: 20 -->
en:retardation
n1=en:dream disorder | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dream enactment ---
r_associated #0: 20 -->
en:retardation
n1=en:dream enactment | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dressing disability ---
r_associated #0: 20 -->
en:retardation
n1=en:dressing disability | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:drooling ---
r_associated #0: 20 -->
en:retardation
n1=en:drooling | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:drop attack ---
r_associated #0: 20 -->
en:retardation
n1=en:drop attack | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:drug abuse ---
r_associated #0: 20 -->
en:retardation
n1=en:drug abuse | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:drug dependence ---
r_associated #0: 20 -->
en:retardation
n1=en:drug dependence | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:drug-resistent seizures (rare) ---
r_associated #0: 20 -->
en:retardation
n1=en:drug-resistent seizures (rare) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dubowitz syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:dubowitz syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:duodenal ulcer ---
r_associated #0: 20 -->
en:retardation
n1=en:duodenal ulcer | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dural and choroid plexus calcifications ---
r_associated #0: 20 -->
en:retardation
n1=en:dural and choroid plexus calcifications | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dural ectasia ---
r_associated #0: 20 -->
en:retardation
n1=en:dural ectasia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dysarthria ---
r_associated #0: 20 -->
en:retardation
n1=en:dysarthria | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dysarthria (1 family) ---
r_associated #0: 20 -->
en:retardation
n1=en:dysarthria (1 family) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dysarthria (1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:dysarthria (1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dysarthria (74%) ---
r_associated #0: 20 -->
en:retardation
n1=en:dysarthria (74%) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dysarthria (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:dysarthria (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dysarthria (less common) ---
r_associated #0: 20 -->
en:retardation
n1=en:dysarthria (less common) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dysarthria (mild) ---
r_associated #0: 20 -->
en:retardation
n1=en:dysarthria (mild) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dysarthria (most common presenting symptom) ---
r_associated #0: 20 -->
en:retardation
n1=en:dysarthria (most common presenting symptom) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dysarthria (onset in third decade) ---
r_associated #0: 20 -->
en:retardation
n1=en:dysarthria (onset in third decade) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dysarthria may occur ---
r_associated #0: 20 -->
en:retardation
n1=en:dysarthria may occur | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dysarthria, mild (1 family) ---
r_associated #0: 20 -->
en:retardation
n1=en:dysarthria, mild (1 family) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dysarthria, mild (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:dysarthria, mild (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dysarthria, slowly progressive ---
r_associated #0: 20 -->
en:retardation
n1=en:dysarthria, slowly progressive | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dysarthrias, spastic ---
r_associated #0: 20 -->
en:retardation
n1=en:dysarthrias, spastic | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dysautonomia ---
r_associated #0: 20 -->
en:retardation
n1=en:dysautonomia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dysautonomia may occur ---
r_associated #0: 20 -->
en:retardation
n1=en:dysautonomia may occur | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dyscalculia ---
r_associated #0: 20 -->
en:retardation
n1=en:dyscalculia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dysdiadochokinesis ---
r_associated #0: 20 -->
en:retardation
n1=en:dysdiadochokinesis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dysdiadochokinesis (1 family) ---
r_associated #0: 20 -->
en:retardation
n1=en:dysdiadochokinesis (1 family) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dysdiadochokinesis (63%) ---
r_associated #0: 20 -->
en:retardation
n1=en:dysdiadochokinesis (63%) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dysequilibrium syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:dysequilibrium syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dysfunction of lateral corticospinal tracts ---
r_associated #0: 20 -->
en:retardation
n1=en:dysfunction of lateral corticospinal tracts | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dysfunction of the autonomic nervous system ---
r_associated #0: 20 -->
en:retardation
n1=en:dysfunction of the autonomic nervous system | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dysgenesis of corpus callosum ---
r_associated #0: 20 -->
en:retardation
n1=en:dysgenesis of corpus callosum | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dysgenesis of the anterior commissure (in some) ---
r_associated #0: 20 -->
en:retardation
n1=en:dysgenesis of the anterior commissure (in some) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dysgenesis of the corpus callosum (1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:dysgenesis of the corpus callosum (1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dysgenesis or agenesis of the cerebellar vermis ---
r_associated #0: 20 -->
en:retardation
n1=en:dysgenesis or agenesis of the cerebellar vermis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dysgenesis or agenesis of the corpus callosum (in some) ---
r_associated #0: 20 -->
en:retardation
n1=en:dysgenesis or agenesis of the corpus callosum (in some) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dysgraphias ---
r_associated #0: 20 -->
en:retardation
n1=en:dysgraphias | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dyshidrosis [pompholyx] ---
r_associated #0: 20 -->
en:retardation
n1=en:dyshidrosis [pompholyx] | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dyskinesia ---
r_associated #0: 20 -->
en:retardation
n1=en:dyskinesia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dyskinesia buccoglossal ---
r_associated #0: 20 -->
en:retardation
n1=en:dyskinesia buccoglossal | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dyskinesia, episodic ---
r_associated #0: 20 -->
en:retardation
n1=en:dyskinesia, episodic | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dyskinesia, limb, exertion-induced ---
r_associated #0: 20 -->
en:retardation
n1=en:dyskinesia, limb, exertion-induced | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dyskinetic movements ---
r_associated #0: 20 -->
en:retardation
n1=en:dyskinetic movements | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dyslexia ---
r_associated #0: 20 -->
en:retardation
n1=en:dyslexia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dysmetria (1 family) ---
r_associated #0: 20 -->
en:retardation
n1=en:dysmetria (1 family) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dysmetria (1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:dysmetria (1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dysmetria (in 1 of 3 families) ---
r_associated #0: 20 -->
en:retardation
n1=en:dysmetria (in 1 of 3 families) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dysmetria (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:dysmetria (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dysmetria (type i) ---
r_associated #0: 20 -->
en:retardation
n1=en:dysmetria (type i) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dysmetria, mild ---
r_associated #0: 20 -->
en:retardation
n1=en:dysmetria, mild | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dysmetrias, cerebellar ---
r_associated #0: 20 -->
en:retardation
n1=en:dysmetrias, cerebellar | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dysmetric saccades ---
r_associated #0: 20 -->
en:retardation
n1=en:dysmetric saccades | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dysmorphic basal ganglia ---
r_associated #0: 20 -->
en:retardation
n1=en:dysmorphic basal ganglia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dysmorphic basal ganglia (1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:dysmorphic basal ganglia (1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dysmorphic basal ganglia (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:dysmorphic basal ganglia (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dysmorphic basal ganglia (in some) ---
r_associated #0: 20 -->
en:retardation
n1=en:dysmorphic basal ganglia (in some) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dysmorphic corpus callosum ---
r_associated #0: 20 -->
en:retardation
n1=en:dysmorphic corpus callosum | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dysmorphism ---
r_associated #0: 20 -->
en:retardation
n1=en:dysmorphism | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dysmyelinating leukodystrophy ---
r_associated #0: 20 -->
en:retardation
n1=en:dysmyelinating leukodystrophy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dysmyelination of the brain and spinal cord ---
r_associated #0: 20 -->
en:retardation
n1=en:dysmyelination of the brain and spinal cord | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dysmyelination of the brain, myelin is not formed properly ---
r_associated #0: 20 -->
en:retardation
n1=en:dysmyelination of the brain, myelin is not formed properly | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dysmyelination with jaundice ---
r_associated #0: 20 -->
en:retardation
n1=en:dysmyelination with jaundice | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dysosteosclerosis ---
r_associated #0: 20 -->
en:retardation
n1=en:dysosteosclerosis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dysphagia ---
r_associated #0: 20 -->
en:retardation
n1=en:dysphagia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dysphasia ---
r_associated #0: 20 -->
en:retardation
n1=en:dysphasia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dysphonia ---
r_associated #0: 20 -->
en:retardation
n1=en:dysphonia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dysplasia of the cerebellar hemispheres ---
r_associated #0: 20 -->
en:retardation
n1=en:dysplasia of the cerebellar hemispheres | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dysplastic basal ganglia ---
r_associated #0: 20 -->
en:retardation
n1=en:dysplastic basal ganglia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dysplastic c-shaped inferior olivary nuclei ---
r_associated #0: 20 -->
en:retardation
n1=en:dysplastic c-shaped inferior olivary nuclei | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dysplastic cerebellar gangliocytoma ---
r_associated #0: 20 -->
en:retardation
n1=en:dysplastic cerebellar gangliocytoma | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dysplastic cerebellar vermis ---
r_associated #0: 20 -->
en:retardation
n1=en:dysplastic cerebellar vermis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dysplastic cerebellum ---
r_associated #0: 20 -->
en:retardation
n1=en:dysplastic cerebellum | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dysplastic pons ---
r_associated #0: 20 -->
en:retardation
n1=en:dysplastic pons | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dysplastic superior cerebellar vermis ---
r_associated #0: 20 -->
en:retardation
n1=en:dysplastic superior cerebellar vermis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dystonia ---
r_associated #0: 20 -->
en:retardation
n1=en:dystonia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dystonia (1 family) ---
r_associated #0: 20 -->
en:retardation
n1=en:dystonia (1 family) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dystonia (1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:dystonia (1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dystonia (14% of patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:dystonia (14% of patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dystonia (57%) ---
r_associated #0: 20 -->
en:retardation
n1=en:dystonia (57%) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dystonia (<20%) (finding) ---
r_associated #0: 20 -->
en:retardation
n1=en:dystonia (<20%) (finding) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dystonia (in 2 patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:dystonia (in 2 patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dystonia (in severe cases) ---
r_associated #0: 20 -->
en:retardation
n1=en:dystonia (in severe cases) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dystonia (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:dystonia (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dystonia (less common) ---
r_associated #0: 20 -->
en:retardation
n1=en:dystonia (less common) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dystonia (may spontaneously remit in childhood or adolescence) ---
r_associated #0: 20 -->
en:retardation
n1=en:dystonia (may spontaneously remit in childhood or adolescence) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dystonia 18 (disorder) ---
r_associated #0: 20 -->
en:retardation
n1=en:dystonia 18 (disorder) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dystonia at onset (16%) ---
r_associated #0: 20 -->
en:retardation
n1=en:dystonia at onset (16%) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dystonia disorders ---
r_associated #0: 20 -->
en:retardation
n1=en:dystonia disorders | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dystonia may become generalized ---
r_associated #0: 20 -->
en:retardation
n1=en:dystonia may become generalized | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dystonia with diurnal variation ---
r_associated #0: 20 -->
en:retardation
n1=en:dystonia with diurnal variation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dystonia, episodic, primary affects hands and feet ---
r_associated #0: 20 -->
en:retardation
n1=en:dystonia, episodic, primary affects hands and feet | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dystonia, focal (at onset) ---
r_associated #0: 20 -->
en:retardation
n1=en:dystonia, focal (at onset) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dystonia, focal, limited to orbicularis oculi muscle (blepharospasm) ---
r_associated #0: 20 -->
en:retardation
n1=en:dystonia, focal, limited to orbicularis oculi muscle (blepharospasm) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dystonia, generalized, dopa-unresponsive ---
r_associated #0: 20 -->
en:retardation
n1=en:dystonia, generalized, dopa-unresponsive | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dystonia, limb, exercise-induced ---
r_associated #0: 20 -->
en:retardation
n1=en:dystonia, limb, exercise-induced | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dystonia, progressive ---
r_associated #0: 20 -->
en:retardation
n1=en:dystonia, progressive | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dystonia, severe (in all limbs) ---
r_associated #0: 20 -->
en:retardation
n1=en:dystonia, severe (in all limbs) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dystonia, trunk and limbs (upper and lower) ---
r_associated #0: 20 -->
en:retardation
n1=en:dystonia, trunk and limbs (upper and lower) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dystonic hand posturing (44% of patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:dystonic hand posturing (44% of patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dystonic movements (in 1 of 6 patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:dystonic movements (in 1 of 6 patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dystonic posture ---
r_associated #0: 20 -->
en:retardation
n1=en:dystonic posture | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dystonic posturing (rare) ---
r_associated #0: 20 -->
en:retardation
n1=en:dystonic posturing (rare) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dystonic posturing of the hands ---
r_associated #0: 20 -->
en:retardation
n1=en:dystonic posturing of the hands | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dystonic tongue protrusion ---
r_associated #0: 20 -->
en:retardation
n1=en:dystonic tongue protrusion | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dystonic tremor ---
r_associated #0: 20 -->
en:retardation
n1=en:dystonic tremor | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dystonic vocal tremor ---
r_associated #0: 20 -->
en:retardation
n1=en:dystonic vocal tremor | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dystonic writer's cramp ---
r_associated #0: 20 -->
en:retardation
n1=en:dystonic writer's cramp | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:dystrophic neurites ---
r_associated #0: 20 -->
en:retardation
n1=en:dystrophic neurites | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ear neoplasm ---
r_associated #0: 20 -->
en:retardation
n1=en:ear neoplasm | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ear, face and neck congenital anomalies ---
r_associated #0: 20 -->
en:retardation
n1=en:ear, face and neck congenital anomalies | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ear, patella, short stature syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:ear, patella, short stature syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:earlier sleep-offset time (earlier awakening) ---
r_associated #0: 20 -->
en:retardation
n1=en:earlier sleep-offset time (earlier awakening) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:early and severe foot extensor muscle involvement ---
r_associated #0: 20 -->
en:retardation
n1=en:early and severe foot extensor muscle involvement | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:early childhood developmental disability ---
r_associated #0: 20 -->
en:retardation
n1=en:early childhood developmental disability | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:early involvement of the corticospinal pathways ---
r_associated #0: 20 -->
en:retardation
n1=en:early involvement of the corticospinal pathways | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:early severe fetal akinesia sequence ---
r_associated #0: 20 -->
en:retardation
n1=en:early severe fetal akinesia sequence | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:early-onset myoclonic seizures ---
r_associated #0: 20 -->
en:retardation
n1=en:early-onset myoclonic seizures | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:eating disorder ---
r_associated #0: 20 -->
en:retardation
n1=en:eating disorder | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:eating problems in children ---
r_associated #0: 20 -->
en:retardation
n1=en:eating problems in children | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:echolalia ---
r_associated #0: 20 -->
en:retardation
n1=en:echolalia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ectodermal dysplasia ---
r_associated #0: 20 -->
en:retardation
n1=en:ectodermal dysplasia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ectopia ---
r_associated #0: 20 -->
en:retardation
n1=en:ectopia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ectopia cordis ---
r_associated #0: 20 -->
en:retardation
n1=en:ectopia cordis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ectopic dorsal pontine transverse bundle of fibers forms the 'cap' ---
r_associated #0: 20 -->
en:retardation
n1=en:ectopic dorsal pontine transverse bundle of fibers forms the 'cap' | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ectopic posterior pituitary ---
r_associated #0: 20 -->
en:retardation
n1=en:ectopic posterior pituitary | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ectopic posterior pituitary (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:ectopic posterior pituitary (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ectopic pregnancy ---
r_associated #0: 20 -->
en:retardation
n1=en:ectopic pregnancy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ectromelia ---
r_associated #0: 20 -->
en:retardation
n1=en:ectromelia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:educationally subnormal ---
r_associated #0: 20 -->
en:retardation
n1=en:educationally subnormal | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:eeg - alpha abolished, continuous spike waves, intense myoclonus on photic stimulation (stage 3) ---
r_associated #0: 20 -->
en:retardation
n1=en:eeg - alpha abolished, continuous spike waves, intense myoclonus on photic stimulation (stage 3) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:eeg - alpha slowing, 4-6 hz spike waves, myoclonus on photic stimulation (stage 2) ---
r_associated #0: 20 -->
en:retardation
n1=en:eeg - alpha slowing, 4-6 hz spike waves, myoclonus on photic stimulation (stage 2) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:eeg - polyspike on photic stimulation (stage 1) ---
r_associated #0: 20 -->
en:retardation
n1=en:eeg - polyspike on photic stimulation (stage 1) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:eeg abnormalities - slow waking background, intermittent rhythmical slowing (3-5hz), epileptiform discharges ---
r_associated #0: 20 -->
en:retardation
n1=en:eeg abnormalities - slow waking background, intermittent rhythmical slowing (3-5hz), epileptiform discharges | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:eeg abnormalities in 20-50% ---
r_associated #0: 20 -->
en:retardation
n1=en:eeg abnormalities in 20-50% | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:eeg abnormalities in 20-50% impaired language development ---
r_associated #0: 20 -->
en:retardation
n1=en:eeg abnormalities in 20-50% impaired language development | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:eeg and symptomatology suggest mesial temporal origin ---
r_associated #0: 20 -->
en:retardation
n1=en:eeg and symptomatology suggest mesial temporal origin | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:eeg during episodes shows desynchronization ---
r_associated #0: 20 -->
en:retardation
n1=en:eeg during episodes shows desynchronization | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:eeg is slowed with polyspike wave discharges ---
r_associated #0: 20 -->
en:retardation
n1=en:eeg is slowed with polyspike wave discharges | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:eeg is usually normal ---
r_associated #0: 20 -->
en:retardation
n1=en:eeg is usually normal | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:eeg later shows generalized spike or polyspike waves and focal spikes ---
r_associated #0: 20 -->
en:retardation
n1=en:eeg later shows generalized spike or polyspike waves and focal spikes | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:eeg may be normal at first ---
r_associated #0: 20 -->
en:retardation
n1=en:eeg may be normal at first | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:eeg may show migrating focal or multifocal origin (in severe cases) ---
r_associated #0: 20 -->
en:retardation
n1=en:eeg may show migrating focal or multifocal origin (in severe cases) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:eeg shows 3-4-hz spike and multispike slow wave complexes ---
r_associated #0: 20 -->
en:retardation
n1=en:eeg shows 3-4-hz spike and multispike slow wave complexes | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:eeg shows 3-4-hz spike waves ---
r_associated #0: 20 -->
en:retardation
n1=en:eeg shows 3-4-hz spike waves | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:eeg shows 3-hz spike-wave discharges ---
r_associated #0: 20 -->
en:retardation
n1=en:eeg shows 3-hz spike-wave discharges | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:eeg shows abundant slow waves and fast spike activity ---
r_associated #0: 20 -->
en:retardation
n1=en:eeg shows abundant slow waves and fast spike activity | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:eeg shows active generalized spike and wave and polyspike pattern ---
r_associated #0: 20 -->
en:retardation
n1=en:eeg shows active generalized spike and wave and polyspike pattern | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:eeg shows burst suppression ---
r_associated #0: 20 -->
en:retardation
n1=en:eeg shows burst suppression | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:eeg shows centrotemporal spike-wave discharges ---
r_associated #0: 20 -->
en:retardation
n1=en:eeg shows centrotemporal spike-wave discharges | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:eeg shows epileptiform activity ---
r_associated #0: 20 -->
en:retardation
n1=en:eeg shows epileptiform activity | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:eeg shows epileptiform discharges ---
r_associated #0: 20 -->
en:retardation
n1=en:eeg shows epileptiform discharges | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:eeg shows frontal lobe origin ---
r_associated #0: 20 -->
en:retardation
n1=en:eeg shows frontal lobe origin | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:eeg shows generalized polyspike and wave discharges (4-5 hz) ---
r_associated #0: 20 -->
en:retardation
n1=en:eeg shows generalized polyspike and wave discharges (4-5 hz) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:eeg shows generalized polyspike and wave discharges (4-6 hz) ---
r_associated #0: 20 -->
en:retardation
n1=en:eeg shows generalized polyspike and wave discharges (4-6 hz) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:eeg shows generalized, bilateral, synchronous, symmetrical discharge ---
r_associated #0: 20 -->
en:retardation
n1=en:eeg shows generalized, bilateral, synchronous, symmetrical discharge | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:eeg shows hypsarrhythmia ---
r_associated #0: 20 -->
en:retardation
n1=en:eeg shows hypsarrhythmia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:eeg shows hypsarrhythmia (in 1 of 6 patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:eeg shows hypsarrhythmia (in 1 of 6 patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:eeg shows multifocal discharges ---
r_associated #0: 20 -->
en:retardation
n1=en:eeg shows multifocal discharges | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:eeg shows multifocal epileptic activity ---
r_associated #0: 20 -->
en:retardation
n1=en:eeg shows multifocal epileptic activity | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:eeg shows nonspecific slow-wave paroxysms ---
r_associated #0: 20 -->
en:retardation
n1=en:eeg shows nonspecific slow-wave paroxysms | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:eeg shows photosensitivity ---
r_associated #0: 20 -->
en:retardation
n1=en:eeg shows photosensitivity | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:eeg shows rolandic sharp waves and spikes ---
r_associated #0: 20 -->
en:retardation
n1=en:eeg shows rolandic sharp waves and spikes | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:eeg shows slow frequency high amplitude waves with high frequency polyspikes ---
r_associated #0: 20 -->
en:retardation
n1=en:eeg shows slow frequency high amplitude waves with high frequency polyspikes | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:eeg shows slowed dysrhythmia and multifocal discharges ---
r_associated #0: 20 -->
en:retardation
n1=en:eeg shows slowed dysrhythmia and multifocal discharges | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:eeg shows spike and multispike waves, 3-4 hz ---
r_associated #0: 20 -->
en:retardation
n1=en:eeg shows spike and multispike waves, 3-4 hz | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:eeg shows spike and wave or polyspike and wave discharges ---
r_associated #0: 20 -->
en:retardation
n1=en:eeg shows spike and wave or polyspike and wave discharges | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:eeg shows suppression with ictal burst activities ---
r_associated #0: 20 -->
en:retardation
n1=en:eeg shows suppression with ictal burst activities | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:eeg shows suppression-burst pattern ---
r_associated #0: 20 -->
en:retardation
n1=en:eeg shows suppression-burst pattern | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:eeg shows unilateral centrotemporal spikes ---
r_associated #0: 20 -->
en:retardation
n1=en:eeg shows unilateral centrotemporal spikes | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:eeg shows with a multifocal pattern with spikes and sharp waves ---
r_associated #0: 20 -->
en:retardation
n1=en:eeg shows with a multifocal pattern with spikes and sharp waves | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:eeg with burst suppression ---
r_associated #0: 20 -->
en:retardation
n1=en:eeg with burst suppression | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:eeg with focal discharge ---
r_associated #0: 20 -->
en:retardation
n1=en:eeg with focal discharge | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:eeg with paroxysmal activity ---
r_associated #0: 20 -->
en:retardation
n1=en:eeg with paroxysmal activity | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:eeg with photoparoxysmal response ---
r_associated #0: 20 -->
en:retardation
n1=en:eeg with photoparoxysmal response | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:effaced gyral pattern ---
r_associated #0: 20 -->
en:retardation
n1=en:effaced gyral pattern | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:effect prosthetic device ---
r_associated #0: 20 -->
en:retardation
n1=en:effect prosthetic device | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ehlers-danlos syndrome, beasley cohen type ---
r_associated #0: 20 -->
en:retardation
n1=en:ehlers-danlos syndrome, beasley cohen type | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:electroencephalogram (eeg) abnormalities ---
r_associated #0: 20 -->
en:retardation
n1=en:electroencephalogram (eeg) abnormalities | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:electroencephalogram abnormal ---
r_associated #0: 20 -->
en:retardation
n1=en:electroencephalogram abnormal | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:electrophysiologic studies indicate cortical origin ---
r_associated #0: 20 -->
en:retardation
n1=en:electrophysiologic studies indicate cortical origin | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:elejalde disease ---
r_associated #0: 20 -->
en:retardation
n1=en:elejalde disease | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:elevated interferon levels in cerebrospinal fluid ---
r_associated #0: 20 -->
en:retardation
n1=en:elevated interferon levels in cerebrospinal fluid | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:elevated pterin levels (tetrahydrobiopterin, neopterin) in cerebrospinal fluid ---
r_associated #0: 20 -->
en:retardation
n1=en:elevated pterin levels (tetrahydrobiopterin, neopterin) in cerebrospinal fluid | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:elevated white cell count in cerebrospinal fluid ---
r_associated #0: 20 -->
en:retardation
n1=en:elevated white cell count in cerebrospinal fluid | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:elevation and splaying of the superior cerebellar peduncles ---
r_associated #0: 20 -->
en:retardation
n1=en:elevation and splaying of the superior cerebellar peduncles | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:elimination disorders ---
r_associated #0: 20 -->
en:retardation
n1=en:elimination disorders | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:elongated superior cerebellar peduncles ---
r_associated #0: 20 -->
en:retardation
n1=en:elongated superior cerebellar peduncles | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:emanuel syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:emanuel syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:embolism, cerebral ---
r_associated #0: 20 -->
en:retardation
n1=en:embolism, cerebral | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:embryological remnant ---
r_associated #0: 20 -->
en:retardation
n1=en:embryological remnant | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:embryonal rest and/or persistent embryonic structure ---
r_associated #0: 20 -->
en:retardation
n1=en:embryonal rest and/or persistent embryonic structure | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:embryonic cyst ---
r_associated #0: 20 -->
en:retardation
n1=en:embryonic cyst | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:emg shows bursts of activity originating in the masseter muscle and spreading to the orbicularis oris and oculi muscles ---
r_associated #0: 20 -->
en:retardation
n1=en:emg shows bursts of activity originating in the masseter muscle and spreading to the orbicularis oris and oculi muscles | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:emg shows continuous motor unit firing at rest ---
r_associated #0: 20 -->
en:retardation
n1=en:emg shows continuous motor unit firing at rest | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:emg shows evidence of denervation ---
r_associated #0: 20 -->
en:retardation
n1=en:emg shows evidence of denervation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:emg shows fibrillation potentials and mixed myopathic and neurogenic motor unit potentials ---
r_associated #0: 20 -->
en:retardation
n1=en:emg shows fibrillation potentials and mixed myopathic and neurogenic motor unit potentials | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:emg shows fibrillations and fasiculations ---
r_associated #0: 20 -->
en:retardation
n1=en:emg shows fibrillations and fasiculations | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:emg shows involuntary continuous motor activity at rest ---
r_associated #0: 20 -->
en:retardation
n1=en:emg shows involuntary continuous motor activity at rest | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:emg shows neurogenic abnormalities ---
r_associated #0: 20 -->
en:retardation
n1=en:emg shows neurogenic abnormalities | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:emg shows neurogenic changes ---
r_associated #0: 20 -->
en:retardation
n1=en:emg shows neurogenic changes | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:emg shows neurogenic changes and denervation ---
r_associated #0: 20 -->
en:retardation
n1=en:emg shows neurogenic changes and denervation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:emg shows neurogenic findings ---
r_associated #0: 20 -->
en:retardation
n1=en:emg shows neurogenic findings | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:emg with spontaneous discharge of normal motor unit potentials ---
r_associated #0: 20 -->
en:retardation
n1=en:emg with spontaneous discharge of normal motor unit potentials | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:empty sella syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:empty sella syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:encephalitis ---
r_associated #0: 20 -->
en:retardation
n1=en:encephalitis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:encephalocele ---
r_associated #0: 20 -->
en:retardation
n1=en:encephalocele | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:encephalocele (1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:encephalocele (1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:encephalocele (rare) ---
r_associated #0: 20 -->
en:retardation
n1=en:encephalocele (rare) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:encephalocele (single case) ---
r_associated #0: 20 -->
en:retardation
n1=en:encephalocele (single case) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:encephalocele (uncommon) ---
r_associated #0: 20 -->
en:retardation
n1=en:encephalocele (uncommon) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:encephalocele of orbit ---
r_associated #0: 20 -->
en:retardation
n1=en:encephalocele of orbit | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:encephaloceles, frontal ---
r_associated #0: 20 -->
en:retardation
n1=en:encephaloceles, frontal | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:encephalomyelopathy ---
r_associated #0: 20 -->
en:retardation
n1=en:encephalomyelopathy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:encephalomyopathy ---
r_associated #0: 20 -->
en:retardation
n1=en:encephalomyopathy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:encephalopathic attacks, episodic, associated with infection ---
r_associated #0: 20 -->
en:retardation
n1=en:encephalopathic attacks, episodic, associated with infection | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:encephalopathic episodes, often associated with infection ---
r_associated #0: 20 -->
en:retardation
n1=en:encephalopathic episodes, often associated with infection | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:encephalopathy ---
r_associated #0: 20 -->
en:retardation
n1=en:encephalopathy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:encephalopathy (in 1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:encephalopathy (in 1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:encephalopathy (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:encephalopathy (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:encephalopathy adverse event ---
r_associated #0: 20 -->
en:retardation
n1=en:encephalopathy adverse event | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:encephalopathy associated with hypoglycemia ---
r_associated #0: 20 -->
en:retardation
n1=en:encephalopathy associated with hypoglycemia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:encephalopathy during episodes ---
r_associated #0: 20 -->
en:retardation
n1=en:encephalopathy during episodes | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:encephalopathy, acute, episodic ---
r_associated #0: 20 -->
en:retardation
n1=en:encephalopathy, acute, episodic | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:encephalopathy, acute, sudden-onset after febrile illness ---
r_associated #0: 20 -->
en:retardation
n1=en:encephalopathy, acute, sudden-onset after febrile illness | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:encephalopathy, acute, sudden-onset during febrile illness ---
r_associated #0: 20 -->
en:retardation
n1=en:encephalopathy, acute, sudden-onset during febrile illness | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:encephalopathy, acute-onset ---
r_associated #0: 20 -->
en:retardation
n1=en:encephalopathy, acute-onset | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:encephalopathy, episodic ---
r_associated #0: 20 -->
en:retardation
n1=en:encephalopathy, episodic | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:encephalopathy, episodic, associated with febrile illnesses ---
r_associated #0: 20 -->
en:retardation
n1=en:encephalopathy, episodic, associated with febrile illnesses | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:encephalopathy, severe, neonatal ---
r_associated #0: 20 -->
en:retardation
n1=en:encephalopathy, severe, neonatal | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:encopresis ---
r_associated #0: 20 -->
en:retardation
n1=en:encopresis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:end-position nystagmus ---
r_associated #0: 20 -->
en:retardation
n1=en:end-position nystagmus | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:endocrine infection ---
r_associated #0: 20 -->
en:retardation
n1=en:endocrine infection | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:endothelial intracytoplasmic globular inclusions ---
r_associated #0: 20 -->
en:retardation
n1=en:endothelial intracytoplasmic globular inclusions | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:enhancement of the c-reflex ---
r_associated #0: 20 -->
en:retardation
n1=en:enhancement of the c-reflex | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:enlarged cerebellar cistern ---
r_associated #0: 20 -->
en:retardation
n1=en:enlarged cerebellar cistern | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:enlarged cerebellum ---
r_associated #0: 20 -->
en:retardation
n1=en:enlarged cerebellum | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:enlarged cisterna magna ---
r_associated #0: 20 -->
en:retardation
n1=en:enlarged cisterna magna | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:enlarged cisterna magna (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:enlarged cisterna magna (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:enlarged corpus callosum ---
r_associated #0: 20 -->
en:retardation
n1=en:enlarged corpus callosum | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:enlarged extraaxial space on brain imaging ---
r_associated #0: 20 -->
en:retardation
n1=en:enlarged extraaxial space on brain imaging | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:enlarged fourth ventricle, mild ---
r_associated #0: 20 -->
en:retardation
n1=en:enlarged fourth ventricle, mild | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:enlarged lateral and third ventricles ---
r_associated #0: 20 -->
en:retardation
n1=en:enlarged lateral and third ventricles | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:enlarged lateral ventricles (occipital>frontal) ---
r_associated #0: 20 -->
en:retardation
n1=en:enlarged lateral ventricles (occipital>frontal) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:enlarged motor unit action potentials ---
r_associated #0: 20 -->
en:retardation
n1=en:enlarged motor unit action potentials | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:enlarged or prominent ventricles (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:enlarged or prominent ventricles (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:enlarged ventricles (1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:enlarged ventricles (1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:enlarged ventricles (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:enlarged ventricles (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:enlarged ventricles (in some) ---
r_associated #0: 20 -->
en:retardation
n1=en:enlarged ventricles (in some) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:enlarged white matter ---
r_associated #0: 20 -->
en:retardation
n1=en:enlarged white matter | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:entire brain ---
r_associated #0: 20 -->
en:retardation
n1=en:entire brain | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:entire central nervous system ---
r_associated #0: 20 -->
en:retardation
n1=en:entire central nervous system | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:entire nucleus of brain ---
r_associated #0: 20 -->
en:retardation
n1=en:entire nucleus of brain | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:eosinophilic 'cotton wool' plaques without dense congophilic core in various brain regions ---
r_associated #0: 20 -->
en:retardation
n1=en:eosinophilic 'cotton wool' plaques without dense congophilic core in various brain regions | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ependymitis ---
r_associated #0: 20 -->
en:retardation
n1=en:ependymitis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:epididymo-orchitis ---
r_associated #0: 20 -->
en:retardation
n1=en:epididymo-orchitis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:epilepsia partialis continua ---
r_associated #0: 20 -->
en:retardation
n1=en:epilepsia partialis continua | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:epilepsies, myoclonic ---
r_associated #0: 20 -->
en:retardation
n1=en:epilepsies, myoclonic | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:epilepsy ---
r_associated #0: 20 -->
en:retardation
n1=en:epilepsy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:epilepsy (in 2 of 3 patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:epilepsy (in 2 of 3 patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:epilepsy (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:epilepsy (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:epilepsy, frontal lobe ---
r_associated #0: 20 -->
en:retardation
n1=en:epilepsy, frontal lobe | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:epilepsy, multifocal, intractable ---
r_associated #0: 20 -->
en:retardation
n1=en:epilepsy, multifocal, intractable | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:epilepsy, myoclonic astatic ---
r_associated #0: 20 -->
en:retardation
n1=en:epilepsy, myoclonic astatic | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:epilepsy, progressive myoclonic 3 ---
r_associated #0: 20 -->
en:retardation
n1=en:epilepsy, progressive myoclonic 3 | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:epilepsy, progressive myoclonic, 8 ---
r_associated #0: 20 -->
en:retardation
n1=en:epilepsy, progressive myoclonic, 8 | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:epilepsy, pyridoxine-dependent ---
r_associated #0: 20 -->
en:retardation
n1=en:epilepsy, pyridoxine-dependent | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:epilepsy, refractory (onset in adolescence or young adulthood) ---
r_associated #0: 20 -->
en:retardation
n1=en:epilepsy, refractory (onset in adolescence or young adulthood) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:epilepsy, rolandic ---
r_associated #0: 20 -->
en:retardation
n1=en:epilepsy, rolandic | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:epilepsy, temporal lobe ---
r_associated #0: 20 -->
en:retardation
n1=en:epilepsy, temporal lobe | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:epileptic drop attack ---
r_associated #0: 20 -->
en:retardation
n1=en:epileptic drop attack | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:epileptic encephalopathy ---
r_associated #0: 20 -->
en:retardation
n1=en:epileptic encephalopathy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:epileptic encephalopathy (in 2 of 3 patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:epileptic encephalopathy (in 2 of 3 patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:epileptic encephalopathy (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:epileptic encephalopathy (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:epileptic encephalopathy with psychomotor retardation (rare) ---
r_associated #0: 20 -->
en:retardation
n1=en:epileptic encephalopathy with psychomotor retardation (rare) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:epileptic encephalopathy, childhood-onset ---
r_associated #0: 20 -->
en:retardation
n1=en:epileptic encephalopathy, childhood-onset | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:epileptic encephalopathy, early infantile, 1 ---
r_associated #0: 20 -->
en:retardation
n1=en:epileptic encephalopathy, early infantile, 1 | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:epileptic encephalopathy, early infantile, 7 ---
r_associated #0: 20 -->
en:retardation
n1=en:epileptic encephalopathy, early infantile, 7 | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:epiphyseal dysplasia hearing loss dysmorphism ---
r_associated #0: 20 -->
en:retardation
n1=en:epiphyseal dysplasia hearing loss dysmorphism | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:episodes begin with muscle tightening ---
r_associated #0: 20 -->
en:retardation
n1=en:episodes begin with muscle tightening | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:episodes last up to 2 minutes ---
r_associated #0: 20 -->
en:retardation
n1=en:episodes last up to 2 minutes | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:episodes may last less than 30 minutes or greater than several hours ---
r_associated #0: 20 -->
en:retardation
n1=en:episodes may last less than 30 minutes or greater than several hours | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:episodes of decreased alertness, hypotonia, and poor respiration requiring mechanical ventilation ---
r_associated #0: 20 -->
en:retardation
n1=en:episodes of decreased alertness, hypotonia, and poor respiration requiring mechanical ventilation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:episodes of weakness can last 1 day to several weeks and can occur 1-3 times per month ---
r_associated #0: 20 -->
en:retardation
n1=en:episodes of weakness can last 1 day to several weeks and can occur 1-3 times per month | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:episodes typically occur several times a week ---
r_associated #0: 20 -->
en:retardation
n1=en:episodes typically occur several times a week | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:episodic absence-like spells ---
r_associated #0: 20 -->
en:retardation
n1=en:episodic absence-like spells | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:episodic acute neurologic deterioration/encephalopathy, recurrent ---
r_associated #0: 20 -->
en:retardation
n1=en:episodic acute neurologic deterioration/encephalopathy, recurrent | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:episodic ataxia ---
r_associated #0: 20 -->
en:retardation
n1=en:episodic ataxia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:episodic confusion ---
r_associated #0: 20 -->
en:retardation
n1=en:episodic confusion | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:episodic generalized skeletal muscle contractions ---
r_associated #0: 20 -->
en:retardation
n1=en:episodic generalized skeletal muscle contractions | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:episodic hemiplegia ---
r_associated #0: 20 -->
en:retardation
n1=en:episodic hemiplegia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:episodic subtype, headaches occur in clusters ---
r_associated #0: 20 -->
en:retardation
n1=en:episodic subtype, headaches occur in clusters | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:episodic sudden headache ---
r_associated #0: 20 -->
en:retardation
n1=en:episodic sudden headache | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:episodic vomiting ---
r_associated #0: 20 -->
en:retardation
n1=en:episodic vomiting | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:equivocal plantar response ---
r_associated #0: 20 -->
en:retardation
n1=en:equivocal plantar response | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:erythrokeratodermia variabilis 3 (disorder) ---
r_associated #0: 20 -->
en:retardation
n1=en:erythrokeratodermia variabilis 3 (disorder) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:esophageal disorder ---
r_associated #0: 20 -->
en:retardation
n1=en:esophageal disorder | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:essential tremor ---
r_associated #0: 20 -->
en:retardation
n1=en:essential tremor | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:essential tremor (1 family) ---
r_associated #0: 20 -->
en:retardation
n1=en:essential tremor (1 family) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ethmocephaly ---
r_associated #0: 20 -->
en:retardation
n1=en:ethmocephaly | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ethylmalonic encephalopathy ---
r_associated #0: 20 -->
en:retardation
n1=en:ethylmalonic encephalopathy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:euphoric mood ---
r_associated #0: 20 -->
en:retardation
n1=en:euphoric mood | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:eustachian tube salpingitis ---
r_associated #0: 20 -->
en:retardation
n1=en:eustachian tube salpingitis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:evolution to severe encephalopathy ---
r_associated #0: 20 -->
en:retardation
n1=en:evolution to severe encephalopathy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:exaggerated acoustic startle response ---
r_associated #0: 20 -->
en:retardation
n1=en:exaggerated acoustic startle response | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:exaggerated moro reflex ---
r_associated #0: 20 -->
en:retardation
n1=en:exaggerated moro reflex | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:exaggerated startle response ---
r_associated #0: 20 -->
en:retardation
n1=en:exaggerated startle response | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:exaggerated startle response to tactile or acoustic stimuli ---
r_associated #0: 20 -->
en:retardation
n1=en:exaggerated startle response to tactile or acoustic stimuli | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:excessive cerumen ---
r_associated #0: 20 -->
en:retardation
n1=en:excessive cerumen | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:excessive daytime somnolence ---
r_associated #0: 20 -->
en:retardation
n1=en:excessive daytime somnolence | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:exencephaly ---
r_associated #0: 20 -->
en:retardation
n1=en:exencephaly | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:expressive aphasia ---
r_associated #0: 20 -->
en:retardation
n1=en:expressive aphasia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:expressive language delay ---
r_associated #0: 20 -->
en:retardation
n1=en:expressive language delay | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:expressive language disorder ---
r_associated #0: 20 -->
en:retardation
n1=en:expressive language disorder | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:expressive speech absent ---
r_associated #0: 20 -->
en:retardation
n1=en:expressive speech absent | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:expressive speech deficit ---
r_associated #0: 20 -->
en:retardation
n1=en:expressive speech deficit | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:exstrophy ---
r_associated #0: 20 -->
en:retardation
n1=en:exstrophy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:extensive melanosis of leptomeninges, amygdala, and cerebellar hemispheres ---
r_associated #0: 20 -->
en:retardation
n1=en:extensive melanosis of leptomeninges, amygdala, and cerebellar hemispheres | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:extensor plantar responses (1 family) ---
r_associated #0: 20 -->
en:retardation
n1=en:extensor plantar responses (1 family) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:extensor plantar responses (1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:extensor plantar responses (1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:extensor plantar responses (early-on) ---
r_associated #0: 20 -->
en:retardation
n1=en:extensor plantar responses (early-on) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:extensor plantar responses (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:extensor plantar responses (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:extensor plantar responses (later) ---
r_associated #0: 20 -->
en:retardation
n1=en:extensor plantar responses (later) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:extensor plantar responses (reported in 1 family) ---
r_associated #0: 20 -->
en:retardation
n1=en:extensor plantar responses (reported in 1 family) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:extensor plantar responses (reported in 1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:extensor plantar responses (reported in 1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:extensor plantar responses (variable) ---
r_associated #0: 20 -->
en:retardation
n1=en:extensor plantar responses (variable) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:extensor posturing ---
r_associated #0: 20 -->
en:retardation
n1=en:extensor posturing | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:external capsule and claustrum may be involved ---
r_associated #0: 20 -->
en:retardation
n1=en:external capsule and claustrum may be involved | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:extra superior temporal gyrus (female) ---
r_associated #0: 20 -->
en:retardation
n1=en:extra superior temporal gyrus (female) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:extraneuronal accumulation of autofluorescent pigmented material in various brain regions ---
r_associated #0: 20 -->
en:retardation
n1=en:extraneuronal accumulation of autofluorescent pigmented material in various brain regions | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:extrapyramidal disorder ---
r_associated #0: 20 -->
en:retardation
n1=en:extrapyramidal disorder | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:extrapyramidal dyskinesia ---
r_associated #0: 20 -->
en:retardation
n1=en:extrapyramidal dyskinesia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:extrapyramidal dyskinesias (1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:extrapyramidal dyskinesias (1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:extrapyramidal features ---
r_associated #0: 20 -->
en:retardation
n1=en:extrapyramidal features | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:extrapyramidal muscular rigidity ---
r_associated #0: 20 -->
en:retardation
n1=en:extrapyramidal muscular rigidity | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:extrapyramidal sign ---
r_associated #0: 20 -->
en:retardation
n1=en:extrapyramidal sign | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:extrapyramidal signs (in 1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:extrapyramidal signs (in 1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:extrapyramidal signs (in some patients) thinning of the corpus callosum ---
r_associated #0: 20 -->
en:retardation
n1=en:extrapyramidal signs (in some patients) thinning of the corpus callosum | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:extrapyramidal signs (less common) ---
r_associated #0: 20 -->
en:retardation
n1=en:extrapyramidal signs (less common) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:extrapyramidal signs may develop ---
r_associated #0: 20 -->
en:retardation
n1=en:extrapyramidal signs may develop | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:extrapyramidal signs, mild ---
r_associated #0: 20 -->
en:retardation
n1=en:extrapyramidal signs, mild | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:extrapyramidal symptoms (later-onset) ---
r_associated #0: 20 -->
en:retardation
n1=en:extrapyramidal symptoms (later-onset) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:extrapyramidal symptoms may occur ---
r_associated #0: 20 -->
en:retardation
n1=en:extrapyramidal symptoms may occur | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:extremity ataxia ---
r_associated #0: 20 -->
en:retardation
n1=en:extremity ataxia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:eye ---
r_associated #0: 20 -->
en:retardation
n1=en:eye | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:facial cleft ---
r_associated #0: 20 -->
en:retardation
n1=en:facial cleft | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:facial muscle sparing ---
r_associated #0: 20 -->
en:retardation
n1=en:facial muscle sparing | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:facial muscle weakness ---
r_associated #0: 20 -->
en:retardation
n1=en:facial muscle weakness | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:facial muscle weakness of muscles innervated by cn vii ---
r_associated #0: 20 -->
en:retardation
n1=en:facial muscle weakness of muscles innervated by cn vii | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:facial myokymia, mild ---
r_associated #0: 20 -->
en:retardation
n1=en:facial myokymia, mild | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:facial myokymias ---
r_associated #0: 20 -->
en:retardation
n1=en:facial myokymias | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:facial nerve palsy ---
r_associated #0: 20 -->
en:retardation
n1=en:facial nerve palsy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:facial nerve weakness ---
r_associated #0: 20 -->
en:retardation
n1=en:facial nerve weakness | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:facial neuralgia ---
r_associated #0: 20 -->
en:retardation
n1=en:facial neuralgia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:facial palsy secondary to cranial hyperostosis ---
r_associated #0: 20 -->
en:retardation
n1=en:facial palsy secondary to cranial hyperostosis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:facial paralysis ---
r_associated #0: 20 -->
en:retardation
n1=en:facial paralysis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:facial paresis, congenital bilateral ---
r_associated #0: 20 -->
en:retardation
n1=en:facial paresis, congenital bilateral | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:facial, pharyngeal, and masticatory muscle diplegia ---
r_associated #0: 20 -->
en:retardation
n1=en:facial, pharyngeal, and masticatory muscle diplegia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:facial-faucial-finger mini-myoclonus (fff) ---
r_associated #0: 20 -->
en:retardation
n1=en:facial-faucial-finger mini-myoclonus (fff) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:facial-lingual fasciculations ---
r_associated #0: 20 -->
en:retardation
n1=en:facial-lingual fasciculations | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:faciocardiomelic syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:faciocardiomelic syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:faciomandibular myoclonus, nocturnal ---
r_associated #0: 20 -->
en:retardation
n1=en:faciomandibular myoclonus, nocturnal | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:factitious disorder ---
r_associated #0: 20 -->
en:retardation
n1=en:factitious disorder | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:failure of opercularization of the frontal and temporal lobes on ct ---
r_associated #0: 20 -->
en:retardation
n1=en:failure of opercularization of the frontal and temporal lobes on ct | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:failure to achieve sitting or walking (severe form) ---
r_associated #0: 20 -->
en:retardation
n1=en:failure to achieve sitting or walking (severe form) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:fall ---
r_associated #0: 20 -->
en:retardation
n1=en:fall | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:falx cerebri, precocious calcification of ---
r_associated #0: 20 -->
en:retardation
n1=en:falx cerebri, precocious calcification of | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:familial scaphocephaly syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:familial scaphocephaly syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:family history of mental retardation ---
r_associated #0: 20 -->
en:retardation
n1=en:family history of mental retardation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:fasciculation ---
r_associated #0: 20 -->
en:retardation
n1=en:fasciculation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:fasciculation-like movements ---
r_associated #0: 20 -->
en:retardation
n1=en:fasciculation-like movements | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:fasciculations (after long disease duration) ---
r_associated #0: 20 -->
en:retardation
n1=en:fasciculations (after long disease duration) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:fasciculations, tongue ---
r_associated #0: 20 -->
en:retardation
n1=en:fasciculations, tongue | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:fatal subacute encephalopathy (1 family) ---
r_associated #0: 20 -->
en:retardation
n1=en:fatal subacute encephalopathy (1 family) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:fatigue ---
r_associated #0: 20 -->
en:retardation
n1=en:fatigue | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:favorable response to levodopa ---
r_associated #0: 20 -->
en:retardation
n1=en:favorable response to levodopa | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:fear of mental disorder ---
r_associated #0: 20 -->
en:retardation
n1=en:fear of mental disorder | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:fearful expression ---
r_associated #0: 20 -->
en:retardation
n1=en:fearful expression | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:febrile seizure ---
r_associated #0: 20 -->
en:retardation
n1=en:febrile seizure | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:febrile seizures (1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:febrile seizures (1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:febrile seizures (in some) ---
r_associated #0: 20 -->
en:retardation
n1=en:febrile seizures (in some) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:febrile seizures (reported in 1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:febrile seizures (reported in 1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:febrile seizures (usually remit by age 6 years) ---
r_associated #0: 20 -->
en:retardation
n1=en:febrile seizures (usually remit by age 6 years) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:febrile seizures in infancy ---
r_associated #0: 20 -->
en:retardation
n1=en:febrile seizures in infancy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:febrile seizures may occur ---
r_associated #0: 20 -->
en:retardation
n1=en:febrile seizures may occur | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:feeding and eating disorders ---
r_associated #0: 20 -->
en:retardation
n1=en:feeding and eating disorders | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:feeding disability ---
r_associated #0: 20 -->
en:retardation
n1=en:feeding disability | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:feeding problem ---
r_associated #0: 20 -->
en:retardation
n1=en:feeding problem | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:feeling anxious/nervous/tense ---
r_associated #0: 20 -->
en:retardation
n1=en:feeling anxious/nervous/tense | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:feeling depressed ---
r_associated #0: 20 -->
en:retardation
n1=en:feeling depressed | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:feeling/behaving irritable ---
r_associated #0: 20 -->
en:retardation
n1=en:feeling/behaving irritable | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:feeling/behaving old/senile ---
r_associated #0: 20 -->
en:retardation
n1=en:feeling/behaving old/senile | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:feingold syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:feingold syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:feingold syndrome 2 ---
r_associated #0: 20 -->
en:retardation
n1=en:feingold syndrome 2 | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:female genital injuries ---
r_associated #0: 20 -->
en:retardation
n1=en:female genital injuries | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:femur fracture ---
r_associated #0: 20 -->
en:retardation
n1=en:femur fracture | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:fenestrated basilar artery ---
r_associated #0: 20 -->
en:retardation
n1=en:fenestrated basilar artery | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:festinating (parkinsonian) gait ---
r_associated #0: 20 -->
en:retardation
n1=en:festinating (parkinsonian) gait | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:fetal akinesia deformation sequence ---
r_associated #0: 20 -->
en:retardation
n1=en:fetal akinesia deformation sequence | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:fetal alcohol syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:fetal alcohol syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:fetal postural deformity ---
r_associated #0: 20 -->
en:retardation
n1=en:fetal postural deformity | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:fg syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:fg syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:fibrillary plaques in the cerebellar cortex ---
r_associated #0: 20 -->
en:retardation
n1=en:fibrillary plaques in the cerebellar cortex | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:fibrillation ---
r_associated #0: 20 -->
en:retardation
n1=en:fibrillation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:fibroid/myoma (uterus/cervix) ---
r_associated #0: 20 -->
en:retardation
n1=en:fibroid/myoma (uterus/cervix) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:fibrous astrocyte ---
r_associated #0: 20 -->
en:retardation
n1=en:fibrous astrocyte | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:fifth ventricle ---
r_associated #0: 20 -->
en:retardation
n1=en:fifth ventricle | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:fine motor delay ---
r_associated #0: 20 -->
en:retardation
n1=en:fine motor delay | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:fine motor disability ---
r_associated #0: 20 -->
en:retardation
n1=en:fine motor disability | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:fine motor impairment ---
r_associated #0: 20 -->
en:retardation
n1=en:fine motor impairment | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:fine motor skills delayed ---
r_associated #0: 20 -->
en:retardation
n1=en:fine motor skills delayed | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:fine motor task disruption ---
r_associated #0: 20 -->
en:retardation
n1=en:fine motor task disruption | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:fine motor/coordination problems (12%) ---
r_associated #0: 20 -->
en:retardation
n1=en:fine motor/coordination problems (12%) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:fine rapid hand tremor, 4-12 hz ---
r_associated #0: 20 -->
en:retardation
n1=en:fine rapid hand tremor, 4-12 hz | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:fine tremors ---
r_associated #0: 20 -->
en:retardation
n1=en:fine tremors | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:finger dysmetria ---
r_associated #0: 20 -->
en:retardation
n1=en:finger dysmetria | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:finger twitching ---
r_associated #0: 20 -->
en:retardation
n1=en:finger twitching | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:first dorsal interossei muscle atrophy ---
r_associated #0: 20 -->
en:retardation
n1=en:first dorsal interossei muscle atrophy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:first dorsal interossei muscle weakness ---
r_associated #0: 20 -->
en:retardation
n1=en:first dorsal interossei muscle weakness | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:flaccidity, episodic ---
r_associated #0: 20 -->
en:retardation
n1=en:flaccidity, episodic | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:flat pons ---
r_associated #0: 20 -->
en:retardation
n1=en:flat pons | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:flattening of the caudate ---
r_associated #0: 20 -->
en:retardation
n1=en:flattening of the caudate | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:flattening of the pons ---
r_associated #0: 20 -->
en:retardation
n1=en:flattening of the pons | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:flexor plantar response ---
r_associated #0: 20 -->
en:retardation
n1=en:flexor plantar response | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:floppiness ---
r_associated #0: 20 -->
en:retardation
n1=en:floppiness | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:floppy infant ---
r_associated #0: 20 -->
en:retardation
n1=en:floppy infant | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:fluctuating neurologic signs ---
r_associated #0: 20 -->
en:retardation
n1=en:fluctuating neurologic signs | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:fluctuations in consciousness ---
r_associated #0: 20 -->
en:retardation
n1=en:fluctuations in consciousness | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:fluid filled posterior fossa ---
r_associated #0: 20 -->
en:retardation
n1=en:fluid filled posterior fossa | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:fluid-filled cavity within the cerebral hemispheres, can be unilateral or bilateral and may or may not communicate with cerebrospinal fluid (csf) spaces ---
r_associated #0: 20 -->
en:retardation
n1=en:fluid-filled cavity within the cerebral hemispheres, can be unilateral or bilateral and may or may not communicate with cerebrospinal fluid (csf) spaces | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:focal cerebellar dysplasia ---
r_associated #0: 20 -->
en:retardation
n1=en:focal cerebellar dysplasia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:focal clonic seizure ---
r_associated #0: 20 -->
en:retardation
n1=en:focal clonic seizure | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:focal cortical dysplasia ---
r_associated #0: 20 -->
en:retardation
n1=en:focal cortical dysplasia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:focal discharges ---
r_associated #0: 20 -->
en:retardation
n1=en:focal discharges | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:focal dyscognitive seizures ---
r_associated #0: 20 -->
en:retardation
n1=en:focal dyscognitive seizures | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:focal dystonia (adult onset) ---
r_associated #0: 20 -->
en:retardation
n1=en:focal dystonia (adult onset) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:focal dystonia (e.g., writer's cramp) ---
r_associated #0: 20 -->
en:retardation
n1=en:focal dystonia (e.g., writer's cramp) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:focal dystonia (rare) ---
r_associated #0: 20 -->
en:retardation
n1=en:focal dystonia (rare) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:focal dystonia, upper limb ---
r_associated #0: 20 -->
en:retardation
n1=en:focal dystonia, upper limb | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:focal dystonia, usually of the hands ---
r_associated #0: 20 -->
en:retardation
n1=en:focal dystonia, usually of the hands | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:focal dystonias ---
r_associated #0: 20 -->
en:retardation
n1=en:focal dystonias | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:focal hyperplasia of the choroid plexus ---
r_associated #0: 20 -->
en:retardation
n1=en:focal hyperplasia of the choroid plexus | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:focal interhemispheric fusion ---
r_associated #0: 20 -->
en:retardation
n1=en:focal interhemispheric fusion | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:focal lissencephaly ---
r_associated #0: 20 -->
en:retardation
n1=en:focal lissencephaly | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:focal microgyria ---
r_associated #0: 20 -->
en:retardation
n1=en:focal microgyria | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:focal neurologic deficit ---
r_associated #0: 20 -->
en:retardation
n1=en:focal neurologic deficit | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:focal neurologic deficits (i.e., hemiparesis) ---
r_associated #0: 20 -->
en:retardation
n1=en:focal neurologic deficits (i.e., hemiparesis) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:focal neurologic signs ---
r_associated #0: 20 -->
en:retardation
n1=en:focal neurologic signs | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:focal nodular heterotopia ---
r_associated #0: 20 -->
en:retardation
n1=en:focal nodular heterotopia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:focal pachygyria ---
r_associated #0: 20 -->
en:retardation
n1=en:focal pachygyria | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:focal parietal pachygyria ---
r_associated #0: 20 -->
en:retardation
n1=en:focal parietal pachygyria | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:focal paroxysmal discharges ---
r_associated #0: 20 -->
en:retardation
n1=en:focal paroxysmal discharges | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:focal thickening of the cortex on mri (in type iib) ---
r_associated #0: 20 -->
en:retardation
n1=en:focal thickening of the cortex on mri (in type iib) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:focal tremor ---
r_associated #0: 20 -->
en:retardation
n1=en:focal tremor | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:focal white matter lesions (in type iib) ---
r_associated #0: 20 -->
en:retardation
n1=en:focal white matter lesions (in type iib) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:focal, segmental or multifocal dystonia ---
r_associated #0: 20 -->
en:retardation
n1=en:focal, segmental or multifocal dystonia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:foot-drop ---
r_associated #0: 20 -->
en:retardation
n1=en:foot-drop | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:forebrain ---
r_associated #0: 20 -->
en:retardation
n1=en:forebrain | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:forebrain defects ---
r_associated #0: 20 -->
en:retardation
n1=en:forebrain defects | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:foreign body in auditory canal ---
r_associated #0: 20 -->
en:retardation
n1=en:foreign body in auditory canal | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:foreign body nose/larynx/bronchus ---
r_associated #0: 20 -->
en:retardation
n1=en:foreign body nose/larynx/bronchus | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:four-repeat tau plaques in the striatum ---
r_associated #0: 20 -->
en:retardation
n1=en:four-repeat tau plaques in the striatum | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:fracture hand/foot bones ---
r_associated #0: 20 -->
en:retardation
n1=en:fracture hand/foot bones | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:fracture of radius and ulna ---
r_associated #0: 20 -->
en:retardation
n1=en:fracture of radius and ulna | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:fracture of tibia and fibula ---
r_associated #0: 20 -->
en:retardation
n1=en:fracture of tibia and fibula | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:fracture other ---
r_associated #0: 20 -->
en:retardation
n1=en:fracture other | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:fragile x syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:fragile x syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:fraser syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:fraser syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:frequency 3.5 hz in midline ---
r_associated #0: 20 -->
en:retardation
n1=en:frequency 3.5 hz in midline | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:frequency 6 hz in lateral gaze ---
r_associated #0: 20 -->
en:retardation
n1=en:frequency 6 hz in lateral gaze | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:frequency of 1 to 20 episodes per day ---
r_associated #0: 20 -->
en:retardation
n1=en:frequency of 1 to 20 episodes per day | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:frequent falls ---
r_associated #0: 20 -->
en:retardation
n1=en:frequent falls | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:frequent falls with preservation of consciousness ---
r_associated #0: 20 -->
en:retardation
n1=en:frequent falls with preservation of consciousness | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:frequent headache ---
r_associated #0: 20 -->
en:retardation
n1=en:frequent headache | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:frightening sensation ---
r_associated #0: 20 -->
en:retardation
n1=en:frightening sensation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:frohlich syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:frohlich syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:frontal cortical atophy ---
r_associated #0: 20 -->
en:retardation
n1=en:frontal cortical atophy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:frontal lobe ---
r_associated #0: 20 -->
en:retardation
n1=en:frontal lobe | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:frontal lobe atrophy ---
r_associated #0: 20 -->
en:retardation
n1=en:frontal lobe atrophy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:frontal lobe hypoplasia ---
r_associated #0: 20 -->
en:retardation
n1=en:frontal lobe hypoplasia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:frontal lobe origin ---
r_associated #0: 20 -->
en:retardation
n1=en:frontal lobe origin | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:frontal lobe syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:frontal lobe syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:frontal release signs ---
r_associated #0: 20 -->
en:retardation
n1=en:frontal release signs | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:frontolimbic dementia ---
r_associated #0: 20 -->
en:retardation
n1=en:frontolimbic dementia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:frontometaphyseal dysplasia ---
r_associated #0: 20 -->
en:retardation
n1=en:frontometaphyseal dysplasia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:frontonasal dysplasia ---
r_associated #0: 20 -->
en:retardation
n1=en:frontonasal dysplasia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:frontoparietal polymicrogyria ---
r_associated #0: 20 -->
en:retardation
n1=en:frontoparietal polymicrogyria | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:frontotemporal atrophy ---
r_associated #0: 20 -->
en:retardation
n1=en:frontotemporal atrophy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:frontotemporal atrophy, mild, seen on mri ---
r_associated #0: 20 -->
en:retardation
n1=en:frontotemporal atrophy, mild, seen on mri | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:frontotemporal dementia ---
r_associated #0: 20 -->
en:retardation
n1=en:frontotemporal dementia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:frontotemporal dementia (1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:frontotemporal dementia (1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:frontotemporal dementia (in 30% of patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:frontotemporal dementia (in 30% of patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:frontotemporal dementia, variable severity ---
r_associated #0: 20 -->
en:retardation
n1=en:frontotemporal dementia, variable severity | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:frontotemporal hypoplasia ---
r_associated #0: 20 -->
en:retardation
n1=en:frontotemporal hypoplasia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:frontotemporal leukoencephalopathy ---
r_associated #0: 20 -->
en:retardation
n1=en:frontotemporal leukoencephalopathy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:frontotemporal lobar atrophy ---
r_associated #0: 20 -->
en:retardation
n1=en:frontotemporal lobar atrophy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:frontotemporal lobar atrophy with 'knife-edge' distinction ---
r_associated #0: 20 -->
en:retardation
n1=en:frontotemporal lobar atrophy with 'knife-edge' distinction | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:frontotemporal pachygyria (1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:frontotemporal pachygyria (1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:frontotemporal polymicrogyria ---
r_associated #0: 20 -->
en:retardation
n1=en:frontotemporal polymicrogyria | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:frontotemporal/subcortical dementia ---
r_associated #0: 20 -->
en:retardation
n1=en:frontotemporal/subcortical dementia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:frontotemporoparietal cortical dysplasia ---
r_associated #0: 20 -->
en:retardation
n1=en:frontotemporoparietal cortical dysplasia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:fucosidosis ---
r_associated #0: 20 -->
en:retardation
n1=en:fucosidosis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:functional quadriplegia ---
r_associated #0: 20 -->
en:retardation
n1=en:functional quadriplegia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:funnel-shaped signal tapering from subcortical white matter to ventricle (in some type iib patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:funnel-shaped signal tapering from subcortical white matter to ventricle (in some type iib patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:fused hemispheres (wws) ---
r_associated #0: 20 -->
en:retardation
n1=en:fused hemispheres (wws) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:fusion of the basal ganglia ---
r_associated #0: 20 -->
en:retardation
n1=en:fusion of the basal ganglia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:fusion of the cerebellar hemispheres ---
r_associated #0: 20 -->
en:retardation
n1=en:fusion of the cerebellar hemispheres | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:fusion of the dentate nuclei and the superior cerebellar peduncles ---
r_associated #0: 20 -->
en:retardation
n1=en:fusion of the dentate nuclei and the superior cerebellar peduncles | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:fusion of the left and right thalami ---
r_associated #0: 20 -->
en:retardation
n1=en:fusion of the left and right thalami | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:gait abnormalities (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:gait abnormalities (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:gait abnormalities (less common) ---
r_associated #0: 20 -->
en:retardation
n1=en:gait abnormalities (less common) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:gait abnormalities due to muscle weakness ---
r_associated #0: 20 -->
en:retardation
n1=en:gait abnormalities due to muscle weakness | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:gait abnormalities may occur ---
r_associated #0: 20 -->
en:retardation
n1=en:gait abnormalities may occur | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:gait and limb ataxia ---
r_associated #0: 20 -->
en:retardation
n1=en:gait and limb ataxia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:gait apraxia ---
r_associated #0: 20 -->
en:retardation
n1=en:gait apraxia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:gait ataxia (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:gait ataxia (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:gait ataxias, cerebellar ---
r_associated #0: 20 -->
en:retardation
n1=en:gait ataxias, cerebellar | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:gait difficulties due to contractures of the lower limbs ---
r_associated #0: 20 -->
en:retardation
n1=en:gait difficulties due to contractures of the lower limbs | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:gait difficulties, late-onset ---
r_associated #0: 20 -->
en:retardation
n1=en:gait difficulties, late-onset | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:gait disability ---
r_associated #0: 20 -->
en:retardation
n1=en:gait disability | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:gait disturbance ---
r_associated #0: 20 -->
en:retardation
n1=en:gait disturbance | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:gait disturbance (ataxia) ---
r_associated #0: 20 -->
en:retardation
n1=en:gait disturbance (ataxia) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:gait imbalance ---
r_associated #0: 20 -->
en:retardation
n1=en:gait imbalance | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:gait impairment ---
r_associated #0: 20 -->
en:retardation
n1=en:gait impairment | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:gait impairment (55%) ---
r_associated #0: 20 -->
en:retardation
n1=en:gait impairment (55%) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:gait instability, worse in the dark ---
r_associated #0: 20 -->
en:retardation
n1=en:gait instability, worse in the dark | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:gait unsteady ---
r_associated #0: 20 -->
en:retardation
n1=en:gait unsteady | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:gait, drop foot ---
r_associated #0: 20 -->
en:retardation
n1=en:gait, drop foot | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:gait, rigid ---
r_associated #0: 20 -->
en:retardation
n1=en:gait, rigid | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:galactosemia ---
r_associated #0: 20 -->
en:retardation
n1=en:galactosemia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:galloway mowat syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:galloway mowat syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:game friedman paradice syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:game friedman paradice syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ganglion joint/tendon ---
r_associated #0: 20 -->
en:retardation
n1=en:ganglion joint/tendon | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:gangliosidosis, generalized gm1, type 1 (disorder) ---
r_associated #0: 20 -->
en:retardation
n1=en:gangliosidosis, generalized gm1, type 1 (disorder) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:gastroenteritis presumed infectious ---
r_associated #0: 20 -->
en:retardation
n1=en:gastroenteritis presumed infectious | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:gastroschisis ---
r_associated #0: 20 -->
en:retardation
n1=en:gastroschisis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:gaucher disease ---
r_associated #0: 20 -->
en:retardation
n1=en:gaucher disease | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:gaze deviation ---
r_associated #0: 20 -->
en:retardation
n1=en:gaze deviation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:general clinical state ---
r_associated #0: 20 -->
en:retardation
n1=en:general clinical state | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:generalized amyotrophy ---
r_associated #0: 20 -->
en:retardation
n1=en:generalized amyotrophy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:generalized and focal spike and wave complexes seen on eeg ---
r_associated #0: 20 -->
en:retardation
n1=en:generalized and focal spike and wave complexes seen on eeg | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:generalized cerebral hypoplasia/atrophy (45%) ---
r_associated #0: 20 -->
en:retardation
n1=en:generalized cerebral hypoplasia/atrophy (45%) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:generalized cerebral, cerebellar, and brainstem atrophy, progressive ---
r_associated #0: 20 -->
en:retardation
n1=en:generalized cerebral, cerebellar, and brainstem atrophy, progressive | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:generalized clonic or tonic-clonic seizures ---
r_associated #0: 20 -->
en:retardation
n1=en:generalized clonic or tonic-clonic seizures | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:generalized cortical atrophy (in one patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:generalized cortical atrophy (in one patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:generalized cortical atrophy, most prominent in the frontal and parietal lobes ---
r_associated #0: 20 -->
en:retardation
n1=en:generalized cortical atrophy, most prominent in the frontal and parietal lobes | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:generalized dystonia ---
r_associated #0: 20 -->
en:retardation
n1=en:generalized dystonia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:generalized hypotonia ---
r_associated #0: 20 -->
en:retardation
n1=en:generalized hypotonia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:generalized myelin loss ---
r_associated #0: 20 -->
en:retardation
n1=en:generalized myelin loss | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:generalized seizures ---
r_associated #0: 20 -->
en:retardation
n1=en:generalized seizures | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:generalized slowing ---
r_associated #0: 20 -->
en:retardation
n1=en:generalized slowing | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:generalized slowing seen on eeg ---
r_associated #0: 20 -->
en:retardation
n1=en:generalized slowing seen on eeg | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:generalized spike wave discharges ---
r_associated #0: 20 -->
en:retardation
n1=en:generalized spike wave discharges | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:generalized spike-wave activity seen on eeg ---
r_associated #0: 20 -->
en:retardation
n1=en:generalized spike-wave activity seen on eeg | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:generalized spike-wave discharges see on eeg ---
r_associated #0: 20 -->
en:retardation
n1=en:generalized spike-wave discharges see on eeg | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:generalized stiffening ---
r_associated #0: 20 -->
en:retardation
n1=en:generalized stiffening | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:generalized tonic-clonic seizures (gtcs) (in most patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:generalized tonic-clonic seizures (gtcs) (in most patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:generalized tonic-clonic seizures (gtcs) on awakening ---
r_associated #0: 20 -->
en:retardation
n1=en:generalized tonic-clonic seizures (gtcs) on awakening | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:generalized tonic-clonic seizures (often develop in adolescence) ---
r_associated #0: 20 -->
en:retardation
n1=en:generalized tonic-clonic seizures (often develop in adolescence) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:generalized tonic-clonic seizures (rare) ---
r_associated #0: 20 -->
en:retardation
n1=en:generalized tonic-clonic seizures (rare) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:generalized tonic-clonic seizures (stage 2 and 3) ---
r_associated #0: 20 -->
en:retardation
n1=en:generalized tonic-clonic seizures (stage 2 and 3) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:generalized tonic-clonic seizures in 50% ---
r_associated #0: 20 -->
en:retardation
n1=en:generalized tonic-clonic seizures in 50% | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:generalized tonic-clonic seizures on awakening ---
r_associated #0: 20 -->
en:retardation
n1=en:generalized tonic-clonic seizures on awakening | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:genital herpes in men ---
r_associated #0: 20 -->
en:retardation
n1=en:genital herpes in men | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:genital herpes in women ---
r_associated #0: 20 -->
en:retardation
n1=en:genital herpes in women | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:germinal cysts over the caudate ---
r_associated #0: 20 -->
en:retardation
n1=en:germinal cysts over the caudate | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:geroderma osteodysplastica ---
r_associated #0: 20 -->
en:retardation
n1=en:geroderma osteodysplastica | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:giant cortical somatosensory evoked potentials (seps) ---
r_associated #0: 20 -->
en:retardation
n1=en:giant cortical somatosensory evoked potentials (seps) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:giant granules in schwann cells ---
r_associated #0: 20 -->
en:retardation
n1=en:giant granules in schwann cells | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:gilles de la tourette syndrome (reported in 1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:gilles de la tourette syndrome (reported in 1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:gingival cyst of newborn ---
r_associated #0: 20 -->
en:retardation
n1=en:gingival cyst of newborn | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:glaucoma ---
r_associated #0: 20 -->
en:retardation
n1=en:glaucoma | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:glial activation ---
r_associated #0: 20 -->
en:retardation
n1=en:glial activation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:glial cell ---
r_associated #0: 20 -->
en:retardation
n1=en:glial cell | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:glial inclusions ---
r_associated #0: 20 -->
en:retardation
n1=en:glial inclusions | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:gliosis ---
r_associated #0: 20 -->
en:retardation
n1=en:gliosis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:gliosis (27%) ---
r_associated #0: 20 -->
en:retardation
n1=en:gliosis (27%) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:gliosis (patient a) ---
r_associated #0: 20 -->
en:retardation
n1=en:gliosis (patient a) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:gliosis in the brainstem ---
r_associated #0: 20 -->
en:retardation
n1=en:gliosis in the brainstem | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:gliosis in the striatum, medial thalamic nuclei, and inferior olives ---
r_associated #0: 20 -->
en:retardation
n1=en:gliosis in the striatum, medial thalamic nuclei, and inferior olives | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:gliosis of the white matter ---
r_associated #0: 20 -->
en:retardation
n1=en:gliosis of the white matter | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:gliosis, necrosis, neuronal loss in basal ganglia, brainstem, and spinal cord ---
r_associated #0: 20 -->
en:retardation
n1=en:gliosis, necrosis, neuronal loss in basal ganglia, brainstem, and spinal cord | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:global and focal neurologic abnormalities (less than 30%) ---
r_associated #0: 20 -->
en:retardation
n1=en:global and focal neurologic abnormalities (less than 30%) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:global brain atrophy ---
r_associated #0: 20 -->
en:retardation
n1=en:global brain atrophy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:global cerebral atrophy, mild (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:global cerebral atrophy, mild (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:global developmental delay ---
r_associated #0: 20 -->
en:retardation
n1=en:global developmental delay | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:global developmental delay if untreated ---
r_associated #0: 20 -->
en:retardation
n1=en:global developmental delay if untreated | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:global developmental delay, variable severity ---
r_associated #0: 20 -->
en:retardation
n1=en:global developmental delay, variable severity | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:global hypotonia ---
r_associated #0: 20 -->
en:retardation
n1=en:global hypotonia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:global reduction in cerebral blood flow on pet scan ---
r_associated #0: 20 -->
en:retardation
n1=en:global reduction in cerebral blood flow on pet scan | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:globally delayed development ---
r_associated #0: 20 -->
en:retardation
n1=en:globally delayed development | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:globular basal ganglia (1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:globular basal ganglia (1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:globular thalamus (1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:globular thalamus (1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:glomeruloid vascular proliferation in brain and spinal cord ---
r_associated #0: 20 -->
en:retardation
n1=en:glomeruloid vascular proliferation in brain and spinal cord | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:glomerulonephritis/nephrosis ---
r_associated #0: 20 -->
en:retardation
n1=en:glomerulonephritis/nephrosis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:glut1 deficiency syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:glut1 deficiency syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:glycine encephalopathy ---
r_associated #0: 20 -->
en:retardation
n1=en:glycine encephalopathy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:glycosuria, renal ---
r_associated #0: 20 -->
en:retardation
n1=en:glycosuria, renal | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:goiter ---
r_associated #0: 20 -->
en:retardation
n1=en:goiter | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:goldberg-shprintzen megacolon syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:goldberg-shprintzen megacolon syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:goldenhar syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:goldenhar syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:gonadal dysgenesis ---
r_associated #0: 20 -->
en:retardation
n1=en:gonadal dysgenesis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:goniodysgenesis-mental retardation-short stature syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:goniodysgenesis-mental retardation-short stature syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:gonorrhea female ---
r_associated #0: 20 -->
en:retardation
n1=en:gonorrhea female | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:gonorrhea male ---
r_associated #0: 20 -->
en:retardation
n1=en:gonorrhea male | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:gout ---
r_associated #0: 20 -->
en:retardation
n1=en:gout | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:gowers sign ---
r_associated #0: 20 -->
en:retardation
n1=en:gowers sign | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:grand mal epilepsy ---
r_associated #0: 20 -->
en:retardation
n1=en:grand mal epilepsy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:grand mal seizure ---
r_associated #0: 20 -->
en:retardation
n1=en:grand mal seizure | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:granular material in neurons ---
r_associated #0: 20 -->
en:retardation
n1=en:granular material in neurons | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:granular osmiophilic cytoplasmic deposits in schwann cells ---
r_associated #0: 20 -->
en:retardation
n1=en:granular osmiophilic cytoplasmic deposits in schwann cells | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:granulovacuolar degeneration ---
r_associated #0: 20 -->
en:retardation
n1=en:granulovacuolar degeneration | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:gray matter ---
r_associated #0: 20 -->
en:retardation
n1=en:gray matter | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:gray matter appears relatively unaffected ---
r_associated #0: 20 -->
en:retardation
n1=en:gray matter appears relatively unaffected | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:gray matter heterotopia (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:gray matter heterotopia (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:gray matter structure of central nervous system ---
r_associated #0: 20 -->
en:retardation
n1=en:gray matter structure of central nervous system | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:greig syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:greig syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:grimaces ---
r_associated #0: 20 -->
en:retardation
n1=en:grimaces | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:griscelli syndrome, type 1 ---
r_associated #0: 20 -->
en:retardation
n1=en:griscelli syndrome, type 1 | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:gross motor delay ---
r_associated #0: 20 -->
en:retardation
n1=en:gross motor delay | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:gross motor delay (in one family) ---
r_associated #0: 20 -->
en:retardation
n1=en:gross motor delay (in one family) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:gross motor delay, mild ---
r_associated #0: 20 -->
en:retardation
n1=en:gross motor delay, mild | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:gross motor disability ---
r_associated #0: 20 -->
en:retardation
n1=en:gross motor disability | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:gross motor skill delay (infancy) ---
r_associated #0: 20 -->
en:retardation
n1=en:gross motor skill delay (infancy) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:growth and development disorder ---
r_associated #0: 20 -->
en:retardation
n1=en:growth and development disorder | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:growth deficiency and mental retardation with facial dysmorphism ---
r_associated #0: 20 -->
en:retardation
n1=en:growth deficiency and mental retardation with facial dysmorphism | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:growth retardation ---
r_associated #0: 20 -->
en:retardation
n1=en:growth retardation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:gtcs during 'leisure' time (evening) ---
r_associated #0: 20 -->
en:retardation
n1=en:gtcs during 'leisure' time (evening) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:guanidinoacetate methyltransferase deficiency ---
r_associated #0: 20 -->
en:retardation
n1=en:guanidinoacetate methyltransferase deficiency | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:gurgling or drooling during seizures ---
r_associated #0: 20 -->
en:retardation
n1=en:gurgling or drooling during seizures | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:gyral disorganization ---
r_associated #0: 20 -->
en:retardation
n1=en:gyral disorganization | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:gyral simplification ---
r_associated #0: 20 -->
en:retardation
n1=en:gyral simplification | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hadziselimovic syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:hadziselimovic syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hall riggs mental retardation syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:hall riggs mental retardation syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hallucination ---
r_associated #0: 20 -->
en:retardation
n1=en:hallucination | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hallucinations (rare) ---
r_associated #0: 20 -->
en:retardation
n1=en:hallucinations (rare) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hamartoma ---
r_associated #0: 20 -->
en:retardation
n1=en:hamartoma | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hamartomatous lesions of the brain ---
r_associated #0: 20 -->
en:retardation
n1=en:hamartomatous lesions of the brain | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hand function disability ---
r_associated #0: 20 -->
en:retardation
n1=en:hand function disability | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hand muscle atrophy ---
r_associated #0: 20 -->
en:retardation
n1=en:hand muscle atrophy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hand muscle weakness ---
r_associated #0: 20 -->
en:retardation
n1=en:hand muscle weakness | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hand tremor (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:hand tremor (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:handicapping condition ---
r_associated #0: 20 -->
en:retardation
n1=en:handicapping condition | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:has tingling sensation ---
r_associated #0: 20 -->
en:retardation
n1=en:has tingling sensation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:haspeslagh fryns muelenaere syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:haspeslagh fryns muelenaere syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:head 'tilt' in infancy ---
r_associated #0: 20 -->
en:retardation
n1=en:head 'tilt' in infancy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:head bobbing ---
r_associated #0: 20 -->
en:retardation
n1=en:head bobbing | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:head lag ---
r_associated #0: 20 -->
en:retardation
n1=en:head lag | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:head movements abnormal ---
r_associated #0: 20 -->
en:retardation
n1=en:head movements abnormal | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:head oscillations ---
r_associated #0: 20 -->
en:retardation
n1=en:head oscillations | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:head titubation ---
r_associated #0: 20 -->
en:retardation
n1=en:head titubation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:head titubations ---
r_associated #0: 20 -->
en:retardation
n1=en:head titubations | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:head tremor ---
r_associated #0: 20 -->
en:retardation
n1=en:head tremor | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:head tremor (14% of patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:head tremor (14% of patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:head tremor (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:head tremor (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:head tremor, mild ---
r_associated #0: 20 -->
en:retardation
n1=en:head tremor, mild | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:head-rolling movements ---
r_associated #0: 20 -->
en:retardation
n1=en:head-rolling movements | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:headache ---
r_associated #0: 20 -->
en:retardation
n1=en:headache | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:headache (with pheochromocytoma) ---
r_associated #0: 20 -->
en:retardation
n1=en:headache (with pheochromocytoma) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:headache is unilateral ---
r_associated #0: 20 -->
en:retardation
n1=en:headache is unilateral | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:headache is usually not a symptom ---
r_associated #0: 20 -->
en:retardation
n1=en:headache is usually not a symptom | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:headache recurrent ---
r_associated #0: 20 -->
en:retardation
n1=en:headache recurrent | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:headache, episodic ---
r_associated #0: 20 -->
en:retardation
n1=en:headache, episodic | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:headache, suboccipital, migraine-like (most common symptom) precipitated by coughing, sneezing, bending forward, lifting, neck extension ---
r_associated #0: 20 -->
en:retardation
n1=en:headache, suboccipital, migraine-like (most common symptom) precipitated by coughing, sneezing, bending forward, lifting, neck extension | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:headaches, severe, unilateral ---
r_associated #0: 20 -->
en:retardation
n1=en:headaches, severe, unilateral | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:heart failure ---
r_associated #0: 20 -->
en:retardation
n1=en:heart failure | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:heart malformation ---
r_associated #0: 20 -->
en:retardation
n1=en:heart malformation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:heart murmur ---
r_associated #0: 20 -->
en:retardation
n1=en:heart murmur | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:heightened sensitivity to external stimuli ---
r_associated #0: 20 -->
en:retardation
n1=en:heightened sensitivity to external stimuli | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hemangiomas and lymphangiomas of any site ---
r_associated #0: 20 -->
en:retardation
n1=en:hemangiomas and lymphangiomas of any site | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hemiclonic seizures ---
r_associated #0: 20 -->
en:retardation
n1=en:hemiclonic seizures | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hemihypertrophy ---
r_associated #0: 20 -->
en:retardation
n1=en:hemihypertrophy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hemihypoasthesia ---
r_associated #0: 20 -->
en:retardation
n1=en:hemihypoasthesia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hemimegalencephaly ---
r_associated #0: 20 -->
en:retardation
n1=en:hemimegalencephaly | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hemiparesis ---
r_associated #0: 20 -->
en:retardation
n1=en:hemiparesis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hemiparesis (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:hemiparesis (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hemiparesis, paroxysmal ---
r_associated #0: 20 -->
en:retardation
n1=en:hemiparesis, paroxysmal | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hemiplegia ---
r_associated #0: 20 -->
en:retardation
n1=en:hemiplegia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hemiplegia (rare) ---
r_associated #0: 20 -->
en:retardation
n1=en:hemiplegia (rare) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hemiplegic migraine ---
r_associated #0: 20 -->
en:retardation
n1=en:hemiplegic migraine | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hemiplegic migraine in some patients ---
r_associated #0: 20 -->
en:retardation
n1=en:hemiplegic migraine in some patients | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hemisensory attacks ---
r_associated #0: 20 -->
en:retardation
n1=en:hemisensory attacks | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hemispheric atrophy ---
r_associated #0: 20 -->
en:retardation
n1=en:hemispheric atrophy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hemivertebra ---
r_associated #0: 20 -->
en:retardation
n1=en:hemivertebra | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hemorrhage ---
r_associated #0: 20 -->
en:retardation
n1=en:hemorrhage | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hemorrhagic cerebrovascular accident ---
r_associated #0: 20 -->
en:retardation
n1=en:hemorrhagic cerebrovascular accident | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hemorrhoid ---
r_associated #0: 20 -->
en:retardation
n1=en:hemorrhoid | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hemosiderin deposition ---
r_associated #0: 20 -->
en:retardation
n1=en:hemosiderin deposition | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hepatic coma ---
r_associated #0: 20 -->
en:retardation
n1=en:hepatic coma | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hepatic encephalopathy ---
r_associated #0: 20 -->
en:retardation
n1=en:hepatic encephalopathy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hepatomegaly ---
r_associated #0: 20 -->
en:retardation
n1=en:hepatomegaly | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hereditary elliptocytosis ---
r_associated #0: 20 -->
en:retardation
n1=en:hereditary elliptocytosis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hereditary hemolytic anemia ---
r_associated #0: 20 -->
en:retardation
n1=en:hereditary hemolytic anemia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hermaphrodite ---
r_associated #0: 20 -->
en:retardation
n1=en:hermaphrodite | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:herniation and elongation of the cerebellar tonsils, cerebellar vermis, brainstem, and fourth ventricle through the foramen magnum ---
r_associated #0: 20 -->
en:retardation
n1=en:herniation and elongation of the cerebellar tonsils, cerebellar vermis, brainstem, and fourth ventricle through the foramen magnum | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:herniation of the cerebellar tonsils through the foramen magnum 5 mm or greater ---
r_associated #0: 20 -->
en:retardation
n1=en:herniation of the cerebellar tonsils through the foramen magnum 5 mm or greater | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:herpes simplex infections ---
r_associated #0: 20 -->
en:retardation
n1=en:herpes simplex infections | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:herpes zoster ---
r_associated #0: 20 -->
en:retardation
n1=en:herpes zoster | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:heterotopic neurons in the white matter (36%) ---
r_associated #0: 20 -->
en:retardation
n1=en:heterotopic neurons in the white matter (36%) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hiatal hernia ---
r_associated #0: 20 -->
en:retardation
n1=en:hiatal hernia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hiccough ---
r_associated #0: 20 -->
en:retardation
n1=en:hiccough | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:high intensity area in white matter on head mri ---
r_associated #0: 20 -->
en:retardation
n1=en:high intensity area in white matter on head mri | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:high pain threshold ---
r_associated #0: 20 -->
en:retardation
n1=en:high pain threshold | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:high risk pregnancy ---
r_associated #0: 20 -->
en:retardation
n1=en:high risk pregnancy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:high signal intensities at gray/white matter junction ---
r_associated #0: 20 -->
en:retardation
n1=en:high signal intensities at gray/white matter junction | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:high signal intensities in periventricular white matter ---
r_associated #0: 20 -->
en:retardation
n1=en:high signal intensities in periventricular white matter | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:high voltage spikes over the temporal and central regions seen on eeg ---
r_associated #0: 20 -->
en:retardation
n1=en:high voltage spikes over the temporal and central regions seen on eeg | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:high voltage, fast rhythms seen on eeg ---
r_associated #0: 20 -->
en:retardation
n1=en:high voltage, fast rhythms seen on eeg | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:high-steppage gait ---
r_associated #0: 20 -->
en:retardation
n1=en:high-steppage gait | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:high-stepping gait ---
r_associated #0: 20 -->
en:retardation
n1=en:high-stepping gait | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hindbrain and midbrain ---
r_associated #0: 20 -->
en:retardation
n1=en:hindbrain and midbrain | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hip osteoarthritis ---
r_associated #0: 20 -->
en:retardation
n1=en:hip osteoarthritis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hippocampal atrophy (1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:hippocampal atrophy (1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hippocampal atrophy (in 2 siblings) ---
r_associated #0: 20 -->
en:retardation
n1=en:hippocampal atrophy (in 2 siblings) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hippocampal hypoplasia ---
r_associated #0: 20 -->
en:retardation
n1=en:hippocampal hypoplasia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:histidinemia ---
r_associated #0: 20 -->
en:retardation
n1=en:histidinemia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hiv/aids ---
r_associated #0: 20 -->
en:retardation
n1=en:hiv/aids | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hodgkin lymphoma ---
r_associated #0: 20 -->
en:retardation
n1=en:hodgkin lymphoma | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:holoprosencephaly ---
r_associated #0: 20 -->
en:retardation
n1=en:holoprosencephaly | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:holoprosencephaly (1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:holoprosencephaly (1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:holoprosencephaly (100%) ---
r_associated #0: 20 -->
en:retardation
n1=en:holoprosencephaly (100%) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:holoprosencephaly (less common) ---
r_associated #0: 20 -->
en:retardation
n1=en:holoprosencephaly (less common) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:holoprosencephaly (variable) ---
r_associated #0: 20 -->
en:retardation
n1=en:holoprosencephaly (variable) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:holoprosencephaly 10 ---
r_associated #0: 20 -->
en:retardation
n1=en:holoprosencephaly 10 | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:holoprosencephaly type 2 ---
r_associated #0: 20 -->
en:retardation
n1=en:holoprosencephaly type 2 | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:holoprosencephaly type 5 ---
r_associated #0: 20 -->
en:retardation
n1=en:holoprosencephaly type 5 | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:homocystinuria ---
r_associated #0: 20 -->
en:retardation
n1=en:homocystinuria | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hooked aspect of the frontal horn of the lateral ventricles due to abnormally shaped basal ganglia ---
r_associated #0: 20 -->
en:retardation
n1=en:hooked aspect of the frontal horn of the lateral ventricles due to abnormally shaped basal ganglia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:horner syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:horner syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hostility ---
r_associated #0: 20 -->
en:retardation
n1=en:hostility | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hunger and thirst disturbances (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:hunger and thirst disturbances (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:huntington's disease ---
r_associated #0: 20 -->
en:retardation
n1=en:huntington's disease | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:huntington's disease pathway ---
r_associated #0: 20 -->
en:retardation
n1=en:huntington's disease pathway | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hurler syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:hurler syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hydranencephaly ---
r_associated #0: 20 -->
en:retardation
n1=en:hydranencephaly | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hydrocephalus ---
r_associated #0: 20 -->
en:retardation
n1=en:hydrocephalus | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hydrocephalus (11%) ---
r_associated #0: 20 -->
en:retardation
n1=en:hydrocephalus (11%) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hydrocephalus (12%) ---
r_associated #0: 20 -->
en:retardation
n1=en:hydrocephalus (12%) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hydrocephalus (in 1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:hydrocephalus (in 1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hydrocephalus (in 2 patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:hydrocephalus (in 2 patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hydrocephalus (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:hydrocephalus (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hydrocephalus (less common) ---
r_associated #0: 20 -->
en:retardation
n1=en:hydrocephalus (less common) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hydrocephalus (rare) ---
r_associated #0: 20 -->
en:retardation
n1=en:hydrocephalus (rare) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hydrocephalus (uncommon) ---
r_associated #0: 20 -->
en:retardation
n1=en:hydrocephalus (uncommon) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hydrocephalus (variable) ---
r_associated #0: 20 -->
en:retardation
n1=en:hydrocephalus (variable) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hydrocephalus, nonsyndromic, autosomal recessive 1 ---
r_associated #0: 20 -->
en:retardation
n1=en:hydrocephalus, nonsyndromic, autosomal recessive 1 | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hydrocephalus, normal pressure ---
r_associated #0: 20 -->
en:retardation
n1=en:hydrocephalus, normal pressure | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hydrocephalus, occasional ---
r_associated #0: 20 -->
en:retardation
n1=en:hydrocephalus, occasional | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hydrocephaly, mild ---
r_associated #0: 20 -->
en:retardation
n1=en:hydrocephaly, mild | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hydroxyacyl-coa dehydrogenase, type 2, deficiency ---
r_associated #0: 20 -->
en:retardation
n1=en:hydroxyacyl-coa dehydrogenase, type 2, deficiency | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hyperactive brainstem reflexes (head retraction, palmomental, snout) ---
r_associated #0: 20 -->
en:retardation
n1=en:hyperactive brainstem reflexes (head retraction, palmomental, snout) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hyperactive deep tendon reflexes ---
r_associated #0: 20 -->
en:retardation
n1=en:hyperactive deep tendon reflexes | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hyperactive deep tendon reflexes in early stage ---
r_associated #0: 20 -->
en:retardation
n1=en:hyperactive deep tendon reflexes in early stage | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hyperactive startle reflex ---
r_associated #0: 20 -->
en:retardation
n1=en:hyperactive startle reflex | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hyperactivity ---
r_associated #0: 20 -->
en:retardation
n1=en:hyperactivity | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hyperekplexia (rare) ---
r_associated #0: 20 -->
en:retardation
n1=en:hyperekplexia (rare) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hyperexplexia ---
r_associated #0: 20 -->
en:retardation
n1=en:hyperexplexia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hyperextension of the neck ---
r_associated #0: 20 -->
en:retardation
n1=en:hyperextension of the neck | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hyperintense lesions in the basal ganglia on mri ---
r_associated #0: 20 -->
en:retardation
n1=en:hyperintense lesions in the basal ganglia on mri | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hyperintense lesions of the globi pallidi ---
r_associated #0: 20 -->
en:retardation
n1=en:hyperintense lesions of the globi pallidi | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hyperintensities in the basal ganglia (rare) ---
r_associated #0: 20 -->
en:retardation
n1=en:hyperintensities in the basal ganglia (rare) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hyperintensities in the basal ganglia and/or thalamus ---
r_associated #0: 20 -->
en:retardation
n1=en:hyperintensities in the basal ganglia and/or thalamus | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hyperirritability ---
r_associated #0: 20 -->
en:retardation
n1=en:hyperirritability | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hyperkinesia ---
r_associated #0: 20 -->
en:retardation
n1=en:hyperkinesia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hyperkinetic involuntary movements ---
r_associated #0: 20 -->
en:retardation
n1=en:hyperkinetic involuntary movements | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypermetric saccades ---
r_associated #0: 20 -->
en:retardation
n1=en:hypermetric saccades | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypermotor automatisms ---
r_associated #0: 20 -->
en:retardation
n1=en:hypermotor automatisms | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypermotor behavior ---
r_associated #0: 20 -->
en:retardation
n1=en:hypermotor behavior | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hyperphenylalaninemia, bh4-deficient, b ---
r_associated #0: 20 -->
en:retardation
n1=en:hyperphenylalaninemia, bh4-deficient, b | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hyperphenylalaninemia, non phenylketonuric ---
r_associated #0: 20 -->
en:retardation
n1=en:hyperphenylalaninemia, non phenylketonuric | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hyperphosphatasia with mental retardation ---
r_associated #0: 20 -->
en:retardation
n1=en:hyperphosphatasia with mental retardation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hyperprolinemia type 2 ---
r_associated #0: 20 -->
en:retardation
n1=en:hyperprolinemia type 2 | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hyperreflexia ---
r_associated #0: 20 -->
en:retardation
n1=en:hyperreflexia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hyperreflexia (2 patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:hyperreflexia (2 patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hyperreflexia (33%) ---
r_associated #0: 20 -->
en:retardation
n1=en:hyperreflexia (33%) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hyperreflexia (70%) ---
r_associated #0: 20 -->
en:retardation
n1=en:hyperreflexia (70%) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hyperreflexia (early) ---
r_associated #0: 20 -->
en:retardation
n1=en:hyperreflexia (early) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hyperreflexia (later) ---
r_associated #0: 20 -->
en:retardation
n1=en:hyperreflexia (later) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hyperreflexia (less common) ---
r_associated #0: 20 -->
en:retardation
n1=en:hyperreflexia (less common) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hyperreflexia (particularly in lower extremities, more prevalent in adolescents and adults) ---
r_associated #0: 20 -->
en:retardation
n1=en:hyperreflexia (particularly in lower extremities, more prevalent in adolescents and adults) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hyperreflexia (some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:hyperreflexia (some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hyperreflexia (type i) ---
r_associated #0: 20 -->
en:retardation
n1=en:hyperreflexia (type i) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hyperreflexia in some ---
r_associated #0: 20 -->
en:retardation
n1=en:hyperreflexia in some | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hyperreflexia in the lower limbs (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:hyperreflexia in the lower limbs (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hyperreflexia may occur ---
r_associated #0: 20 -->
en:retardation
n1=en:hyperreflexia may occur | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hyperreflexia proximally ---
r_associated #0: 20 -->
en:retardation
n1=en:hyperreflexia proximally | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hyperreflexia, especially of the lower limbs ---
r_associated #0: 20 -->
en:retardation
n1=en:hyperreflexia, especially of the lower limbs | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hyperreflexia, lower limbs more than upper limbs ---
r_associated #0: 20 -->
en:retardation
n1=en:hyperreflexia, lower limbs more than upper limbs | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hyperreflexia, lower limbs, mild ---
r_associated #0: 20 -->
en:retardation
n1=en:hyperreflexia, lower limbs, mild | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypersensitive to stimuli ---
r_associated #0: 20 -->
en:retardation
n1=en:hypersensitive to stimuli | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypersensitivity to sound ---
r_associated #0: 20 -->
en:retardation
n1=en:hypersensitivity to sound | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypersomnia disorder related to another mental disorder ---
r_associated #0: 20 -->
en:retardation
n1=en:hypersomnia disorder related to another mental disorder | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypersomnolent ---
r_associated #0: 20 -->
en:retardation
n1=en:hypersomnolent | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypertelorism ---
r_associated #0: 20 -->
en:retardation
n1=en:hypertelorism | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypertension with involvement target organs ---
r_associated #0: 20 -->
en:retardation
n1=en:hypertension with involvement target organs | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypertensive encephalopathy ---
r_associated #0: 20 -->
en:retardation
n1=en:hypertensive encephalopathy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hyperthermia ---
r_associated #0: 20 -->
en:retardation
n1=en:hyperthermia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hyperthyroidism, nonautoimmune ---
r_associated #0: 20 -->
en:retardation
n1=en:hyperthyroidism, nonautoimmune | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypertonia ---
r_associated #0: 20 -->
en:retardation
n1=en:hypertonia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypertonia (after age 2 years) ---
r_associated #0: 20 -->
en:retardation
n1=en:hypertonia (after age 2 years) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypertonia (childhood) ---
r_associated #0: 20 -->
en:retardation
n1=en:hypertonia (childhood) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypertonia (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:hypertonia (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypertonia (older children and adolescents) ---
r_associated #0: 20 -->
en:retardation
n1=en:hypertonia (older children and adolescents) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypertonia (type ii) ---
r_associated #0: 20 -->
en:retardation
n1=en:hypertonia (type ii) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypertonia and rigidity during seizures ---
r_associated #0: 20 -->
en:retardation
n1=en:hypertonia and rigidity during seizures | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypertonia in early stage ---
r_associated #0: 20 -->
en:retardation
n1=en:hypertonia in early stage | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypertonia in neonatal period ---
r_associated #0: 20 -->
en:retardation
n1=en:hypertonia in neonatal period | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypertonia late ---
r_associated #0: 20 -->
en:retardation
n1=en:hypertonia late | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypertonia of lower limbs, later ---
r_associated #0: 20 -->
en:retardation
n1=en:hypertonia of lower limbs, later | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypertonia of the extremities ---
r_associated #0: 20 -->
en:retardation
n1=en:hypertonia of the extremities | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypertonia, mild, transient ---
r_associated #0: 20 -->
en:retardation
n1=en:hypertonia, mild, transient | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypertonia, peripheral dystonia ---
r_associated #0: 20 -->
en:retardation
n1=en:hypertonia, peripheral dystonia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypertonic seizures ---
r_associated #0: 20 -->
en:retardation
n1=en:hypertonic seizures | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypertonicity ---
r_associated #0: 20 -->
en:retardation
n1=en:hypertonicity | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypertrophy of clitoris ---
r_associated #0: 20 -->
en:retardation
n1=en:hypertrophy of clitoris | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypertrophy of tonsils and adenoids ---
r_associated #0: 20 -->
en:retardation
n1=en:hypertrophy of tonsils and adenoids | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hyperventilation ---
r_associated #0: 20 -->
en:retardation
n1=en:hyperventilation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypnagogic hallucinations ---
r_associated #0: 20 -->
en:retardation
n1=en:hypnagogic hallucinations | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypnapompic hallucinations ---
r_associated #0: 20 -->
en:retardation
n1=en:hypnapompic hallucinations | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypo- and demyelination of the brain ---
r_associated #0: 20 -->
en:retardation
n1=en:hypo- and demyelination of the brain | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypocalcemic seizures ---
r_associated #0: 20 -->
en:retardation
n1=en:hypocalcemic seizures | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypocalcemic tetany ---
r_associated #0: 20 -->
en:retardation
n1=en:hypocalcemic tetany | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypodensity of caudate ---
r_associated #0: 20 -->
en:retardation
n1=en:hypodensity of caudate | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypodensity of cerebral white matter seen on mri ---
r_associated #0: 20 -->
en:retardation
n1=en:hypodensity of cerebral white matter seen on mri | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypodensity of lenticular nuclei ---
r_associated #0: 20 -->
en:retardation
n1=en:hypodensity of lenticular nuclei | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypodensity of the white matter ---
r_associated #0: 20 -->
en:retardation
n1=en:hypodensity of the white matter | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypodysplasia of the corpus callosum ---
r_associated #0: 20 -->
en:retardation
n1=en:hypodysplasia of the corpus callosum | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypogenesis of the corpus callosum ---
r_associated #0: 20 -->
en:retardation
n1=en:hypogenesis of the corpus callosum | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypoglycemia ---
r_associated #0: 20 -->
en:retardation
n1=en:hypoglycemia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypoglycemia, leucine-induced ---
r_associated #0: 20 -->
en:retardation
n1=en:hypoglycemia, leucine-induced | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypoglycemia-related seizures ---
r_associated #0: 20 -->
en:retardation
n1=en:hypoglycemia-related seizures | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypoglycemic coma ---
r_associated #0: 20 -->
en:retardation
n1=en:hypoglycemic coma | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypoglycemic encephalopathy ---
r_associated #0: 20 -->
en:retardation
n1=en:hypoglycemic encephalopathy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypoglycemic seizures ---
r_associated #0: 20 -->
en:retardation
n1=en:hypoglycemic seizures | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypokinesia ---
r_associated #0: 20 -->
en:retardation
n1=en:hypokinesia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypokinesia in infancy ---
r_associated #0: 20 -->
en:retardation
n1=en:hypokinesia in infancy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypokinetic movements ---
r_associated #0: 20 -->
en:retardation
n1=en:hypokinetic movements | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypometabolism of the frontal lobe and thalamic regions ---
r_associated #0: 20 -->
en:retardation
n1=en:hypometabolism of the frontal lobe and thalamic regions | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypomimia ---
r_associated #0: 20 -->
en:retardation
n1=en:hypomimia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypomyelinating leukoencephalopathy ---
r_associated #0: 20 -->
en:retardation
n1=en:hypomyelinating leukoencephalopathy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypomyelination ---
r_associated #0: 20 -->
en:retardation
n1=en:hypomyelination | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypomyelination (1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:hypomyelination (1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypomyelination (patient a) metabolic : hypochloremia metabolic alkalosis (patient a) ---
r_associated #0: 20 -->
en:retardation
n1=en:hypomyelination (patient a) metabolic : hypochloremia metabolic alkalosis (patient a) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypomyelination of the brain white matter, diffuse ---
r_associated #0: 20 -->
en:retardation
n1=en:hypomyelination of the brain white matter, diffuse | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypoparathyroidism-retardation-dysmorphism syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:hypoparathyroidism-retardation-dysmorphism syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypoplasia ---
r_associated #0: 20 -->
en:retardation
n1=en:hypoplasia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypoplasia and displacement of the corticospinal fibers within the brainstem ---
r_associated #0: 20 -->
en:retardation
n1=en:hypoplasia and displacement of the corticospinal fibers within the brainstem | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypoplasia of anterior or entire pituitary gland (frequent) ---
r_associated #0: 20 -->
en:retardation
n1=en:hypoplasia of anterior or entire pituitary gland (frequent) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypoplasia of corpus callosum ---
r_associated #0: 20 -->
en:retardation
n1=en:hypoplasia of corpus callosum | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypoplasia of corpus callosum and cerebellar vermis ---
r_associated #0: 20 -->
en:retardation
n1=en:hypoplasia of corpus callosum and cerebellar vermis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypoplasia of dentate nucleus ---
r_associated #0: 20 -->
en:retardation
n1=en:hypoplasia of dentate nucleus | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypoplasia of olfactory tract ---
r_associated #0: 20 -->
en:retardation
n1=en:hypoplasia of olfactory tract | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypoplasia of septum pellucidum ---
r_associated #0: 20 -->
en:retardation
n1=en:hypoplasia of septum pellucidum | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypoplasia of the brainstem ---
r_associated #0: 20 -->
en:retardation
n1=en:hypoplasia of the brainstem | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypoplasia of the corpus callosum (2 patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:hypoplasia of the corpus callosum (2 patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypoplasia of the hypothalamus ---
r_associated #0: 20 -->
en:retardation
n1=en:hypoplasia of the hypothalamus | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypoplasia of the medulla oblongata ---
r_associated #0: 20 -->
en:retardation
n1=en:hypoplasia of the medulla oblongata | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypoplasia of the mesencephalic tectum ---
r_associated #0: 20 -->
en:retardation
n1=en:hypoplasia of the mesencephalic tectum | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypoplasia of the optic chiasm ---
r_associated #0: 20 -->
en:retardation
n1=en:hypoplasia of the optic chiasm | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypoplasia of the optic tract ---
r_associated #0: 20 -->
en:retardation
n1=en:hypoplasia of the optic tract | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypoplasia of the pons ---
r_associated #0: 20 -->
en:retardation
n1=en:hypoplasia of the pons | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypoplasia of the posterior corpus callosum (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:hypoplasia of the posterior corpus callosum (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypoplasia of the pyramidal tract ---
r_associated #0: 20 -->
en:retardation
n1=en:hypoplasia of the pyramidal tract | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypoplasia of the ventral pons ---
r_associated #0: 20 -->
en:retardation
n1=en:hypoplasia of the ventral pons | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypoplasia or dysgenesis of the corpus callosum (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:hypoplasia or dysgenesis of the corpus callosum (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypoplastic anterior pituitary (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:hypoplastic anterior pituitary (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypoplastic anterior pituitary gland ---
r_associated #0: 20 -->
en:retardation
n1=en:hypoplastic anterior pituitary gland | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypoplastic brainstem with loss of demarcation at the pontomedullary junction ---
r_associated #0: 20 -->
en:retardation
n1=en:hypoplastic brainstem with loss of demarcation at the pontomedullary junction | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypoplastic cerebellar vermis (rare) ---
r_associated #0: 20 -->
en:retardation
n1=en:hypoplastic cerebellar vermis (rare) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypoplastic cerebrum ---
r_associated #0: 20 -->
en:retardation
n1=en:hypoplastic cerebrum | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypoplastic corpus callosum (1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:hypoplastic corpus callosum (1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypoplastic corpus callosum (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:hypoplastic corpus callosum (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypoplastic corpus callosum (in some) ---
r_associated #0: 20 -->
en:retardation
n1=en:hypoplastic corpus callosum (in some) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypoplastic corpus callosum (rare) ---
r_associated #0: 20 -->
en:retardation
n1=en:hypoplastic corpus callosum (rare) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypoplastic internal capsule (in some) ---
r_associated #0: 20 -->
en:retardation
n1=en:hypoplastic internal capsule (in some) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypoplastic olfactory lobes ---
r_associated #0: 20 -->
en:retardation
n1=en:hypoplastic olfactory lobes | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypoplastic or absent middle cerebellar peduncles ---
r_associated #0: 20 -->
en:retardation
n1=en:hypoplastic or absent middle cerebellar peduncles | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypoplastic or absent optic chiasm ---
r_associated #0: 20 -->
en:retardation
n1=en:hypoplastic or absent optic chiasm | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypoplastic pituitary gland (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:hypoplastic pituitary gland (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypoplastic pons ---
r_associated #0: 20 -->
en:retardation
n1=en:hypoplastic pons | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypoplastic/atrophic corpus callosum (55%) ---
r_associated #0: 20 -->
en:retardation
n1=en:hypoplastic/atrophic corpus callosum (55%) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hyporeflexia ---
r_associated #0: 20 -->
en:retardation
n1=en:hyporeflexia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hyporeflexia (early) ---
r_associated #0: 20 -->
en:retardation
n1=en:hyporeflexia (early) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hyporeflexia (occurs later) ---
r_associated #0: 20 -->
en:retardation
n1=en:hyporeflexia (occurs later) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hyporeflexia of lower limbs ---
r_associated #0: 20 -->
en:retardation
n1=en:hyporeflexia of lower limbs | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hyporeflexia or areflexia ---
r_associated #0: 20 -->
en:retardation
n1=en:hyporeflexia or areflexia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hyporeflexia to hyperreflexia ---
r_associated #0: 20 -->
en:retardation
n1=en:hyporeflexia to hyperreflexia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hyposmia/anosmia ---
r_associated #0: 20 -->
en:retardation
n1=en:hyposmia/anosmia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hyposmia/anosmia (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:hyposmia/anosmia (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hyposomnia co-occurrent and due to psychological disorder ---
r_associated #0: 20 -->
en:retardation
n1=en:hyposomnia co-occurrent and due to psychological disorder | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypospadias ---
r_associated #0: 20 -->
en:retardation
n1=en:hypospadias | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypothalamic hamartoma ---
r_associated #0: 20 -->
en:retardation
n1=en:hypothalamic hamartoma | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypothalamus ---
r_associated #0: 20 -->
en:retardation
n1=en:hypothalamus | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypotonia ---
r_associated #0: 20 -->
en:retardation
n1=en:hypotonia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypotonia (1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:hypotonia (1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypotonia (93%) ---
r_associated #0: 20 -->
en:retardation
n1=en:hypotonia (93%) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypotonia (96%) ---
r_associated #0: 20 -->
en:retardation
n1=en:hypotonia (96%) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypotonia (congenital form) ---
r_associated #0: 20 -->
en:retardation
n1=en:hypotonia (congenital form) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypotonia (early infancy) ---
r_associated #0: 20 -->
en:retardation
n1=en:hypotonia (early infancy) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypotonia (early-onset form) ---
r_associated #0: 20 -->
en:retardation
n1=en:hypotonia (early-onset form) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypotonia (hcs and 2p21del) ---
r_associated #0: 20 -->
en:retardation
n1=en:hypotonia (hcs and 2p21del) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypotonia (in 1/4 patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:hypotonia (in 1/4 patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypotonia (in males) ---
r_associated #0: 20 -->
en:retardation
n1=en:hypotonia (in males) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypotonia (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:hypotonia (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypotonia (less common) ---
r_associated #0: 20 -->
en:retardation
n1=en:hypotonia (less common) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypotonia (newborn) ---
r_associated #0: 20 -->
en:retardation
n1=en:hypotonia (newborn) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypotonia (rare) ---
r_associated #0: 20 -->
en:retardation
n1=en:hypotonia (rare) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypotonia (type i and type ii, infantile) ---
r_associated #0: 20 -->
en:retardation
n1=en:hypotonia (type i and type ii, infantile) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypotonia at birth ---
r_associated #0: 20 -->
en:retardation
n1=en:hypotonia at birth | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypotonia changing to hypertonia ---
r_associated #0: 20 -->
en:retardation
n1=en:hypotonia changing to hypertonia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypotonia in infancy and early childhood ---
r_associated #0: 20 -->
en:retardation
n1=en:hypotonia in infancy and early childhood | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypotonia in later stages ---
r_associated #0: 20 -->
en:retardation
n1=en:hypotonia in later stages | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypotonia progressing to hypertonia ---
r_associated #0: 20 -->
en:retardation
n1=en:hypotonia progressing to hypertonia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypotonia, axial, severe ---
r_associated #0: 20 -->
en:retardation
n1=en:hypotonia, axial, severe | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypotonia, global, severe ---
r_associated #0: 20 -->
en:retardation
n1=en:hypotonia, global, severe | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypotonia, mild ---
r_associated #0: 20 -->
en:retardation
n1=en:hypotonia, mild | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypotonia, mild, transient ---
r_associated #0: 20 -->
en:retardation
n1=en:hypotonia, mild, transient | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypotonia, neonatal (> 90%) ---
r_associated #0: 20 -->
en:retardation
n1=en:hypotonia, neonatal (> 90%) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypotonia, poor moro reflex ---
r_associated #0: 20 -->
en:retardation
n1=en:hypotonia, poor moro reflex | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypotonia, profound muscular (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:hypotonia, profound muscular (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypotonia, proximal, severe ---
r_associated #0: 20 -->
en:retardation
n1=en:hypotonia, proximal, severe | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypotonia, severe (rare) ---
r_associated #0: 20 -->
en:retardation
n1=en:hypotonia, severe (rare) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypotonic ---
r_associated #0: 20 -->
en:retardation
n1=en:hypotonic | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypotonic seizures ---
r_associated #0: 20 -->
en:retardation
n1=en:hypotonic seizures | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypotonicity (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:hypotonicity (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypotrophic brainstem ---
r_associated #0: 20 -->
en:retardation
n1=en:hypotrophic brainstem | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypoxic convulsions ---
r_associated #0: 20 -->
en:retardation
n1=en:hypoxic convulsions | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypperreflexia ---
r_associated #0: 20 -->
en:retardation
n1=en:hypperreflexia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypsarrhythmia ---
r_associated #0: 20 -->
en:retardation
n1=en:hypsarrhythmia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypsarrhythmia (1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:hypsarrhythmia (1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypsarrhythmia (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:hypsarrhythmia (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypsarrhythmia or severe multifocal epileptic abnormalities with poor background activity on eeg ---
r_associated #0: 20 -->
en:retardation
n1=en:hypsarrhythmia or severe multifocal epileptic abnormalities with poor background activity on eeg | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hypsarrhythmia seen on eeg ---
r_associated #0: 20 -->
en:retardation
n1=en:hypsarrhythmia seen on eeg | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hysteria ---
r_associated #0: 20 -->
en:retardation
n1=en:hysteria | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:hysterical/hypochondriacal disease ---
r_associated #0: 20 -->
en:retardation
n1=en:hysterical/hypochondriacal disease | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ichthyosiform erythroderma, corneal involvement, deafness ---
r_associated #0: 20 -->
en:retardation
n1=en:ichthyosiform erythroderma, corneal involvement, deafness | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ichthyosis follicularis atrichia photophobia syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:ichthyosis follicularis atrichia photophobia syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ictal eeg showed partial seizures with frontal lobe origin ---
r_associated #0: 20 -->
en:retardation
n1=en:ictal eeg showed partial seizures with frontal lobe origin | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ictal eeg shows diffuse slow delta and theta activity ---
r_associated #0: 20 -->
en:retardation
n1=en:ictal eeg shows diffuse slow delta and theta activity | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ictal eeg shows focal onset in central, parietal, or temporal regions ---
r_associated #0: 20 -->
en:retardation
n1=en:ictal eeg shows focal onset in central, parietal, or temporal regions | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ictal eeg shows focal onset, often posterior region of brain ---
r_associated #0: 20 -->
en:retardation
n1=en:ictal eeg shows focal onset, often posterior region of brain | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ictal eeg shows focal, temporal, unilateral, rhythmic slow wave activity of high amplitude ---
r_associated #0: 20 -->
en:retardation
n1=en:ictal eeg shows focal, temporal, unilateral, rhythmic slow wave activity of high amplitude | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ictal eeg with bisynchronous spike waves ---
r_associated #0: 20 -->
en:retardation
n1=en:ictal eeg with bisynchronous spike waves | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:identity problem ---
r_associated #0: 20 -->
en:retardation
n1=en:identity problem | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:idiopathic generalized epilepsy in childhood (homozygous patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:idiopathic generalized epilepsy in childhood (homozygous patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:idiopathic torsion dystonia ---
r_associated #0: 20 -->
en:retardation
n1=en:idiopathic torsion dystonia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:idiot ---
r_associated #0: 20 -->
en:retardation
n1=en:idiot | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:illegible handwriting ---
r_associated #0: 20 -->
en:retardation
n1=en:illegible handwriting | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:imaging shows noncalcified subependymal periventricular heterotopic nodules of gray matter ---
r_associated #0: 20 -->
en:retardation
n1=en:imaging shows noncalcified subependymal periventricular heterotopic nodules of gray matter | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:imaging shows signal abnormalities in basal ganglia ---
r_associated #0: 20 -->
en:retardation
n1=en:imaging shows signal abnormalities in basal ganglia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:imbalance ---
r_associated #0: 20 -->
en:retardation
n1=en:imbalance | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:imbecility ---
r_associated #0: 20 -->
en:retardation
n1=en:imbecility | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:immature brain with no gyral development ---
r_associated #0: 20 -->
en:retardation
n1=en:immature brain with no gyral development | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:immature myelination ---
r_associated #0: 20 -->
en:retardation
n1=en:immature myelination | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:immobile ---
r_associated #0: 20 -->
en:retardation
n1=en:immobile | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:immunodeficiency-centromeric instability-facial anomalies syndrome 2 ---
r_associated #0: 20 -->
en:retardation
n1=en:immunodeficiency-centromeric instability-facial anomalies syndrome 2 | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:impaired ambulation due to muscle weakness ---
r_associated #0: 20 -->
en:retardation
n1=en:impaired ambulation due to muscle weakness | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:impaired balance ---
r_associated #0: 20 -->
en:retardation
n1=en:impaired balance | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:impaired balance (2 patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:impaired balance (2 patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:impaired cognition (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:impaired cognition (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:impaired executive function (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:impaired executive function (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:impaired expression of language ---
r_associated #0: 20 -->
en:retardation
n1=en:impaired expression of language | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:impaired expressive speech ---
r_associated #0: 20 -->
en:retardation
n1=en:impaired expressive speech | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:impaired fine motor skills ---
r_associated #0: 20 -->
en:retardation
n1=en:impaired fine motor skills | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:impaired gait due to peripheral neuropathy ---
r_associated #0: 20 -->
en:retardation
n1=en:impaired gait due to peripheral neuropathy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:impaired horizontal smooth pursuit ---
r_associated #0: 20 -->
en:retardation
n1=en:impaired horizontal smooth pursuit | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:impaired insight ---
r_associated #0: 20 -->
en:retardation
n1=en:impaired insight | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:impaired language development ---
r_associated #0: 20 -->
en:retardation
n1=en:impaired language development | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:impaired long-term verbal memory ---
r_associated #0: 20 -->
en:retardation
n1=en:impaired long-term verbal memory | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:impaired motor control, mild ---
r_associated #0: 20 -->
en:retardation
n1=en:impaired motor control, mild | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:impaired processing of language ---
r_associated #0: 20 -->
en:retardation
n1=en:impaired processing of language | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:impaired proprioception ---
r_associated #0: 20 -->
en:retardation
n1=en:impaired proprioception | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:impaired psychomotor development ---
r_associated #0: 20 -->
en:retardation
n1=en:impaired psychomotor development | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:impaired tandem gait ---
r_associated #0: 20 -->
en:retardation
n1=en:impaired tandem gait | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:impaired use of nonverbal behaviors, such as eye-to-eye gaze, facial expression, body posture, and gestures ---
r_associated #0: 20 -->
en:retardation
n1=en:impaired use of nonverbal behaviors, such as eye-to-eye gaze, facial expression, body posture, and gestures | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:impaired vertical visual pursuit ---
r_associated #0: 20 -->
en:retardation
n1=en:impaired vertical visual pursuit | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:impaired vibration sensation at ankles ---
r_associated #0: 20 -->
en:retardation
n1=en:impaired vibration sensation at ankles | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:impaired vibration sensation in the lower limbs ---
r_associated #0: 20 -->
en:retardation
n1=en:impaired vibration sensation in the lower limbs | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:impaired visuospatial skills ---
r_associated #0: 20 -->
en:retardation
n1=en:impaired visuospatial skills | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:impaired voluntary movement ---
r_associated #0: 20 -->
en:retardation
n1=en:impaired voluntary movement | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:impaired walking ability (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:impaired walking ability (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:impairment of balance ---
r_associated #0: 20 -->
en:retardation
n1=en:impairment of balance | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:impairment of gross and fine motor coordination ---
r_associated #0: 20 -->
en:retardation
n1=en:impairment of gross and fine motor coordination | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:imperforate anus ---
r_associated #0: 20 -->
en:retardation
n1=en:imperforate anus | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:impetigo ---
r_associated #0: 20 -->
en:retardation
n1=en:impetigo | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:impulse control disorder nec (disorder) in snomedct_us_2016_03_01 ---
r_associated #0: 20 -->
en:retardation
n1=en:impulse control disorder nec (disorder) in snomedct_us_2016_03_01 | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:impulse-control disorder ---
r_associated #0: 20 -->
en:retardation
n1=en:impulse-control disorder | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:inability to communicate ---
r_associated #0: 20 -->
en:retardation
n1=en:inability to communicate | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:inability to generate syntactic grammar rules (i.e., tense, gender, number) ---
r_associated #0: 20 -->
en:retardation
n1=en:inability to generate syntactic grammar rules (i.e., tense, gender, number) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:inability to hold head ---
r_associated #0: 20 -->
en:retardation
n1=en:inability to hold head | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:inability to hold head up ---
r_associated #0: 20 -->
en:retardation
n1=en:inability to hold head up | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:inability to hold neck up ('limber neck') onset at 6 months ---
r_associated #0: 20 -->
en:retardation
n1=en:inability to hold neck up ('limber neck') onset at 6 months | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:inability to reach ---
r_associated #0: 20 -->
en:retardation
n1=en:inability to reach | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:inability to run ---
r_associated #0: 20 -->
en:retardation
n1=en:inability to run | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:inability to run (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:inability to run (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:inability to sit ---
r_associated #0: 20 -->
en:retardation
n1=en:inability to sit | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:inability to sit or control head ---
r_associated #0: 20 -->
en:retardation
n1=en:inability to sit or control head | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:inability to sit or stand independently ---
r_associated #0: 20 -->
en:retardation
n1=en:inability to sit or stand independently | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:inability to sit or walk independently ---
r_associated #0: 20 -->
en:retardation
n1=en:inability to sit or walk independently | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:inability to stand on toes ---
r_associated #0: 20 -->
en:retardation
n1=en:inability to stand on toes | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:inability to stand without assistance ---
r_associated #0: 20 -->
en:retardation
n1=en:inability to stand without assistance | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:inability to walk independently ---
r_associated #0: 20 -->
en:retardation
n1=en:inability to walk independently | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:inability to walk unaided ---
r_associated #0: 20 -->
en:retardation
n1=en:inability to walk unaided | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:inability to walk unsupported ---
r_associated #0: 20 -->
en:retardation
n1=en:inability to walk unsupported | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:inarticulate speech delayed gross motor skills ---
r_associated #0: 20 -->
en:retardation
n1=en:inarticulate speech delayed gross motor skills | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:incomplete anencephaly, hemicrania ---
r_associated #0: 20 -->
en:retardation
n1=en:incomplete anencephaly, hemicrania | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:incomplete myelination ---
r_associated #0: 20 -->
en:retardation
n1=en:incomplete myelination | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:incomprehensible speech ---
r_associated #0: 20 -->
en:retardation
n1=en:incomprehensible speech | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:incontinentia pigmenti, familial male-lethal type ---
r_associated #0: 20 -->
en:retardation
n1=en:incontinentia pigmenti, familial male-lethal type | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:incoordination of the hands ---
r_associated #0: 20 -->
en:retardation
n1=en:incoordination of the hands | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:incoordination of trunk and limbs ---
r_associated #0: 20 -->
en:retardation
n1=en:incoordination of trunk and limbs | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:increase in blood pressure ---
r_associated #0: 20 -->
en:retardation
n1=en:increase in blood pressure | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:increased activity period ---
r_associated #0: 20 -->
en:retardation
n1=en:increased activity period | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:increased cerebral lactate ---
r_associated #0: 20 -->
en:retardation
n1=en:increased cerebral lactate | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:increased csf lactate ---
r_associated #0: 20 -->
en:retardation
n1=en:increased csf lactate | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:increased csf protein ---
r_associated #0: 20 -->
en:retardation
n1=en:increased csf protein | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:increased csf protein with normal cell count ---
r_associated #0: 20 -->
en:retardation
n1=en:increased csf protein with normal cell count | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:increased deep tendon reflexes (if left untreated) ---
r_associated #0: 20 -->
en:retardation
n1=en:increased deep tendon reflexes (if left untreated) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:increased falls ---
r_associated #0: 20 -->
en:retardation
n1=en:increased falls | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:increased intracranial pressure preoperatively (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:increased intracranial pressure preoperatively (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:increased iron deposition in the basal ganglia ---
r_associated #0: 20 -->
en:retardation
n1=en:increased iron deposition in the basal ganglia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:increased iron deposition in the basal ganglia (40%) ---
r_associated #0: 20 -->
en:retardation
n1=en:increased iron deposition in the basal ganglia (40%) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:increased lactate in the brain ---
r_associated #0: 20 -->
en:retardation
n1=en:increased lactate in the brain | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:increased muscle tone in the lower limbs ---
r_associated #0: 20 -->
en:retardation
n1=en:increased muscle tone in the lower limbs | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:increased neurologic sequelae of infections (rare) ---
r_associated #0: 20 -->
en:retardation
n1=en:increased neurologic sequelae of infections (rare) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:increased risk of seizures in childhood or adulthood (11-16%) ---
r_associated #0: 20 -->
en:retardation
n1=en:increased risk of seizures in childhood or adulthood (11-16%) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:increased signal intensity on t(2)-weighted scans in the periventricular and centrum ovale area ---
r_associated #0: 20 -->
en:retardation
n1=en:increased signal intensity on t(2)-weighted scans in the periventricular and centrum ovale area | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:increased startle response ---
r_associated #0: 20 -->
en:retardation
n1=en:increased startle response | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:increased subdural space around frontal lobes ---
r_associated #0: 20 -->
en:retardation
n1=en:increased subdural space around frontal lobes | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:increased t2 signal intensities in the middle cerebellar peduncles ---
r_associated #0: 20 -->
en:retardation
n1=en:increased t2 signal intensities in the middle cerebellar peduncles | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:increased tone in the upper limbs (occur later) ---
r_associated #0: 20 -->
en:retardation
n1=en:increased tone in the upper limbs (occur later) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:increased white matter abnormalities on t2 signalling (in type iib) ---
r_associated #0: 20 -->
en:retardation
n1=en:increased white matter abnormalities on t2 signalling (in type iib) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:independent walking never achieved ---
r_associated #0: 20 -->
en:retardation
n1=en:independent walking never achieved | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:indication for modification of patient status ---
r_associated #0: 20 -->
en:retardation
n1=en:indication for modification of patient status | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:individuals can stand or walk with support by 4 to 6 years of age ---
r_associated #0: 20 -->
en:retardation
n1=en:individuals can stand or walk with support by 4 to 6 years of age | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:individuals require less sleep in a 24-hour period compared to age-matched controls ---
r_associated #0: 20 -->
en:retardation
n1=en:individuals require less sleep in a 24-hour period compared to age-matched controls | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:induced abortion finding ---
r_associated #0: 20 -->
en:retardation
n1=en:induced abortion finding | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:infantile encephalopathy ---
r_associated #0: 20 -->
en:retardation
n1=en:infantile encephalopathy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:infantile encephalopathy, progressive ---
r_associated #0: 20 -->
en:retardation
n1=en:infantile encephalopathy, progressive | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:infantile hemiplegias ---
r_associated #0: 20 -->
en:retardation
n1=en:infantile hemiplegias | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:infantile irritability (if left untreated) ---
r_associated #0: 20 -->
en:retardation
n1=en:infantile irritability (if left untreated) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:infantile muscular hypotonia ---
r_associated #0: 20 -->
en:retardation
n1=en:infantile muscular hypotonia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:infantile neuroaxonal dystrophy ---
r_associated #0: 20 -->
en:retardation
n1=en:infantile neuroaxonal dystrophy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:infantile nystagmus ---
r_associated #0: 20 -->
en:retardation
n1=en:infantile nystagmus | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:infantile seizures ---
r_associated #0: 20 -->
en:retardation
n1=en:infantile seizures | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:infantile seizures (approximately 80% of patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:infantile seizures (approximately 80% of patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:infantile seizures, afebrile, with no neurologic sequelae (in 40% of patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:infantile seizures, afebrile, with no neurologic sequelae (in 40% of patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:infantile spasm ---
r_associated #0: 20 -->
en:retardation
n1=en:infantile spasm | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:infantilism ---
r_associated #0: 20 -->
en:retardation
n1=en:infantilism | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:infarction ---
r_associated #0: 20 -->
en:retardation
n1=en:infarction | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:infections of musculoskeletal system ---
r_associated #0: 20 -->
en:retardation
n1=en:infections of musculoskeletal system | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:infectious conjunctivitis ---
r_associated #0: 20 -->
en:retardation
n1=en:infectious conjunctivitis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:infectious diarrhea/dysentery ---
r_associated #0: 20 -->
en:retardation
n1=en:infectious diarrhea/dysentery | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:infectious disease circulatory system ---
r_associated #0: 20 -->
en:retardation
n1=en:infectious disease circulatory system | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:infectious mononucleosis ---
r_associated #0: 20 -->
en:retardation
n1=en:infectious mononucleosis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:inferior olivary nuclei show fetal pattern ---
r_associated #0: 20 -->
en:retardation
n1=en:inferior olivary nuclei show fetal pattern | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:inferior vermis hypoplasia ---
r_associated #0: 20 -->
en:retardation
n1=en:inferior vermis hypoplasia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:inflexible adherence to routines or rituals ---
r_associated #0: 20 -->
en:retardation
n1=en:inflexible adherence to routines or rituals | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:influenza (proven) without pneumonia ---
r_associated #0: 20 -->
en:retardation
n1=en:influenza (proven) without pneumonia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:infrequent generalized seizures ---
r_associated #0: 20 -->
en:retardation
n1=en:infrequent generalized seizures | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ingrown toenail/other disease of nail ---
r_associated #0: 20 -->
en:retardation
n1=en:ingrown toenail/other disease of nail | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:inguinal hernia ---
r_associated #0: 20 -->
en:retardation
n1=en:inguinal hernia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:inhibition/loss sexual fulfillment ---
r_associated #0: 20 -->
en:retardation
n1=en:inhibition/loss sexual fulfillment | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:initial hypotonia, followed by spasticity ---
r_associated #0: 20 -->
en:retardation
n1=en:initial hypotonia, followed by spasticity | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:initial normal development ---
r_associated #0: 20 -->
en:retardation
n1=en:initial normal development | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:injuries complicating pregnancy ---
r_associated #0: 20 -->
en:retardation
n1=en:injuries complicating pregnancy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:insomnia adverse event ---
r_associated #0: 20 -->
en:retardation
n1=en:insomnia adverse event | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:insomnia related to...[indicate the axis i or axis ii disorder] ---
r_associated #0: 20 -->
en:retardation
n1=en:insomnia related to...[indicate the axis i or axis ii disorder] | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:insomnia, refractory ---
r_associated #0: 20 -->
en:retardation
n1=en:insomnia, refractory | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:insulin-like growth factor i deficiency ---
r_associated #0: 20 -->
en:retardation
n1=en:insulin-like growth factor i deficiency | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:intellect high (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:intellect high (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:intellectual delay ---
r_associated #0: 20 -->
en:retardation
n1=en:intellectual delay | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:intellectual development ---
r_associated #0: 20 -->
en:retardation
n1=en:intellectual development | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:intellectual disabilities (in 1 family) ---
r_associated #0: 20 -->
en:retardation
n1=en:intellectual disabilities (in 1 family) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:intellectual disability (in 1 ashkenazi patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:intellectual disability (in 1 ashkenazi patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:intellectual disability (in most patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:intellectual disability (in most patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:intellectual disability (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:intellectual disability (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:intellectual disability, mild (1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:intellectual disability, mild (1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:intellectual disability, mild (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:intellectual disability, mild (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:intellectual disability, mild (uncommon) ---
r_associated #0: 20 -->
en:retardation
n1=en:intellectual disability, mild (uncommon) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:intellectual disability, mild to moderate ---
r_associated #0: 20 -->
en:retardation
n1=en:intellectual disability, mild to moderate | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:intellectual disability, mild to moderate (in homozygotes) ---
r_associated #0: 20 -->
en:retardation
n1=en:intellectual disability, mild to moderate (in homozygotes) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:intellectual disability, mild to severe ---
r_associated #0: 20 -->
en:retardation
n1=en:intellectual disability, mild to severe | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:intellectual disability, moderate (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:intellectual disability, moderate (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:intellectual disability, moderate to severe ---
r_associated #0: 20 -->
en:retardation
n1=en:intellectual disability, moderate to severe | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:intellectual disability, progressive ---
r_associated #0: 20 -->
en:retardation
n1=en:intellectual disability, progressive | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:intellectual function may be high in milder cases ---
r_associated #0: 20 -->
en:retardation
n1=en:intellectual function may be high in milder cases | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:intellectual impairment (rare) ---
r_associated #0: 20 -->
en:retardation
n1=en:intellectual impairment (rare) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:intellectual impairment, mild ---
r_associated #0: 20 -->
en:retardation
n1=en:intellectual impairment, mild | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:intellectual impairment, mild (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:intellectual impairment, mild (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:intelligence ---
r_associated #0: 20 -->
en:retardation
n1=en:intelligence | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:intelligence and ability ---
r_associated #0: 20 -->
en:retardation
n1=en:intelligence and ability | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:intensive care psychiatric disorder ---
r_associated #0: 20 -->
en:retardation
n1=en:intensive care psychiatric disorder | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:intention tremor (1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:intention tremor (1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:intention tremor (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:intention tremor (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:intention tremor in those who survive ---
r_associated #0: 20 -->
en:retardation
n1=en:intention tremor in those who survive | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:intentional trauma ---
r_associated #0: 20 -->
en:retardation
n1=en:intentional trauma | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:interhemispheric cysts ---
r_associated #0: 20 -->
en:retardation
n1=en:interhemispheric cysts | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:interhemispheric lipoma ---
r_associated #0: 20 -->
en:retardation
n1=en:interhemispheric lipoma | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:interictal ataxia may occur later in disease course ---
r_associated #0: 20 -->
en:retardation
n1=en:interictal ataxia may occur later in disease course | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:interictal downbeat nystagmus ---
r_associated #0: 20 -->
en:retardation
n1=en:interictal downbeat nystagmus | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:interictal dystonia may occur later in disease course ---
r_associated #0: 20 -->
en:retardation
n1=en:interictal dystonia may occur later in disease course | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:interictal eeg is usually normal ---
r_associated #0: 20 -->
en:retardation
n1=en:interictal eeg is usually normal | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:interictal eeg may be normal or abnormal ---
r_associated #0: 20 -->
en:retardation
n1=en:interictal eeg may be normal or abnormal | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:interictal eeg may show nonspecific changes in 15 to 20% ---
r_associated #0: 20 -->
en:retardation
n1=en:interictal eeg may show nonspecific changes in 15 to 20% | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:interictal eeg shows 3-4 hz general spike-wave complexes ---
r_associated #0: 20 -->
en:retardation
n1=en:interictal eeg shows 3-4 hz general spike-wave complexes | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:interictal neurologic impairment ---
r_associated #0: 20 -->
en:retardation
n1=en:interictal neurologic impairment | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:interictal periods of normal health ---
r_associated #0: 20 -->
en:retardation
n1=en:interictal periods of normal health | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:intermittent episodes associated with lethargy, vomiting ---
r_associated #0: 20 -->
en:retardation
n1=en:intermittent episodes associated with lethargy, vomiting | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:intermittent migraine headaches ---
r_associated #0: 20 -->
en:retardation
n1=en:intermittent migraine headaches | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:intermittent wheelchair dependence (stage 3) ---
r_associated #0: 20 -->
en:retardation
n1=en:intermittent wheelchair dependence (stage 3) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:intermittent, transient episodes of worsening of ataxia ---
r_associated #0: 20 -->
en:retardation
n1=en:intermittent, transient episodes of worsening of ataxia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:interosseus muscle atrophy ---
r_associated #0: 20 -->
en:retardation
n1=en:interosseus muscle atrophy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:interventricular cysts ---
r_associated #0: 20 -->
en:retardation
n1=en:interventricular cysts | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:intestinal malrotation ---
r_associated #0: 20 -->
en:retardation
n1=en:intestinal malrotation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:intracellular accumulation of material resulting in curvilinear profiles on ultrastructural analysis ---
r_associated #0: 20 -->
en:retardation
n1=en:intracellular accumulation of material resulting in curvilinear profiles on ultrastructural analysis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:intracellular accumulation of material resulting in fingerprint profiles on ultrastructural analysis ---
r_associated #0: 20 -->
en:retardation
n1=en:intracellular accumulation of material resulting in fingerprint profiles on ultrastructural analysis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:intracellular accumulation of material resulting in rectilinear profiles on ultrastructural analysis ---
r_associated #0: 20 -->
en:retardation
n1=en:intracellular accumulation of material resulting in rectilinear profiles on ultrastructural analysis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:intracellular lewy bodies ---
r_associated #0: 20 -->
en:retardation
n1=en:intracellular lewy bodies | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:intracellular pas-positive polyglucosan inclusion bodies ('lafora' bodies) ---
r_associated #0: 20 -->
en:retardation
n1=en:intracellular pas-positive polyglucosan inclusion bodies ('lafora' bodies) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:intracerebral calcifications (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:intracerebral calcifications (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:intracerebral cysts (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:intracerebral cysts (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:intracerebral periventricular calcifications ---
r_associated #0: 20 -->
en:retardation
n1=en:intracerebral periventricular calcifications | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:intracranial bleeding (1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:intracranial bleeding (1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:intracranial calcification affecting the basal ganglia (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:intracranial calcification affecting the basal ganglia (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:intracranial calcification by x-ray or ct ---
r_associated #0: 20 -->
en:retardation
n1=en:intracranial calcification by x-ray or ct | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:intracranial calcifications (1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:intracranial calcifications (1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:intracranial calcifications (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:intracranial calcifications (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:intracranial calcifications in the anterior mesial temporal lobes ---
r_associated #0: 20 -->
en:retardation
n1=en:intracranial calcifications in the anterior mesial temporal lobes | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:intracranial calcifications, band-like, particularly periventricular and in the basal ganglia and thalamus ---
r_associated #0: 20 -->
en:retardation
n1=en:intracranial calcifications, band-like, particularly periventricular and in the basal ganglia and thalamus | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:intracranial cysts ---
r_associated #0: 20 -->
en:retardation
n1=en:intracranial cysts | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:intracranial hemorrhage ---
r_associated #0: 20 -->
en:retardation
n1=en:intracranial hemorrhage | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:intracranial hypertension ---
r_associated #0: 20 -->
en:retardation
n1=en:intracranial hypertension | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:intracranial lipoma (cerebello-pontine) ---
r_associated #0: 20 -->
en:retardation
n1=en:intracranial lipoma (cerebello-pontine) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:intracranial thin-walled sinusoidal vessel (cavernous) malformations ---
r_associated #0: 20 -->
en:retardation
n1=en:intracranial thin-walled sinusoidal vessel (cavernous) malformations | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:intractable epilepsy ---
r_associated #0: 20 -->
en:retardation
n1=en:intractable epilepsy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:intraneuronal inclusions ---
r_associated #0: 20 -->
en:retardation
n1=en:intraneuronal inclusions | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:intraparenchymal brain hemorrhage, multifocal ---
r_associated #0: 20 -->
en:retardation
n1=en:intraparenchymal brain hemorrhage, multifocal | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:intraspinal neoplasm ---
r_associated #0: 20 -->
en:retardation
n1=en:intraspinal neoplasm | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:invalidism ---
r_associated #0: 20 -->
en:retardation
n1=en:invalidism | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:involuntary dystonic or choreiform movements ---
r_associated #0: 20 -->
en:retardation
n1=en:involuntary dystonic or choreiform movements | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:involuntary jerking movements ---
r_associated #0: 20 -->
en:retardation
n1=en:involuntary jerking movements | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:involuntary movement and habit disorder ---
r_associated #0: 20 -->
en:retardation
n1=en:involuntary movement and habit disorder | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:involuntary movements ---
r_associated #0: 20 -->
en:retardation
n1=en:involuntary movements | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:involuntary movements may be precipitated by exertion or anxiety ---
r_associated #0: 20 -->
en:retardation
n1=en:involuntary movements may be precipitated by exertion or anxiety | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:involuntary movements of extremities, neck, trunk, and/or face ---
r_associated #0: 20 -->
en:retardation
n1=en:involuntary movements of extremities, neck, trunk, and/or face | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:involuntary movements, asymmetric ---
r_associated #0: 20 -->
en:retardation
n1=en:involuntary movements, asymmetric | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:involuntary repetitive movements ---
r_associated #0: 20 -->
en:retardation
n1=en:involuntary repetitive movements | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:involuntary rhythmic myoclonic movements ('tremor') of the distal extremities, usually fingers ---
r_associated #0: 20 -->
en:retardation
n1=en:involuntary rhythmic myoclonic movements ('tremor') of the distal extremities, usually fingers | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:involuntary rhythmic myoclonic movements ('tremor'), upper extremities ---
r_associated #0: 20 -->
en:retardation
n1=en:involuntary rhythmic myoclonic movements ('tremor'), upper extremities | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:involuntary writhing movements ---
r_associated #0: 20 -->
en:retardation
n1=en:involuntary writhing movements | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ipsilateral brain hypoplasia ---
r_associated #0: 20 -->
en:retardation
n1=en:ipsilateral brain hypoplasia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ipsilateral cranial nerve hypoplasia ---
r_associated #0: 20 -->
en:retardation
n1=en:ipsilateral cranial nerve hypoplasia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:iq 85-115 (female) ---
r_associated #0: 20 -->
en:retardation
n1=en:iq 85-115 (female) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:iron accumulation in the basal ganglia seen on mri ---
r_associated #0: 20 -->
en:retardation
n1=en:iron accumulation in the basal ganglia seen on mri | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:iron accumulation in the globus pallidus and substantia nigra seen on mri ---
r_associated #0: 20 -->
en:retardation
n1=en:iron accumulation in the globus pallidus and substantia nigra seen on mri | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:iron deposition in pallidal nuclei ---
r_associated #0: 20 -->
en:retardation
n1=en:iron deposition in pallidal nuclei | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:iron deposition in the basal ganglia (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:iron deposition in the basal ganglia (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:iron deposition in the globus pallidus (variable) ---
r_associated #0: 20 -->
en:retardation
n1=en:iron deposition in the globus pallidus (variable) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:iron deposition in the globus pallidus and substantia nigra seen on mri ---
r_associated #0: 20 -->
en:retardation
n1=en:iron deposition in the globus pallidus and substantia nigra seen on mri | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:iron deposits in the globus pallidus, caudate, and substantia nigra ---
r_associated #0: 20 -->
en:retardation
n1=en:iron deposits in the globus pallidus, caudate, and substantia nigra | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:iron-containing deposits in various brain regions ---
r_associated #0: 20 -->
en:retardation
n1=en:iron-containing deposits in various brain regions | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:iron-deficiency anemia ---
r_associated #0: 20 -->
en:retardation
n1=en:iron-deficiency anemia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:irregular cortical ribbon ---
r_associated #0: 20 -->
en:retardation
n1=en:irregular cortical ribbon | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:irregular folding of the cortex ---
r_associated #0: 20 -->
en:retardation
n1=en:irregular folding of the cortex | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:irregular spike and slow waves ---
r_associated #0: 20 -->
en:retardation
n1=en:irregular spike and slow waves | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:irresistible desire to move the legs ---
r_associated #0: 20 -->
en:retardation
n1=en:irresistible desire to move the legs | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:irritable bowel syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:irritable bowel syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:irritation ---
r_associated #0: 20 -->
en:retardation
n1=en:irritation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ischemic cerebrovascular accident ---
r_associated #0: 20 -->
en:retardation
n1=en:ischemic cerebrovascular accident | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ischemic infarct of brain ---
r_associated #0: 20 -->
en:retardation
n1=en:ischemic infarct of brain | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ischemic infarction (rare) ---
r_associated #0: 20 -->
en:retardation
n1=en:ischemic infarction (rare) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ischemic necrotic lesions ---
r_associated #0: 20 -->
en:retardation
n1=en:ischemic necrotic lesions | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ischemic stroke (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:ischemic stroke (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ischemic stroke in the basal ganglia (rare) ---
r_associated #0: 20 -->
en:retardation
n1=en:ischemic stroke in the basal ganglia (rare) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:isolated absence of pain sensation ---
r_associated #0: 20 -->
en:retardation
n1=en:isolated absence of pain sensation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:isolated focal dystonia may occur ---
r_associated #0: 20 -->
en:retardation
n1=en:isolated focal dystonia may occur | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:jacksonian seizure ---
r_associated #0: 20 -->
en:retardation
n1=en:jacksonian seizure | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:jacobsen syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:jacobsen syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:jerk-locked premyoclonus spikes ---
r_associated #0: 20 -->
en:retardation
n1=en:jerk-locked premyoclonus spikes | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:jerking may be unidirectional, periodically alternating, or mixed pendular and jerk-like ---
r_associated #0: 20 -->
en:retardation
n1=en:jerking may be unidirectional, periodically alternating, or mixed pendular and jerk-like | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:jerking movements ---
r_associated #0: 20 -->
en:retardation
n1=en:jerking movements | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:jerky head movements ---
r_associated #0: 20 -->
en:retardation
n1=en:jerky head movements | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:jerky limb movements ---
r_associated #0: 20 -->
en:retardation
n1=en:jerky limb movements | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:jerky movements in infancy ---
r_associated #0: 20 -->
en:retardation
n1=en:jerky movements in infancy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:johanson-blizzard syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:johanson-blizzard syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:joubert syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:joubert syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:joubert syndrome 15 ---
r_associated #0: 20 -->
en:retardation
n1=en:joubert syndrome 15 | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:joubert syndrome 18 ---
r_associated #0: 20 -->
en:retardation
n1=en:joubert syndrome 18 | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:joubert syndrome 2 ---
r_associated #0: 20 -->
en:retardation
n1=en:joubert syndrome 2 | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:joubert syndrome 21 ---
r_associated #0: 20 -->
en:retardation
n1=en:joubert syndrome 21 | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:joubert syndrome 3 ---
r_associated #0: 20 -->
en:retardation
n1=en:joubert syndrome 3 | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:joubert syndrome 5 ---
r_associated #0: 20 -->
en:retardation
n1=en:joubert syndrome 5 | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:joubert syndrome 6 ---
r_associated #0: 20 -->
en:retardation
n1=en:joubert syndrome 6 | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:kabuki syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:kabuki syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:kaufman oculocerebrofacial syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:kaufman oculocerebrofacial syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:kbg syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:kbg syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:kearns-sayre syndrome (530000), in a subset of patients ---
r_associated #0: 20 -->
en:retardation
n1=en:kearns-sayre syndrome (530000), in a subset of patients | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:kernicterus ---
r_associated #0: 20 -->
en:retardation
n1=en:kernicterus | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:klinefelter syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:klinefelter syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:klippel-trenaunay-weber syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:klippel-trenaunay-weber syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:knee and ankle clonus ---
r_associated #0: 20 -->
en:retardation
n1=en:knee and ankle clonus | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:known or suspected fetal abnormality affecting management of mother ---
r_associated #0: 20 -->
en:retardation
n1=en:known or suspected fetal abnormality affecting management of mother | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:kuzniecky syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:kuzniecky syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lack of bunina bodies ---
r_associated #0: 20 -->
en:retardation
n1=en:lack of bunina bodies | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lack of communication ---
r_associated #0: 20 -->
en:retardation
n1=en:lack of communication | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lack of development ---
r_associated #0: 20 -->
en:retardation
n1=en:lack of development | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lack of developmental development ---
r_associated #0: 20 -->
en:retardation
n1=en:lack of developmental development | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lack of developmental milestones ---
r_associated #0: 20 -->
en:retardation
n1=en:lack of developmental milestones | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lack of ependymal cells ---
r_associated #0: 20 -->
en:retardation
n1=en:lack of ependymal cells | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lack of expressive speech ---
r_associated #0: 20 -->
en:retardation
n1=en:lack of expressive speech | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lack of head control ---
r_associated #0: 20 -->
en:retardation
n1=en:lack of head control | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lack of head or postural control (in severe cases) ---
r_associated #0: 20 -->
en:retardation
n1=en:lack of head or postural control (in severe cases) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lack of independent ambulation ---
r_associated #0: 20 -->
en:retardation
n1=en:lack of independent ambulation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lack of independent ambulation (1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:lack of independent ambulation (1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lack of independent sitting or walking ---
r_associated #0: 20 -->
en:retardation
n1=en:lack of independent sitting or walking | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lack of independent walking (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:lack of independent walking (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lack of inflammatory infiltrate ---
r_associated #0: 20 -->
en:retardation
n1=en:lack of inflammatory infiltrate | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lack of motor development ---
r_associated #0: 20 -->
en:retardation
n1=en:lack of motor development | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lack of motor development (wws) ---
r_associated #0: 20 -->
en:retardation
n1=en:lack of motor development (wws) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lack of motor milestones ---
r_associated #0: 20 -->
en:retardation
n1=en:lack of motor milestones | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lack of neurologic development ---
r_associated #0: 20 -->
en:retardation
n1=en:lack of neurologic development | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lack of peer relationships ---
r_associated #0: 20 -->
en:retardation
n1=en:lack of peer relationships | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lack of psychomotor development (1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:lack of psychomotor development (1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lack of psychomotor development (severe connatal form) ---
r_associated #0: 20 -->
en:retardation
n1=en:lack of psychomotor development (severe connatal form) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lack of skein-like inclusions ---
r_associated #0: 20 -->
en:retardation
n1=en:lack of skein-like inclusions | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lack of speech (in severe cases) ---
r_associated #0: 20 -->
en:retardation
n1=en:lack of speech (in severe cases) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lack of speech acquisition ---
r_associated #0: 20 -->
en:retardation
n1=en:lack of speech acquisition | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lack of speech development ---
r_associated #0: 20 -->
en:retardation
n1=en:lack of speech development | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lack of speech development (some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:lack of speech development (some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lack of speech or only a few words ---
r_associated #0: 20 -->
en:retardation
n1=en:lack of speech or only a few words | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lack of speech or poor speech ---
r_associated #0: 20 -->
en:retardation
n1=en:lack of speech or poor speech | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lack of spontaneous movement ---
r_associated #0: 20 -->
en:retardation
n1=en:lack of spontaneous movement | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lack of spontaneous play ---
r_associated #0: 20 -->
en:retardation
n1=en:lack of spontaneous play | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lack of upper motor neuron signs ---
r_associated #0: 20 -->
en:retardation
n1=en:lack of upper motor neuron signs | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lack of verbal communication ---
r_associated #0: 20 -->
en:retardation
n1=en:lack of verbal communication | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lack of visual attention ---
r_associated #0: 20 -->
en:retardation
n1=en:lack of visual attention | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lack of volitional movement ---
r_associated #0: 20 -->
en:retardation
n1=en:lack of volitional movement | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lacunar infarcts develop after age 40 years ---
r_associated #0: 20 -->
en:retardation
n1=en:lacunar infarcts develop after age 40 years | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lacunar infarcts in the deep-brain nuclei, brainstem, internal capsule seen on imaging ---
r_associated #0: 20 -->
en:retardation
n1=en:lacunar infarcts in the deep-brain nuclei, brainstem, internal capsule seen on imaging | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:laminar necrosis ---
r_associated #0: 20 -->
en:retardation
n1=en:laminar necrosis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:language acquisition difficulties (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:language acquisition difficulties (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:language delay ---
r_associated #0: 20 -->
en:retardation
n1=en:language delay | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:language delay (55%) ---
r_associated #0: 20 -->
en:retardation
n1=en:language delay (55%) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:language delay/disorder ---
r_associated #0: 20 -->
en:retardation
n1=en:language delay/disorder | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:language development limited to a few words ---
r_associated #0: 20 -->
en:retardation
n1=en:language development limited to a few words | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:language disorder ---
r_associated #0: 20 -->
en:retardation
n1=en:language disorder | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:language or speech disorder ---
r_associated #0: 20 -->
en:retardation
n1=en:language or speech disorder | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:large basal ganglia ---
r_associated #0: 20 -->
en:retardation
n1=en:large basal ganglia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:large cavum vergae ---
r_associated #0: 20 -->
en:retardation
n1=en:large cavum vergae | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:large cerebellum, progressive ---
r_associated #0: 20 -->
en:retardation
n1=en:large cerebellum, progressive | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:large sella turcica ---
r_associated #0: 20 -->
en:retardation
n1=en:large sella turcica | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:large subcortical cysts in frontal and temporal lobes ---
r_associated #0: 20 -->
en:retardation
n1=en:large subcortical cysts in frontal and temporal lobes | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:larnygeotracheoesophageal cleft ---
r_associated #0: 20 -->
en:retardation
n1=en:larnygeotracheoesophageal cleft | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:larsen syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:larsen syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:laryngeal atresia ---
r_associated #0: 20 -->
en:retardation
n1=en:laryngeal atresia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:laryngocele ---
r_associated #0: 20 -->
en:retardation
n1=en:laryngocele | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:late ambulation ---
r_associated #0: 20 -->
en:retardation
n1=en:late ambulation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:late diaphragmatic involvement ---
r_associated #0: 20 -->
en:retardation
n1=en:late diaphragmatic involvement | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:late effect of trauma ---
r_associated #0: 20 -->
en:retardation
n1=en:late effect of trauma | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:late-onset spinocerebellar degeneration ---
r_associated #0: 20 -->
en:retardation
n1=en:late-onset spinocerebellar degeneration | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lateral corticospinal tracts show atrophy, pallor, and degeneration ---
r_associated #0: 20 -->
en:retardation
n1=en:lateral corticospinal tracts show atrophy, pallor, and degeneration | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lateral epicondylitis ---
r_associated #0: 20 -->
en:retardation
n1=en:lateral epicondylitis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lathosterolosis ---
r_associated #0: 20 -->
en:retardation
n1=en:lathosterolosis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:laurence-moon syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:laurence-moon syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:learning and developmental delay (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:learning and developmental delay (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:learning difficulties ---
r_associated #0: 20 -->
en:retardation
n1=en:learning difficulties | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:learning difficulties (in 1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:learning difficulties (in 1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:learning difficulties (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:learning difficulties (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:learning difficulties (less common) ---
r_associated #0: 20 -->
en:retardation
n1=en:learning difficulties (less common) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:learning difficulties (seen in recessive form) ---
r_associated #0: 20 -->
en:retardation
n1=en:learning difficulties (seen in recessive form) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:learning difficulties in affected females ---
r_associated #0: 20 -->
en:retardation
n1=en:learning difficulties in affected females | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:learning difficulties, mild (1 family) ---
r_associated #0: 20 -->
en:retardation
n1=en:learning difficulties, mild (1 family) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:learning disabilities ---
r_associated #0: 20 -->
en:retardation
n1=en:learning disabilities | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:learning disabilities (1 family) ---
r_associated #0: 20 -->
en:retardation
n1=en:learning disabilities (1 family) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:learning disabilities (30%) ---
r_associated #0: 20 -->
en:retardation
n1=en:learning disabilities (30%) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:learning disabilities (in females) ---
r_associated #0: 20 -->
en:retardation
n1=en:learning disabilities (in females) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:learning disabilities (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:learning disabilities (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:learning disabilities (in some) ---
r_associated #0: 20 -->
en:retardation
n1=en:learning disabilities (in some) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:learning disabilities (major) ---
r_associated #0: 20 -->
en:retardation
n1=en:learning disabilities (major) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:learning disability (90% patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:learning disability (90% patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:learning disability (early in life) ---
r_associated #0: 20 -->
en:retardation
n1=en:learning disability (early in life) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:learning disorder ---
r_associated #0: 20 -->
en:retardation
n1=en:learning disorder | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:learning problems ---
r_associated #0: 20 -->
en:retardation
n1=en:learning problems | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:leber optic atrophy and dystonia ---
r_associated #0: 20 -->
en:retardation
n1=en:leber optic atrophy and dystonia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:leg cramp ---
r_associated #0: 20 -->
en:retardation
n1=en:leg cramp | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:leg pain ---
r_associated #0: 20 -->
en:retardation
n1=en:leg pain | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:leg stiffness ---
r_associated #0: 20 -->
en:retardation
n1=en:leg stiffness | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:leigh disease ---
r_associated #0: 20 -->
en:retardation
n1=en:leigh disease | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:leigh syndrome (245000), in a subset of patients ---
r_associated #0: 20 -->
en:retardation
n1=en:leigh syndrome (245000), in a subset of patients | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:leigh syndrome (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:leigh syndrome (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:leptomeningeal melanocytosis (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:leptomeningeal melanocytosis (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:leptomeningeal thickening ---
r_associated #0: 20 -->
en:retardation
n1=en:leptomeningeal thickening | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lesch-nyhan syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:lesch-nyhan syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lesions are symmetrical ---
r_associated #0: 20 -->
en:retardation
n1=en:lesions are symmetrical | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lesions characterized by demyelination, necrosis, gliosis, spongiosis, and capillary proliferation ---
r_associated #0: 20 -->
en:retardation
n1=en:lesions characterized by demyelination, necrosis, gliosis, spongiosis, and capillary proliferation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lesions in basal ganglia, brainstem, cerebellum, thalamus, spinal cord ---
r_associated #0: 20 -->
en:retardation
n1=en:lesions in basal ganglia, brainstem, cerebellum, thalamus, spinal cord | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lesions in basal ganglia, brainstem, cerebellum, thalamus, spinal cord characterized by demyelination, necrosis, gliosis, spongiosis, and capillary proliferation ---
r_associated #0: 20 -->
en:retardation
n1=en:lesions in basal ganglia, brainstem, cerebellum, thalamus, spinal cord characterized by demyelination, necrosis, gliosis, spongiosis, and capillary proliferation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lesions in the anterior pituitary (less common) ---
r_associated #0: 20 -->
en:retardation
n1=en:lesions in the anterior pituitary (less common) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lesions in the basal ganglia ---
r_associated #0: 20 -->
en:retardation
n1=en:lesions in the basal ganglia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lesions in the caudate and putamen ---
r_associated #0: 20 -->
en:retardation
n1=en:lesions in the caudate and putamen | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lesions in the caudate and putamen seen on mri ---
r_associated #0: 20 -->
en:retardation
n1=en:lesions in the caudate and putamen seen on mri | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lesions in the internal capsule after age 40 years ---
r_associated #0: 20 -->
en:retardation
n1=en:lesions in the internal capsule after age 40 years | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lesions show signal increase on t2- and signal decrease on t1-weighted images ---
r_associated #0: 20 -->
en:retardation
n1=en:lesions show signal increase on t2- and signal decrease on t1-weighted images | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lethargy ---
r_associated #0: 20 -->
en:retardation
n1=en:lethargy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lethargy associated with hypoglycemia ---
r_associated #0: 20 -->
en:retardation
n1=en:lethargy associated with hypoglycemia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lethargy, neonatal ---
r_associated #0: 20 -->
en:retardation
n1=en:lethargy, neonatal | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:leukemia ---
r_associated #0: 20 -->
en:retardation
n1=en:leukemia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:leukoaraiosis ---
r_associated #0: 20 -->
en:retardation
n1=en:leukoaraiosis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:leukodystrophy ---
r_associated #0: 20 -->
en:retardation
n1=en:leukodystrophy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:leukodystrophy (in 1 of 2 patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:leukodystrophy (in 1 of 2 patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:leukodystrophy (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:leukodystrophy (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:leukodystrophy and white matter changes, which improve with age ---
r_associated #0: 20 -->
en:retardation
n1=en:leukodystrophy and white matter changes, which improve with age | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:leukodystrophy, demyelinating ---
r_associated #0: 20 -->
en:retardation
n1=en:leukodystrophy, demyelinating | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:leukodystrophy, hypomyelinating ---
r_associated #0: 20 -->
en:retardation
n1=en:leukodystrophy, hypomyelinating | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:leukoencephalopathy ---
r_associated #0: 20 -->
en:retardation
n1=en:leukoencephalopathy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:leukoencephalopathy in the frontal and parietal lobes (later) ---
r_associated #0: 20 -->
en:retardation
n1=en:leukoencephalopathy in the frontal and parietal lobes (later) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:leukoencephalopathy in the periventricular and deep white matter and brainstem, cerebellum, and spinal cord tracts ---
r_associated #0: 20 -->
en:retardation
n1=en:leukoencephalopathy in the periventricular and deep white matter and brainstem, cerebellum, and spinal cord tracts | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:leukoencephalopathy on ct and mri ---
r_associated #0: 20 -->
en:retardation
n1=en:leukoencephalopathy on ct and mri | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:leukoencephalopathy with metaphyseal chondrodysplasia ---
r_associated #0: 20 -->
en:retardation
n1=en:leukoencephalopathy with metaphyseal chondrodysplasia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:leukoencephalopathy, severe ---
r_associated #0: 20 -->
en:retardation
n1=en:leukoencephalopathy, severe | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:leukomalacia (rare) ---
r_associated #0: 20 -->
en:retardation
n1=en:leukomalacia (rare) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lewy bodies ---
r_associated #0: 20 -->
en:retardation
n1=en:lewy bodies | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lewy bodies (not always present) ---
r_associated #0: 20 -->
en:retardation
n1=en:lewy bodies (not always present) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lewy bodies in the substantia nigra ---
r_associated #0: 20 -->
en:retardation
n1=en:lewy bodies in the substantia nigra | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lewy bodies throughout the brain ---
r_associated #0: 20 -->
en:retardation
n1=en:lewy bodies throughout the brain | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:light-induced sneezing ---
r_associated #0: 20 -->
en:retardation
n1=en:light-induced sneezing | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lightheadedness ---
r_associated #0: 20 -->
en:retardation
n1=en:lightheadedness | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:limb ataxia, progressive ---
r_associated #0: 20 -->
en:retardation
n1=en:limb ataxia, progressive | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:limb deformities, congenital ---
r_associated #0: 20 -->
en:retardation
n1=en:limb deformities, congenital | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:limb dysmetria ---
r_associated #0: 20 -->
en:retardation
n1=en:limb dysmetria | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:limb dystonia ---
r_associated #0: 20 -->
en:retardation
n1=en:limb dystonia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:limb dystonia (18%) ---
r_associated #0: 20 -->
en:retardation
n1=en:limb dystonia (18%) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:limb fasciculations ---
r_associated #0: 20 -->
en:retardation
n1=en:limb fasciculations | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:limb hypertonia ---
r_associated #0: 20 -->
en:retardation
n1=en:limb hypertonia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:limb hypertonia (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:limb hypertonia (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:limb incoordination (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:limb incoordination (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:limb muscle stiffness is often asymmetric ---
r_associated #0: 20 -->
en:retardation
n1=en:limb muscle stiffness is often asymmetric | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:limb muscle weakness (distal greater than proximal) ---
r_associated #0: 20 -->
en:retardation
n1=en:limb muscle weakness (distal greater than proximal) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:limb posturing (if left untreated) ---
r_associated #0: 20 -->
en:retardation
n1=en:limb posturing (if left untreated) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:limb spasticity ---
r_associated #0: 20 -->
en:retardation
n1=en:limb spasticity | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:limb-girdle muscular dystrophy type 2p ---
r_associated #0: 20 -->
en:retardation
n1=en:limb-girdle muscular dystrophy type 2p | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:limbic malformations ---
r_associated #0: 20 -->
en:retardation
n1=en:limbic malformations | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:limbic system ---
r_associated #0: 20 -->
en:retardation
n1=en:limbic system | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:limited expressive language ---
r_associated #0: 20 -->
en:retardation
n1=en:limited expressive language | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:limited memory, attention, language ---
r_associated #0: 20 -->
en:retardation
n1=en:limited memory, attention, language | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:limited psychological function ---
r_associated #0: 20 -->
en:retardation
n1=en:limited psychological function | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:limited verbal comprehension ---
r_associated #0: 20 -->
en:retardation
n1=en:limited verbal comprehension | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:limited walking ability ---
r_associated #0: 20 -->
en:retardation
n1=en:limited walking ability | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lingual-facial-buccal dyskinesia ---
r_associated #0: 20 -->
en:retardation
n1=en:lingual-facial-buccal dyskinesia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lipid metabolism disorder ---
r_associated #0: 20 -->
en:retardation
n1=en:lipid metabolism disorder | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lipodystrophy, generalized, with mental retardation, deafness, short stature, and slender bones ---
r_associated #0: 20 -->
en:retardation
n1=en:lipodystrophy, generalized, with mental retardation, deafness, short stature, and slender bones | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lipoidosis ---
r_associated #0: 20 -->
en:retardation
n1=en:lipoidosis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lipoma ---
r_associated #0: 20 -->
en:retardation
n1=en:lipoma | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lipoma, anterior sacral ---
r_associated #0: 20 -->
en:retardation
n1=en:lipoma, anterior sacral | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lipomyelocystoceles ---
r_associated #0: 20 -->
en:retardation
n1=en:lipomyelocystoceles | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lissencephaly ---
r_associated #0: 20 -->
en:retardation
n1=en:lissencephaly | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lissencephaly (anterior to posterior decreasing gradient of severity, more prominent in anterior brain regions) ---
r_associated #0: 20 -->
en:retardation
n1=en:lissencephaly (anterior to posterior decreasing gradient of severity, more prominent in anterior brain regions) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lissencephaly (anterior to posterior increasing gradient of severity and more prominent in posterior brain regions) ---
r_associated #0: 20 -->
en:retardation
n1=en:lissencephaly (anterior to posterior increasing gradient of severity and more prominent in posterior brain regions) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lissencephaly (reported in 1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:lissencephaly (reported in 1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lissencephaly, posterior to anterior gradient ---
r_associated #0: 20 -->
en:retardation
n1=en:lissencephaly, posterior to anterior gradient | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lithium induced birth defect ---
r_associated #0: 20 -->
en:retardation
n1=en:lithium induced birth defect | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:little or no speech acquisition ---
r_associated #0: 20 -->
en:retardation
n1=en:little or no speech acquisition | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:little polarity in remaining neurons ---
r_associated #0: 20 -->
en:retardation
n1=en:little polarity in remaining neurons | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:little spontaneous limb movement ---
r_associated #0: 20 -->
en:retardation
n1=en:little spontaneous limb movement | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:little spontaneous movement ---
r_associated #0: 20 -->
en:retardation
n1=en:little spontaneous movement | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lobar dysmorphism ---
r_associated #0: 20 -->
en:retardation
n1=en:lobar dysmorphism | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lobar holoprosencephalies ---
r_associated #0: 20 -->
en:retardation
n1=en:lobar holoprosencephalies | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lobar hpe shows clear interhemispheric fissure and 2 lateral ventricles ---
r_associated #0: 20 -->
en:retardation
n1=en:lobar hpe shows clear interhemispheric fissure and 2 lateral ventricles | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:locomotor delay (early-onset form) ---
r_associated #0: 20 -->
en:retardation
n1=en:locomotor delay (early-onset form) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:long perforating arteries of the brain are affected ---
r_associated #0: 20 -->
en:retardation
n1=en:long perforating arteries of the brain are affected | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:long, thickened cerebellar peduncles ---
r_associated #0: 20 -->
en:retardation
n1=en:long, thickened cerebellar peduncles | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:long-tract signs ---
r_associated #0: 20 -->
en:retardation
n1=en:long-tract signs | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:loss of ability to walk ---
r_associated #0: 20 -->
en:retardation
n1=en:loss of ability to walk | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:loss of ability to walk in first decade ---
r_associated #0: 20 -->
en:retardation
n1=en:loss of ability to walk in first decade | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:loss of ability to walk later ---
r_associated #0: 20 -->
en:retardation
n1=en:loss of ability to walk later | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:loss of ambulation ---
r_associated #0: 20 -->
en:retardation
n1=en:loss of ambulation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:loss of ankle reflexes ---
r_associated #0: 20 -->
en:retardation
n1=en:loss of ankle reflexes | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:loss of anterior horn cells and gliosis in the spinal cord ---
r_associated #0: 20 -->
en:retardation
n1=en:loss of anterior horn cells and gliosis in the spinal cord | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:loss of any acquired abilities in early childhood ---
r_associated #0: 20 -->
en:retardation
n1=en:loss of any acquired abilities in early childhood | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:loss of balance may occur ---
r_associated #0: 20 -->
en:retardation
n1=en:loss of balance may occur | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:loss of cerebellar granular cells ---
r_associated #0: 20 -->
en:retardation
n1=en:loss of cerebellar granular cells | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:loss of cerebellar purkinje cells ---
r_associated #0: 20 -->
en:retardation
n1=en:loss of cerebellar purkinje cells | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:loss of cerebral white matter (in 1 of 3 patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:loss of cerebral white matter (in 1 of 3 patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:loss of consciousness ---
r_associated #0: 20 -->
en:retardation
n1=en:loss of consciousness | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:loss of consciousness (1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:loss of consciousness (1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:loss of coordination ---
r_associated #0: 20 -->
en:retardation
n1=en:loss of coordination | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:loss of deep tendon reflexes (later) ---
r_associated #0: 20 -->
en:retardation
n1=en:loss of deep tendon reflexes (later) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:loss of developmental milestones ---
r_associated #0: 20 -->
en:retardation
n1=en:loss of developmental milestones | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:loss of dopaminergic neurons ---
r_associated #0: 20 -->
en:retardation
n1=en:loss of dopaminergic neurons | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:loss of dopaminergic neurons in the substantia nigra ---
r_associated #0: 20 -->
en:retardation
n1=en:loss of dopaminergic neurons in the substantia nigra | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:loss of dorsal root ganglion cells ---
r_associated #0: 20 -->
en:retardation
n1=en:loss of dorsal root ganglion cells | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:loss of executive functions ---
r_associated #0: 20 -->
en:retardation
n1=en:loss of executive functions | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:loss of fine motor skills ---
r_associated #0: 20 -->
en:retardation
n1=en:loss of fine motor skills | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:loss of gait (in some) ---
r_associated #0: 20 -->
en:retardation
n1=en:loss of gait (in some) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:loss of hypocretin (orexin)-secreting neurons in the hypothalamus ---
r_associated #0: 20 -->
en:retardation
n1=en:loss of hypocretin (orexin)-secreting neurons in the hypothalamus | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:loss of independent ambulation ---
r_associated #0: 20 -->
en:retardation
n1=en:loss of independent ambulation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:loss of independent ambulation (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:loss of independent ambulation (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:loss of independent ambulation approximately 30 years after onset ---
r_associated #0: 20 -->
en:retardation
n1=en:loss of independent ambulation approximately 30 years after onset | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:loss of independent ambulation by age 10 years ---
r_associated #0: 20 -->
en:retardation
n1=en:loss of independent ambulation by age 10 years | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:loss of independent ambulation within a few years ---
r_associated #0: 20 -->
en:retardation
n1=en:loss of independent ambulation within a few years | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:loss of language ability ---
r_associated #0: 20 -->
en:retardation
n1=en:loss of language ability | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:loss of lower alpha-motor neurons in the anterior horn of the spinal cord and lower brainstem ---
r_associated #0: 20 -->
en:retardation
n1=en:loss of lower alpha-motor neurons in the anterior horn of the spinal cord and lower brainstem | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:loss of motor functions ---
r_associated #0: 20 -->
en:retardation
n1=en:loss of motor functions | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:loss of motor milestones ---
r_associated #0: 20 -->
en:retardation
n1=en:loss of motor milestones | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:loss of motor neurons in the anterior horn of the spinal cord ---
r_associated #0: 20 -->
en:retardation
n1=en:loss of motor neurons in the anterior horn of the spinal cord | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:loss of motor neurons in the spinal cord ---
r_associated #0: 20 -->
en:retardation
n1=en:loss of motor neurons in the spinal cord | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:loss of motor skills ---
r_associated #0: 20 -->
en:retardation
n1=en:loss of motor skills | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:loss of myelin ---
r_associated #0: 20 -->
en:retardation
n1=en:loss of myelin | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:loss of myelin and oligodendroglia ---
r_associated #0: 20 -->
en:retardation
n1=en:loss of myelin and oligodendroglia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:loss of myelin in the cerebral and cerebellar white matter ---
r_associated #0: 20 -->
en:retardation
n1=en:loss of myelin in the cerebral and cerebellar white matter | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:loss of myelin in the descending lateral spinal cord tracts ---
r_associated #0: 20 -->
en:retardation
n1=en:loss of myelin in the descending lateral spinal cord tracts | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:loss of myelin in the pyramidal tracts ---
r_associated #0: 20 -->
en:retardation
n1=en:loss of myelin in the pyramidal tracts | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:loss of myelinated fibers in spinal cord roots ---
r_associated #0: 20 -->
en:retardation
n1=en:loss of myelinated fibers in spinal cord roots | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:loss of myelinated fibers with regenerative clusters on biopsy ---
r_associated #0: 20 -->
en:retardation
n1=en:loss of myelinated fibers with regenerative clusters on biopsy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:loss of neurons affecting all cortical layers ---
r_associated #0: 20 -->
en:retardation
n1=en:loss of neurons affecting all cortical layers | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:loss of neurons and gliosis in basal ganglia, cranial nerve nuclei, and spinal cord ---
r_associated #0: 20 -->
en:retardation
n1=en:loss of neurons and gliosis in basal ganglia, cranial nerve nuclei, and spinal cord | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:loss of pain and temperature in a cape-like distribution ---
r_associated #0: 20 -->
en:retardation
n1=en:loss of pain and temperature in a cape-like distribution | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:loss of pigmented neurons in the substantia nigra ---
r_associated #0: 20 -->
en:retardation
n1=en:loss of pigmented neurons in the substantia nigra | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:loss of postural tone ---
r_associated #0: 20 -->
en:retardation
n1=en:loss of postural tone | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:loss of primary reflexes ---
r_associated #0: 20 -->
en:retardation
n1=en:loss of primary reflexes | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:loss of purkinje cells ---
r_associated #0: 20 -->
en:retardation
n1=en:loss of purkinje cells | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:loss of purkinje cells in the cerebellar vermis ---
r_associated #0: 20 -->
en:retardation
n1=en:loss of purkinje cells in the cerebellar vermis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:loss of purkinje cells in the cerebellum ---
r_associated #0: 20 -->
en:retardation
n1=en:loss of purkinje cells in the cerebellum | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:loss of purposeful hand movements ---
r_associated #0: 20 -->
en:retardation
n1=en:loss of purposeful hand movements | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:loss of reflexes due to myopathy ---
r_associated #0: 20 -->
en:retardation
n1=en:loss of reflexes due to myopathy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:loss of speech ---
r_associated #0: 20 -->
en:retardation
n1=en:loss of speech | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:loss of speech (1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:loss of speech (1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:loss of speech development ---
r_associated #0: 20 -->
en:retardation
n1=en:loss of speech development | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:loss of spontaneous movements ---
r_associated #0: 20 -->
en:retardation
n1=en:loss of spontaneous movements | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:loss of very early milestones ---
r_associated #0: 20 -->
en:retardation
n1=en:loss of very early milestones | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:loss of white matter ---
r_associated #0: 20 -->
en:retardation
n1=en:loss of white matter | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:low apparent diffusion coefficient (adc) values ---
r_associated #0: 20 -->
en:retardation
n1=en:low apparent diffusion coefficient (adc) values | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:low densities in the basal ganglia similar to leigh syndrome (256000) ---
r_associated #0: 20 -->
en:retardation
n1=en:low densities in the basal ganglia similar to leigh syndrome (256000) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:low density white matter on ct scan ---
r_associated #0: 20 -->
en:retardation
n1=en:low density white matter on ct scan | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:low iq ---
r_associated #0: 20 -->
en:retardation
n1=en:low iq | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:low-lying cerebellar tonsils ---
r_associated #0: 20 -->
en:retardation
n1=en:low-lying cerebellar tonsils | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:low-normal intelligence ---
r_associated #0: 20 -->
en:retardation
n1=en:low-normal intelligence | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:low-normal iq ---
r_associated #0: 20 -->
en:retardation
n1=en:low-normal iq | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lower extremity weakness with febrile episodes (rare) ---
r_associated #0: 20 -->
en:retardation
n1=en:lower extremity weakness with febrile episodes (rare) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lower limb atrophy ---
r_associated #0: 20 -->
en:retardation
n1=en:lower limb atrophy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lower limb dystonia ---
r_associated #0: 20 -->
en:retardation
n1=en:lower limb dystonia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lower limb hyperreflexia ---
r_associated #0: 20 -->
en:retardation
n1=en:lower limb hyperreflexia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lower limb hyperreflexia (reported in 1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:lower limb hyperreflexia (reported in 1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lower limb hypertonia ---
r_associated #0: 20 -->
en:retardation
n1=en:lower limb hypertonia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lower limb hypotrophy ---
r_associated #0: 20 -->
en:retardation
n1=en:lower limb hypotrophy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lower limb muscle atrophy ---
r_associated #0: 20 -->
en:retardation
n1=en:lower limb muscle atrophy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lower limb muscle weakness (occurs later) ---
r_associated #0: 20 -->
en:retardation
n1=en:lower limb muscle weakness (occurs later) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lower limb spasticity ---
r_associated #0: 20 -->
en:retardation
n1=en:lower limb spasticity | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lower limb spasticity, mild ---
r_associated #0: 20 -->
en:retardation
n1=en:lower limb spasticity, mild | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lower limb weakness, proximal ---
r_associated #0: 20 -->
en:retardation
n1=en:lower limb weakness, proximal | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lower limbs affected before upper limbs ---
r_associated #0: 20 -->
en:retardation
n1=en:lower limbs affected before upper limbs | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lower limbs weakness and atrophy, distal ---
r_associated #0: 20 -->
en:retardation
n1=en:lower limbs weakness and atrophy, distal | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lower motor neuron degeneration ---
r_associated #0: 20 -->
en:retardation
n1=en:lower motor neuron degeneration | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lower motor neuron disease affecting upper and lower limbs ---
r_associated #0: 20 -->
en:retardation
n1=en:lower motor neuron disease affecting upper and lower limbs | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lower motor neuron dysfunction ---
r_associated #0: 20 -->
en:retardation
n1=en:lower motor neuron dysfunction | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lower motor neuron dysfunction involving upper and lower limbs ---
r_associated #0: 20 -->
en:retardation
n1=en:lower motor neuron dysfunction involving upper and lower limbs | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lower motor neuron involvement after long disease duration ---
r_associated #0: 20 -->
en:retardation
n1=en:lower motor neuron involvement after long disease duration | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lower motor neuron involvement, mild, seen on emg (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:lower motor neuron involvement, mild, seen on emg (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lower motor neuron signs, later ---
r_associated #0: 20 -->
en:retardation
n1=en:lower motor neuron signs, later | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lower motor neuron symptoms ---
r_associated #0: 20 -->
en:retardation
n1=en:lower motor neuron symptoms | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lower motor signs ---
r_associated #0: 20 -->
en:retardation
n1=en:lower motor signs | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lumbar disc lesion/radiation ---
r_associated #0: 20 -->
en:retardation
n1=en:lumbar disc lesion/radiation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lumbar paraspinal rigidity causes exaggerated lumbar lordosis ---
r_associated #0: 20 -->
en:retardation
n1=en:lumbar paraspinal rigidity causes exaggerated lumbar lordosis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lumbosacral meningocele ---
r_associated #0: 20 -->
en:retardation
n1=en:lumbosacral meningocele | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lymphatic abnormalities ---
r_associated #0: 20 -->
en:retardation
n1=en:lymphatic abnormalities | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:lymphocytic infiltration of the brain ---
r_associated #0: 20 -->
en:retardation
n1=en:lymphocytic infiltration of the brain | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:macrocephaly (due to dandy-walker malformation) ---
r_associated #0: 20 -->
en:retardation
n1=en:macrocephaly (due to dandy-walker malformation) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:macroencephaly ---
r_associated #0: 20 -->
en:retardation
n1=en:macroencephaly | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:macrosomia obesity macrocephaly ocular abnormalities ---
r_associated #0: 20 -->
en:retardation
n1=en:macrosomia obesity macrocephaly ocular abnormalities | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:macular degeneration ---
r_associated #0: 20 -->
en:retardation
n1=en:macular degeneration | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:madokoro ohdo sonoda syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:madokoro ohdo sonoda syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:magnetic resonance spectroscopy (mrs) shows decreased n-acetylaspartic acid in unaffected white matter ---
r_associated #0: 20 -->
en:retardation
n1=en:magnetic resonance spectroscopy (mrs) shows decreased n-acetylaspartic acid in unaffected white matter | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:magnetic resonance spectroscopy (mrs) shows increased lactate in the central nervous system ---
r_associated #0: 20 -->
en:retardation
n1=en:magnetic resonance spectroscopy (mrs) shows increased lactate in the central nervous system | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:magnetic resonance spectroscopy shows increased lactate in white matter ---
r_associated #0: 20 -->
en:retardation
n1=en:magnetic resonance spectroscopy shows increased lactate in white matter | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:major congenital anomaly ---
r_associated #0: 20 -->
en:retardation
n1=en:major congenital anomaly | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:major developmental delay ---
r_associated #0: 20 -->
en:retardation
n1=en:major developmental delay | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:major developmental milestones are not attained ---
r_associated #0: 20 -->
en:retardation
n1=en:major developmental milestones are not attained | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:malaria ---
r_associated #0: 20 -->
en:retardation
n1=en:malaria | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:male genital injuries ---
r_associated #0: 20 -->
en:retardation
n1=en:male genital injuries | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:malformation of the insula ---
r_associated #0: 20 -->
en:retardation
n1=en:malformation of the insula | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:malformation, cerebral arteriovenous ---
r_associated #0: 20 -->
en:retardation
n1=en:malformation, cerebral arteriovenous | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:malformations of cortical development ---
r_associated #0: 20 -->
en:retardation
n1=en:malformations of cortical development | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:malformations of cortical development, variable ---
r_associated #0: 20 -->
en:retardation
n1=en:malformations of cortical development, variable | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:malformations of the mid- and hindbrain ---
r_associated #0: 20 -->
en:retardation
n1=en:malformations of the mid- and hindbrain | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:malignant bladder neoplasm ---
r_associated #0: 20 -->
en:retardation
n1=en:malignant bladder neoplasm | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:malignant cervical neoplasm ---
r_associated #0: 20 -->
en:retardation
n1=en:malignant cervical neoplasm | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:malignant gastric neoplasm ---
r_associated #0: 20 -->
en:retardation
n1=en:malignant gastric neoplasm | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:malignant kidney neoplasm ---
r_associated #0: 20 -->
en:retardation
n1=en:malignant kidney neoplasm | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:malignant neoplasm of colon with rectum ---
r_associated #0: 20 -->
en:retardation
n1=en:malignant neoplasm of colon with rectum | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:malignant neoplasm of female breast ---
r_associated #0: 20 -->
en:retardation
n1=en:malignant neoplasm of female breast | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:malignant neoplasm other/unspecified ---
r_associated #0: 20 -->
en:retardation
n1=en:malignant neoplasm other/unspecified | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:malignant neoplasm: bronchus or lung, unspecified ---
r_associated #0: 20 -->
en:retardation
n1=en:malignant neoplasm: bronchus or lung, unspecified | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:malignant nervous system neoplasm ---
r_associated #0: 20 -->
en:retardation
n1=en:malignant nervous system neoplasm | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:malignant obstetric neoplasm ---
r_associated #0: 20 -->
en:retardation
n1=en:malignant obstetric neoplasm | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:malignant pancreatic neoplasm ---
r_associated #0: 20 -->
en:retardation
n1=en:malignant pancreatic neoplasm | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:malignant prostate neoplasm ---
r_associated #0: 20 -->
en:retardation
n1=en:malignant prostate neoplasm | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:malignant skin neoplasm ---
r_associated #0: 20 -->
en:retardation
n1=en:malignant skin neoplasm | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:malignant thyroid gland neoplasm ---
r_associated #0: 20 -->
en:retardation
n1=en:malignant thyroid gland neoplasm | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:malpuech facial clefting syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:malpuech facial clefting syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mandibular cleft ---
r_associated #0: 20 -->
en:retardation
n1=en:mandibular cleft | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:manic and bipolar mood disorders and disturbances ---
r_associated #0: 20 -->
en:retardation
n1=en:manic and bipolar mood disorders and disturbances | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:manic psychosis ---
r_associated #0: 20 -->
en:retardation
n1=en:manic psychosis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mannosidosis ---
r_associated #0: 20 -->
en:retardation
n1=en:mannosidosis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:maple syrup urine disease ---
r_associated #0: 20 -->
en:retardation
n1=en:maple syrup urine disease | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:markedly delayed nerve conduction velocities ---
r_associated #0: 20 -->
en:retardation
n1=en:markedly delayed nerve conduction velocities | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:marshall-smith syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:marshall-smith syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:masa syndrome (disorder) ---
r_associated #0: 20 -->
en:retardation
n1=en:masa syndrome (disorder) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mask-like facies ---
r_associated #0: 20 -->
en:retardation
n1=en:mask-like facies | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mastitis, postpartum ---
r_associated #0: 20 -->
en:retardation
n1=en:mastitis, postpartum | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mean sleep latency is less than 5 to 8 minutes ---
r_associated #0: 20 -->
en:retardation
n1=en:mean sleep latency is less than 5 to 8 minutes | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:measles ---
r_associated #0: 20 -->
en:retardation
n1=en:measles | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:medical history:find:pt:^patient:nom:phenx ---
r_associated #0: 20 -->
en:retardation
n1=en:medical history:find:pt:^patient:nom:phenx | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:medication abuse ---
r_associated #0: 20 -->
en:retardation
n1=en:medication abuse | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:medulloblastoma ---
r_associated #0: 20 -->
en:retardation
n1=en:medulloblastoma | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mega cisterna magna ---
r_associated #0: 20 -->
en:retardation
n1=en:mega cisterna magna | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mega-aeroesophagus sign ---
r_associated #0: 20 -->
en:retardation
n1=en:mega-aeroesophagus sign | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:megacisterna magna (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:megacisterna magna (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:megacisterna magna (rare) ---
r_associated #0: 20 -->
en:retardation
n1=en:megacisterna magna (rare) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:megalencephalic leukoencephalopathy with subcortical cysts 2a ---
r_associated #0: 20 -->
en:retardation
n1=en:megalencephalic leukoencephalopathy with subcortical cysts 2a | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:megalencephaly cutis marmorata telangiectatica congenita ---
r_associated #0: 20 -->
en:retardation
n1=en:megalencephaly cutis marmorata telangiectatica congenita | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:memory defects ---
r_associated #0: 20 -->
en:retardation
n1=en:memory defects | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:memory dysfunction ---
r_associated #0: 20 -->
en:retardation
n1=en:memory dysfunction | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:memory impairment ---
r_associated #0: 20 -->
en:retardation
n1=en:memory impairment | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:memory impairment, progressive ---
r_associated #0: 20 -->
en:retardation
n1=en:memory impairment, progressive | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:memory loss ---
r_associated #0: 20 -->
en:retardation
n1=en:memory loss | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:meninges ---
r_associated #0: 20 -->
en:retardation
n1=en:meninges | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:meningioma ---
r_associated #0: 20 -->
en:retardation
n1=en:meningioma | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:meningioma (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:meningioma (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:meningitis ---
r_associated #0: 20 -->
en:retardation
n1=en:meningitis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:meningitis/encephalitis ---
r_associated #0: 20 -->
en:retardation
n1=en:meningitis/encephalitis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:meningoceles, multiple, lateral ---
r_associated #0: 20 -->
en:retardation
n1=en:meningoceles, multiple, lateral | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:meningoencephalitis ---
r_associated #0: 20 -->
en:retardation
n1=en:meningoencephalitis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:meningoencephalocele (wws) ---
r_associated #0: 20 -->
en:retardation
n1=en:meningoencephalocele (wws) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:menkes disease ---
r_associated #0: 20 -->
en:retardation
n1=en:menkes disease | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental aberration ---
r_associated #0: 20 -->
en:retardation
n1=en:mental aberration | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental abnormality acute transient ---
r_associated #0: 20 -->
en:retardation
n1=en:mental abnormality acute transient | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental and behavioural disorders ---
r_associated #0: 20 -->
en:retardation
n1=en:mental and behavioural disorders | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental and behavioural disorders due to psychoactive substance use ---
r_associated #0: 20 -->
en:retardation
n1=en:mental and behavioural disorders due to psychoactive substance use | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental delay or retardation (uncommon) ---
r_associated #0: 20 -->
en:retardation
n1=en:mental delay or retardation (uncommon) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental deterioration ---
r_associated #0: 20 -->
en:retardation
n1=en:mental deterioration | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental deterioration beginning 2 to 5 years after onset of seizures ---
r_associated #0: 20 -->
en:retardation
n1=en:mental deterioration beginning 2 to 5 years after onset of seizures | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental deterioration in a subset of patients ---
r_associated #0: 20 -->
en:retardation
n1=en:mental deterioration in a subset of patients | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental deterioration in childhood ---
r_associated #0: 20 -->
en:retardation
n1=en:mental deterioration in childhood | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental disorder and/or culture bound syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:mental disorder and/or culture bound syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental disorder diagnosis ---
r_associated #0: 20 -->
en:retardation
n1=en:mental disorder diagnosis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental disorder due to a general medical condition ---
r_associated #0: 20 -->
en:retardation
n1=en:mental disorder due to a general medical condition | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental disorder due to drug ---
r_associated #0: 20 -->
en:retardation
n1=en:mental disorder due to drug | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental disorder in mother complicating childbirth ---
r_associated #0: 20 -->
en:retardation
n1=en:mental disorder in mother complicating childbirth | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental disorder transient ---
r_associated #0: 20 -->
en:retardation
n1=en:mental disorder transient | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental disorder usually first evident in infancy, childhood and/or adolescence ---
r_associated #0: 20 -->
en:retardation
n1=en:mental disorder usually first evident in infancy, childhood and/or adolescence | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental disorders complicating pregnancy, childbirth, or the puerperium ---
r_associated #0: 20 -->
en:retardation
n1=en:mental disorders complicating pregnancy, childbirth, or the puerperium | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental disorders during pregnancy, childbirth and the puerperium ---
r_associated #0: 20 -->
en:retardation
n1=en:mental disorders during pregnancy, childbirth and the puerperium | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental disorders of mother ---
r_associated #0: 20 -->
en:retardation
n1=en:mental disorders of mother | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental disorders of mother, antepartum condition or complication ---
r_associated #0: 20 -->
en:retardation
n1=en:mental disorders of mother, antepartum condition or complication | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental disorders of mother, delivered, with mention of postpartum complication ---
r_associated #0: 20 -->
en:retardation
n1=en:mental disorders of mother, delivered, with mention of postpartum complication | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental disorders of mother, delivered, with or without mention of antepartum condition ---
r_associated #0: 20 -->
en:retardation
n1=en:mental disorders of mother, delivered, with or without mention of antepartum condition | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental disorders of mother, postpartum condition or complication ---
r_associated #0: 20 -->
en:retardation
n1=en:mental disorders of mother, postpartum condition or complication | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental disorders of mother, unspecified as to episode of care or not applicable ---
r_associated #0: 20 -->
en:retardation
n1=en:mental disorders of mother, unspecified as to episode of care or not applicable | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental dysequilibrium ---
r_associated #0: 20 -->
en:retardation
n1=en:mental dysequilibrium | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental impairment ---
r_associated #0: 20 -->
en:retardation
n1=en:mental impairment | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental impairment may develop with repeated acute episodes ---
r_associated #0: 20 -->
en:retardation
n1=en:mental impairment may develop with repeated acute episodes | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental impairment, mild to moderate ---
r_associated #0: 20 -->
en:retardation
n1=en:mental impairment, mild to moderate | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental lethargy ---
r_associated #0: 20 -->
en:retardation
n1=en:mental lethargy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation (1 family) ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation (1 family) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation (15%) ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation (15%) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation (18% of patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation (18% of patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation (2 patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation (2 patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation (2/3 patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation (2/3 patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation (20%) ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation (20%) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation (25%) ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation (25%) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation (3 patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation (3 patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation (30%) ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation (30%) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation (31%) ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation (31%) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation (38%) ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation (38%) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation (47%) ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation (47%) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation (50% patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation (50% patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation (6%) ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation (6%) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation (7%) ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation (7%) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation (70%) ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation (70%) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation (about 40%) ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation (about 40%) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation (average iq 51) ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation (average iq 51) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation (average iq 56) ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation (average iq 56) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation (cvs+) ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation (cvs+) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation (develops later) ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation (develops later) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation (early-onset form) ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation (early-onset form) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation (if left untreated) ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation (if left untreated) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation (if untreated in infancy) ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation (if untreated in infancy) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation (in 2 of 6 patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation (in 2 of 6 patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation (in 2 patients) learning disability (in 1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation (in 2 patients) learning disability (in 1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation (in a subset of patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation (in a subset of patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation (in most patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation (in most patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation (in most) ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation (in most) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation (in some cases) ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation (in some cases) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation (in some) ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation (in some) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation (in type iia) ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation (in type iia) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation (iq 20-78) ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation (iq 20-78) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation (iq 24-85) (variable) ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation (iq 24-85) (variable) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation (iq 45-75) ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation (iq 45-75) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation (iq 50-60 combined griffiths and stanford-binet scale) ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation (iq 50-60 combined griffiths and stanford-binet scale) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation (less common) ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation (less common) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation (males) ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation (males) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation (moderate to severe in males) ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation (moderate to severe in males) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation (one patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation (one patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation (one-third) ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation (one-third) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation (range mild to severe) ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation (range mild to severe) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation (rare less than 1% of cases) ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation (rare less than 1% of cases) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation (rare) ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation (rare) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation (rarely noted) ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation (rarely noted) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation (reported in 1 family) ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation (reported in 1 family) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation (reported in 1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation (reported in 1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation (secondary to intracranial bleed) ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation (secondary to intracranial bleed) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation (seen in hhs variant) ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation (seen in hhs variant) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation (some) ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation (some) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation (sometimes) ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation (sometimes) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation (type i) ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation (type i) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation (uncommon) ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation (uncommon) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation (untreated hypothyroidism) ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation (untreated hypothyroidism) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation (variable expression) ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation (variable expression) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation by age 30 years ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation by age 30 years | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation by the age of 7 years ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation by the age of 7 years | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation can occur in patients with repeated episodes of dehydration ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation can occur in patients with repeated episodes of dehydration | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation due to repeated episodes of hypoglycemia ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation due to repeated episodes of hypoglycemia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation from rapid mental regression ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation from rapid mental regression | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation has been reported ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation has been reported | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation if untreated ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation if untreated | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation in 5-13% ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation in 5-13% | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation in 75% ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation in 75% | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation in survivors ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation in survivors | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation may occur ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation may occur | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation screen ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation screen | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation severity unspecified ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation severity unspecified | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation with psychosis, pyramidal signs, and macroorchidism ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation with psychosis, pyramidal signs, and macroorchidism | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation with spastic paraplegia ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation with spastic paraplegia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation wolff type ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation wolff type | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation, autosomal dominant 1 ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation, autosomal dominant 1 | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation, autosomal dominant 22 ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation, autosomal dominant 22 | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation, autosomal recessive 36 ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation, autosomal recessive 36 | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation, autosomal recessive 38 ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation, autosomal recessive 38 | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation, autosomal recessive 40 ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation, autosomal recessive 40 | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation, autosomal recessive 46 ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation, autosomal recessive 46 | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation, borderline (1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation, borderline (1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation, borderline to severe ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation, borderline to severe | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation, borderline-mild in carrier females ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation, borderline-mild in carrier females | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation, buenos aires type ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation, buenos aires type | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation, fra12a type ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation, fra12a type | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation, in subgroup of patients ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation, in subgroup of patients | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation, microcephaly, growth retardation, joint contractures, and facial dysmorphism ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation, microcephaly, growth retardation, joint contractures, and facial dysmorphism | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation, mild (1 family) ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation, mild (1 family) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation, mild (1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation, mild (1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation, mild (10%) ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation, mild (10%) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation, mild (11%) ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation, mild (11%) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation, mild (18%) ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation, mild (18%) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation, mild (2 families) ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation, mild (2 families) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation, mild (20% have more severe mental retardation) ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation, mild (20% have more severe mental retardation) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation, mild (carrier females) ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation, mild (carrier females) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation, mild (in some females) ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation, mild (in some females) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation, mild (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation, mild (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation, mild (iq range from 50 to 70) ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation, mild (iq range from 50 to 70) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation, mild (rare) ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation, mild (rare) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation, mild to moderate ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation, mild to moderate | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation, mild to moderate (20% of patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation, mild to moderate (20% of patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation, mild to moderate (in 12%) ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation, mild to moderate (in 12%) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation, mild to moderate (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation, mild to moderate (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation, mild to moderate (iq 30-76) ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation, mild to moderate (iq 30-76) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation, mild to profound ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation, mild to profound | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation, mild to severe ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation, mild to severe | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation, mild, in most carrier females ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation, mild, in most carrier females | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation, mild, some patients (iq 70-80) ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation, mild, some patients (iq 70-80) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation, mild-borderline, nonprogressive ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation, mild-borderline, nonprogressive | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation, mild-moderate (28%, usually in males) ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation, mild-moderate (28%, usually in males) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation, mild-moderate (some) ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation, mild-moderate (some) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation, moderate (apparent by age 4 years) ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation, moderate (apparent by age 4 years) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation, moderate (in 1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation, moderate (in 1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation, moderate (in sister) ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation, moderate (in sister) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation, moderate (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation, moderate (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation, moderate to profound ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation, moderate to profound | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation, moderate to severe ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation, moderate to severe | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation, moderate to severe (10-15% of patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation, moderate to severe (10-15% of patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation, moderate to severe (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation, moderate to severe (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation, moderate to severe (iq 35-50) ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation, moderate to severe (iq 35-50) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation, moderate to severe (iq 40 to 60) ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation, moderate to severe (iq 40 to 60) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation, moderate to severe (type ii, infantile and juvenile) ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation, moderate to severe (type ii, infantile and juvenile) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation, moderate-severe (2p21del) ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation, moderate-severe (2p21del) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation, occasional ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation, occasional | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation, profound (wws) ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation, profound (wws) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation, progressive (50% of patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation, progressive (50% of patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation, residual mild-to-severe (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation, residual mild-to-severe (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation, severe (if untreated) ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation, severe (if untreated) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation, severe (meb) ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation, severe (meb) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation, severe in some patients ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation, severe in some patients | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation, severe to profound ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation, severe to profound | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation, severe, profound ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation, severe, profound | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation, variable (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation, variable (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation, variable degree (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation, variable degree (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation, variable severity ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation, variable severity | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation, x-linked ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation, x-linked | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation, x-linked 101 ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation, x-linked 101 | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation, x-linked 3 ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation, x-linked 3 | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation, x-linked 93 (disorder) ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation, x-linked 93 (disorder) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation, x-linked 98 ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation, x-linked 98 | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation, x-linked 99 ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation, x-linked 99 | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation, x-linked, syndromic 17 ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation, x-linked, syndromic 17 | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation, x-linked, syndromic, nascimento type ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation, x-linked, syndromic, nascimento type | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation, x-linked, with epilepsy ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation, x-linked, with epilepsy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation, x-linked, with short stature (disorder) ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation, x-linked, with short stature (disorder) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental retardation, x-linked, with short stature, hypogonadism, and abnormal gait ---
r_associated #0: 20 -->
en:retardation
n1=en:mental retardation, x-linked, with short stature, hypogonadism, and abnormal gait | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental state abnormal aggravated ---
r_associated #0: 20 -->
en:retardation
n1=en:mental state abnormal aggravated | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mental symptom ---
r_associated #0: 20 -->
en:retardation
n1=en:mental symptom | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mentally disabled persons ---
r_associated #0: 20 -->
en:retardation
n1=en:mentally disabled persons | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mentally late developer ---
r_associated #0: 20 -->
en:retardation
n1=en:mentally late developer | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mesial temporal brain malformations ---
r_associated #0: 20 -->
en:retardation
n1=en:mesial temporal brain malformations | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mesial temporal sclerosis (in 1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:mesial temporal sclerosis (in 1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:metaphyseal acroscyphodysplasia ---
r_associated #0: 20 -->
en:retardation
n1=en:metaphyseal acroscyphodysplasia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:methylcrotonyl-coa carboxylase deficiency ---
r_associated #0: 20 -->
en:retardation
n1=en:methylcrotonyl-coa carboxylase deficiency | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:methylmalonic acidemia with homocystinuria ---
r_associated #0: 20 -->
en:retardation
n1=en:methylmalonic acidemia with homocystinuria | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:methylmalonic aciduria and homocystinuria, cbld type ---
r_associated #0: 20 -->
en:retardation
n1=en:methylmalonic aciduria and homocystinuria, cbld type | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mevalonic aciduria ---
r_associated #0: 20 -->
en:retardation
n1=en:mevalonic aciduria | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:microbleeds ---
r_associated #0: 20 -->
en:retardation
n1=en:microbleeds | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:microbleeds (most smaller than 5 mm) occur after age 40 years ---
r_associated #0: 20 -->
en:retardation
n1=en:microbleeds (most smaller than 5 mm) occur after age 40 years | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:microcephalic osteodysplastic primordial dwarfism, type 3 ---
r_associated #0: 20 -->
en:retardation
n1=en:microcephalic osteodysplastic primordial dwarfism, type 3 | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:microcephalic osteodysplastic primordial dwarfism, type i ---
r_associated #0: 20 -->
en:retardation
n1=en:microcephalic osteodysplastic primordial dwarfism, type i | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:microcephalic osteodysplastic primordial dwarfism, type ii ---
r_associated #0: 20 -->
en:retardation
n1=en:microcephalic osteodysplastic primordial dwarfism, type ii | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:microcephalic primordial dwarfism toriello type ---
r_associated #0: 20 -->
en:retardation
n1=en:microcephalic primordial dwarfism toriello type | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:microcephaly ---
r_associated #0: 20 -->
en:retardation
n1=en:microcephaly | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:microcephaly and chorioretinopathy, autosomal recessive, 1 ---
r_associated #0: 20 -->
en:retardation
n1=en:microcephaly and chorioretinopathy, autosomal recessive, 1 | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:microcephaly and chorioretinopathy, autosomal recessive, 2 ---
r_associated #0: 20 -->
en:retardation
n1=en:microcephaly and chorioretinopathy, autosomal recessive, 2 | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:microcephaly with mental retardation and digital anomalies ---
r_associated #0: 20 -->
en:retardation
n1=en:microcephaly with mental retardation and digital anomalies | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:microcephaly, primary autosomal recessive, 2 (disorder) ---
r_associated #0: 20 -->
en:retardation
n1=en:microcephaly, primary autosomal recessive, 2 (disorder) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:microcephaly, short stature, and impaired glucose metabolism ---
r_associated #0: 20 -->
en:retardation
n1=en:microcephaly, short stature, and impaired glucose metabolism | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:microcystic degeneration ---
r_associated #0: 20 -->
en:retardation
n1=en:microcystic degeneration | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:micrographia ---
r_associated #0: 20 -->
en:retardation
n1=en:micrographia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:microgyria ---
r_associated #0: 20 -->
en:retardation
n1=en:microgyria | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:microlissencephalies ---
r_associated #0: 20 -->
en:retardation
n1=en:microlissencephalies | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:microphthalmia, syndromic 13 ---
r_associated #0: 20 -->
en:retardation
n1=en:microphthalmia, syndromic 13 | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:microvacuolation ---
r_associated #0: 20 -->
en:retardation
n1=en:microvacuolation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:microvascular spaces, dilated ---
r_associated #0: 20 -->
en:retardation
n1=en:microvascular spaces, dilated | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:midbrain atrophy ---
r_associated #0: 20 -->
en:retardation
n1=en:midbrain atrophy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:midline brain calcifications ---
r_associated #0: 20 -->
en:retardation
n1=en:midline brain calcifications | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:midline forebrain defects ---
r_associated #0: 20 -->
en:retardation
n1=en:midline forebrain defects | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:migraine ---
r_associated #0: 20 -->
en:retardation
n1=en:migraine | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:migraine (40% of patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:migraine (40% of patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:migraine (in affected males) ---
r_associated #0: 20 -->
en:retardation
n1=en:migraine (in affected males) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:migraine (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:migraine (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:migraine (uncommon) ---
r_associated #0: 20 -->
en:retardation
n1=en:migraine (uncommon) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:migraine headache (less common) ---
r_associated #0: 20 -->
en:retardation
n1=en:migraine headache (less common) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:migraine headaches (cvs+) ---
r_associated #0: 20 -->
en:retardation
n1=en:migraine headaches (cvs+) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:migraine headaches (ipsilateral to facial hemangioma) ---
r_associated #0: 20 -->
en:retardation
n1=en:migraine headaches (ipsilateral to facial hemangioma) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:migraine headaches (onset in adolescence) ---
r_associated #0: 20 -->
en:retardation
n1=en:migraine headaches (onset in adolescence) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:migraine with aura ---
r_associated #0: 20 -->
en:retardation
n1=en:migraine with aura | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:migraine with aura, usually visual (in 50% of patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:migraine with aura, usually visual (in 50% of patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:migraine without aura ---
r_associated #0: 20 -->
en:retardation
n1=en:migraine without aura | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:migraine, with or without aura ---
r_associated #0: 20 -->
en:retardation
n1=en:migraine, with or without aura | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:migraines (less common) ---
r_associated #0: 20 -->
en:retardation
n1=en:migraines (less common) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:migrating clonic jerks (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:migrating clonic jerks (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:migrating discharges from one cortical region to another seen on eeg (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:migrating discharges from one cortical region to another seen on eeg (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:migrating focal discharges from one cortical region to another seen on eeg ---
r_associated #0: 20 -->
en:retardation
n1=en:migrating focal discharges from one cortical region to another seen on eeg | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:migrating partial seizures ---
r_associated #0: 20 -->
en:retardation
n1=en:migrating partial seizures | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mild brain anomalies on mri (e.g., dilated ventricles) (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:mild brain anomalies on mri (e.g., dilated ventricles) (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mild cerebellar hypoplasia ---
r_associated #0: 20 -->
en:retardation
n1=en:mild cerebellar hypoplasia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mild cognitive decline (1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:mild cognitive decline (1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mild cognitive deterioration in adults ---
r_associated #0: 20 -->
en:retardation
n1=en:mild cognitive deterioration in adults | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mild cognitive disorder ---
r_associated #0: 20 -->
en:retardation
n1=en:mild cognitive disorder | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mild cognitive impairment (in 2 patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:mild cognitive impairment (in 2 patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mild cognitive impairment (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:mild cognitive impairment (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mild cognitive impairment (less common) ---
r_associated #0: 20 -->
en:retardation
n1=en:mild cognitive impairment (less common) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mild cortical atrophy (in 1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:mild cortical atrophy (in 1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mild cortical atrophy on ct or mri ---
r_associated #0: 20 -->
en:retardation
n1=en:mild cortical atrophy on ct or mri | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mild distal sensory deficits ---
r_associated #0: 20 -->
en:retardation
n1=en:mild distal sensory deficits | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mild global developmental delay ---
r_associated #0: 20 -->
en:retardation
n1=en:mild global developmental delay | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mild loss of neurons in the cerebellum ---
r_associated #0: 20 -->
en:retardation
n1=en:mild loss of neurons in the cerebellum | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mild memory loss ---
r_associated #0: 20 -->
en:retardation
n1=en:mild memory loss | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mild mental decline ---
r_associated #0: 20 -->
en:retardation
n1=en:mild mental decline | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mild mental deterioration ---
r_associated #0: 20 -->
en:retardation
n1=en:mild mental deterioration | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mild mental retardation ---
r_associated #0: 20 -->
en:retardation
n1=en:mild mental retardation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mild mental retardation (39%) feeding problems/weak suck (43%) ---
r_associated #0: 20 -->
en:retardation
n1=en:mild mental retardation (39%) feeding problems/weak suck (43%) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mild mental retardation (in 1/4 patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:mild mental retardation (in 1/4 patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mild mental retardation (some) ---
r_associated #0: 20 -->
en:retardation
n1=en:mild mental retardation (some) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mild motor development delay ---
r_associated #0: 20 -->
en:retardation
n1=en:mild motor development delay | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mild paraparesis ---
r_associated #0: 20 -->
en:retardation
n1=en:mild paraparesis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mild psychomotor delay ---
r_associated #0: 20 -->
en:retardation
n1=en:mild psychomotor delay | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mild pyramidal signs (variable expression) ---
r_associated #0: 20 -->
en:retardation
n1=en:mild pyramidal signs (variable expression) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mild sensorimotor neuropathy ---
r_associated #0: 20 -->
en:retardation
n1=en:mild sensorimotor neuropathy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mild spasticity ---
r_associated #0: 20 -->
en:retardation
n1=en:mild spasticity | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mild structural abnormalities seen mri (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:mild structural abnormalities seen mri (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mild to moderate learning difficulties ---
r_associated #0: 20 -->
en:retardation
n1=en:mild to moderate learning difficulties | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mild to severe mental retardation (24%) ---
r_associated #0: 20 -->
en:retardation
n1=en:mild to severe mental retardation (24%) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mild upper limb involvement ---
r_associated #0: 20 -->
en:retardation
n1=en:mild upper limb involvement | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mild-moderate mental retardation (80% affected males) ---
r_associated #0: 20 -->
en:retardation
n1=en:mild-moderate mental retardation (80% affected males) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mild-moderate ventricular dilatation ---
r_associated #0: 20 -->
en:retardation
n1=en:mild-moderate ventricular dilatation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mild-severe mental retardation (20%) ---
r_associated #0: 20 -->
en:retardation
n1=en:mild-severe mental retardation (20%) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:milder cases have isolated recurrent daytime sleepiness and/or lapses into sleep without cataplexy ---
r_associated #0: 20 -->
en:retardation
n1=en:milder cases have isolated recurrent daytime sleepiness and/or lapses into sleep without cataplexy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mildly decreased intelligence has been reported ---
r_associated #0: 20 -->
en:retardation
n1=en:mildly decreased intelligence has been reported | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mildly delayed developmental milestones ---
r_associated #0: 20 -->
en:retardation
n1=en:mildly delayed developmental milestones | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mildly delayed motor development ---
r_associated #0: 20 -->
en:retardation
n1=en:mildly delayed motor development | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mildly delayed motor development due to vestibular dysfunction ---
r_associated #0: 20 -->
en:retardation
n1=en:mildly delayed motor development due to vestibular dysfunction | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mildly enlarged ventricles ---
r_associated #0: 20 -->
en:retardation
n1=en:mildly enlarged ventricles | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mildly thin corpus callosum ---
r_associated #0: 20 -->
en:retardation
n1=en:mildly thin corpus callosum | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:miller-dieker syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:miller-dieker syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:minimal brain dysfunction ---
r_associated #0: 20 -->
en:retardation
n1=en:minimal brain dysfunction | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:minimal gliosis ---
r_associated #0: 20 -->
en:retardation
n1=en:minimal gliosis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:minimal or lack of speech ---
r_associated #0: 20 -->
en:retardation
n1=en:minimal or lack of speech | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:minimal to absent speech ---
r_associated #0: 20 -->
en:retardation
n1=en:minimal to absent speech | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:minor motor impairment (stage 2) ---
r_associated #0: 20 -->
en:retardation
n1=en:minor motor impairment (stage 2) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mirror hand movements (bimanual synkinesis, in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:mirror hand movements (bimanual synkinesis, in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mirror movements disorder ---
r_associated #0: 20 -->
en:retardation
n1=en:mirror movements disorder | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mirror movements, involuntary, affecting the hand and fingers ---
r_associated #0: 20 -->
en:retardation
n1=en:mirror movements, involuntary, affecting the hand and fingers | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mirror movements, involuntary, usually of the upper limb and hand ---
r_associated #0: 20 -->
en:retardation
n1=en:mirror movements, involuntary, usually of the upper limb and hand | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:miscellaneous mental disorders ---
r_associated #0: 20 -->
en:retardation
n1=en:miscellaneous mental disorders | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:misorientation of pyramidal fibers ---
r_associated #0: 20 -->
en:retardation
n1=en:misorientation of pyramidal fibers | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:misshapen posterior fossa ---
r_associated #0: 20 -->
en:retardation
n1=en:misshapen posterior fossa | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mitochondrial complex iii deficiency, nuclear type 1 ---
r_associated #0: 20 -->
en:retardation
n1=en:mitochondrial complex iii deficiency, nuclear type 1 | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mitochondrial dna depletion in brain tissue ---
r_associated #0: 20 -->
en:retardation
n1=en:mitochondrial dna depletion in brain tissue | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mitochondrial dna depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria) ---
r_associated #0: 20 -->
en:retardation
n1=en:mitochondrial dna depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mitochondrial dna depletion syndrome 8a (encephalomyopathic type with renal tubulopathy) ---
r_associated #0: 20 -->
en:retardation
n1=en:mitochondrial dna depletion syndrome 8a (encephalomyopathic type with renal tubulopathy) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mitochondrial encephalopathy ---
r_associated #0: 20 -->
en:retardation
n1=en:mitochondrial encephalopathy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mixed cerebellar/pseudobulbar dysarthria ---
r_associated #0: 20 -->
en:retardation
n1=en:mixed cerebellar/pseudobulbar dysarthria | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mixed developmental disorder ---
r_associated #0: 20 -->
en:retardation
n1=en:mixed developmental disorder | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mobility poor ---
r_associated #0: 20 -->
en:retardation
n1=en:mobility poor | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mobius syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:mobius syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:moderate cortical atrophy (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:moderate cortical atrophy (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:moderate learning difficulties ---
r_associated #0: 20 -->
en:retardation
n1=en:moderate learning difficulties | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:moderate mental retardation (i.q. 35-49) ---
r_associated #0: 20 -->
en:retardation
n1=en:moderate mental retardation (i.q. 35-49) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:moderate to severe hypotonia ---
r_associated #0: 20 -->
en:retardation
n1=en:moderate to severe hypotonia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:moderately thickened cortex ---
r_associated #0: 20 -->
en:retardation
n1=en:moderately thickened cortex | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:molar tooth sign on brain mri ---
r_associated #0: 20 -->
en:retardation
n1=en:molar tooth sign on brain mri | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:molar tooth sign on brain mri (subset of patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:molar tooth sign on brain mri (subset of patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:molar tooth sign on mri ---
r_associated #0: 20 -->
en:retardation
n1=en:molar tooth sign on mri | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:molar tooth sign seen on mri ---
r_associated #0: 20 -->
en:retardation
n1=en:molar tooth sign seen on mri | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:molluscum contagiosum ---
r_associated #0: 20 -->
en:retardation
n1=en:molluscum contagiosum | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:momes syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:momes syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:moniliasis genital female ---
r_associated #0: 20 -->
en:retardation
n1=en:moniliasis genital female | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:moniliasis/candida (excluding x72 y75) ---
r_associated #0: 20 -->
en:retardation
n1=en:moniliasis/candida (excluding x72 y75) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:monopareses ---
r_associated #0: 20 -->
en:retardation
n1=en:monopareses | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:monotone speech ---
r_associated #0: 20 -->
en:retardation
n1=en:monotone speech | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:monotonous speech ---
r_associated #0: 20 -->
en:retardation
n1=en:monotonous speech | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:monster (disorder) ---
r_associated #0: 20 -->
en:retardation
n1=en:monster (disorder) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mood disorder ---
r_associated #0: 20 -->
en:retardation
n1=en:mood disorder | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mood disorders and disturbances nec ---
r_associated #0: 20 -->
en:retardation
n1=en:mood disorders and disturbances nec | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mood lability ---
r_associated #0: 20 -->
en:retardation
n1=en:mood lability | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:morning myoclonic jerks ---
r_associated #0: 20 -->
en:retardation
n1=en:morning myoclonic jerks | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:moro reflex absent ---
r_associated #0: 20 -->
en:retardation
n1=en:moro reflex absent | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:moronity ---
r_associated #0: 20 -->
en:retardation
n1=en:moronity | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:most never acquire independent ambulation ---
r_associated #0: 20 -->
en:retardation
n1=en:most never acquire independent ambulation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:most patients achieve walking with aid ---
r_associated #0: 20 -->
en:retardation
n1=en:most patients achieve walking with aid | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:most patients are wheelchair-bound ---
r_associated #0: 20 -->
en:retardation
n1=en:most patients are wheelchair-bound | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:most patients do not achieve independent sitting or walking ---
r_associated #0: 20 -->
en:retardation
n1=en:most patients do not achieve independent sitting or walking | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:most patients remain stable or improve in years after the abrupt onset of symptoms ---
r_associated #0: 20 -->
en:retardation
n1=en:most patients remain stable or improve in years after the abrupt onset of symptoms | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mosy patients become wheelchair-bound after 10 years ---
r_associated #0: 20 -->
en:retardation
n1=en:mosy patients become wheelchair-bound after 10 years | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:motor abnormalities ---
r_associated #0: 20 -->
en:retardation
n1=en:motor abnormalities | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:motor and intellectual disability, severe ---
r_associated #0: 20 -->
en:retardation
n1=en:motor and intellectual disability, severe | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:motor and vocal tics ---
r_associated #0: 20 -->
en:retardation
n1=en:motor and vocal tics | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:motor automatisms ---
r_associated #0: 20 -->
en:retardation
n1=en:motor automatisms | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:motor delay (in one patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:motor delay (in one patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:motor deterioration ---
r_associated #0: 20 -->
en:retardation
n1=en:motor deterioration | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:motor deterioration in second decade ---
r_associated #0: 20 -->
en:retardation
n1=en:motor deterioration in second decade | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:motor development delay (83%) ---
r_associated #0: 20 -->
en:retardation
n1=en:motor development delay (83%) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:motor development delayed (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:motor development delayed (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:motor developmental delay ---
r_associated #0: 20 -->
en:retardation
n1=en:motor developmental delay | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:motor developmental delay, severe ---
r_associated #0: 20 -->
en:retardation
n1=en:motor developmental delay, severe | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:motor disorders ---
r_associated #0: 20 -->
en:retardation
n1=en:motor disorders | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:motor disturbances ---
r_associated #0: 20 -->
en:retardation
n1=en:motor disturbances | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:motor dysfunction ---
r_associated #0: 20 -->
en:retardation
n1=en:motor dysfunction | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:motor dyspraxia ---
r_associated #0: 20 -->
en:retardation
n1=en:motor dyspraxia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:motor incoordination ---
r_associated #0: 20 -->
en:retardation
n1=en:motor incoordination | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:motor neuron disease ---
r_associated #0: 20 -->
en:retardation
n1=en:motor neuron disease | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:motor neuron disease (less common) ---
r_associated #0: 20 -->
en:retardation
n1=en:motor neuron disease (less common) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:motor neuron disease, lower ---
r_associated #0: 20 -->
en:retardation
n1=en:motor neuron disease, lower | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:motor regression ---
r_associated #0: 20 -->
en:retardation
n1=en:motor regression | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:motor retardation, mild ---
r_associated #0: 20 -->
en:retardation
n1=en:motor retardation, mild | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:motor seizures, nocturnal, usually occur in clusters (up to 8 per night) during dozing or on awakening ---
r_associated #0: 20 -->
en:retardation
n1=en:motor seizures, nocturnal, usually occur in clusters (up to 8 per night) during dozing or on awakening | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:motor stereotypy ---
r_associated #0: 20 -->
en:retardation
n1=en:motor stereotypy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:motor symptoms may be present ---
r_associated #0: 20 -->
en:retardation
n1=en:motor symptoms may be present | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:motor tic ---
r_associated #0: 20 -->
en:retardation
n1=en:motor tic | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mouth movements ---
r_associated #0: 20 -->
en:retardation
n1=en:mouth movements | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:movement abnormalities of the extremities ---
r_associated #0: 20 -->
en:retardation
n1=en:movement abnormalities of the extremities | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:movement disorder ---
r_associated #0: 20 -->
en:retardation
n1=en:movement disorder | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:movement of visual image - finding ---
r_associated #0: 20 -->
en:retardation
n1=en:movement of visual image - finding | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:movements ('tremors') characterized by 8 to 10-hz discharges ---
r_associated #0: 20 -->
en:retardation
n1=en:movements ('tremors') characterized by 8 to 10-hz discharges | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:movements are exacerbated by anxiety ---
r_associated #0: 20 -->
en:retardation
n1=en:movements are exacerbated by anxiety | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:moyamoya disease ---
r_associated #0: 20 -->
en:retardation
n1=en:moyamoya disease | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mr spectroscopy shows decreased n-acetyl aspartate ---
r_associated #0: 20 -->
en:retardation
n1=en:mr spectroscopy shows decreased n-acetyl aspartate | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mri - diffuse or focal cerebral and cerebellar white matter disease ---
r_associated #0: 20 -->
en:retardation
n1=en:mri - diffuse or focal cerebral and cerebellar white matter disease | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mri imaging shows cavitation of the basal ganglia ---
r_associated #0: 20 -->
en:retardation
n1=en:mri imaging shows cavitation of the basal ganglia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mri is best imaging modality to detect lesions ---
r_associated #0: 20 -->
en:retardation
n1=en:mri is best imaging modality to detect lesions | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mri may be normal, especially in type iib ---
r_associated #0: 20 -->
en:retardation
n1=en:mri may be normal, especially in type iib | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mri may show atrophy of the cerebrum ---
r_associated #0: 20 -->
en:retardation
n1=en:mri may show atrophy of the cerebrum | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mri may show lesions in basal ganglia, thalamus, and white matter ---
r_associated #0: 20 -->
en:retardation
n1=en:mri may show lesions in basal ganglia, thalamus, and white matter | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mri shows absence of the facial nerve ---
r_associated #0: 20 -->
en:retardation
n1=en:mri shows absence of the facial nerve | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mri shows atretic occipital cephalocele with bony skull defect ---
r_associated #0: 20 -->
en:retardation
n1=en:mri shows atretic occipital cephalocele with bony skull defect | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mri shows brain asymmetry ---
r_associated #0: 20 -->
en:retardation
n1=en:mri shows brain asymmetry | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mri shows brainstem hypoplasia ---
r_associated #0: 20 -->
en:retardation
n1=en:mri shows brainstem hypoplasia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mri shows cerebellar atrophy ---
r_associated #0: 20 -->
en:retardation
n1=en:mri shows cerebellar atrophy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mri shows cerebral atrophy ---
r_associated #0: 20 -->
en:retardation
n1=en:mri shows cerebral atrophy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mri shows congenital abnormalities of the posterior fossa ---
r_associated #0: 20 -->
en:retardation
n1=en:mri shows congenital abnormalities of the posterior fossa | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mri shows decreased signal intensities in the basal ganglia ---
r_associated #0: 20 -->
en:retardation
n1=en:mri shows decreased signal intensities in the basal ganglia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mri shows decreased signal intensity in the pallidal nuclei with central hyperintensity ('eye of the tiger' sign) ---
r_associated #0: 20 -->
en:retardation
n1=en:mri shows decreased signal intensity in the pallidal nuclei with central hyperintensity ('eye of the tiger' sign) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mri shows defects of the corpus callosum ---
r_associated #0: 20 -->
en:retardation
n1=en:mri shows defects of the corpus callosum | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mri shows delayed myelination (1 of 6 patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:mri shows delayed myelination (1 of 6 patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mri shows diffuse white matter hyperintensities on t2-weighted imaging ---
r_associated #0: 20 -->
en:retardation
n1=en:mri shows diffuse white matter hyperintensities on t2-weighted imaging | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mri shows dysmyelination ---
r_associated #0: 20 -->
en:retardation
n1=en:mri shows dysmyelination | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mri shows frontal and temporal cortical atrophy ---
r_associated #0: 20 -->
en:retardation
n1=en:mri shows frontal and temporal cortical atrophy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mri shows generalized atrophy ---
r_associated #0: 20 -->
en:retardation
n1=en:mri shows generalized atrophy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mri shows global lack of myelination in the cerebral hemispheres ---
r_associated #0: 20 -->
en:retardation
n1=en:mri shows global lack of myelination in the cerebral hemispheres | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mri shows globus pallidus signal abnormalities ---
r_associated #0: 20 -->
en:retardation
n1=en:mri shows globus pallidus signal abnormalities | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mri shows high signal intensity of the white matter later ---
r_associated #0: 20 -->
en:retardation
n1=en:mri shows high signal intensity of the white matter later | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mri shows hypointensity of the thalami early-on ---
r_associated #0: 20 -->
en:retardation
n1=en:mri shows hypointensity of the thalami early-on | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mri shows increased t2-weighted signals in the globus pallidi ---
r_associated #0: 20 -->
en:retardation
n1=en:mri shows increased t2-weighted signals in the globus pallidi | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mri shows leukoencephalopathy ---
r_associated #0: 20 -->
en:retardation
n1=en:mri shows leukoencephalopathy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mri shows no normal myelination ---
r_associated #0: 20 -->
en:retardation
n1=en:mri shows no normal myelination | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mri shows short, thick corpus callosum ---
r_associated #0: 20 -->
en:retardation
n1=en:mri shows short, thick corpus callosum | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mri shows subcortical leukoencephalopathy with cavitation ---
r_associated #0: 20 -->
en:retardation
n1=en:mri shows subcortical leukoencephalopathy with cavitation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mri shows symmetric lesions of the basal ganglia (particularly caudate and putamen) ---
r_associated #0: 20 -->
en:retardation
n1=en:mri shows symmetric lesions of the basal ganglia (particularly caudate and putamen) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mri shows symmetric, diffuse lesions with csf-like signal intensity ---
r_associated #0: 20 -->
en:retardation
n1=en:mri shows symmetric, diffuse lesions with csf-like signal intensity | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mri shows t2-weighted signals in the basal ganglia ---
r_associated #0: 20 -->
en:retardation
n1=en:mri shows t2-weighted signals in the basal ganglia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mri shows white matter lesions ---
r_associated #0: 20 -->
en:retardation
n1=en:mri shows white matter lesions | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mrs shows decreased choline in affected white matter ---
r_associated #0: 20 -->
en:retardation
n1=en:mrs shows decreased choline in affected white matter | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mrs shows decreased creatine in white matter ---
r_associated #0: 20 -->
en:retardation
n1=en:mrs shows decreased creatine in white matter | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mrx78 gene ---
r_associated #0: 20 -->
en:retardation
n1=en:mrx78 gene | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mucolipidosis type iv ---
r_associated #0: 20 -->
en:retardation
n1=en:mucolipidosis type iv | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mucopolysaccharidosis type iiia ---
r_associated #0: 20 -->
en:retardation
n1=en:mucopolysaccharidosis type iiia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mucopolysaccharidosis type iiib ---
r_associated #0: 20 -->
en:retardation
n1=en:mucopolysaccharidosis type iiib | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mucopolysaccharidosis type iiic ---
r_associated #0: 20 -->
en:retardation
n1=en:mucopolysaccharidosis type iiic | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mucopolysaccharidosis type iiid ---
r_associated #0: 20 -->
en:retardation
n1=en:mucopolysaccharidosis type iiid | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:muenke syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:muenke syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:multifocal areas of laminar dysmorphic neurons (in type iia) ---
r_associated #0: 20 -->
en:retardation
n1=en:multifocal areas of laminar dysmorphic neurons (in type iia) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:multifocal cerebral white matter abnormalities ---
r_associated #0: 20 -->
en:retardation
n1=en:multifocal cerebral white matter abnormalities | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:multifocal discharges ---
r_associated #0: 20 -->
en:retardation
n1=en:multifocal discharges | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:multifocal discharges associated with contralateral jerky movements ---
r_associated #0: 20 -->
en:retardation
n1=en:multifocal discharges associated with contralateral jerky movements | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:multifocal discharges seen on eeg (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:multifocal discharges seen on eeg (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:multifocal epileptic activity ---
r_associated #0: 20 -->
en:retardation
n1=en:multifocal epileptic activity | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:multifocal epileptiform discharges on diffuse slow background ---
r_associated #0: 20 -->
en:retardation
n1=en:multifocal epileptiform discharges on diffuse slow background | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:multifocal epileptiform spikes seen on eeg ---
r_associated #0: 20 -->
en:retardation
n1=en:multifocal epileptiform spikes seen on eeg | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:multifocal intractable seizures ---
r_associated #0: 20 -->
en:retardation
n1=en:multifocal intractable seizures | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:multifocal seizure ---
r_associated #0: 20 -->
en:retardation
n1=en:multifocal seizure | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:multifocal spike and wave activity ---
r_associated #0: 20 -->
en:retardation
n1=en:multifocal spike and wave activity | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:multifocal spike waves ---
r_associated #0: 20 -->
en:retardation
n1=en:multifocal spike waves | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:multifocal spikes ---
r_associated #0: 20 -->
en:retardation
n1=en:multifocal spikes | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:multifocal spikes and progressive slowing of background activity seen on eeg ---
r_associated #0: 20 -->
en:retardation
n1=en:multifocal spikes and progressive slowing of background activity seen on eeg | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:multifocal white matter lesions ---
r_associated #0: 20 -->
en:retardation
n1=en:multifocal white matter lesions | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:multiple aneurysms ---
r_associated #0: 20 -->
en:retardation
n1=en:multiple aneurysms | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:multiple congenital anomalies ---
r_associated #0: 20 -->
en:retardation
n1=en:multiple congenital anomalies | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:multiple disability ---
r_associated #0: 20 -->
en:retardation
n1=en:multiple disability | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:multiple independent spike foci ---
r_associated #0: 20 -->
en:retardation
n1=en:multiple independent spike foci | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:multiple lesions in the white matter ---
r_associated #0: 20 -->
en:retardation
n1=en:multiple lesions in the white matter | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:multiple sclerosis ---
r_associated #0: 20 -->
en:retardation
n1=en:multiple sclerosis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:multiple sclerosis-like illness (516003.0001) ---
r_associated #0: 20 -->
en:retardation
n1=en:multiple sclerosis-like illness (516003.0001) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:multiple sulfatase deficiency disease ---
r_associated #0: 20 -->
en:retardation
n1=en:multiple sulfatase deficiency disease | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:multiple trauma/internal injury ---
r_associated #0: 20 -->
en:retardation
n1=en:multiple trauma/internal injury | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mumps ---
r_associated #0: 20 -->
en:retardation
n1=en:mumps | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:muscle atrophy ---
r_associated #0: 20 -->
en:retardation
n1=en:muscle atrophy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:muscle biopsy shows neurogenic changes ---
r_associated #0: 20 -->
en:retardation
n1=en:muscle biopsy shows neurogenic changes | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:muscle cramp ---
r_associated #0: 20 -->
en:retardation
n1=en:muscle cramp | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:muscle stiffness and rigidity, chronic, fluctuating ---
r_associated #0: 20 -->
en:retardation
n1=en:muscle stiffness and rigidity, chronic, fluctuating | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:muscle weakness ---
r_associated #0: 20 -->
en:retardation
n1=en:muscle weakness | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:muscle weakness lower limb ---
r_associated #0: 20 -->
en:retardation
n1=en:muscle weakness lower limb | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:muscle weakness of limb ---
r_associated #0: 20 -->
en:retardation
n1=en:muscle weakness of limb | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:muscle weakness, distal (lower limbs more affected than upper limbs), due to motor neuronopathy ---
r_associated #0: 20 -->
en:retardation
n1=en:muscle weakness, distal (lower limbs more affected than upper limbs), due to motor neuronopathy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:muscle weakness, distal, upper and lower ---
r_associated #0: 20 -->
en:retardation
n1=en:muscle weakness, distal, upper and lower | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:muscle weakness, proximal, due to neuronopathy begins in the lower limbs and then progresses to upper limbs ---
r_associated #0: 20 -->
en:retardation
n1=en:muscle weakness, proximal, due to neuronopathy begins in the lower limbs and then progresses to upper limbs | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:muscle weakness, proximal, symmetric (lower limbs more affected than upper limbs) due to motor neuronopathy ---
r_associated #0: 20 -->
en:retardation
n1=en:muscle weakness, proximal, symmetric (lower limbs more affected than upper limbs) due to motor neuronopathy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:muscle weakness, symmetric, proximal due to motor neuronopathy ---
r_associated #0: 20 -->
en:retardation
n1=en:muscle weakness, symmetric, proximal due to motor neuronopathy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:muscular dystrophy, congenital, 1c ---
r_associated #0: 20 -->
en:retardation
n1=en:muscular dystrophy, congenital, 1c | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:muscular dystrophy, congenital, megaconial type ---
r_associated #0: 20 -->
en:retardation
n1=en:muscular dystrophy, congenital, megaconial type | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) type a, 4 ---
r_associated #0: 20 -->
en:retardation
n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) type a, 4 | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) type a, 6 ---
r_associated #0: 20 -->
en:retardation
n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) type a, 6 | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 3 ---
r_associated #0: 20 -->
en:retardation
n1=en:muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 3 | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:muscular hypotonia of the trunk ---
r_associated #0: 20 -->
en:retardation
n1=en:muscular hypotonia of the trunk | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:muscular rigidity ---
r_associated #0: 20 -->
en:retardation
n1=en:muscular rigidity | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:musician's cramp ---
r_associated #0: 20 -->
en:retardation
n1=en:musician's cramp | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:mutism ---
r_associated #0: 20 -->
en:retardation
n1=en:mutism | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:myclonus (rare) ---
r_associated #0: 20 -->
en:retardation
n1=en:myclonus (rare) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:myelin loss in the corticospinal tracts ---
r_associated #0: 20 -->
en:retardation
n1=en:myelin loss in the corticospinal tracts | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:myelin microvacuolation ---
r_associated #0: 20 -->
en:retardation
n1=en:myelin microvacuolation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:myelin-like lamellar structures in schwann cells ---
r_associated #0: 20 -->
en:retardation
n1=en:myelin-like lamellar structures in schwann cells | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:myelination defect ---
r_associated #0: 20 -->
en:retardation
n1=en:myelination defect | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:myelination defects (type ii) ---
r_associated #0: 20 -->
en:retardation
n1=en:myelination defects (type ii) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:myelomeningocele ---
r_associated #0: 20 -->
en:retardation
n1=en:myelomeningocele | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:myelomeningocele (less common) ---
r_associated #0: 20 -->
en:retardation
n1=en:myelomeningocele (less common) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:myelomeningocele (rare) ---
r_associated #0: 20 -->
en:retardation
n1=en:myelomeningocele (rare) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:myhre syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:myhre syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:myoclonic epilepsy (1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:myoclonic epilepsy (1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:myoclonic jerk ---
r_associated #0: 20 -->
en:retardation
n1=en:myoclonic jerk | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:myoclonic jerks (less common) ---
r_associated #0: 20 -->
en:retardation
n1=en:myoclonic jerks (less common) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:myoclonic jerks (rare) ---
r_associated #0: 20 -->
en:retardation
n1=en:myoclonic jerks (rare) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:myoclonic seizure, refractory ---
r_associated #0: 20 -->
en:retardation
n1=en:myoclonic seizure, refractory | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:myoclonic seizures (1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:myoclonic seizures (1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:myoclonic seizures (subtype 3a) ---
r_associated #0: 20 -->
en:retardation
n1=en:myoclonic seizures (subtype 3a) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:myoclonic seizures may occur ---
r_associated #0: 20 -->
en:retardation
n1=en:myoclonic seizures may occur | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:myoclonic seizures, frequent, long-lasting (many hours) ---
r_associated #0: 20 -->
en:retardation
n1=en:myoclonic seizures, frequent, long-lasting (many hours) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:myoclonic seizures, progressive ---
r_associated #0: 20 -->
en:retardation
n1=en:myoclonic seizures, progressive | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:myoclonic spasms, superimposed episodic, severe, painful (characterized by activation of antagonistic muscle pairs, may involve facial muscles) ---
r_associated #0: 20 -->
en:retardation
n1=en:myoclonic spasms, superimposed episodic, severe, painful (characterized by activation of antagonistic muscle pairs, may involve facial muscles) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:myoclonic-astatic seizures ---
r_associated #0: 20 -->
en:retardation
n1=en:myoclonic-astatic seizures | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:myoclonus (in 1 family) ---
r_associated #0: 20 -->
en:retardation
n1=en:myoclonus (in 1 family) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:myoclonus (in a subset of patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:myoclonus (in a subset of patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:myoclonus (less common) ---
r_associated #0: 20 -->
en:retardation
n1=en:myoclonus (less common) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:myoclonus (subtype 3a) ---
r_associated #0: 20 -->
en:retardation
n1=en:myoclonus (subtype 3a) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:myoclonus (type i and type ii, infantile and juvenile) ---
r_associated #0: 20 -->
en:retardation
n1=en:myoclonus (type i and type ii, infantile and juvenile) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:myoclonus, axial (predominantly in upper limbs, occurs at rest and increases with activity or changes in posture) ---
r_associated #0: 20 -->
en:retardation
n1=en:myoclonus, axial (predominantly in upper limbs, occurs at rest and increases with activity or changes in posture) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:myoclonus, cortical, multifocal ---
r_associated #0: 20 -->
en:retardation
n1=en:myoclonus, cortical, multifocal | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:myoclonus, paroxysmal ---
r_associated #0: 20 -->
en:retardation
n1=en:myoclonus, paroxysmal | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:myokymia ---
r_associated #0: 20 -->
en:retardation
n1=en:myokymia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:myokymia (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:myokymia (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:myokymia, especially facial ---
r_associated #0: 20 -->
en:retardation
n1=en:myokymia, especially facial | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:myopathy ---
r_associated #0: 20 -->
en:retardation
n1=en:myopathy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:myotonia ---
r_associated #0: 20 -->
en:retardation
n1=en:myotonia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:myotonia (in 1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:myotonia (in 1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:myotonic seizures ---
r_associated #0: 20 -->
en:retardation
n1=en:myotonic seizures | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:myxedema ---
r_associated #0: 20 -->
en:retardation
n1=en:myxedema | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:narcolepsy ---
r_associated #0: 20 -->
en:retardation
n1=en:narcolepsy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neck drop ---
r_associated #0: 20 -->
en:retardation
n1=en:neck drop | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neck pain ---
r_associated #0: 20 -->
en:retardation
n1=en:neck pain | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:necrotic process ---
r_associated #0: 20 -->
en:retardation
n1=en:necrotic process | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:necrotic white matter lesions throughout the brain and brainstem ---
r_associated #0: 20 -->
en:retardation
n1=en:necrotic white matter lesions throughout the brain and brainstem | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neocortical atrophy ---
r_associated #0: 20 -->
en:retardation
n1=en:neocortical atrophy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neocortical dysplasia (27%) ---
r_associated #0: 20 -->
en:retardation
n1=en:neocortical dysplasia (27%) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neonatal deformity ---
r_associated #0: 20 -->
en:retardation
n1=en:neonatal deformity | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neonatal epileptic encephalopathy (nee) ---
r_associated #0: 20 -->
en:retardation
n1=en:neonatal epileptic encephalopathy (nee) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neonatal hearing impairment ---
r_associated #0: 20 -->
en:retardation
n1=en:neonatal hearing impairment | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neonatal hypotonia ---
r_associated #0: 20 -->
en:retardation
n1=en:neonatal hypotonia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neonatal irresponsiveness ---
r_associated #0: 20 -->
en:retardation
n1=en:neonatal irresponsiveness | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neonatal irritability ---
r_associated #0: 20 -->
en:retardation
n1=en:neonatal irritability | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neonatal jaundice ---
r_associated #0: 20 -->
en:retardation
n1=en:neonatal jaundice | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neonatal/early-infantile onset encephalopathy ---
r_associated #0: 20 -->
en:retardation
n1=en:neonatal/early-infantile onset encephalopathy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neoplasm ---
r_associated #0: 20 -->
en:retardation
n1=en:neoplasm | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neoplasm of ocular adnexa ---
r_associated #0: 20 -->
en:retardation
n1=en:neoplasm of ocular adnexa | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:nerve cells show ballooning with membrane-bound vesicles with reticulogranular pattern ---
r_associated #0: 20 -->
en:retardation
n1=en:nerve cells show ballooning with membrane-bound vesicles with reticulogranular pattern | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:nerve degeneration ---
r_associated #0: 20 -->
en:retardation
n1=en:nerve degeneration | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:nerve paralysis ---
r_associated #0: 20 -->
en:retardation
n1=en:nerve paralysis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:nervous breakdown ---
r_associated #0: 20 -->
en:retardation
n1=en:nervous breakdown | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:nervousness ---
r_associated #0: 20 -->
en:retardation
n1=en:nervousness | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neuhauser syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:neuhauser syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neural tube defect ---
r_associated #0: 20 -->
en:retardation
n1=en:neural tube defect | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neural tube defect (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:neural tube defect (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neural tube defects (4%) ---
r_associated #0: 20 -->
en:retardation
n1=en:neural tube defects (4%) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neural tube defects may occur ---
r_associated #0: 20 -->
en:retardation
n1=en:neural tube defects may occur | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neurasthenia/surmenage ---
r_associated #0: 20 -->
en:retardation
n1=en:neurasthenia/surmenage | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neuroaxonal abnormalities ---
r_associated #0: 20 -->
en:retardation
n1=en:neuroaxonal abnormalities | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neuroaxonal dystrophies ---
r_associated #0: 20 -->
en:retardation
n1=en:neuroaxonal dystrophies | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neuroaxonal spheroids ---
r_associated #0: 20 -->
en:retardation
n1=en:neuroaxonal spheroids | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neurobehavioral changes associated with hyperammonemia ---
r_associated #0: 20 -->
en:retardation
n1=en:neurobehavioral changes associated with hyperammonemia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neurocognitive disorders ---
r_associated #0: 20 -->
en:retardation
n1=en:neurocognitive disorders | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neurocognitive impairment, mild (homozygous patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:neurocognitive impairment, mild (homozygous patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neurodegeneration (patient a) ---
r_associated #0: 20 -->
en:retardation
n1=en:neurodegeneration (patient a) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neurodegeneration in the basal ganglia ---
r_associated #0: 20 -->
en:retardation
n1=en:neurodegeneration in the basal ganglia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neurodegeneration in the cerebellum ---
r_associated #0: 20 -->
en:retardation
n1=en:neurodegeneration in the cerebellum | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neurodegeneration in the substantia nigra ---
r_associated #0: 20 -->
en:retardation
n1=en:neurodegeneration in the substantia nigra | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neurodegeneration leading to profound mental retardation ---
r_associated #0: 20 -->
en:retardation
n1=en:neurodegeneration leading to profound mental retardation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neurodegeneration with brain iron accumulation 5 ---
r_associated #0: 20 -->
en:retardation
n1=en:neurodegeneration with brain iron accumulation 5 | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neurodevelopmental anomaly ---
r_associated #0: 20 -->
en:retardation
n1=en:neurodevelopmental anomaly | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neurodevelopmental disorder ---
r_associated #0: 20 -->
en:retardation
n1=en:neurodevelopmental disorder | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neurodevelopmental impairment (early-onset form) ---
r_associated #0: 20 -->
en:retardation
n1=en:neurodevelopmental impairment (early-onset form) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neurodevelopmental regression ---
r_associated #0: 20 -->
en:retardation
n1=en:neurodevelopmental regression | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neurofibrillary degeneration (morphologic abnormality) ---
r_associated #0: 20 -->
en:retardation
n1=en:neurofibrillary degeneration (morphologic abnormality) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neurofibrillary mapt (tau)-positive tangles ---
r_associated #0: 20 -->
en:retardation
n1=en:neurofibrillary mapt (tau)-positive tangles | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neurofibrillary tangles composed of disordered microtubules ---
r_associated #0: 20 -->
en:retardation
n1=en:neurofibrillary tangles composed of disordered microtubules | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neurofibrillary tangles may be present ---
r_associated #0: 20 -->
en:retardation
n1=en:neurofibrillary tangles may be present | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neurofibromas can occur at cervical, thoracic, lumbar, and sacral levels ---
r_associated #0: 20 -->
en:retardation
n1=en:neurofibromas can occur at cervical, thoracic, lumbar, and sacral levels | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neurogenic bladder ---
r_associated #0: 20 -->
en:retardation
n1=en:neurogenic bladder | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neurogenic muscle atrophy, especially in the lower limbs ---
r_associated #0: 20 -->
en:retardation
n1=en:neurogenic muscle atrophy, especially in the lower limbs | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neuroimaging shows cortical atrophy ---
r_associated #0: 20 -->
en:retardation
n1=en:neuroimaging shows cortical atrophy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neurologic abnormalities in about 7% ---
r_associated #0: 20 -->
en:retardation
n1=en:neurologic abnormalities in about 7% | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neurologic crises with coma (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:neurologic crises with coma (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neurologic decompensation ---
r_associated #0: 20 -->
en:retardation
n1=en:neurologic decompensation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neurologic degeneration ---
r_associated #0: 20 -->
en:retardation
n1=en:neurologic degeneration | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neurologic deterioration in longterm survivors ---
r_associated #0: 20 -->
en:retardation
n1=en:neurologic deterioration in longterm survivors | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neurologic dysfunction, progressive ---
r_associated #0: 20 -->
en:retardation
n1=en:neurologic dysfunction, progressive | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neurologic involvement (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:neurologic involvement (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neurologic involvement is rare ---
r_associated #0: 20 -->
en:retardation
n1=en:neurologic involvement is rare | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neurologic regression ---
r_associated #0: 20 -->
en:retardation
n1=en:neurologic regression | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neurologic regression after age 2 years ---
r_associated #0: 20 -->
en:retardation
n1=en:neurologic regression after age 2 years | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neurologic regression after prolonged episodes ---
r_associated #0: 20 -->
en:retardation
n1=en:neurologic regression after prolonged episodes | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neurologic regression around age 3 months ---
r_associated #0: 20 -->
en:retardation
n1=en:neurologic regression around age 3 months | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neurologic regression following seizure onset ---
r_associated #0: 20 -->
en:retardation
n1=en:neurologic regression following seizure onset | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neurologic sequelae not always present ---
r_associated #0: 20 -->
en:retardation
n1=en:neurologic sequelae not always present | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neurologic sequelae of stroke ---
r_associated #0: 20 -->
en:retardation
n1=en:neurologic sequelae of stroke | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neurologic symptoms, if present, usually result from associated syringomyelia ---
r_associated #0: 20 -->
en:retardation
n1=en:neurologic symptoms, if present, usually result from associated syringomyelia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neurological development terminology ---
r_associated #0: 20 -->
en:retardation
n1=en:neurological development terminology | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neuromuscular disturbances, progressive ---
r_associated #0: 20 -->
en:retardation
n1=en:neuromuscular disturbances, progressive | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neuron apoptotic process ---
r_associated #0: 20 -->
en:retardation
n1=en:neuron apoptotic process | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neuron loss ---
r_associated #0: 20 -->
en:retardation
n1=en:neuron loss | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neuronal and vascular calcifications ---
r_associated #0: 20 -->
en:retardation
n1=en:neuronal and vascular calcifications | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neuronal ceroid lipofuscinosis ---
r_associated #0: 20 -->
en:retardation
n1=en:neuronal ceroid lipofuscinosis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neuronal ceroid lipofuscinosis type 3 ---
r_associated #0: 20 -->
en:retardation
n1=en:neuronal ceroid lipofuscinosis type 3 | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neuronal heterotopia ---
r_associated #0: 20 -->
en:retardation
n1=en:neuronal heterotopia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neuronal inclusion bodies stain for neuroserpin ---
r_associated #0: 20 -->
en:retardation
n1=en:neuronal inclusion bodies stain for neuroserpin | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neuronal loss (patient a) ---
r_associated #0: 20 -->
en:retardation
n1=en:neuronal loss (patient a) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neuronal loss and gliosis in caudate and putamen ---
r_associated #0: 20 -->
en:retardation
n1=en:neuronal loss and gliosis in caudate and putamen | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neuronal loss and gliosis in the cerebral cortex ---
r_associated #0: 20 -->
en:retardation
n1=en:neuronal loss and gliosis in the cerebral cortex | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neuronal loss and gliosis in the dentate nucleus ---
r_associated #0: 20 -->
en:retardation
n1=en:neuronal loss and gliosis in the dentate nucleus | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neuronal loss and gliosis in the inferior olives ---
r_associated #0: 20 -->
en:retardation
n1=en:neuronal loss and gliosis in the inferior olives | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neuronal loss and gliosis in the substantia nigra pars compacta ---
r_associated #0: 20 -->
en:retardation
n1=en:neuronal loss and gliosis in the substantia nigra pars compacta | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neuronal loss in basal ganglia ---
r_associated #0: 20 -->
en:retardation
n1=en:neuronal loss in basal ganglia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neuronal loss in central nervous system ---
r_associated #0: 20 -->
en:retardation
n1=en:neuronal loss in central nervous system | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neuronal loss in the brainstem ---
r_associated #0: 20 -->
en:retardation
n1=en:neuronal loss in the brainstem | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neuronal loss in the cerebral cortex ---
r_associated #0: 20 -->
en:retardation
n1=en:neuronal loss in the cerebral cortex | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neuronal loss in the cerebrum and cerebellum ---
r_associated #0: 20 -->
en:retardation
n1=en:neuronal loss in the cerebrum and cerebellum | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neuronal loss in the dentate nuclei ---
r_associated #0: 20 -->
en:retardation
n1=en:neuronal loss in the dentate nuclei | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neuronal loss in the hippocampus ---
r_associated #0: 20 -->
en:retardation
n1=en:neuronal loss in the hippocampus | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neuronal loss in the inferior olives ---
r_associated #0: 20 -->
en:retardation
n1=en:neuronal loss in the inferior olives | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neuronal loss in the locus ceruleus ---
r_associated #0: 20 -->
en:retardation
n1=en:neuronal loss in the locus ceruleus | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neuronal loss in the purkinje cell layer of the cerebellar vermis ---
r_associated #0: 20 -->
en:retardation
n1=en:neuronal loss in the purkinje cell layer of the cerebellar vermis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neuronal loss in the striatum, cerebral cortex, and cerebellum (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:neuronal loss in the striatum, cerebral cortex, and cerebellum (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neuronal loss in the striatum, medial thalamic nuclei, and inferior olives ---
r_associated #0: 20 -->
en:retardation
n1=en:neuronal loss in the striatum, medial thalamic nuclei, and inferior olives | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neuronal loss in the substantia nigra ---
r_associated #0: 20 -->
en:retardation
n1=en:neuronal loss in the substantia nigra | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neuronal loss, diffuse ---
r_associated #0: 20 -->
en:retardation
n1=en:neuronal loss, diffuse | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neuronal loss, particularly of cerebellar purkinje cells ---
r_associated #0: 20 -->
en:retardation
n1=en:neuronal loss, particularly of cerebellar purkinje cells | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neuronal migration defect ---
r_associated #0: 20 -->
en:retardation
n1=en:neuronal migration defect | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neuronal migration disorder ---
r_associated #0: 20 -->
en:retardation
n1=en:neuronal migration disorder | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neuropathologic examination shows calcification of the small brain vessels ---
r_associated #0: 20 -->
en:retardation
n1=en:neuropathologic examination shows calcification of the small brain vessels | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neuropathologic examination shows extensive spongiosis and gliosis ---
r_associated #0: 20 -->
en:retardation
n1=en:neuropathologic examination shows extensive spongiosis and gliosis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neuropathologic examination shows severe demyelination ---
r_associated #0: 20 -->
en:retardation
n1=en:neuropathologic examination shows severe demyelination | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neuropathologic findings include leukoencephalopathy, predominantly in the upper corticospinal tract and cerebellar peduncles (initially) ---
r_associated #0: 20 -->
en:retardation
n1=en:neuropathologic findings include leukoencephalopathy, predominantly in the upper corticospinal tract and cerebellar peduncles (initially) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neuropathology shows alpha-synuclein-containing cytoplasmic inclusions in glial cells ---
r_associated #0: 20 -->
en:retardation
n1=en:neuropathology shows alpha-synuclein-containing cytoplasmic inclusions in glial cells | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neuropathology shows diffuse demyelination of the cerebral white matter ---
r_associated #0: 20 -->
en:retardation
n1=en:neuropathology shows diffuse demyelination of the cerebral white matter | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neuropathology shows fmr1 mrna-positive inclusions in neurons and astrocytes ---
r_associated #0: 20 -->
en:retardation
n1=en:neuropathology shows fmr1 mrna-positive inclusions in neurons and astrocytes | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neuropathology shows neuronal degeneration ---
r_associated #0: 20 -->
en:retardation
n1=en:neuropathology shows neuronal degeneration | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neuropathology shows neuronal loss in basal ganglia, brainstem, and cerebellum ---
r_associated #0: 20 -->
en:retardation
n1=en:neuropathology shows neuronal loss in basal ganglia, brainstem, and cerebellum | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neuropathology shows severe neuronal loss in the inner granular layer of the cerebellum ---
r_associated #0: 20 -->
en:retardation
n1=en:neuropathology shows severe neuronal loss in the inner granular layer of the cerebellum | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neurophysiologic abnormalities (eeg, sep, vep) ---
r_associated #0: 20 -->
en:retardation
n1=en:neurophysiologic abnormalities (eeg, sep, vep) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neurophysiologic abnormalities (eeg, vep, sep) ---
r_associated #0: 20 -->
en:retardation
n1=en:neurophysiologic abnormalities (eeg, vep, sep) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neurophysiologic studies show evidence of denervation and renervation ---
r_associated #0: 20 -->
en:retardation
n1=en:neurophysiologic studies show evidence of denervation and renervation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neuropil ---
r_associated #0: 20 -->
en:retardation
n1=en:neuropil | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neuropsychologic cognitive abnormalities ---
r_associated #0: 20 -->
en:retardation
n1=en:neuropsychologic cognitive abnormalities | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neuropsychologic impairment ---
r_associated #0: 20 -->
en:retardation
n1=en:neuropsychologic impairment | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neurosarcoidosis (5-16% of patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:neurosarcoidosis (5-16% of patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neurosis ---
r_associated #0: 20 -->
en:retardation
n1=en:neurosis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neurotic, personality, or other mental disorder ---
r_associated #0: 20 -->
en:retardation
n1=en:neurotic, personality, or other mental disorder | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:neurotic, stress-related and somatoform disorders ---
r_associated #0: 20 -->
en:retardation
n1=en:neurotic, stress-related and somatoform disorders | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:never able to walk ---
r_associated #0: 20 -->
en:retardation
n1=en:never able to walk | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:never learn to walk (some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:never learn to walk (some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:nevus of ito ---
r_associated #0: 20 -->
en:retardation
n1=en:nevus of ito | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:nevus/mole ---
r_associated #0: 20 -->
en:retardation
n1=en:nevus/mole | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:nicolaides baraitser syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:nicolaides baraitser syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:niemann-pick disease, type a ---
r_associated #0: 20 -->
en:retardation
n1=en:niemann-pick disease, type a | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:nigrostriatal degeneration ---
r_associated #0: 20 -->
en:retardation
n1=en:nigrostriatal degeneration | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:no amyloid plaques ---
r_associated #0: 20 -->
en:retardation
n1=en:no amyloid plaques | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:no autistic features ---
r_associated #0: 20 -->
en:retardation
n1=en:no autistic features | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:no bulbar involvement ---
r_associated #0: 20 -->
en:retardation
n1=en:no bulbar involvement | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:no central nervous system abnormalities ---
r_associated #0: 20 -->
en:retardation
n1=en:no central nervous system abnormalities | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:no cerebellar signs ---
r_associated #0: 20 -->
en:retardation
n1=en:no cerebellar signs | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:no cerebellar vermis aplasia/hypoplasia ---
r_associated #0: 20 -->
en:retardation
n1=en:no cerebellar vermis aplasia/hypoplasia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:no cognitive decline ---
r_associated #0: 20 -->
en:retardation
n1=en:no cognitive decline | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:no dementia ---
r_associated #0: 20 -->
en:retardation
n1=en:no dementia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:no development ---
r_associated #0: 20 -->
en:retardation
n1=en:no development | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:no developmental progress ---
r_associated #0: 20 -->
en:retardation
n1=en:no developmental progress | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:no disease ---
r_associated #0: 20 -->
en:retardation
n1=en:no disease | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:no gaze contact ---
r_associated #0: 20 -->
en:retardation
n1=en:no gaze contact | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:no head control ---
r_associated #0: 20 -->
en:retardation
n1=en:no head control | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:no hippocampal sclerosis ---
r_associated #0: 20 -->
en:retardation
n1=en:no hippocampal sclerosis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:no hydrocephalus ---
r_associated #0: 20 -->
en:retardation
n1=en:no hydrocephalus | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:no language ---
r_associated #0: 20 -->
en:retardation
n1=en:no language | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:no language development ---
r_associated #0: 20 -->
en:retardation
n1=en:no language development | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:no lewy bodies ---
r_associated #0: 20 -->
en:retardation
n1=en:no lewy bodies | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:no mental retardation ---
r_associated #0: 20 -->
en:retardation
n1=en:no mental retardation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:no motor skills acquired (in some) ---
r_associated #0: 20 -->
en:retardation
n1=en:no motor skills acquired (in some) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:no myoclonus ---
r_associated #0: 20 -->
en:retardation
n1=en:no myoclonus | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:no neurofibrillary tangles ---
r_associated #0: 20 -->
en:retardation
n1=en:no neurofibrillary tangles | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:no neurofibromas ---
r_associated #0: 20 -->
en:retardation
n1=en:no neurofibromas | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:no other neurologic deficits ---
r_associated #0: 20 -->
en:retardation
n1=en:no other neurologic deficits | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:no other neurologic disorder ---
r_associated #0: 20 -->
en:retardation
n1=en:no other neurologic disorder | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:no overt seizures ---
r_associated #0: 20 -->
en:retardation
n1=en:no overt seizures | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:no pick bodies or lewy bodies ---
r_associated #0: 20 -->
en:retardation
n1=en:no pick bodies or lewy bodies | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:no response to l-dopa treatment ---
r_associated #0: 20 -->
en:retardation
n1=en:no response to l-dopa treatment | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:no seizures ---
r_associated #0: 20 -->
en:retardation
n1=en:no seizures | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:no seizures (hcs) ---
r_associated #0: 20 -->
en:retardation
n1=en:no seizures (hcs) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:no sensory deficit ---
r_associated #0: 20 -->
en:retardation
n1=en:no sensory deficit | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:no sensory symptoms ---
r_associated #0: 20 -->
en:retardation
n1=en:no sensory symptoms | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:no speech acquisition ---
r_associated #0: 20 -->
en:retardation
n1=en:no speech acquisition | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:no speech development (in most patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:no speech development (in most patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:no speech problem ---
r_associated #0: 20 -->
en:retardation
n1=en:no speech problem | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:no spontaneous movements ---
r_associated #0: 20 -->
en:retardation
n1=en:no spontaneous movements | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:no structural brain abnormalities seen on mri ---
r_associated #0: 20 -->
en:retardation
n1=en:no structural brain abnormalities seen on mri | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:no structural brain anomalies ---
r_associated #0: 20 -->
en:retardation
n1=en:no structural brain anomalies | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:no tau pathology ---
r_associated #0: 20 -->
en:retardation
n1=en:no tau pathology | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:no tremor ---
r_associated #0: 20 -->
en:retardation
n1=en:no tremor | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:no visual fixation ---
r_associated #0: 20 -->
en:retardation
n1=en:no visual fixation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:no voluntary movement ---
r_associated #0: 20 -->
en:retardation
n1=en:no voluntary movement | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:nocturnal enuresis ---
r_associated #0: 20 -->
en:retardation
n1=en:nocturnal enuresis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:nocturnal occurrence ---
r_associated #0: 20 -->
en:retardation
n1=en:nocturnal occurrence | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:nocturnal occurrence, usually during light sleep ---
r_associated #0: 20 -->
en:retardation
n1=en:nocturnal occurrence, usually during light sleep | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:nocturnal seizures ---
r_associated #0: 20 -->
en:retardation
n1=en:nocturnal seizures | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:nocturnal seizures (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:nocturnal seizures (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:nocturnal sleep disruption ---
r_associated #0: 20 -->
en:retardation
n1=en:nocturnal sleep disruption | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:nodding of head ---
r_associated #0: 20 -->
en:retardation
n1=en:nodding of head | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:nodular heterotopia ---
r_associated #0: 20 -->
en:retardation
n1=en:nodular heterotopia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:nodular heterotopia (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:nodular heterotopia (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:nodular heterotopia (less common) ---
r_associated #0: 20 -->
en:retardation
n1=en:nodular heterotopia (less common) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:nodular heterotopia (rare) ---
r_associated #0: 20 -->
en:retardation
n1=en:nodular heterotopia (rare) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:nodular heterotopia of the grey matter ---
r_associated #0: 20 -->
en:retardation
n1=en:nodular heterotopia of the grey matter | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:non-febrile seizures later ---
r_associated #0: 20 -->
en:retardation
n1=en:non-febrile seizures later | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:non-gonococcal urethritis ---
r_associated #0: 20 -->
en:retardation
n1=en:non-gonococcal urethritis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:non-purposeful arm movements, choreoathetoid-like ---
r_associated #0: 20 -->
en:retardation
n1=en:non-purposeful arm movements, choreoathetoid-like | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:non-rheum heart valve disease ---
r_associated #0: 20 -->
en:retardation
n1=en:non-rheum heart valve disease | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:nonprogressive cerebellar ataxia ---
r_associated #0: 20 -->
en:retardation
n1=en:nonprogressive cerebellar ataxia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:nonspecific leukoencephalopathy (52%) ---
r_associated #0: 20 -->
en:retardation
n1=en:nonspecific leukoencephalopathy (52%) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:nonspecific spongiform degeneration ---
r_associated #0: 20 -->
en:retardation
n1=en:nonspecific spongiform degeneration | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:nonverbal (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:nonverbal (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:noonan-like syndrome with loose anagen hair ---
r_associated #0: 20 -->
en:retardation
n1=en:noonan-like syndrome with loose anagen hair | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:normal brain mri or ct scan ---
r_associated #0: 20 -->
en:retardation
n1=en:normal brain mri or ct scan | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:normal cognition (1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:normal cognition (1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:normal cognition (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:normal cognition (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:normal cognition (reported in 1 patient who survived to age 20 years) ---
r_associated #0: 20 -->
en:retardation
n1=en:normal cognition (reported in 1 patient who survived to age 20 years) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:normal cognition (reported in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:normal cognition (reported in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:normal cognition and intellectual function ---
r_associated #0: 20 -->
en:retardation
n1=en:normal cognition and intellectual function | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:normal delivery deadborn ---
r_associated #0: 20 -->
en:retardation
n1=en:normal delivery deadborn | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:normal delivery liveborn ---
r_associated #0: 20 -->
en:retardation
n1=en:normal delivery liveborn | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:normal development ---
r_associated #0: 20 -->
en:retardation
n1=en:normal development | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:normal development (in 2 of 6 patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:normal development (in 2 of 6 patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:normal development in some patients ---
r_associated #0: 20 -->
en:retardation
n1=en:normal development in some patients | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:normal development until 6-18 months ---
r_associated #0: 20 -->
en:retardation
n1=en:normal development until 6-18 months | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:normal early development ---
r_associated #0: 20 -->
en:retardation
n1=en:normal early development | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:normal early development, up to 8 to 15 months of age ---
r_associated #0: 20 -->
en:retardation
n1=en:normal early development, up to 8 to 15 months of age | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:normal early developmental milestones ---
r_associated #0: 20 -->
en:retardation
n1=en:normal early developmental milestones | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:normal early psychomotor development ---
r_associated #0: 20 -->
en:retardation
n1=en:normal early psychomotor development | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:normal fine motor activity ---
r_associated #0: 20 -->
en:retardation
n1=en:normal fine motor activity | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:normal initial psychomotor development ---
r_associated #0: 20 -->
en:retardation
n1=en:normal initial psychomotor development | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:normal intellectual development ---
r_associated #0: 20 -->
en:retardation
n1=en:normal intellectual development | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:normal intellectual function ---
r_associated #0: 20 -->
en:retardation
n1=en:normal intellectual function | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:normal intelligence (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:normal intelligence (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:normal intelligence (majority) ---
r_associated #0: 20 -->
en:retardation
n1=en:normal intelligence (majority) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:normal intelligence in carrier females ---
r_associated #0: 20 -->
en:retardation
n1=en:normal intelligence in carrier females | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:normal intelligence in iib ---
r_associated #0: 20 -->
en:retardation
n1=en:normal intelligence in iib | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:normal intelligence in majority ---
r_associated #0: 20 -->
en:retardation
n1=en:normal intelligence in majority | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:normal intelligence in most cases ---
r_associated #0: 20 -->
en:retardation
n1=en:normal intelligence in most cases | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:normal intelligence to mild or moderate mental retardation ---
r_associated #0: 20 -->
en:retardation
n1=en:normal intelligence to mild or moderate mental retardation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:normal interictal eeg ---
r_associated #0: 20 -->
en:retardation
n1=en:normal interictal eeg | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:normal interictal neurologic examination ---
r_associated #0: 20 -->
en:retardation
n1=en:normal interictal neurologic examination | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:normal iq in infancy, then iq drops with age ---
r_associated #0: 20 -->
en:retardation
n1=en:normal iq in infancy, then iq drops with age | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:normal mental development ---
r_associated #0: 20 -->
en:retardation
n1=en:normal mental development | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:normal motor conduction studies (initially) ---
r_associated #0: 20 -->
en:retardation
n1=en:normal motor conduction studies (initially) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:normal motor development ---
r_associated #0: 20 -->
en:retardation
n1=en:normal motor development | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:normal muscle strength ---
r_associated #0: 20 -->
en:retardation
n1=en:normal muscle strength | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:normal neurologic development in most cases ---
r_associated #0: 20 -->
en:retardation
n1=en:normal neurologic development in most cases | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:normal neurological development is possible ---
r_associated #0: 20 -->
en:retardation
n1=en:normal neurological development is possible | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:normal neuromuscular studies ---
r_associated #0: 20 -->
en:retardation
n1=en:normal neuromuscular studies | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:normal psychomotor development ---
r_associated #0: 20 -->
en:retardation
n1=en:normal psychomotor development | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:normal psychomotor development in most ---
r_associated #0: 20 -->
en:retardation
n1=en:normal psychomotor development in most | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:normal psychomotor development until age 2 to 3 years ---
r_associated #0: 20 -->
en:retardation
n1=en:normal psychomotor development until age 2 to 3 years | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:normal sleep-onset time (normal time of falling asleep) ---
r_associated #0: 20 -->
en:retardation
n1=en:normal sleep-onset time (normal time of falling asleep) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:normal to mild mental retardation ---
r_associated #0: 20 -->
en:retardation
n1=en:normal to mild mental retardation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:normal to mildly delayed development ---
r_associated #0: 20 -->
en:retardation
n1=en:normal to mildly delayed development | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:normal, timely language development ---
r_associated #0: 20 -->
en:retardation
n1=en:normal, timely language development | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:norrie syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:norrie syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:nuclear magnetic resonance imaging brain normal ---
r_associated #0: 20 -->
en:retardation
n1=en:nuclear magnetic resonance imaging brain normal | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:numbness ---
r_associated #0: 20 -->
en:retardation
n1=en:numbness | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:nystagmus ---
r_associated #0: 20 -->
en:retardation
n1=en:nystagmus | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:nystagmus decreases on convergence ---
r_associated #0: 20 -->
en:retardation
n1=en:nystagmus decreases on convergence | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:nystagmus is accentuated by fixation, lateral gaze, smooth pursuit ---
r_associated #0: 20 -->
en:retardation
n1=en:nystagmus is accentuated by fixation, lateral gaze, smooth pursuit | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:nystagmus, horizontal ---
r_associated #0: 20 -->
en:retardation
n1=en:nystagmus, horizontal | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:nystagmus, jerky, horizontal, congenital ---
r_associated #0: 20 -->
en:retardation
n1=en:nystagmus, jerky, horizontal, congenital | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:nystagmus, mild ---
r_associated #0: 20 -->
en:retardation
n1=en:nystagmus, mild | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:obsessive compulsive behavior ---
r_associated #0: 20 -->
en:retardation
n1=en:obsessive compulsive behavior | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:obstruction of the foramen of monro (variable) ---
r_associated #0: 20 -->
en:retardation
n1=en:obstruction of the foramen of monro (variable) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:obtundation ---
r_associated #0: 20 -->
en:retardation
n1=en:obtundation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:occasional degeneration of the globus pallidus ---
r_associated #0: 20 -->
en:retardation
n1=en:occasional degeneration of the globus pallidus | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:occipital dermal sinus tract ---
r_associated #0: 20 -->
en:retardation
n1=en:occipital dermal sinus tract | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:occipital encephalocele (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:occipital encephalocele (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:occipital encephalocele (wws) ---
r_associated #0: 20 -->
en:retardation
n1=en:occipital encephalocele (wws) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:occipital encephaloceles ---
r_associated #0: 20 -->
en:retardation
n1=en:occipital encephaloceles | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:occipital headache ---
r_associated #0: 20 -->
en:retardation
n1=en:occipital headache | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:occipital lobe ---
r_associated #0: 20 -->
en:retardation
n1=en:occipital lobe | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:occipital lobe atrophy ---
r_associated #0: 20 -->
en:retardation
n1=en:occipital lobe atrophy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:occipital lobe infarct (rare) ---
r_associated #0: 20 -->
en:retardation
n1=en:occipital lobe infarct (rare) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:occipital meningocele ---
r_associated #0: 20 -->
en:retardation
n1=en:occipital meningocele | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:occipital meningocele (less common) ---
r_associated #0: 20 -->
en:retardation
n1=en:occipital meningocele (less common) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:occipital myelomeningocele (less common) ---
r_associated #0: 20 -->
en:retardation
n1=en:occipital myelomeningocele (less common) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:occipital neural tube defects ---
r_associated #0: 20 -->
en:retardation
n1=en:occipital neural tube defects | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:occlusive hydrocephalus, congenital ---
r_associated #0: 20 -->
en:retardation
n1=en:occlusive hydrocephalus, congenital | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:occurs most often during the night or early morning ---
r_associated #0: 20 -->
en:retardation
n1=en:occurs most often during the night or early morning | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ocular foreign body ---
r_associated #0: 20 -->
en:retardation
n1=en:ocular foreign body | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ocular motility spared ---
r_associated #0: 20 -->
en:retardation
n1=en:ocular motility spared | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ocular muscle abnormalities ---
r_associated #0: 20 -->
en:retardation
n1=en:ocular muscle abnormalities | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ocular palsies ---
r_associated #0: 20 -->
en:retardation
n1=en:ocular palsies | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:oculocerebrocutaneous syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:oculocerebrocutaneous syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:oculocerebrorenal syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:oculocerebrorenal syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:oculogyric crisis ---
r_associated #0: 20 -->
en:retardation
n1=en:oculogyric crisis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:oculomotor apraxia ---
r_associated #0: 20 -->
en:retardation
n1=en:oculomotor apraxia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:odontogenic cyst ---
r_associated #0: 20 -->
en:retardation
n1=en:odontogenic cyst | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ohdo syndrome, maat-kievit-brunner type ---
r_associated #0: 20 -->
en:retardation
n1=en:ohdo syndrome, maat-kievit-brunner type | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:olfactory lobe agenesis ---
r_associated #0: 20 -->
en:retardation
n1=en:olfactory lobe agenesis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:olfactory or auditory hallucinations ---
r_associated #0: 20 -->
en:retardation
n1=en:olfactory or auditory hallucinations | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:oligodendrocytes with foamy cytoplasm ---
r_associated #0: 20 -->
en:retardation
n1=en:oligodendrocytes with foamy cytoplasm | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:olivopontocerebellar atrophy ---
r_associated #0: 20 -->
en:retardation
n1=en:olivopontocerebellar atrophy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:olivopontocerebellar hypoplasia, fetal-onset ---
r_associated #0: 20 -->
en:retardation
n1=en:olivopontocerebellar hypoplasia, fetal-onset | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:olivopontocerebellar hypoplasia, severe ---
r_associated #0: 20 -->
en:retardation
n1=en:olivopontocerebellar hypoplasia, severe | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:omphalocele ---
r_associated #0: 20 -->
en:retardation
n1=en:omphalocele | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:onat syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:onat syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:only some achieve rolling or sitting ---
r_associated #0: 20 -->
en:retardation
n1=en:only some achieve rolling or sitting | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:only walking achieved ---
r_associated #0: 20 -->
en:retardation
n1=en:only walking achieved | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:onset may be triggered by emotional stress, fever, exercise, exposure to heat ---
r_associated #0: 20 -->
en:retardation
n1=en:onset may be triggered by emotional stress, fever, exercise, exposure to heat | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:open operculum ---
r_associated #0: 20 -->
en:retardation
n1=en:open operculum | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:open spina bifida (myelomeningocele, 182940) ---
r_associated #0: 20 -->
en:retardation
n1=en:open spina bifida (myelomeningocele, 182940) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:open sylvian fissures ---
r_associated #0: 20 -->
en:retardation
n1=en:open sylvian fissures | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:opisthotonic posturing ---
r_associated #0: 20 -->
en:retardation
n1=en:opisthotonic posturing | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:opisthotonos (type ii) ---
r_associated #0: 20 -->
en:retardation
n1=en:opisthotonos (type ii) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:opisthotonus ---
r_associated #0: 20 -->
en:retardation
n1=en:opisthotonus | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:opitz-g syndrome, type 2 ---
r_associated #0: 20 -->
en:retardation
n1=en:opitz-g syndrome, type 2 | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:opsoclonus ---
r_associated #0: 20 -->
en:retardation
n1=en:opsoclonus | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:optic ataxia (in a subset of patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:optic ataxia (in a subset of patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:optic nerve hypoplasia ---
r_associated #0: 20 -->
en:retardation
n1=en:optic nerve hypoplasia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:optic tract agenesis ---
r_associated #0: 20 -->
en:retardation
n1=en:optic tract agenesis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:optic tract and chiasm hypoplasia ---
r_associated #0: 20 -->
en:retardation
n1=en:optic tract and chiasm hypoplasia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:organic mental disorder ---
r_associated #0: 20 -->
en:retardation
n1=en:organic mental disorder | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:organic writer's cramp ---
r_associated #0: 20 -->
en:retardation
n1=en:organic writer's cramp | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:organic, including symptomatic, mental disorders ---
r_associated #0: 20 -->
en:retardation
n1=en:organic, including symptomatic, mental disorders | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:organoid nevus ---
r_associated #0: 20 -->
en:retardation
n1=en:organoid nevus | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ornithine carbamoyltransferase deficiency disease ---
r_associated #0: 20 -->
en:retardation
n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:orofacial dyspraxia, linguistic and nonlinguistic ---
r_associated #0: 20 -->
en:retardation
n1=en:orofacial dyspraxia, linguistic and nonlinguistic | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:orofacial dystonia ---
r_associated #0: 20 -->
en:retardation
n1=en:orofacial dystonia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndrome 11 ---
r_associated #0: 20 -->
en:retardation
n1=en:orofaciodigital syndrome 11 | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndrome 3 ---
r_associated #0: 20 -->
en:retardation
n1=en:orofaciodigital syndrome 3 | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndrome type 6 ---
r_associated #0: 20 -->
en:retardation
n1=en:orofaciodigital syndrome type 6 | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:oromandibular dystonia ---
r_associated #0: 20 -->
en:retardation
n1=en:oromandibular dystonia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:orotic aciduria ---
r_associated #0: 20 -->
en:retardation
n1=en:orotic aciduria | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:orthostatic hypotension ---
r_associated #0: 20 -->
en:retardation
n1=en:orthostatic hypotension | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:orthostatic proteinuria ---
r_associated #0: 20 -->
en:retardation
n1=en:orthostatic proteinuria | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:osgood-schlatter's disease ---
r_associated #0: 20 -->
en:retardation
n1=en:osgood-schlatter's disease | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ossification of the faux cerebri (less common) ---
r_associated #0: 20 -->
en:retardation
n1=en:ossification of the faux cerebri (less common) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:osteoarthritis, knee ---
r_associated #0: 20 -->
en:retardation
n1=en:osteoarthritis, knee | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:osteoarthritis, spine ---
r_associated #0: 20 -->
en:retardation
n1=en:osteoarthritis, spine | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:osteolysis syndrome recessive ---
r_associated #0: 20 -->
en:retardation
n1=en:osteolysis syndrome recessive | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:osteoporosis ---
r_associated #0: 20 -->
en:retardation
n1=en:osteoporosis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:osteoporosis with pseudoglioma ---
r_associated #0: 20 -->
en:retardation
n1=en:osteoporosis with pseudoglioma | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:other abdominal hernia ---
r_associated #0: 20 -->
en:retardation
n1=en:other abdominal hernia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:other anaemias ---
r_associated #0: 20 -->
en:retardation
n1=en:other anaemias | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:other and unspecified congenital anomalies ---
r_associated #0: 20 -->
en:retardation
n1=en:other and unspecified congenital anomalies | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:other and unspecified disorders of the circulatory system ---
r_associated #0: 20 -->
en:retardation
n1=en:other and unspecified disorders of the circulatory system | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:other and unspecified special symptoms or syndromes, nec in mdr18_1 ---
r_associated #0: 20 -->
en:retardation
n1=en:other and unspecified special symptoms or syndromes, nec in mdr18_1 | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:other arterial obstructive/peripheral vascular disease ---
r_associated #0: 20 -->
en:retardation
n1=en:other arterial obstructive/peripheral vascular disease | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:other auditory injuries ---
r_associated #0: 20 -->
en:retardation
n1=en:other auditory injuries | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:other auras may occur ---
r_associated #0: 20 -->
en:retardation
n1=en:other auras may occur | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:other benign neoplasm female genital ---
r_associated #0: 20 -->
en:retardation
n1=en:other benign neoplasm female genital | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:other benign neoplasm of skin, unspecified ---
r_associated #0: 20 -->
en:retardation
n1=en:other benign neoplasm of skin, unspecified | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:other complications of the puerperium ---
r_associated #0: 20 -->
en:retardation
n1=en:other complications of the puerperium | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:other concern behavior adolescence ---
r_associated #0: 20 -->
en:retardation
n1=en:other concern behavior adolescence | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:other concern behavior childhood ---
r_associated #0: 20 -->
en:retardation
n1=en:other concern behavior childhood | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:other congenital anomalies of limbs ---
r_associated #0: 20 -->
en:retardation
n1=en:other congenital anomalies of limbs | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:other congenital anomalies of nervous system ---
r_associated #0: 20 -->
en:retardation
n1=en:other congenital anomalies of nervous system | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:other congenital malformations of circulatory system ---
r_associated #0: 20 -->
en:retardation
n1=en:other congenital malformations of circulatory system | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:other congenital malformations of digestive system ---
r_associated #0: 20 -->
en:retardation
n1=en:other congenital malformations of digestive system | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:other congenital malformations of eye ---
r_associated #0: 20 -->
en:retardation
n1=en:other congenital malformations of eye | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:other congenital malformations of heart ---
r_associated #0: 20 -->
en:retardation
n1=en:other congenital malformations of heart | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:other congenital musculoskeletal deformities ---
r_associated #0: 20 -->
en:retardation
n1=en:other congenital musculoskeletal deformities | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:other congenital upper alimentary tract anomalies ---
r_associated #0: 20 -->
en:retardation
n1=en:other congenital upper alimentary tract anomalies | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:other cranial nerves may be involved ---
r_associated #0: 20 -->
en:retardation
n1=en:other cranial nerves may be involved | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:other dermatologic congenital anomalies ---
r_associated #0: 20 -->
en:retardation
n1=en:other dermatologic congenital anomalies | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:other digestive system injuries ---
r_associated #0: 20 -->
en:retardation
n1=en:other digestive system injuries | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:other disease blood/lymph/spleen ---
r_associated #0: 20 -->
en:retardation
n1=en:other disease blood/lymph/spleen | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:other disease male genital including breast ---
r_associated #0: 20 -->
en:retardation
n1=en:other disease male genital including breast | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:other disease of neurological system ---
r_associated #0: 20 -->
en:retardation
n1=en:other disease of neurological system | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:other disease of pregnancy/delivery/puerperium ---
r_associated #0: 20 -->
en:retardation
n1=en:other disease of pregnancy/delivery/puerperium | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:other diseases female genital system ---
r_associated #0: 20 -->
en:retardation
n1=en:other diseases female genital system | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:other diseases of digestive system ---
r_associated #0: 20 -->
en:retardation
n1=en:other diseases of digestive system | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:other diseases of ear/mastoid ---
r_associated #0: 20 -->
en:retardation
n1=en:other diseases of ear/mastoid | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:other disorders of eye ---
r_associated #0: 20 -->
en:retardation
n1=en:other disorders of eye | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:other disorders of the skin and subcutaneous tissue ---
r_associated #0: 20 -->
en:retardation
n1=en:other disorders of the skin and subcutaneous tissue | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:other disorders of urinary system ---
r_associated #0: 20 -->
en:retardation
n1=en:other disorders of urinary system | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:other endocrine or metabolic congenital anomalies ---
r_associated #0: 20 -->
en:retardation
n1=en:other endocrine or metabolic congenital anomalies | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:other endocrine/metabolic nutritional disease ---
r_associated #0: 20 -->
en:retardation
n1=en:other endocrine/metabolic nutritional disease | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:other female genital malignant neoplasms ---
r_associated #0: 20 -->
en:retardation
n1=en:other female genital malignant neoplasms | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:other forms of chronic ischaemic heart disease ---
r_associated #0: 20 -->
en:retardation
n1=en:other forms of chronic ischaemic heart disease | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:other forms of heart disease ---
r_associated #0: 20 -->
en:retardation
n1=en:other forms of heart disease | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:other general/unspecified diseases ---
r_associated #0: 20 -->
en:retardation
n1=en:other general/unspecified diseases | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:other head injury without skull fracture ---
r_associated #0: 20 -->
en:retardation
n1=en:other head injury without skull fracture | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:other hematologic congenital anomalies ---
r_associated #0: 20 -->
en:retardation
n1=en:other hematologic congenital anomalies | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:other hematologic injuries ---
r_associated #0: 20 -->
en:retardation
n1=en:other hematologic injuries | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:other hematologic malignant neoplasms ---
r_associated #0: 20 -->
en:retardation
n1=en:other hematologic malignant neoplasms | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:other hematological abnormality ---
r_associated #0: 20 -->
en:retardation
n1=en:other hematological abnormality | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:other infection neurological system ---
r_associated #0: 20 -->
en:retardation
n1=en:other infection neurological system | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:other infection/inflammation of eye (excluding herpes) ---
r_associated #0: 20 -->
en:retardation
n1=en:other infection/inflammation of eye (excluding herpes) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:other infections of respiratory system ---
r_associated #0: 20 -->
en:retardation
n1=en:other infections of respiratory system | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:other infectious diseases ---
r_associated #0: 20 -->
en:retardation
n1=en:other infectious diseases | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:other infectious skin disease ---
r_associated #0: 20 -->
en:retardation
n1=en:other infectious skin disease | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:other male genital malignant neoplasm ---
r_associated #0: 20 -->
en:retardation
n1=en:other male genital malignant neoplasm | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:other malignant neoplasm urinary tract ---
r_associated #0: 20 -->
en:retardation
n1=en:other malignant neoplasm urinary tract | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:other malignant respiratory neoplasm ---
r_associated #0: 20 -->
en:retardation
n1=en:other malignant respiratory neoplasm | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:other mental retardation ---
r_associated #0: 20 -->
en:retardation
n1=en:other mental retardation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:other mental/psychological disorders ---
r_associated #0: 20 -->
en:retardation
n1=en:other mental/psychological disorders | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:other musculoskeletal disorder ---
r_associated #0: 20 -->
en:retardation
n1=en:other musculoskeletal disorder | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:other neurologic injuries ---
r_associated #0: 20 -->
en:retardation
n1=en:other neurologic injuries | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:other neurotic disorders ---
r_associated #0: 20 -->
en:retardation
n1=en:other neurotic disorders | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:other non-obstetrical conditions ---
r_associated #0: 20 -->
en:retardation
n1=en:other non-obstetrical conditions | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:other ocular injuries ---
r_associated #0: 20 -->
en:retardation
n1=en:other ocular injuries | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:other organic psychosis ---
r_associated #0: 20 -->
en:retardation
n1=en:other organic psychosis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:other osteoarthritis ---
r_associated #0: 20 -->
en:retardation
n1=en:other osteoarthritis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:other peptic ulcers ---
r_associated #0: 20 -->
en:retardation
n1=en:other peptic ulcers | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:other peripheral neuritis ---
r_associated #0: 20 -->
en:retardation
n1=en:other peripheral neuritis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:other psychological symptom/complaint ---
r_associated #0: 20 -->
en:retardation
n1=en:other psychological symptom/complaint | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:other psychoses ---
r_associated #0: 20 -->
en:retardation
n1=en:other psychoses | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:other respiratory injuries ---
r_associated #0: 20 -->
en:retardation
n1=en:other respiratory injuries | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:other respiratory system diseases ---
r_associated #0: 20 -->
en:retardation
n1=en:other respiratory system diseases | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:other seizure types (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:other seizure types (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:other specified congenital malformations ---
r_associated #0: 20 -->
en:retardation
n1=en:other specified congenital malformations | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:other specified drug-induced mental disorders ---
r_associated #0: 20 -->
en:retardation
n1=en:other specified drug-induced mental disorders | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:other specified intellectual disabilities ---
r_associated #0: 20 -->
en:retardation
n1=en:other specified intellectual disabilities | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:other specified mental retardation ---
r_associated #0: 20 -->
en:retardation
n1=en:other specified mental retardation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:other specified psychophysiological malfunction ---
r_associated #0: 20 -->
en:retardation
n1=en:other specified psychophysiological malfunction | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:other specified transient mental disorders due to conditions classified elsewhere, other ---
r_associated #0: 20 -->
en:retardation
n1=en:other specified transient mental disorders due to conditions classified elsewhere, other | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:other viral disease with exanthems ---
r_associated #0: 20 -->
en:retardation
n1=en:other viral disease with exanthems | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:other viral diseases ---
r_associated #0: 20 -->
en:retardation
n1=en:other viral diseases | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:other/unspecified neoplasm female genital ---
r_associated #0: 20 -->
en:retardation
n1=en:other/unspecified neoplasm female genital | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:other/unspecified neoplasm skin ---
r_associated #0: 20 -->
en:retardation
n1=en:other/unspecified neoplasm skin | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:other/unspecified neoplasms ---
r_associated #0: 20 -->
en:retardation
n1=en:other/unspecified neoplasms | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:otitis externa ---
r_associated #0: 20 -->
en:retardation
n1=en:otitis externa | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:otocephaly ---
r_associated #0: 20 -->
en:retardation
n1=en:otocephaly | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:otopalatodigital syndrome, type ii ---
r_associated #0: 20 -->
en:retardation
n1=en:otopalatodigital syndrome, type ii | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:otosclerosis ---
r_associated #0: 20 -->
en:retardation
n1=en:otosclerosis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:over time, white matter vanishes and is replaced by csf ---
r_associated #0: 20 -->
en:retardation
n1=en:over time, white matter vanishes and is replaced by csf | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:overactive child/hyperkinetic ---
r_associated #0: 20 -->
en:retardation
n1=en:overactive child/hyperkinetic | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:overlapping lesion of brain ---
r_associated #0: 20 -->
en:retardation
n1=en:overlapping lesion of brain | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:overweight ---
r_associated #0: 20 -->
en:retardation
n1=en:overweight | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pachygyria (1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:pachygyria (1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pachygyria (less common) ---
r_associated #0: 20 -->
en:retardation
n1=en:pachygyria (less common) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pachygyria (posterior-to-anterior gradient) ---
r_associated #0: 20 -->
en:retardation
n1=en:pachygyria (posterior-to-anterior gradient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pachygyria (rare) ---
r_associated #0: 20 -->
en:retardation
n1=en:pachygyria (rare) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pachygyria with preferential frontoparietal involvement (meb) ---
r_associated #0: 20 -->
en:retardation
n1=en:pachygyria with preferential frontoparietal involvement (meb) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pachygyria, bilateral frontotemporal ---
r_associated #0: 20 -->
en:retardation
n1=en:pachygyria, bilateral frontotemporal | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pachygyria, frontoparietal ---
r_associated #0: 20 -->
en:retardation
n1=en:pachygyria, frontoparietal | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pachygyria, most prominent in the frontal lobes ---
r_associated #0: 20 -->
en:retardation
n1=en:pachygyria, most prominent in the frontal lobes | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pachygyria, occipital ---
r_associated #0: 20 -->
en:retardation
n1=en:pachygyria, occipital | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pachygyria, usually posterior ---
r_associated #0: 20 -->
en:retardation
n1=en:pachygyria, usually posterior | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pachygyrias ---
r_associated #0: 20 -->
en:retardation
n1=en:pachygyrias | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pachymacrogyria ---
r_associated #0: 20 -->
en:retardation
n1=en:pachymacrogyria | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pachymeningitis cervicalis (cervical cord compression due to thickened dura) ---
r_associated #0: 20 -->
en:retardation
n1=en:pachymeningitis cervicalis (cervical cord compression due to thickened dura) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pain ---
r_associated #0: 20 -->
en:retardation
n1=en:pain | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pain (sharp, boring, drilling, piercing) ---
r_associated #0: 20 -->
en:retardation
n1=en:pain (sharp, boring, drilling, piercing) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pain affects upper body ---
r_associated #0: 20 -->
en:retardation
n1=en:pain affects upper body | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pain, episodic ---
r_associated #0: 20 -->
en:retardation
n1=en:pain, episodic | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:palatal myoclonus ---
r_associated #0: 20 -->
en:retardation
n1=en:palatal myoclonus | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pallidal degeneration ---
r_associated #0: 20 -->
en:retardation
n1=en:pallidal degeneration | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pallor of dorsal columns of the spinal cord ---
r_associated #0: 20 -->
en:retardation
n1=en:pallor of dorsal columns of the spinal cord | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:paradoxical cerebral emboli ---
r_associated #0: 20 -->
en:retardation
n1=en:paradoxical cerebral emboli | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:paralysis ---
r_associated #0: 20 -->
en:retardation
n1=en:paralysis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:paralysis, episodic, after strenuous exercise ---
r_associated #0: 20 -->
en:retardation
n1=en:paralysis, episodic, after strenuous exercise | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:paraneoplastic syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:paraneoplastic syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:paranoid reaction ---
r_associated #0: 20 -->
en:retardation
n1=en:paranoid reaction | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:paraparesis ---
r_associated #0: 20 -->
en:retardation
n1=en:paraparesis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:paraparesis, spastic ---
r_associated #0: 20 -->
en:retardation
n1=en:paraparesis, spastic | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:paraphilias ---
r_associated #0: 20 -->
en:retardation
n1=en:paraphilias | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:paraplegia ---
r_associated #0: 20 -->
en:retardation
n1=en:paraplegia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:paraplegia secondary to spinal cord compression due to severe kyphosis ---
r_associated #0: 20 -->
en:retardation
n1=en:paraplegia secondary to spinal cord compression due to severe kyphosis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:paraspinal masses ---
r_associated #0: 20 -->
en:retardation
n1=en:paraspinal masses | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:paraventricular cysts ---
r_associated #0: 20 -->
en:retardation
n1=en:paraventricular cysts | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:parenchymal neuromelanosis ---
r_associated #0: 20 -->
en:retardation
n1=en:parenchymal neuromelanosis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:paresis (hcp) ---
r_associated #0: 20 -->
en:retardation
n1=en:paresis (hcp) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:paresis of extensor muscles of the big toe is presenting symptom ---
r_associated #0: 20 -->
en:retardation
n1=en:paresis of extensor muscles of the big toe is presenting symptom | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:paresthesia ---
r_associated #0: 20 -->
en:retardation
n1=en:paresthesia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:parietal lobe ---
r_associated #0: 20 -->
en:retardation
n1=en:parietal lobe | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:parietal lobe epilepsy ---
r_associated #0: 20 -->
en:retardation
n1=en:parietal lobe epilepsy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:paris trousseau thrombocytopenia ---
r_associated #0: 20 -->
en:retardation
n1=en:paris trousseau thrombocytopenia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:parkinsonism ---
r_associated #0: 20 -->
en:retardation
n1=en:parkinsonism | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:parkinsonism (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:parkinsonism (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:parkinsonism (in some) ---
r_associated #0: 20 -->
en:retardation
n1=en:parkinsonism (in some) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:parkinsonism (later onset) ---
r_associated #0: 20 -->
en:retardation
n1=en:parkinsonism (later onset) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:parkinsonism (later) ---
r_associated #0: 20 -->
en:retardation
n1=en:parkinsonism (later) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:parkinsonism (less common) ---
r_associated #0: 20 -->
en:retardation
n1=en:parkinsonism (less common) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:parkinsonism has been described in 1 family ---
r_associated #0: 20 -->
en:retardation
n1=en:parkinsonism has been described in 1 family | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:parkinsonism may occur ---
r_associated #0: 20 -->
en:retardation
n1=en:parkinsonism may occur | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:parkinsonism, early-onset ---
r_associated #0: 20 -->
en:retardation
n1=en:parkinsonism, early-onset | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:parkinsonism, l-dopa responsive ---
r_associated #0: 20 -->
en:retardation
n1=en:parkinsonism, l-dopa responsive | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:parkinsonism, levodopa-responsive (occurs at later stages, may replace dystonia symptoms) ---
r_associated #0: 20 -->
en:retardation
n1=en:parkinsonism, levodopa-responsive (occurs at later stages, may replace dystonia symptoms) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:paroxysmal choreoathetosis ---
r_associated #0: 20 -->
en:retardation
n1=en:paroxysmal choreoathetosis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:paroxysmal dystonia ---
r_associated #0: 20 -->
en:retardation
n1=en:paroxysmal dystonia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:paroxysmal lethargy ---
r_associated #0: 20 -->
en:retardation
n1=en:paroxysmal lethargy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:paroxysmal nonkinesigenic dyskinesia ---
r_associated #0: 20 -->
en:retardation
n1=en:paroxysmal nonkinesigenic dyskinesia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:paroxysmal oculogyric crises ---
r_associated #0: 20 -->
en:retardation
n1=en:paroxysmal oculogyric crises | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:partial absence of the corpus callosum (in one patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:partial absence of the corpus callosum (in one patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:partial agenesis of corpus callosum ---
r_associated #0: 20 -->
en:retardation
n1=en:partial agenesis of corpus callosum | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:partial agenesis of corpus callosum (rare, in males) ---
r_associated #0: 20 -->
en:retardation
n1=en:partial agenesis of corpus callosum (rare, in males) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:partial agenesis of the corpus callosum (in 1 of 2 sibs) ---
r_associated #0: 20 -->
en:retardation
n1=en:partial agenesis of the corpus callosum (in 1 of 2 sibs) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:partial agenesis of the corpus callosum (rare) ---
r_associated #0: 20 -->
en:retardation
n1=en:partial agenesis of the corpus callosum (rare) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:partial empty sella turcica ---
r_associated #0: 20 -->
en:retardation
n1=en:partial empty sella turcica | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:partial epilepsy ---
r_associated #0: 20 -->
en:retardation
n1=en:partial epilepsy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:partial migrating seizures seen on eeg (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:partial migrating seizures seen on eeg (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:partial or complete absence of the cerebellar vermis consistent with dandy walker malformation ---
r_associated #0: 20 -->
en:retardation
n1=en:partial or complete absence of the cerebellar vermis consistent with dandy walker malformation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:partial or complete agenesis of corpus callosum ---
r_associated #0: 20 -->
en:retardation
n1=en:partial or complete agenesis of corpus callosum | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:partial or total agenesis of the corpus callosum (33%) ---
r_associated #0: 20 -->
en:retardation
n1=en:partial or total agenesis of the corpus callosum (33%) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:partial pachygyria ---
r_associated #0: 20 -->
en:retardation
n1=en:partial pachygyria | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:partial response to pyridoxine ---
r_associated #0: 20 -->
en:retardation
n1=en:partial response to pyridoxine | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:partial seizure ---
r_associated #0: 20 -->
en:retardation
n1=en:partial seizure | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:partial seizures, simple and complex ---
r_associated #0: 20 -->
en:retardation
n1=en:partial seizures, simple and complex | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:partington x-linked mental retardation syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:partington x-linked mental retardation syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:patchy demyelination of subcortical white matter ---
r_associated #0: 20 -->
en:retardation
n1=en:patchy demyelination of subcortical white matter | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:patchy diffuse hyperintensities on t2-weighted mri ---
r_associated #0: 20 -->
en:retardation
n1=en:patchy diffuse hyperintensities on t2-weighted mri | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:patellar and ankle clonus ---
r_associated #0: 20 -->
en:retardation
n1=en:patellar and ankle clonus | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:patellar tendon reflexes hyperactive ---
r_associated #0: 20 -->
en:retardation
n1=en:patellar tendon reflexes hyperactive | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:patent ductus arteriosus - persisting type ---
r_associated #0: 20 -->
en:retardation
n1=en:patent ductus arteriosus - persisting type | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pathologic calcification, calcified structure ---
r_associated #0: 20 -->
en:retardation
n1=en:pathologic calcification, calcified structure | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pathologic changes in anterior horn cells and lateral corticospinal tracts ---
r_associated #0: 20 -->
en:retardation
n1=en:pathologic changes in anterior horn cells and lateral corticospinal tracts | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pathology includes spongiform changes, diffuse nerve cell degeneration and glial proliferation ---
r_associated #0: 20 -->
en:retardation
n1=en:pathology includes spongiform changes, diffuse nerve cell degeneration and glial proliferation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:patients 20-30 years old have hyperintense lesions on t2-weighted mri in the frontal and anterior temporal lobes ---
r_associated #0: 20 -->
en:retardation
n1=en:patients 20-30 years old have hyperintense lesions on t2-weighted mri in the frontal and anterior temporal lobes | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:patients 30-40 years old have hyperintense lesions in periventricular areas, the external capsule, basal ganglia, thalamus, and brainstem ---
r_associated #0: 20 -->
en:retardation
n1=en:patients 30-40 years old have hyperintense lesions in periventricular areas, the external capsule, basal ganglia, thalamus, and brainstem | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:patients achieve ambulation ---
r_associated #0: 20 -->
en:retardation
n1=en:patients achieve ambulation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:patients may develop a seizure disorder later in life ---
r_associated #0: 20 -->
en:retardation
n1=en:patients may develop a seizure disorder later in life | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:patients may have no structural abnormalities in the central nervous system ---
r_associated #0: 20 -->
en:retardation
n1=en:patients may have no structural abnormalities in the central nervous system | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:patients may only achieve sitting or walking ---
r_associated #0: 20 -->
en:retardation
n1=en:patients may only achieve sitting or walking | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:patients older than 50 years have hyperintensities, lacunar infarcts, and microbleeds ---
r_associated #0: 20 -->
en:retardation
n1=en:patients older than 50 years have hyperintensities, lacunar infarcts, and microbleeds | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:patients show normal psychomotor development ---
r_associated #0: 20 -->
en:retardation
n1=en:patients show normal psychomotor development | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:paucity of anterior horn motor neurons ---
r_associated #0: 20 -->
en:retardation
n1=en:paucity of anterior horn motor neurons | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:peak frequency of vomiting every 10 to 15 minutes ---
r_associated #0: 20 -->
en:retardation
n1=en:peak frequency of vomiting every 10 to 15 minutes | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:peculiar gait (if left untreated) ---
r_associated #0: 20 -->
en:retardation
n1=en:peculiar gait (if left untreated) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:peculiar stance and sitting posture (if left untreated) ---
r_associated #0: 20 -->
en:retardation
n1=en:peculiar stance and sitting posture (if left untreated) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pediatric adverse events terminology ---
r_associated #0: 20 -->
en:retardation
n1=en:pediatric adverse events terminology | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pediatric failure to thrive ---
r_associated #0: 20 -->
en:retardation
n1=en:pediatric failure to thrive | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pediatric immunization terminology ---
r_associated #0: 20 -->
en:retardation
n1=en:pediatric immunization terminology | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pediatric psychiatric disorder ---
r_associated #0: 20 -->
en:retardation
n1=en:pediatric psychiatric disorder | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pediatric terminology ---
r_associated #0: 20 -->
en:retardation
n1=en:pediatric terminology | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pediculosis/other skin infestation ---
r_associated #0: 20 -->
en:retardation
n1=en:pediculosis/other skin infestation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pelizaeus-merzbacher disease ---
r_associated #0: 20 -->
en:retardation
n1=en:pelizaeus-merzbacher disease | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pelvic inflammatory disease ---
r_associated #0: 20 -->
en:retardation
n1=en:pelvic inflammatory disease | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:perception disturbance ---
r_associated #0: 20 -->
en:retardation
n1=en:perception disturbance | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pericystic abnormal myelination ---
r_associated #0: 20 -->
en:retardation
n1=en:pericystic abnormal myelination | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:perinatal mortality ---
r_associated #0: 20 -->
en:retardation
n1=en:perinatal mortality | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:periodic paralysis (finding) ---
r_associated #0: 20 -->
en:retardation
n1=en:periodic paralysis (finding) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:periodic paralysis, usually hypokalemic ---
r_associated #0: 20 -->
en:retardation
n1=en:periodic paralysis, usually hypokalemic | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:periodic stiffness ---
r_associated #0: 20 -->
en:retardation
n1=en:periodic stiffness | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:peripheral demyelinating neuropathy, central dysmyelination, waardenburg syndrome, and hirschsprung disease ---
r_associated #0: 20 -->
en:retardation
n1=en:peripheral demyelinating neuropathy, central dysmyelination, waardenburg syndrome, and hirschsprung disease | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:peripheral hypertonia ---
r_associated #0: 20 -->
en:retardation
n1=en:peripheral hypertonia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:peripheral motor neuropathy ---
r_associated #0: 20 -->
en:retardation
n1=en:peripheral motor neuropathy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:peripheral nervous system disorder ---
r_associated #0: 20 -->
en:retardation
n1=en:peripheral nervous system disorder | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:peripheral sensory neuropathy ---
r_associated #0: 20 -->
en:retardation
n1=en:peripheral sensory neuropathy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:perisylvian polymicrogyria ---
r_associated #0: 20 -->
en:retardation
n1=en:perisylvian polymicrogyria | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:perivascular spaces ---
r_associated #0: 20 -->
en:retardation
n1=en:perivascular spaces | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:periventricular and subcortical white matter abnormalities ---
r_associated #0: 20 -->
en:retardation
n1=en:periventricular and subcortical white matter abnormalities | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:periventricular calcifications ---
r_associated #0: 20 -->
en:retardation
n1=en:periventricular calcifications | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:periventricular cysts ---
r_associated #0: 20 -->
en:retardation
n1=en:periventricular cysts | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:periventricular gray matter heterotopia ---
r_associated #0: 20 -->
en:retardation
n1=en:periventricular gray matter heterotopia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:periventricular hemorrhagic infarction ---
r_associated #0: 20 -->
en:retardation
n1=en:periventricular hemorrhagic infarction | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:periventricular leukomalacia ---
r_associated #0: 20 -->
en:retardation
n1=en:periventricular leukomalacia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:periventricular leukomalacia (reported in 2 patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:periventricular leukomalacia (reported in 2 patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:periventricular nodular heterotopia ---
r_associated #0: 20 -->
en:retardation
n1=en:periventricular nodular heterotopia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:periventricular nodular heterotopia seen on mri ---
r_associated #0: 20 -->
en:retardation
n1=en:periventricular nodular heterotopia seen on mri | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:periventricular white matter abnormalities ---
r_associated #0: 20 -->
en:retardation
n1=en:periventricular white matter abnormalities | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:periventricular white matter abnormalities (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:periventricular white matter abnormalities (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:periventricular white matter changes ---
r_associated #0: 20 -->
en:retardation
n1=en:periventricular white matter changes | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:periventricular white matter changes (meb) ---
r_associated #0: 20 -->
en:retardation
n1=en:periventricular white matter changes (meb) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:periventricular white matter gliosis (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:periventricular white matter gliosis (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:periventricular white matter hyperintensities, bilateral ---
r_associated #0: 20 -->
en:retardation
n1=en:periventricular white matter hyperintensities, bilateral | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:periventricular white matter lesions ---
r_associated #0: 20 -->
en:retardation
n1=en:periventricular white matter lesions | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pernicious/folate deficiency anemias ---
r_associated #0: 20 -->
en:retardation
n1=en:pernicious/folate deficiency anemias | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:peroxisomal fatty acyl-coa reductase 1 disorder ---
r_associated #0: 20 -->
en:retardation
n1=en:peroxisomal fatty acyl-coa reductase 1 disorder | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:peroxisome biogenesis disorder 3b ---
r_associated #0: 20 -->
en:retardation
n1=en:peroxisome biogenesis disorder 3b | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:perseveration ---
r_associated #0: 20 -->
en:retardation
n1=en:perseveration | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:persistent cavum septum pellucidum ---
r_associated #0: 20 -->
en:retardation
n1=en:persistent cavum septum pellucidum | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:persistent cavus septum pellucidum ---
r_associated #0: 20 -->
en:retardation
n1=en:persistent cavus septum pellucidum | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:persistent cloaca ---
r_associated #0: 20 -->
en:retardation
n1=en:persistent cloaca | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:persistent falcine venous sinus ---
r_associated #0: 20 -->
en:retardation
n1=en:persistent falcine venous sinus | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:personal care disability ---
r_associated #0: 20 -->
en:retardation
n1=en:personal care disability | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:personal hygiene disability ---
r_associated #0: 20 -->
en:retardation
n1=en:personal hygiene disability | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:personality change ---
r_associated #0: 20 -->
en:retardation
n1=en:personality change | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:personality disorder ---
r_associated #0: 20 -->
en:retardation
n1=en:personality disorder | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:personality disorders and disturbances in behaviour ---
r_associated #0: 20 -->
en:retardation
n1=en:personality disorders and disturbances in behaviour | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pervasive developmental disorder ---
r_associated #0: 20 -->
en:retardation
n1=en:pervasive developmental disorder | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:petit mal epilepsy ---
r_associated #0: 20 -->
en:retardation
n1=en:petit mal epilepsy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pettigrew syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:pettigrew syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pharyngeal gag reflex negative ---
r_associated #0: 20 -->
en:retardation
n1=en:pharyngeal gag reflex negative | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:phase of life problem adult ---
r_associated #0: 20 -->
en:retardation
n1=en:phase of life problem adult | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:phenylketonuria ---
r_associated #0: 20 -->
en:retardation
n1=en:phenylketonuria | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:phenylketonuria ii ---
r_associated #0: 20 -->
en:retardation
n1=en:phenylketonuria ii | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:phlebitis and thrombophlebitis ---
r_associated #0: 20 -->
en:retardation
n1=en:phlebitis and thrombophlebitis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:phonology deficits ---
r_associated #0: 20 -->
en:retardation
n1=en:phonology deficits | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:phonophobia ---
r_associated #0: 20 -->
en:retardation
n1=en:phonophobia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:phosphoglycerate dehydrogenase deficiency ---
r_associated #0: 20 -->
en:retardation
n1=en:phosphoglycerate dehydrogenase deficiency | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:phosphoglycerate kinase 1 deficiency ---
r_associated #0: 20 -->
en:retardation
n1=en:phosphoglycerate kinase 1 deficiency | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:photoparoxysmal and photomyoclonic responses ---
r_associated #0: 20 -->
en:retardation
n1=en:photoparoxysmal and photomyoclonic responses | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:photoparoxysmal response (in some) ---
r_associated #0: 20 -->
en:retardation
n1=en:photoparoxysmal response (in some) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:photophobia ---
r_associated #0: 20 -->
en:retardation
n1=en:photophobia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:photosensitive tonic-clonic seizures ---
r_associated #0: 20 -->
en:retardation
n1=en:photosensitive tonic-clonic seizures | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:photosensitivity in one-third of patients ---
r_associated #0: 20 -->
en:retardation
n1=en:photosensitivity in one-third of patients | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:physical disability ---
r_associated #0: 20 -->
en:retardation
n1=en:physical disability | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pick bodies found in neocortical layers, granule cells of the dentate gyrus, and throughout the hippocampus ---
r_associated #0: 20 -->
en:retardation
n1=en:pick bodies found in neocortical layers, granule cells of the dentate gyrus, and throughout the hippocampus | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pigmentary loss in the substantia nigra ---
r_associated #0: 20 -->
en:retardation
n1=en:pigmentary loss in the substantia nigra | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pilonidal cyst/fistula ---
r_associated #0: 20 -->
en:retardation
n1=en:pilonidal cyst/fistula | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pineal gland ---
r_associated #0: 20 -->
en:retardation
n1=en:pineal gland | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pineal hypertrophy ---
r_associated #0: 20 -->
en:retardation
n1=en:pineal hypertrophy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pitt-hopkins syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:pitt-hopkins syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pituitary agenesis ---
r_associated #0: 20 -->
en:retardation
n1=en:pituitary agenesis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pituitary agenesis (rare) ---
r_associated #0: 20 -->
en:retardation
n1=en:pituitary agenesis (rare) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pituitary aplasia or dysplasia ---
r_associated #0: 20 -->
en:retardation
n1=en:pituitary aplasia or dysplasia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pituitary gland adenoma ---
r_associated #0: 20 -->
en:retardation
n1=en:pituitary gland adenoma | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pituitary gland hypoplasia ---
r_associated #0: 20 -->
en:retardation
n1=en:pituitary gland hypoplasia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pituitary hypoplasia (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:pituitary hypoplasia (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pityriasis rosea ---
r_associated #0: 20 -->
en:retardation
n1=en:pityriasis rosea | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:plaque, amyloid ---
r_associated #0: 20 -->
en:retardation
n1=en:plaque, amyloid | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:platybasia ---
r_associated #0: 20 -->
en:retardation
n1=en:platybasia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pleural effusion ---
r_associated #0: 20 -->
en:retardation
n1=en:pleural effusion | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pleurisy with pleural effusion ---
r_associated #0: 20 -->
en:retardation
n1=en:pleurisy with pleural effusion | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pneumonia ---
r_associated #0: 20 -->
en:retardation
n1=en:pneumonia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:poisoning by medical agent ---
r_associated #0: 20 -->
en:retardation
n1=en:poisoning by medical agent | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:poliomyelitis/other enterovirus ---
r_associated #0: 20 -->
en:retardation
n1=en:poliomyelitis/other enterovirus | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:polycystic kidney disease ---
r_associated #0: 20 -->
en:retardation
n1=en:polycystic kidney disease | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:polyglucosan bodies (round intracellular inclusions) found in neuronal and astrocytic processes ---
r_associated #0: 20 -->
en:retardation
n1=en:polyglucosan bodies (round intracellular inclusions) found in neuronal and astrocytic processes | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:polygyria ---
r_associated #0: 20 -->
en:retardation
n1=en:polygyria | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:polymicrogyria ---
r_associated #0: 20 -->
en:retardation
n1=en:polymicrogyria | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:polymicrogyria (64%) ---
r_associated #0: 20 -->
en:retardation
n1=en:polymicrogyria (64%) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:polymicrogyria (meb) ---
r_associated #0: 20 -->
en:retardation
n1=en:polymicrogyria (meb) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:polymicrogyria (rare) ---
r_associated #0: 20 -->
en:retardation
n1=en:polymicrogyria (rare) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:polymicrogyria (reported in 1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:polymicrogyria (reported in 1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:polymicrogyria, anterior to posterior gradient ---
r_associated #0: 20 -->
en:retardation
n1=en:polymicrogyria, anterior to posterior gradient | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:polymicrogyria, asymmetric or symmetric ---
r_associated #0: 20 -->
en:retardation
n1=en:polymicrogyria, asymmetric or symmetric | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:polymicrogyria, bilateral frontoparietal ---
r_associated #0: 20 -->
en:retardation
n1=en:polymicrogyria, bilateral frontoparietal | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:polymicrogyria, diffuse, asymmetric ---
r_associated #0: 20 -->
en:retardation
n1=en:polymicrogyria, diffuse, asymmetric | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:polymicrogyria, frontal ---
r_associated #0: 20 -->
en:retardation
n1=en:polymicrogyria, frontal | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:polymicrogyria, most severe in the frontoparietal regions ---
r_associated #0: 20 -->
en:retardation
n1=en:polymicrogyria, most severe in the frontoparietal regions | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:polymicrogyria, occipital ---
r_associated #0: 20 -->
en:retardation
n1=en:polymicrogyria, occipital | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:polymicrogyria, predominantly frontal and perisylvian ---
r_associated #0: 20 -->
en:retardation
n1=en:polymicrogyria, predominantly frontal and perisylvian | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:polymicrogyria, symmetric or asymmetric ---
r_associated #0: 20 -->
en:retardation
n1=en:polymicrogyria, symmetric or asymmetric | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:polymicrogyria, temporo-occipital ---
r_associated #0: 20 -->
en:retardation
n1=en:polymicrogyria, temporo-occipital | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:polymicrogyria, usually frontal (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:polymicrogyria, usually frontal (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:polyneuropathies, motor ---
r_associated #0: 20 -->
en:retardation
n1=en:polyneuropathies, motor | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:polyneuropathy ---
r_associated #0: 20 -->
en:retardation
n1=en:polyneuropathy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:polysyndactyly ---
r_associated #0: 20 -->
en:retardation
n1=en:polysyndactyly | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pons damage ---
r_associated #0: 20 -->
en:retardation
n1=en:pons damage | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pontine atrophy ---
r_associated #0: 20 -->
en:retardation
n1=en:pontine atrophy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pontine dysraphia ---
r_associated #0: 20 -->
en:retardation
n1=en:pontine dysraphia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pontine hypoplasia (1 family) ---
r_associated #0: 20 -->
en:retardation
n1=en:pontine hypoplasia (1 family) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pontine hypoplasia, mild ---
r_associated #0: 20 -->
en:retardation
n1=en:pontine hypoplasia, mild | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pontocerebellar arachnoid cyst (reported in 2 patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:pontocerebellar arachnoid cyst (reported in 2 patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pontocerebellar atrophy ---
r_associated #0: 20 -->
en:retardation
n1=en:pontocerebellar atrophy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pontocerebellar hypoplasia type 1 ---
r_associated #0: 20 -->
en:retardation
n1=en:pontocerebellar hypoplasia type 1 | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pontocerebellar hypoplasia, type 8 ---
r_associated #0: 20 -->
en:retardation
n1=en:pontocerebellar hypoplasia, type 8 | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pontoneocerebellar hypoplasia ---
r_associated #0: 20 -->
en:retardation
n1=en:pontoneocerebellar hypoplasia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:poor adaptation to disability ---
r_associated #0: 20 -->
en:retardation
n1=en:poor adaptation to disability | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:poor adaptive skills ---
r_associated #0: 20 -->
en:retardation
n1=en:poor adaptive skills | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:poor balance (finding) ---
r_associated #0: 20 -->
en:retardation
n1=en:poor balance (finding) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:poor cognition ---
r_associated #0: 20 -->
en:retardation
n1=en:poor cognition | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:poor communication ---
r_associated #0: 20 -->
en:retardation
n1=en:poor communication | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:poor concentration ---
r_associated #0: 20 -->
en:retardation
n1=en:poor concentration | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:poor coordination ---
r_associated #0: 20 -->
en:retardation
n1=en:poor coordination | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:poor coordination (83%) ---
r_associated #0: 20 -->
en:retardation
n1=en:poor coordination (83%) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:poor delineation of cerebral cortical regions ---
r_associated #0: 20 -->
en:retardation
n1=en:poor delineation of cerebral cortical regions | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:poor dendritic maturation ---
r_associated #0: 20 -->
en:retardation
n1=en:poor dendritic maturation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:poor differentiation of gray and white matter on t2-weighted mri ---
r_associated #0: 20 -->
en:retardation
n1=en:poor differentiation of gray and white matter on t2-weighted mri | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:poor eye contact ---
r_associated #0: 20 -->
en:retardation
n1=en:poor eye contact | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:poor feeding (congenital form form) ---
r_associated #0: 20 -->
en:retardation
n1=en:poor feeding (congenital form form) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:poor fine and gross motor coordination ---
r_associated #0: 20 -->
en:retardation
n1=en:poor fine and gross motor coordination | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:poor fine motor coordination ---
r_associated #0: 20 -->
en:retardation
n1=en:poor fine motor coordination | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:poor fine motor skills ---
r_associated #0: 20 -->
en:retardation
n1=en:poor fine motor skills | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:poor gross motor coordination ---
r_associated #0: 20 -->
en:retardation
n1=en:poor gross motor coordination | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:poor hand-eye coordination ---
r_associated #0: 20 -->
en:retardation
n1=en:poor hand-eye coordination | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:poor head and trunk control in infancy ---
r_associated #0: 20 -->
en:retardation
n1=en:poor head and trunk control in infancy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:poor head control ---
r_associated #0: 20 -->
en:retardation
n1=en:poor head control | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:poor language ---
r_associated #0: 20 -->
en:retardation
n1=en:poor language | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:poor language and speech development ---
r_associated #0: 20 -->
en:retardation
n1=en:poor language and speech development | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:poor motor coordination ---
r_associated #0: 20 -->
en:retardation
n1=en:poor motor coordination | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:poor motor development ---
r_associated #0: 20 -->
en:retardation
n1=en:poor motor development | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:poor myelination ---
r_associated #0: 20 -->
en:retardation
n1=en:poor myelination | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:poor neonatal suck and swallow reflexes ---
r_associated #0: 20 -->
en:retardation
n1=en:poor neonatal suck and swallow reflexes | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:poor or absent independent walking ---
r_associated #0: 20 -->
en:retardation
n1=en:poor or absent independent walking | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:poor or absent smooth pursuit ---
r_associated #0: 20 -->
en:retardation
n1=en:poor or absent smooth pursuit | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:poor or absent speech ---
r_associated #0: 20 -->
en:retardation
n1=en:poor or absent speech | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:poor or absent speech acquisition ---
r_associated #0: 20 -->
en:retardation
n1=en:poor or absent speech acquisition | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:poor or absent speech development ---
r_associated #0: 20 -->
en:retardation
n1=en:poor or absent speech development | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:poor responsiveness ---
r_associated #0: 20 -->
en:retardation
n1=en:poor responsiveness | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:poor school performance ---
r_associated #0: 20 -->
en:retardation
n1=en:poor school performance | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:poor speech ---
r_associated #0: 20 -->
en:retardation
n1=en:poor speech | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:poor speech or lack of speech development ---
r_associated #0: 20 -->
en:retardation
n1=en:poor speech or lack of speech development | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:poor speech or no speech ---
r_associated #0: 20 -->
en:retardation
n1=en:poor speech or no speech | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:poor spontaneous movements ---
r_associated #0: 20 -->
en:retardation
n1=en:poor spontaneous movements | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:poor vestibuloocular reflex ---
r_associated #0: 20 -->
en:retardation
n1=en:poor vestibuloocular reflex | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:poor visual-motor integration (range 41-80) ---
r_associated #0: 20 -->
en:retardation
n1=en:poor visual-motor integration (range 41-80) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:poor visual-spatial construction ---
r_associated #0: 20 -->
en:retardation
n1=en:poor visual-spatial construction | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:poor-absent neurologic development ---
r_associated #0: 20 -->
en:retardation
n1=en:poor-absent neurologic development | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:porencephalic changes ---
r_associated #0: 20 -->
en:retardation
n1=en:porencephalic changes | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:porencephalic cyst ---
r_associated #0: 20 -->
en:retardation
n1=en:porencephalic cyst | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:porencephaly (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:porencephaly (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:porencephaly, familial ---
r_associated #0: 20 -->
en:retardation
n1=en:porencephaly, familial | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:posterior column degeneration ---
r_associated #0: 20 -->
en:retardation
n1=en:posterior column degeneration | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:posterior column sensory loss ---
r_associated #0: 20 -->
en:retardation
n1=en:posterior column sensory loss | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:posterior fossa abnormalities (rare) ---
r_associated #0: 20 -->
en:retardation
n1=en:posterior fossa abnormalities (rare) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:posterior fossa arachnoid cyst ---
r_associated #0: 20 -->
en:retardation
n1=en:posterior fossa arachnoid cyst | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:posterior fossa compression syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:posterior fossa compression syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:posterior fossa crowding, progressive ---
r_associated #0: 20 -->
en:retardation
n1=en:posterior fossa crowding, progressive | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:posterior fossa cyst ---
r_associated #0: 20 -->
en:retardation
n1=en:posterior fossa cyst | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:posterior fossa cyst (in 1 of 2 patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:posterior fossa cyst (in 1 of 2 patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:posterior fossa cyst continuous with the fourth ventricle ---
r_associated #0: 20 -->
en:retardation
n1=en:posterior fossa cyst continuous with the fourth ventricle | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:posterior fossa cysts (wws) ---
r_associated #0: 20 -->
en:retardation
n1=en:posterior fossa cysts (wws) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:posterior fossa malformations ---
r_associated #0: 20 -->
en:retardation
n1=en:posterior fossa malformations | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:posterior pachygyria ---
r_associated #0: 20 -->
en:retardation
n1=en:posterior pachygyria | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:posterior slow-wave activity on eeg ---
r_associated #0: 20 -->
en:retardation
n1=en:posterior slow-wave activity on eeg | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:posterior urethral valve ---
r_associated #0: 20 -->
en:retardation
n1=en:posterior urethral valve | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:postnatal development of hypertonic extremities ---
r_associated #0: 20 -->
en:retardation
n1=en:postnatal development of hypertonic extremities | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:postural dystonia (onset is restricted to 1 extremity, usually lower, with foot dystonia) ---
r_associated #0: 20 -->
en:retardation
n1=en:postural dystonia (onset is restricted to 1 extremity, usually lower, with foot dystonia) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:postural hand tremor ---
r_associated #0: 20 -->
en:retardation
n1=en:postural hand tremor | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:postural instability ---
r_associated #0: 20 -->
en:retardation
n1=en:postural instability | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:postural instability (63%) ---
r_associated #0: 20 -->
en:retardation
n1=en:postural instability (63%) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:postural tremor (later onset, spreads to all limbs and neck) ---
r_associated #0: 20 -->
en:retardation
n1=en:postural tremor (later onset, spreads to all limbs and neck) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:postural tremor, slow, irregular (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:postural tremor, slow, irregular (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:posturing ---
r_associated #0: 20 -->
en:retardation
n1=en:posturing | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:prader-willi syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:prader-willi syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:praxis ---
r_associated #0: 20 -->
en:retardation
n1=en:praxis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pre-senile dementia ---
r_associated #0: 20 -->
en:retardation
n1=en:pre-senile dementia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:precocious puberty ---
r_associated #0: 20 -->
en:retardation
n1=en:precocious puberty | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pregnancy complications, infectious ---
r_associated #0: 20 -->
en:retardation
n1=en:pregnancy complications, infectious | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:premature birth of newborn ---
r_associated #0: 20 -->
en:retardation
n1=en:premature birth of newborn | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:premature epiphyseal fusion ---
r_associated #0: 20 -->
en:retardation
n1=en:premature epiphyseal fusion | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:premature stroke ---
r_associated #0: 20 -->
en:retardation
n1=en:premature stroke | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:premenstrual tension ---
r_associated #0: 20 -->
en:retardation
n1=en:premenstrual tension | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:prenatal disorder ---
r_associated #0: 20 -->
en:retardation
n1=en:prenatal disorder | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:presbycusis ---
r_associated #0: 20 -->
en:retardation
n1=en:presbycusis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:presence of rosenthal fibers (eosinophilic bodies near astrocyte filaments) ---
r_associated #0: 20 -->
en:retardation
n1=en:presence of rosenthal fibers (eosinophilic bodies near astrocyte filaments) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:presenile and senile dementia ---
r_associated #0: 20 -->
en:retardation
n1=en:presenile and senile dementia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:preservation of u fibers ---
r_associated #0: 20 -->
en:retardation
n1=en:preservation of u fibers | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:prieto x-linked mental retardation syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:prieto x-linked mental retardation syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:primarily affects distal lower limbs ---
r_associated #0: 20 -->
en:retardation
n1=en:primarily affects distal lower limbs | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:primitive reflex ---
r_associated #0: 20 -->
en:retardation
n1=en:primitive reflex | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:primitive reflexes (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:primitive reflexes (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:primitive reflexes (palmomental, snout, glabellar) ---
r_associated #0: 20 -->
en:retardation
n1=en:primitive reflexes (palmomental, snout, glabellar) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:primitive sylvian fissures ---
r_associated #0: 20 -->
en:retardation
n1=en:primitive sylvian fissures | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:primrose syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:primrose syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:prion protein-positive senile plaques ---
r_associated #0: 20 -->
en:retardation
n1=en:prion protein-positive senile plaques | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:prnp-immunoreactive cerebral amyloid angiopathy (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:prnp-immunoreactive cerebral amyloid angiopathy (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:profound global developmental delay ---
r_associated #0: 20 -->
en:retardation
n1=en:profound global developmental delay | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:profound intellectual disabilities ---
r_associated #0: 20 -->
en:retardation
n1=en:profound intellectual disabilities | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:profound mental retardation and hypotonia in survivors ---
r_associated #0: 20 -->
en:retardation
n1=en:profound mental retardation and hypotonia in survivors | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:progression to paralysis and atrophy of distal lower limb muscles ---
r_associated #0: 20 -->
en:retardation
n1=en:progression to paralysis and atrophy of distal lower limb muscles | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:progression to tetraplegia and decerebrate state ---
r_associated #0: 20 -->
en:retardation
n1=en:progression to tetraplegia and decerebrate state | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:progressive ataxia (onset second year of life) ---
r_associated #0: 20 -->
en:retardation
n1=en:progressive ataxia (onset second year of life) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:progressive bulbar palsy ---
r_associated #0: 20 -->
en:retardation
n1=en:progressive bulbar palsy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:progressive cerebellar ataxia ---
r_associated #0: 20 -->
en:retardation
n1=en:progressive cerebellar ataxia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:progressive cerebellar degeneration ---
r_associated #0: 20 -->
en:retardation
n1=en:progressive cerebellar degeneration | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:progressive cerebral atrophy seen on mri ---
r_associated #0: 20 -->
en:retardation
n1=en:progressive cerebral atrophy seen on mri | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:progressive choreoathetosis ---
r_associated #0: 20 -->
en:retardation
n1=en:progressive choreoathetosis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:progressive cns degeneration ---
r_associated #0: 20 -->
en:retardation
n1=en:progressive cns degeneration | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:progressive cognitive decline following normal development in childhood (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:progressive cognitive decline following normal development in childhood (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:progressive encephalopathy ---
r_associated #0: 20 -->
en:retardation
n1=en:progressive encephalopathy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:progressive extrapyramidal movement disorder ---
r_associated #0: 20 -->
en:retardation
n1=en:progressive extrapyramidal movement disorder | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:progressive forgetfulness ---
r_associated #0: 20 -->
en:retardation
n1=en:progressive forgetfulness | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:progressive gait ataxia ---
r_associated #0: 20 -->
en:retardation
n1=en:progressive gait ataxia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:progressive impairment of gait ---
r_associated #0: 20 -->
en:retardation
n1=en:progressive impairment of gait | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:progressive inability to walk ---
r_associated #0: 20 -->
en:retardation
n1=en:progressive inability to walk | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:progressive intellectual decline ---
r_associated #0: 20 -->
en:retardation
n1=en:progressive intellectual decline | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:progressive language deterioration ---
r_associated #0: 20 -->
en:retardation
n1=en:progressive language deterioration | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:progressive leukoencephalopathy ---
r_associated #0: 20 -->
en:retardation
n1=en:progressive leukoencephalopathy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:progressive loss of movement control ---
r_associated #0: 20 -->
en:retardation
n1=en:progressive loss of movement control | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:progressive myoclonus epilepsy ---
r_associated #0: 20 -->
en:retardation
n1=en:progressive myoclonus epilepsy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:progressive neurologic deterioration ---
r_associated #0: 20 -->
en:retardation
n1=en:progressive neurologic deterioration | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:progressive psychomotor deterioration ---
r_associated #0: 20 -->
en:retardation
n1=en:progressive psychomotor deterioration | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:progressive pyramidal and cerebellar signs ---
r_associated #0: 20 -->
en:retardation
n1=en:progressive pyramidal and cerebellar signs | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:progressive spastic diplegia to quadriplegia ---
r_associated #0: 20 -->
en:retardation
n1=en:progressive spastic diplegia to quadriplegia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:progressive spastic paraplegia ---
r_associated #0: 20 -->
en:retardation
n1=en:progressive spastic paraplegia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:progressive spastic quadriplegia ---
r_associated #0: 20 -->
en:retardation
n1=en:progressive spastic quadriplegia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:progressive spasticity ---
r_associated #0: 20 -->
en:retardation
n1=en:progressive spasticity | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:progressive truncal ataxia ---
r_associated #0: 20 -->
en:retardation
n1=en:progressive truncal ataxia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:progressive ventriculomegaly ---
r_associated #0: 20 -->
en:retardation
n1=en:progressive ventriculomegaly | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:progressive white matter lesions in the brain ---
r_associated #0: 20 -->
en:retardation
n1=en:progressive white matter lesions in the brain | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:progressive, symmetric degeneration of the caudate and putamen ---
r_associated #0: 20 -->
en:retardation
n1=en:progressive, symmetric degeneration of the caudate and putamen | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:prolonged seizure ---
r_associated #0: 20 -->
en:retardation
n1=en:prolonged seizure | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:prolonged somatosensory evoked potentials (seps) ---
r_associated #0: 20 -->
en:retardation
n1=en:prolonged somatosensory evoked potentials (seps) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:prominent cortical sulci ---
r_associated #0: 20 -->
en:retardation
n1=en:prominent cortical sulci | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:prominent csf spaces (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:prominent csf spaces (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:prominent perivascular spaces ---
r_associated #0: 20 -->
en:retardation
n1=en:prominent perivascular spaces | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:prominent perivascular spaces with surrounding gliosis in periatrial white matter ---
r_associated #0: 20 -->
en:retardation
n1=en:prominent perivascular spaces with surrounding gliosis in periatrial white matter | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:prominent sulci ---
r_associated #0: 20 -->
en:retardation
n1=en:prominent sulci | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:prominent trigone and occipital horns ---
r_associated #0: 20 -->
en:retardation
n1=en:prominent trigone and occipital horns | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:prominent ventricles (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:prominent ventricles (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:prosoposchisis ---
r_associated #0: 20 -->
en:retardation
n1=en:prosoposchisis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:prostatitis/seminal vesiculitis ---
r_associated #0: 20 -->
en:retardation
n1=en:prostatitis/seminal vesiculitis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:proximal amyotrophy ---
r_associated #0: 20 -->
en:retardation
n1=en:proximal amyotrophy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:proximal limb muscle stiffness ---
r_associated #0: 20 -->
en:retardation
n1=en:proximal limb muscle stiffness | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:proximal muscle weakness ---
r_associated #0: 20 -->
en:retardation
n1=en:proximal muscle weakness | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:proximal muscle weakness in lower limbs ---
r_associated #0: 20 -->
en:retardation
n1=en:proximal muscle weakness in lower limbs | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:proximal weakness occurs first ---
r_associated #0: 20 -->
en:retardation
n1=en:proximal weakness occurs first | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:proximal weakness occurs later ---
r_associated #0: 20 -->
en:retardation
n1=en:proximal weakness occurs later | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:proximal weakness of the lower extremities ---
r_associated #0: 20 -->
en:retardation
n1=en:proximal weakness of the lower extremities | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:prp immunoreactivity limited to cerebellum and putamen ---
r_associated #0: 20 -->
en:retardation
n1=en:prp immunoreactivity limited to cerebellum and putamen | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pseudo-hurler polydystrophy ---
r_associated #0: 20 -->
en:retardation
n1=en:pseudo-hurler polydystrophy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pseudobulbar palsy ---
r_associated #0: 20 -->
en:retardation
n1=en:pseudobulbar palsy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pseudobulbar palsy (e.g. involuntary weeping or laughter) ---
r_associated #0: 20 -->
en:retardation
n1=en:pseudobulbar palsy (e.g. involuntary weeping or laughter) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pseudobulbar signs ---
r_associated #0: 20 -->
en:retardation
n1=en:pseudobulbar signs | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pseudobulbar symptoms (uncontrolled laughter, weeping) ---
r_associated #0: 20 -->
en:retardation
n1=en:pseudobulbar symptoms (uncontrolled laughter, weeping) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pseudohypoparathyroidism type 1c ---
r_associated #0: 20 -->
en:retardation
n1=en:pseudohypoparathyroidism type 1c | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pseudolaminar spongiform changes ---
r_associated #0: 20 -->
en:retardation
n1=en:pseudolaminar spongiform changes | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pseudotumor ---
r_associated #0: 20 -->
en:retardation
n1=en:pseudotumor | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pseudotumor cerebri ---
r_associated #0: 20 -->
en:retardation
n1=en:pseudotumor cerebri | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:psoriasis ---
r_associated #0: 20 -->
en:retardation
n1=en:psoriasis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:psychiatric and behavioural symptoms nec ---
r_associated #0: 20 -->
en:retardation
n1=en:psychiatric and behavioural symptoms nec | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:psychiatric behavioral disability ---
r_associated #0: 20 -->
en:retardation
n1=en:psychiatric behavioral disability | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:psychiatric disorder ---
r_associated #0: 20 -->
en:retardation
n1=en:psychiatric disorder | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:psychiatric disorders nec ---
r_associated #0: 20 -->
en:retardation
n1=en:psychiatric disorders nec | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:psychiatric problem ---
r_associated #0: 20 -->
en:retardation
n1=en:psychiatric problem | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:psychiatric symptoms (delusions, hallucinations) ---
r_associated #0: 20 -->
en:retardation
n1=en:psychiatric symptoms (delusions, hallucinations) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:psychic disease ---
r_associated #0: 20 -->
en:retardation
n1=en:psychic disease | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:psychic factors associated with diseases classified elsewhere ---
r_associated #0: 20 -->
en:retardation
n1=en:psychic factors associated with diseases classified elsewhere | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:psychomotor agitation ---
r_associated #0: 20 -->
en:retardation
n1=en:psychomotor agitation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:psychomotor arrest and regression ---
r_associated #0: 20 -->
en:retardation
n1=en:psychomotor arrest and regression | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:psychomotor delay (evident at 3 months) ---
r_associated #0: 20 -->
en:retardation
n1=en:psychomotor delay (evident at 3 months) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:psychomotor delay (in one family) ---
r_associated #0: 20 -->
en:retardation
n1=en:psychomotor delay (in one family) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:psychomotor delay (rare) ---
r_associated #0: 20 -->
en:retardation
n1=en:psychomotor delay (rare) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:psychomotor delay after second year ---
r_associated #0: 20 -->
en:retardation
n1=en:psychomotor delay after second year | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:psychomotor delay, mild to moderate ---
r_associated #0: 20 -->
en:retardation
n1=en:psychomotor delay, mild to moderate | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:psychomotor delay, severe ---
r_associated #0: 20 -->
en:retardation
n1=en:psychomotor delay, severe | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:psychomotor deterioration ---
r_associated #0: 20 -->
en:retardation
n1=en:psychomotor deterioration | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:psychomotor deterioration (classical form) ---
r_associated #0: 20 -->
en:retardation
n1=en:psychomotor deterioration (classical form) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:psychomotor disorders ---
r_associated #0: 20 -->
en:retardation
n1=en:psychomotor disorders | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:psychomotor impairments ---
r_associated #0: 20 -->
en:retardation
n1=en:psychomotor impairments | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:psychomotor regression ---
r_associated #0: 20 -->
en:retardation
n1=en:psychomotor regression | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:psychomotor regression (in milder cases) ---
r_associated #0: 20 -->
en:retardation
n1=en:psychomotor regression (in milder cases) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:psychomotor regression (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:psychomotor regression (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:psychomotor regression (in some) ---
r_associated #0: 20 -->
en:retardation
n1=en:psychomotor regression (in some) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:psychomotor regression (onset within first year of life) ---
r_associated #0: 20 -->
en:retardation
n1=en:psychomotor regression (onset within first year of life) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:psychomotor regression beginning in infancy ---
r_associated #0: 20 -->
en:retardation
n1=en:psychomotor regression beginning in infancy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:psychomotor regression in infants ---
r_associated #0: 20 -->
en:retardation
n1=en:psychomotor regression in infants | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:psychomotor regression may occur ---
r_associated #0: 20 -->
en:retardation
n1=en:psychomotor regression may occur | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:psychomotor regression, episodic, often associated with common childhood infections ---
r_associated #0: 20 -->
en:retardation
n1=en:psychomotor regression, episodic, often associated with common childhood infections | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:psychomotor regression, progressive ---
r_associated #0: 20 -->
en:retardation
n1=en:psychomotor regression, progressive | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:psychomotor regression, severe ---
r_associated #0: 20 -->
en:retardation
n1=en:psychomotor regression, severe | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:psychomotor retardation ---
r_associated #0: 20 -->
en:retardation
n1=en:psychomotor retardation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:psychomotor retardation (2/4 patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:psychomotor retardation (2/4 patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:psychomotor retardation (in 1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:psychomotor retardation (in 1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:psychomotor retardation (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:psychomotor retardation (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:psychomotor retardation in those that survive ---
r_associated #0: 20 -->
en:retardation
n1=en:psychomotor retardation in those that survive | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:psychomotor retardation, mild ---
r_associated #0: 20 -->
en:retardation
n1=en:psychomotor retardation, mild | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:psychomotor retardation, mild to moderate ---
r_associated #0: 20 -->
en:retardation
n1=en:psychomotor retardation, mild to moderate | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:psychomotor retardation, moderate ---
r_associated #0: 20 -->
en:retardation
n1=en:psychomotor retardation, moderate | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:psychomotor retardation, profound ---
r_associated #0: 20 -->
en:retardation
n1=en:psychomotor retardation, profound | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:psychomotor retardation, profound, in those who survive ---
r_associated #0: 20 -->
en:retardation
n1=en:psychomotor retardation, profound, in those who survive | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:psychomotor retardation, severe to profound ---
r_associated #0: 20 -->
en:retardation
n1=en:psychomotor retardation, severe to profound | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:psychomotor retardation, variable ---
r_associated #0: 20 -->
en:retardation
n1=en:psychomotor retardation, variable | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:psychoneuropathy nos ---
r_associated #0: 20 -->
en:retardation
n1=en:psychoneuropathy nos | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:psychopathology ---
r_associated #0: 20 -->
en:retardation
n1=en:psychopathology | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:psychophysiologic disorders ---
r_associated #0: 20 -->
en:retardation
n1=en:psychophysiologic disorders | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:psychosexual disorders ---
r_associated #0: 20 -->
en:retardation
n1=en:psychosexual disorders | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:psychosis ---
r_associated #0: 20 -->
en:retardation
n1=en:psychosis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:psychosis (rare) ---
r_associated #0: 20 -->
en:retardation
n1=en:psychosis (rare) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:psychosis with origin in childhood ---
r_associated #0: 20 -->
en:retardation
n1=en:psychosis with origin in childhood | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:psychotic episodes ---
r_associated #0: 20 -->
en:retardation
n1=en:psychotic episodes | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pterygium colli ---
r_associated #0: 20 -->
en:retardation
n1=en:pterygium colli | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:puerperal infection/sepsis ---
r_associated #0: 20 -->
en:retardation
n1=en:puerperal infection/sepsis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pulmonary embolism ---
r_associated #0: 20 -->
en:retardation
n1=en:pulmonary embolism | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pulmonary emphysema ---
r_associated #0: 20 -->
en:retardation
n1=en:pulmonary emphysema | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pulmonary tuberculosis ---
r_associated #0: 20 -->
en:retardation
n1=en:pulmonary tuberculosis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pulsating quality ---
r_associated #0: 20 -->
en:retardation
n1=en:pulsating quality | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:purposeless movements (if left untreated) ---
r_associated #0: 20 -->
en:retardation
n1=en:purposeless movements (if left untreated) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:purpura/coagulation defects/abnormal platelets ---
r_associated #0: 20 -->
en:retardation
n1=en:purpura/coagulation defects/abnormal platelets | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:putamen atrophy ---
r_associated #0: 20 -->
en:retardation
n1=en:putamen atrophy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pyelonephritis/pyelitis acute ---
r_associated #0: 20 -->
en:retardation
n1=en:pyelonephritis/pyelitis acute | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pyloric stenosis ---
r_associated #0: 20 -->
en:retardation
n1=en:pyloric stenosis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pyramidal features (rare) ---
r_associated #0: 20 -->
en:retardation
n1=en:pyramidal features (rare) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pyramidal hypertonia ---
r_associated #0: 20 -->
en:retardation
n1=en:pyramidal hypertonia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pyramidal sign ---
r_associated #0: 20 -->
en:retardation
n1=en:pyramidal sign | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pyramidal signs (1 family) ---
r_associated #0: 20 -->
en:retardation
n1=en:pyramidal signs (1 family) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pyramidal signs (1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:pyramidal signs (1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pyramidal signs (21% of patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:pyramidal signs (21% of patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pyramidal signs (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:pyramidal signs (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pyramidal signs (in some) ---
r_associated #0: 20 -->
en:retardation
n1=en:pyramidal signs (in some) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pyramidal signs (less common) ---
r_associated #0: 20 -->
en:retardation
n1=en:pyramidal signs (less common) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pyramidal signs, mild ---
r_associated #0: 20 -->
en:retardation
n1=en:pyramidal signs, mild | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pyramidal signs, mild (uncommon) ---
r_associated #0: 20 -->
en:retardation
n1=en:pyramidal signs, mild (uncommon) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pyramidal symptoms ---
r_associated #0: 20 -->
en:retardation
n1=en:pyramidal symptoms | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pyramidal syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:pyramidal syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pyramidal syndrome of the lower limbs ---
r_associated #0: 20 -->
en:retardation
n1=en:pyramidal syndrome of the lower limbs | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pyramidal system ---
r_associated #0: 20 -->
en:retardation
n1=en:pyramidal system | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pyramidal tetraparesis ---
r_associated #0: 20 -->
en:retardation
n1=en:pyramidal tetraparesis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pyramidal tract dysfunction (juvenile-onset, less common) ---
r_associated #0: 20 -->
en:retardation
n1=en:pyramidal tract dysfunction (juvenile-onset, less common) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pyramidal tract involvement ---
r_associated #0: 20 -->
en:retardation
n1=en:pyramidal tract involvement | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pyramidal tract signs (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:pyramidal tract signs (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pyruvate carboxylase deficiency ---
r_associated #0: 20 -->
en:retardation
n1=en:pyruvate carboxylase deficiency | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pyruvate dehydrogenase e3-binding protein deficiency ---
r_associated #0: 20 -->
en:retardation
n1=en:pyruvate dehydrogenase e3-binding protein deficiency | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:pyruvate dehydrogenase phosphatase deficiency ---
r_associated #0: 20 -->
en:retardation
n1=en:pyruvate dehydrogenase phosphatase deficiency | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:quadriparesis ---
r_associated #0: 20 -->
en:retardation
n1=en:quadriparesis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:quadriplegia ---
r_associated #0: 20 -->
en:retardation
n1=en:quadriplegia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:quadriplegia, episodic ---
r_associated #0: 20 -->
en:retardation
n1=en:quadriplegia, episodic | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:quadriplegia, flaccid ---
r_associated #0: 20 -->
en:retardation
n1=en:quadriplegia, flaccid | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:quadriplegic dyskinesia ---
r_associated #0: 20 -->
en:retardation
n1=en:quadriplegic dyskinesia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:quadrupedal gait ---
r_associated #0: 20 -->
en:retardation
n1=en:quadrupedal gait | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:quadrupedal gait (in some) ---
r_associated #0: 20 -->
en:retardation
n1=en:quadrupedal gait (in some) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:quadrupedal gait (palm of hands, legs straight) with diagonal walking ---
r_associated #0: 20 -->
en:retardation
n1=en:quadrupedal gait (palm of hands, legs straight) with diagonal walking | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:quadrupedal locomotion (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:quadrupedal locomotion (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ramon syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:ramon syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ramos arroyo clark syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:ramos arroyo clark syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:rapid complete resolution of symptoms ---
r_associated #0: 20 -->
en:retardation
n1=en:rapid complete resolution of symptoms | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:rapid initial onset of symptoms (hours to weeks) ---
r_associated #0: 20 -->
en:retardation
n1=en:rapid initial onset of symptoms (hours to weeks) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:rapid onset ---
r_associated #0: 20 -->
en:retardation
n1=en:rapid onset | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:rapid regression ---
r_associated #0: 20 -->
en:retardation
n1=en:rapid regression | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:rapid, instantaneous neurologic decline may occur after fright ---
r_associated #0: 20 -->
en:retardation
n1=en:rapid, instantaneous neurologic decline may occur after fright | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:rapid, jerky movements ---
r_associated #0: 20 -->
en:retardation
n1=en:rapid, jerky movements | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:rapidly progressive brainstem degeneration ---
r_associated #0: 20 -->
en:retardation
n1=en:rapidly progressive brainstem degeneration | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:rare dementia ---
r_associated #0: 20 -->
en:retardation
n1=en:rare dementia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:rare secondary generalization ---
r_associated #0: 20 -->
en:retardation
n1=en:rare secondary generalization | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:reactive attachment disorder of infancy or early childhood ---
r_associated #0: 20 -->
en:retardation
n1=en:reactive attachment disorder of infancy or early childhood | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:reactive gliosis ---
r_associated #0: 20 -->
en:retardation
n1=en:reactive gliosis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:recurrent bacterial meningitis ---
r_associated #0: 20 -->
en:retardation
n1=en:recurrent bacterial meningitis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:recurrent encephalopathy ---
r_associated #0: 20 -->
en:retardation
n1=en:recurrent encephalopathy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:recurrent meningitis ---
r_associated #0: 20 -->
en:retardation
n1=en:recurrent meningitis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:recurrent muscle twitches (symptom) ---
r_associated #0: 20 -->
en:retardation
n1=en:recurrent muscle twitches (symptom) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:recurrent seizures nos ---
r_associated #0: 20 -->
en:retardation
n1=en:recurrent seizures nos | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:recurrent subcortical infarcts (strokes) ---
r_associated #0: 20 -->
en:retardation
n1=en:recurrent subcortical infarcts (strokes) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:reduced brain gyri ---
r_associated #0: 20 -->
en:retardation
n1=en:reduced brain gyri | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:reduced brain size ---
r_associated #0: 20 -->
en:retardation
n1=en:reduced brain size | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:reduced cerebral white matter ---
r_associated #0: 20 -->
en:retardation
n1=en:reduced cerebral white matter | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:reduced concentration span ---
r_associated #0: 20 -->
en:retardation
n1=en:reduced concentration span | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:reduced consciousness ---
r_associated #0: 20 -->
en:retardation
n1=en:reduced consciousness | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:reduced consciousness, hypoglycemia-related ---
r_associated #0: 20 -->
en:retardation
n1=en:reduced consciousness, hypoglycemia-related | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:reduced numbers of neurons ---
r_associated #0: 20 -->
en:retardation
n1=en:reduced numbers of neurons | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:reduced posterior white matter volume (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:reduced posterior white matter volume (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:reduced size of the pituitary gland ---
r_associated #0: 20 -->
en:retardation
n1=en:reduced size of the pituitary gland | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:reduced sleep latency ---
r_associated #0: 20 -->
en:retardation
n1=en:reduced sleep latency | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:reduced tendon reflexes ---
r_associated #0: 20 -->
en:retardation
n1=en:reduced tendon reflexes | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:reduced white matter ---
r_associated #0: 20 -->
en:retardation
n1=en:reduced white matter | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:reduced white matter volume ---
r_associated #0: 20 -->
en:retardation
n1=en:reduced white matter volume | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:reduction of white matter, generalized ---
r_associated #0: 20 -->
en:retardation
n1=en:reduction of white matter, generalized | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:reduction or loss of acquired skills (e.g., purposeful hand use, speech) ---
r_associated #0: 20 -->
en:retardation
n1=en:reduction or loss of acquired skills (e.g., purposeful hand use, speech) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:redundant prepuce and phimosis ---
r_associated #0: 20 -->
en:retardation
n1=en:redundant prepuce and phimosis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:reflex epilepsy, photosensitive ---
r_associated #0: 20 -->
en:retardation
n1=en:reflex epilepsy, photosensitive | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:reflex, deep tendon, absent ---
r_associated #0: 20 -->
en:retardation
n1=en:reflex, deep tendon, absent | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:refractive error ---
r_associated #0: 20 -->
en:retardation
n1=en:refractive error | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:registered disabled ---
r_associated #0: 20 -->
en:retardation
n1=en:registered disabled | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:regression of development ---
r_associated #0: 20 -->
en:retardation
n1=en:regression of development | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:regression of early motor skills ---
r_associated #0: 20 -->
en:retardation
n1=en:regression of early motor skills | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:regression of motor development ---
r_associated #0: 20 -->
en:retardation
n1=en:regression of motor development | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:relative preservation of purkinje cells, but they are deformed and disaligned ---
r_associated #0: 20 -->
en:retardation
n1=en:relative preservation of purkinje cells, but they are deformed and disaligned | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:relative preservation of the cerebellar folia ---
r_associated #0: 20 -->
en:retardation
n1=en:relative preservation of the cerebellar folia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:relative preservation of the cerebellum ---
r_associated #0: 20 -->
en:retardation
n1=en:relative preservation of the cerebellum | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:relative sparing of language ---
r_associated #0: 20 -->
en:retardation
n1=en:relative sparing of language | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:relief with motor activation ---
r_associated #0: 20 -->
en:retardation
n1=en:relief with motor activation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:rem sleep behavior disorder ---
r_associated #0: 20 -->
en:retardation
n1=en:rem sleep behavior disorder | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:renal tubular acidosis, proximal, with ocular abnormalities and mental retardation ---
r_associated #0: 20 -->
en:retardation
n1=en:renal tubular acidosis, proximal, with ocular abnormalities and mental retardation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:renpenning syndrome 1 ---
r_associated #0: 20 -->
en:retardation
n1=en:renpenning syndrome 1 | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:residual ataxia ---
r_associated #0: 20 -->
en:retardation
n1=en:residual ataxia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:response to pyridoxal phosphate ---
r_associated #0: 20 -->
en:retardation
n1=en:response to pyridoxal phosphate | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:resting myoclonus ---
r_associated #0: 20 -->
en:retardation
n1=en:resting myoclonus | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:resting tremor (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:resting tremor (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:resting tremors ---
r_associated #0: 20 -->
en:retardation
n1=en:resting tremors | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:restlessness at birth ---
r_associated #0: 20 -->
en:retardation
n1=en:restlessness at birth | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:restrictive behavior, interests, and activities ---
r_associated #0: 20 -->
en:retardation
n1=en:restrictive behavior, interests, and activities | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:results in nocturnal insomnia and chronic sleep deprivation ---
r_associated #0: 20 -->
en:retardation
n1=en:results in nocturnal insomnia and chronic sleep deprivation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:retardations, psychosocial mental ---
r_associated #0: 20 -->
en:retardation
n1=en:retardations, psychosocial mental | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:retinal detachment ---
r_associated #0: 20 -->
en:retardation
n1=en:retinal detachment | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:retinitis pigmentosa, deafness, mental retardation, and hypogonadism ---
r_associated #0: 20 -->
en:retardation
n1=en:retinitis pigmentosa, deafness, mental retardation, and hypogonadism | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:retinopathy ---
r_associated #0: 20 -->
en:retardation
n1=en:retinopathy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:retrocerebellar cyst ---
r_associated #0: 20 -->
en:retardation
n1=en:retrocerebellar cyst | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:retrocerebellar cyst (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:retrocerebellar cyst (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:retrocerebellar cyst (rare) ---
r_associated #0: 20 -->
en:retardation
n1=en:retrocerebellar cyst (rare) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:retrocollis ---
r_associated #0: 20 -->
en:retardation
n1=en:retrocollis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:retroflexion of the neck ---
r_associated #0: 20 -->
en:retardation
n1=en:retroflexion of the neck | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:rett syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:rett syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:reye syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:reye syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:rheumatic heart disease ---
r_associated #0: 20 -->
en:retardation
n1=en:rheumatic heart disease | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:rhinitis seasonal ---
r_associated #0: 20 -->
en:retardation
n1=en:rhinitis seasonal | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:rhinocephaly ---
r_associated #0: 20 -->
en:retardation
n1=en:rhinocephaly | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:rhizomelic chondrodysplasia punctata, type 1 ---
r_associated #0: 20 -->
en:retardation
n1=en:rhizomelic chondrodysplasia punctata, type 1 | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:rhizomelic chondrodysplasia punctata, type 2 ---
r_associated #0: 20 -->
en:retardation
n1=en:rhizomelic chondrodysplasia punctata, type 2 | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:rhombencephalosynapsis ---
r_associated #0: 20 -->
en:retardation
n1=en:rhombencephalosynapsis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:richards-rundle syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:richards-rundle syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:rigidity (juvenile form) ---
r_associated #0: 20 -->
en:retardation
n1=en:rigidity (juvenile form) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:rigidity (later) ---
r_associated #0: 20 -->
en:retardation
n1=en:rigidity (later) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:rigidity during seizures ---
r_associated #0: 20 -->
en:retardation
n1=en:rigidity during seizures | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:rigidity of limbs ---
r_associated #0: 20 -->
en:retardation
n1=en:rigidity of limbs | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:rigidity, axial and limb ---
r_associated #0: 20 -->
en:retardation
n1=en:rigidity, axial and limb | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:roberts syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:roberts syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:robin sequence with distinctive facial appearance and brachydactyly ---
r_associated #0: 20 -->
en:retardation
n1=en:robin sequence with distinctive facial appearance and brachydactyly | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:romberg's sign positive ---
r_associated #0: 20 -->
en:retardation
n1=en:romberg's sign positive | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:rotary head movements ('rolling,' 'tremor') ---
r_associated #0: 20 -->
en:retardation
n1=en:rotary head movements ('rolling,' 'tremor') | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:roving eye movements (infancy) ---
r_associated #0: 20 -->
en:retardation
n1=en:roving eye movements (infancy) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:rubella infection ---
r_associated #0: 20 -->
en:retardation
n1=en:rubella infection | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:rubinstein-taybi syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:rubinstein-taybi syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:rudimentary white matter ---
r_associated #0: 20 -->
en:retardation
n1=en:rudimentary white matter | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ruvalcaba syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:ruvalcaba syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:sabinas brittle hair syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:sabinas brittle hair syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:sacral dimple ---
r_associated #0: 20 -->
en:retardation
n1=en:sacral dimple | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:sagittal sinus thrombosis ---
r_associated #0: 20 -->
en:retardation
n1=en:sagittal sinus thrombosis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:salaam seizures ---
r_associated #0: 20 -->
en:retardation
n1=en:salaam seizures | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:say meyer syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:say meyer syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:scabies and other acariases ---
r_associated #0: 20 -->
en:retardation
n1=en:scabies and other acariases | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:scanning speech ---
r_associated #0: 20 -->
en:retardation
n1=en:scanning speech | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:scant iron deposition in the brain (1 family) ---
r_associated #0: 20 -->
en:retardation
n1=en:scant iron deposition in the brain (1 family) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:scattered cns demyelination ---
r_associated #0: 20 -->
en:retardation
n1=en:scattered cns demyelination | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:schinzel-giedion midface-retraction syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:schinzel-giedion midface-retraction syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:schizencephaly ---
r_associated #0: 20 -->
en:retardation
n1=en:schizencephaly | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:schizophrenia ---
r_associated #0: 20 -->
en:retardation
n1=en:schizophrenia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:schizophrenia and other psychotic disorders ---
r_associated #0: 20 -->
en:retardation
n1=en:schizophrenia and other psychotic disorders | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:schizophrenia mental retardation deafness retinitis ---
r_associated #0: 20 -->
en:retardation
n1=en:schizophrenia mental retardation deafness retinitis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:schizophrenia spectrum and other psychotic disorders ---
r_associated #0: 20 -->
en:retardation
n1=en:schizophrenia spectrum and other psychotic disorders | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:schizophrenia, schizotypal and delusional disorders ---
r_associated #0: 20 -->
en:retardation
n1=en:schizophrenia, schizotypal and delusional disorders | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:schizophrenic reaction ---
r_associated #0: 20 -->
en:retardation
n1=en:schizophrenic reaction | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:school problem (finding) ---
r_associated #0: 20 -->
en:retardation
n1=en:school problem (finding) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:scissoring ---
r_associated #0: 20 -->
en:retardation
n1=en:scissoring | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:scissors gait ---
r_associated #0: 20 -->
en:retardation
n1=en:scissors gait | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:scott bryant graham syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:scott bryant graham syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:screening and history of mental health and substance abuse codes ---
r_associated #0: 20 -->
en:retardation
n1=en:screening and history of mental health and substance abuse codes | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:sebaceous cyst ---
r_associated #0: 20 -->
en:retardation
n1=en:sebaceous cyst | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seborrheic dermatitis ---
r_associated #0: 20 -->
en:retardation
n1=en:seborrheic dermatitis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seckel syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:seckel syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:secondary generalization ---
r_associated #0: 20 -->
en:retardation
n1=en:secondary generalization | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:secondary generalization may occur ---
r_associated #0: 20 -->
en:retardation
n1=en:secondary generalization may occur | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:secondary generalization occurs in about 33% of patients ---
r_associated #0: 20 -->
en:retardation
n1=en:secondary generalization occurs in about 33% of patients | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:secondary generalized tonic-clonic seizures may occur ---
r_associated #0: 20 -->
en:retardation
n1=en:secondary generalized tonic-clonic seizures may occur | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:secondary hand muscle weakness predominating at the wrist and finger extensor muscles ---
r_associated #0: 20 -->
en:retardation
n1=en:secondary hand muscle weakness predominating at the wrist and finger extensor muscles | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:secondary hypertonia ---
r_associated #0: 20 -->
en:retardation
n1=en:secondary hypertonia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:secondary involvement of proximal and trunk muscles ---
r_associated #0: 20 -->
en:retardation
n1=en:secondary involvement of proximal and trunk muscles | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:secondary motor complications develop in 50% of those on levodopa therapy ---
r_associated #0: 20 -->
en:retardation
n1=en:secondary motor complications develop in 50% of those on levodopa therapy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:secondary seizures (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:secondary seizures (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:secondary spinal cord compression may occur ---
r_associated #0: 20 -->
en:retardation
n1=en:secondary spinal cord compression may occur | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:secretory otitis media ---
r_associated #0: 20 -->
en:retardation
n1=en:secretory otitis media | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:see juvenile myoclonic epilepsy (606904) ---
r_associated #0: 20 -->
en:retardation
n1=en:see juvenile myoclonic epilepsy (606904) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:see spg5a (270800) ---
r_associated #0: 20 -->
en:retardation
n1=en:see spg5a (270800) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:segmental callosal hypoplasia, mild ---
r_associated #0: 20 -->
en:retardation
n1=en:segmental callosal hypoplasia, mild | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:segmental odontomaxillary dysplasia ---
r_associated #0: 20 -->
en:retardation
n1=en:segmental odontomaxillary dysplasia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:segmental sensory loss, especially of pain and temperature ---
r_associated #0: 20 -->
en:retardation
n1=en:segmental sensory loss, especially of pain and temperature | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizure (in a subset of patients in infancy) ---
r_associated #0: 20 -->
en:retardation
n1=en:seizure (in a subset of patients in infancy) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizure disorder ---
r_associated #0: 20 -->
en:retardation
n1=en:seizure disorder | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizure disorder (homozygote) ---
r_associated #0: 20 -->
en:retardation
n1=en:seizure disorder (homozygote) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizure including seizure-like activity in utero starting around 18 weeks gestation ---
r_associated #0: 20 -->
en:retardation
n1=en:seizure including seizure-like activity in utero starting around 18 weeks gestation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizure, febrile (2/3 children) ---
r_associated #0: 20 -->
en:retardation
n1=en:seizure, febrile (2/3 children) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizure, focal or multifocal onset ---
r_associated #0: 20 -->
en:retardation
n1=en:seizure, focal or multifocal onset | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizures (1 family) ---
r_associated #0: 20 -->
en:retardation
n1=en:seizures (1 family) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizures (1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:seizures (1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizures (2-10% of patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:seizures (2-10% of patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizures (3 patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:seizures (3 patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizures (40%) ---
r_associated #0: 20 -->
en:retardation
n1=en:seizures (40%) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizures (50% of patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:seizures (50% of patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizures (50%) ---
r_associated #0: 20 -->
en:retardation
n1=en:seizures (50%) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizures (> 90%) ---
r_associated #0: 20 -->
en:retardation
n1=en:seizures (> 90%) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizures (about 50% of patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:seizures (about 50% of patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizures (adult) ---
r_associated #0: 20 -->
en:retardation
n1=en:seizures (adult) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizures (cvs+) ---
r_associated #0: 20 -->
en:retardation
n1=en:seizures (cvs+) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizures (eclampsia) ---
r_associated #0: 20 -->
en:retardation
n1=en:seizures (eclampsia) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizures (if left untreated) ---
r_associated #0: 20 -->
en:retardation
n1=en:seizures (if left untreated) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizures (in 1 of 2 sibs) ---
r_associated #0: 20 -->
en:retardation
n1=en:seizures (in 1 of 2 sibs) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizures (in 1 of 3 patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:seizures (in 1 of 3 patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizures (in 2 of 6 patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:seizures (in 2 of 6 patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizures (in 2 of 9 patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:seizures (in 2 of 9 patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizures (in 35%) ---
r_associated #0: 20 -->
en:retardation
n1=en:seizures (in 35%) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizures (in one patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:seizures (in one patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizures (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:seizures (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizures (in some) ---
r_associated #0: 20 -->
en:retardation
n1=en:seizures (in some) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizures (juvenile form) ---
r_associated #0: 20 -->
en:retardation
n1=en:seizures (juvenile form) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizures (less common) ---
r_associated #0: 20 -->
en:retardation
n1=en:seizures (less common) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizures (may be difficult to control) ---
r_associated #0: 20 -->
en:retardation
n1=en:seizures (may be difficult to control) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizures (mean onset 4-5 months) ---
r_associated #0: 20 -->
en:retardation
n1=en:seizures (mean onset 4-5 months) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizures (meb) ---
r_associated #0: 20 -->
en:retardation
n1=en:seizures (meb) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizures (onset <2 years) ---
r_associated #0: 20 -->
en:retardation
n1=en:seizures (onset <2 years) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizures (rare) ---
r_associated #0: 20 -->
en:retardation
n1=en:seizures (rare) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizures (rare, in males) ---
r_associated #0: 20 -->
en:retardation
n1=en:seizures (rare, in males) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizures (reported in 1 family) ---
r_associated #0: 20 -->
en:retardation
n1=en:seizures (reported in 1 family) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizures (reported in 2 patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:seizures (reported in 2 patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizures (tetany) ---
r_associated #0: 20 -->
en:retardation
n1=en:seizures (tetany) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizures (type i and type ii, juvenile) ---
r_associated #0: 20 -->
en:retardation
n1=en:seizures (type i and type ii, juvenile) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizures (uncommon) ---
r_associated #0: 20 -->
en:retardation
n1=en:seizures (uncommon) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizures (variable) ---
r_associated #0: 20 -->
en:retardation
n1=en:seizures (variable) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizures affect the vocal cords, lips, mouth, and face ---
r_associated #0: 20 -->
en:retardation
n1=en:seizures affect the vocal cords, lips, mouth, and face | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizures are poorly controlled ---
r_associated #0: 20 -->
en:retardation
n1=en:seizures are poorly controlled | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizures in 15-30% ---
r_associated #0: 20 -->
en:retardation
n1=en:seizures in 15-30% | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizures in the newborn, refractory ---
r_associated #0: 20 -->
en:retardation
n1=en:seizures in the newborn, refractory | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizures may occur during hypotensive episodes ---
r_associated #0: 20 -->
en:retardation
n1=en:seizures may occur during hypotensive episodes | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizures occur in absence of intracranial infection or defined pathologic or traumatic cause ---
r_associated #0: 20 -->
en:retardation
n1=en:seizures occur in absence of intracranial infection or defined pathologic or traumatic cause | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizures occur in clusters ---
r_associated #0: 20 -->
en:retardation
n1=en:seizures occur in clusters | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizures occur in clusters over 1 or several days ---
r_associated #0: 20 -->
en:retardation
n1=en:seizures occur in clusters over 1 or several days | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizures occur multiple times per day ---
r_associated #0: 20 -->
en:retardation
n1=en:seizures occur multiple times per day | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizures often associated with infections ---
r_associated #0: 20 -->
en:retardation
n1=en:seizures often associated with infections | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizures often begin focally with head and eye deviation ---
r_associated #0: 20 -->
en:retardation
n1=en:seizures often begin focally with head and eye deviation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizures often begin with head and eye deviation ---
r_associated #0: 20 -->
en:retardation
n1=en:seizures often begin with head and eye deviation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizures provoked by tactile stimulation or extreme emotion ---
r_associated #0: 20 -->
en:retardation
n1=en:seizures provoked by tactile stimulation or extreme emotion | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizures recur in 33% of patients ---
r_associated #0: 20 -->
en:retardation
n1=en:seizures recur in 33% of patients | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizures usually last 1 to 5 minutes (less commonly up to 10 minutes) ---
r_associated #0: 20 -->
en:retardation
n1=en:seizures usually last 1 to 5 minutes (less commonly up to 10 minutes) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizures usually last less than 15 minutes ---
r_associated #0: 20 -->
en:retardation
n1=en:seizures usually last less than 15 minutes | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizures usually occur less than 3 times ---
r_associated #0: 20 -->
en:retardation
n1=en:seizures usually occur less than 3 times | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizures, complex partial, episodic ---
r_associated #0: 20 -->
en:retardation
n1=en:seizures, complex partial, episodic | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizures, complex, myoclonic ---
r_associated #0: 20 -->
en:retardation
n1=en:seizures, complex, myoclonic | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizures, continuous, refractory ---
r_associated #0: 20 -->
en:retardation
n1=en:seizures, continuous, refractory | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizures, diurnal partial, rare (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:seizures, diurnal partial, rare (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizures, early onset ---
r_associated #0: 20 -->
en:retardation
n1=en:seizures, early onset | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizures, early-onset (1 family) ---
r_associated #0: 20 -->
en:retardation
n1=en:seizures, early-onset (1 family) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizures, febrile (1 family) ---
r_associated #0: 20 -->
en:retardation
n1=en:seizures, febrile (1 family) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizures, focal, partial, motor ---
r_associated #0: 20 -->
en:retardation
n1=en:seizures, focal, partial, motor | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizures, generalized tonic/clonic, myoclonic, atonic, or atypical absence, aggravated by fatigue and fasting with frequency ranges from daily to monthly (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:seizures, generalized tonic/clonic, myoclonic, atonic, or atypical absence, aggravated by fatigue and fasting with frequency ranges from daily to monthly (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizures, generalized, afebrile ---
r_associated #0: 20 -->
en:retardation
n1=en:seizures, generalized, afebrile | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizures, generalized, may occur ---
r_associated #0: 20 -->
en:retardation
n1=en:seizures, generalized, may occur | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizures, hypoglycemic (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:seizures, hypoglycemic (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizures, infantile-onset ---
r_associated #0: 20 -->
en:retardation
n1=en:seizures, infantile-onset | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizures, intractable ---
r_associated #0: 20 -->
en:retardation
n1=en:seizures, intractable | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizures, intractable (in 1 family) ---
r_associated #0: 20 -->
en:retardation
n1=en:seizures, intractable (in 1 family) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizures, juvenile myoclonic ---
r_associated #0: 20 -->
en:retardation
n1=en:seizures, juvenile myoclonic | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizures, mild ---
r_associated #0: 20 -->
en:retardation
n1=en:seizures, mild | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizures, multiple types ---
r_associated #0: 20 -->
en:retardation
n1=en:seizures, multiple types | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizures, neonatal (2p21del) ---
r_associated #0: 20 -->
en:retardation
n1=en:seizures, neonatal (2p21del) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizures, nocturnal, usually occur in daily clusters ---
r_associated #0: 20 -->
en:retardation
n1=en:seizures, nocturnal, usually occur in daily clusters | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizures, onset age 5 to 10 years ---
r_associated #0: 20 -->
en:retardation
n1=en:seizures, onset age 5 to 10 years | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizures, partial complex (rare) ---
r_associated #0: 20 -->
en:retardation
n1=en:seizures, partial complex (rare) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizures, partial with secondary generalization, focal at onset, usually motor ---
r_associated #0: 20 -->
en:retardation
n1=en:seizures, partial with secondary generalization, focal at onset, usually motor | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizures, partial, often hemifacial ---
r_associated #0: 20 -->
en:retardation
n1=en:seizures, partial, often hemifacial | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizures, partial, unilateral ---
r_associated #0: 20 -->
en:retardation
n1=en:seizures, partial, unilateral | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizures, particularly absence (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:seizures, particularly absence (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizures, poorly controlled ---
r_associated #0: 20 -->
en:retardation
n1=en:seizures, poorly controlled | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizures, recurrent, refractory ---
r_associated #0: 20 -->
en:retardation
n1=en:seizures, recurrent, refractory | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizures, refractory ---
r_associated #0: 20 -->
en:retardation
n1=en:seizures, refractory | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizures, refractory to treatment ---
r_associated #0: 20 -->
en:retardation
n1=en:seizures, refractory to treatment | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizures, refractory, infantile-onset ---
r_associated #0: 20 -->
en:retardation
n1=en:seizures, refractory, infantile-onset | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizures, severe, drug-resistant, intractable ---
r_associated #0: 20 -->
en:retardation
n1=en:seizures, severe, drug-resistant, intractable | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizures, severe, intractable ---
r_associated #0: 20 -->
en:retardation
n1=en:seizures, severe, intractable | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizures, sudden-onset, drug-resistant ---
r_associated #0: 20 -->
en:retardation
n1=en:seizures, sudden-onset, drug-resistant | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizures, tonic, clonic, focal ---
r_associated #0: 20 -->
en:retardation
n1=en:seizures, tonic, clonic, focal | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizures, tonic, hyperekplectic ---
r_associated #0: 20 -->
en:retardation
n1=en:seizures, tonic, hyperekplectic | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizures, tonic-clonic (1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:seizures, tonic-clonic (1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizures, tonic-clonic (rare) ---
r_associated #0: 20 -->
en:retardation
n1=en:seizures, tonic-clonic (rare) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seizures, tonic-clonic or absence (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:seizures, tonic-clonic or absence (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:selective loss of cerebellar purkinje cells ---
r_associated #0: 20 -->
en:retardation
n1=en:selective loss of cerebellar purkinje cells | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:self mutilation ---
r_associated #0: 20 -->
en:retardation
n1=en:self mutilation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:self-injurious behavior, median onset age 2 years ---
r_associated #0: 20 -->
en:retardation
n1=en:self-injurious behavior, median onset age 2 years | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:semilobar holoprosencephalies ---
r_associated #0: 20 -->
en:retardation
n1=en:semilobar holoprosencephalies | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:semilobar hpe shows posterior interhemispheric fissure with rudimentary cerebral hemispheres and single ventricle ---
r_associated #0: 20 -->
en:retardation
n1=en:semilobar hpe shows posterior interhemispheric fissure with rudimentary cerebral hemispheres and single ventricle | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:sensitivity to neuroleptic medication ---
r_associated #0: 20 -->
en:retardation
n1=en:sensitivity to neuroleptic medication | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:sensorineural hearing loss ---
r_associated #0: 20 -->
en:retardation
n1=en:sensorineural hearing loss | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:sensory ataxia (less common) ---
r_associated #0: 20 -->
en:retardation
n1=en:sensory ataxia (less common) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:sensory aura may occur ---
r_associated #0: 20 -->
en:retardation
n1=en:sensory aura may occur | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:sensory disability ---
r_associated #0: 20 -->
en:retardation
n1=en:sensory disability | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:septum pellucidum deficient or cavum ---
r_associated #0: 20 -->
en:retardation
n1=en:septum pellucidum deficient or cavum | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:seropositive rheumatoid arthritis ---
r_associated #0: 20 -->
en:retardation
n1=en:seropositive rheumatoid arthritis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:sesame syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:sesame syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:severe behavioral problems at age 3-4 ---
r_associated #0: 20 -->
en:retardation
n1=en:severe behavioral problems at age 3-4 | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:severe brain damage ---
r_associated #0: 20 -->
en:retardation
n1=en:severe brain damage | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:severe cognitive deficits (develop later) ---
r_associated #0: 20 -->
en:retardation
n1=en:severe cognitive deficits (develop later) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:severe cognitive impairment ---
r_associated #0: 20 -->
en:retardation
n1=en:severe cognitive impairment | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:severe delay in myelination ---
r_associated #0: 20 -->
en:retardation
n1=en:severe delay in myelination | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:severe demyelination of the white matter ---
r_associated #0: 20 -->
en:retardation
n1=en:severe demyelination of the white matter | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:severe developmental delay in survivors ---
r_associated #0: 20 -->
en:retardation
n1=en:severe developmental delay in survivors | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:severe expressive language delay ---
r_associated #0: 20 -->
en:retardation
n1=en:severe expressive language delay | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:severe expressive speech delay ---
r_associated #0: 20 -->
en:retardation
n1=en:severe expressive speech delay | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:severe form may never achieve sitting or walking ---
r_associated #0: 20 -->
en:retardation
n1=en:severe form may never achieve sitting or walking | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:severe global developmental delay ---
r_associated #0: 20 -->
en:retardation
n1=en:severe global developmental delay | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:severe hydrocephalus ---
r_associated #0: 20 -->
en:retardation
n1=en:severe hydrocephalus | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:severe involvement of globus pallidus ---
r_associated #0: 20 -->
en:retardation
n1=en:severe involvement of globus pallidus | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:severe mental retardation (congenital form) ---
r_associated #0: 20 -->
en:retardation
n1=en:severe mental retardation (congenital form) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:severe mental retardation (i.q. 20-34) ---
r_associated #0: 20 -->
en:retardation
n1=en:severe mental retardation (i.q. 20-34) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:severe mental retardation (iq 10-40) ---
r_associated #0: 20 -->
en:retardation
n1=en:severe mental retardation (iq 10-40) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:severe muscular hypotonia ---
r_associated #0: 20 -->
en:retardation
n1=en:severe muscular hypotonia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:severe neonatal hypotonia improving with age ---
r_associated #0: 20 -->
en:retardation
n1=en:severe neonatal hypotonia improving with age | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:severe prenatal onset hydrocephalus ---
r_associated #0: 20 -->
en:retardation
n1=en:severe prenatal onset hydrocephalus | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:severe psychomotor retardation ---
r_associated #0: 20 -->
en:retardation
n1=en:severe psychomotor retardation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:severe psychomotor retardation (iq 35-65) ---
r_associated #0: 20 -->
en:retardation
n1=en:severe psychomotor retardation (iq 35-65) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:severe psychomotor retardation from birth ---
r_associated #0: 20 -->
en:retardation
n1=en:severe psychomotor retardation from birth | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:severe speech delay ---
r_associated #0: 20 -->
en:retardation
n1=en:severe speech delay | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:severe speech impairment ---
r_associated #0: 20 -->
en:retardation
n1=en:severe speech impairment | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:severely delayed psychomotor development ---
r_associated #0: 20 -->
en:retardation
n1=en:severely delayed psychomotor development | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:severely impaired or absent speech ---
r_associated #0: 20 -->
en:retardation
n1=en:severely impaired or absent speech | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:severity of symptoms peak in the second decade and do not progress ---
r_associated #0: 20 -->
en:retardation
n1=en:severity of symptoms peak in the second decade and do not progress | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:sex behavior disorder ---
r_associated #0: 20 -->
en:retardation
n1=en:sex behavior disorder | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:sex maturation female accelerated ---
r_associated #0: 20 -->
en:retardation
n1=en:sex maturation female accelerated | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:sex maturation male accelerated ---
r_associated #0: 20 -->
en:retardation
n1=en:sex maturation male accelerated | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:sexual and gender identity disorders ---
r_associated #0: 20 -->
en:retardation
n1=en:sexual and gender identity disorders | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:sexual dysfunctions, disturbances and gender identity disorders ---
r_associated #0: 20 -->
en:retardation
n1=en:sexual dysfunctions, disturbances and gender identity disorders | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:shaheen syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:shaheen syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:shivering sensation ---
r_associated #0: 20 -->
en:retardation
n1=en:shivering sensation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:short pons ---
r_associated #0: 20 -->
en:retardation
n1=en:short pons | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:short-rib thoracic dysplasia 10 with or without polydactyly ---
r_associated #0: 20 -->
en:retardation
n1=en:short-rib thoracic dysplasia 10 with or without polydactyly | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:shorter daily total sleep times compared to age-matched controls ---
r_associated #0: 20 -->
en:retardation
n1=en:shorter daily total sleep times compared to age-matched controls | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:shoulder syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:shoulder syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:shprintzen-goldberg craniosynostosis syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:shprintzen-goldberg craniosynostosis syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:shrunken inferior olivary nuclei ---
r_associated #0: 20 -->
en:retardation
n1=en:shrunken inferior olivary nuclei | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:shuffling gaits ---
r_associated #0: 20 -->
en:retardation
n1=en:shuffling gaits | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:sialic acid storage disease, finnish type (disorder) ---
r_associated #0: 20 -->
en:retardation
n1=en:sialic acid storage disease, finnish type (disorder) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:signal abnormalities in the posterior limbs of the internal capsules, middle cerebral peduncles, pyramidal tracts in the pons, and middle cerebellar peduncles seen on mri ---
r_associated #0: 20 -->
en:retardation
n1=en:signal abnormalities in the posterior limbs of the internal capsules, middle cerebral peduncles, pyramidal tracts in the pons, and middle cerebellar peduncles seen on mri | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:signal changes in the caudate and putamen ---
r_associated #0: 20 -->
en:retardation
n1=en:signal changes in the caudate and putamen | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:simple partial seizures ---
r_associated #0: 20 -->
en:retardation
n1=en:simple partial seizures | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:simple partial seizures with secondary generalization ---
r_associated #0: 20 -->
en:retardation
n1=en:simple partial seizures with secondary generalization | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:simplified cortical gyral pattern ---
r_associated #0: 20 -->
en:retardation
n1=en:simplified cortical gyral pattern | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:simplified cortical gyration pattern ---
r_associated #0: 20 -->
en:retardation
n1=en:simplified cortical gyration pattern | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:simplified gyral pattern (1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:simplified gyral pattern (1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:simplified gyral pattern (in 1 of 2 sibs) ---
r_associated #0: 20 -->
en:retardation
n1=en:simplified gyral pattern (in 1 of 2 sibs) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:simplified gyral pattern (in one patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:simplified gyral pattern (in one patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:simplified gyral pattern (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:simplified gyral pattern (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:simplified gyration in the frontal cortex (less common) ---
r_associated #0: 20 -->
en:retardation
n1=en:simplified gyration in the frontal cortex (less common) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:simplified gyration pattern ---
r_associated #0: 20 -->
en:retardation
n1=en:simplified gyration pattern | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:single congenital anomaly ---
r_associated #0: 20 -->
en:retardation
n1=en:single congenital anomaly | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:sinus pericranii (rare) ---
r_associated #0: 20 -->
en:retardation
n1=en:sinus pericranii (rare) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:sinusitis acute/chronic ---
r_associated #0: 20 -->
en:retardation
n1=en:sinusitis acute/chronic | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:sirenomelia ---
r_associated #0: 20 -->
en:retardation
n1=en:sirenomelia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:situs inversus ---
r_associated #0: 20 -->
en:retardation
n1=en:situs inversus | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:sjogren-larsson syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:sjogren-larsson syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:skeletal defects, genital hypoplasia, and mental retardation ---
r_associated #0: 20 -->
en:retardation
n1=en:skeletal defects, genital hypoplasia, and mental retardation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:skin photosensitivity ---
r_associated #0: 20 -->
en:retardation
n1=en:skin photosensitivity | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:sleep abnormalities ---
r_associated #0: 20 -->
en:retardation
n1=en:sleep abnormalities | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:sleep apnea ---
r_associated #0: 20 -->
en:retardation
n1=en:sleep apnea | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:sleep apnea (in 1/4 patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:sleep apnea (in 1/4 patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:sleep benefit (31%) ---
r_associated #0: 20 -->
en:retardation
n1=en:sleep benefit (31%) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:sleep disorder ---
r_associated #0: 20 -->
en:retardation
n1=en:sleep disorder | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:sleep disorder (rare) ---
r_associated #0: 20 -->
en:retardation
n1=en:sleep disorder (rare) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:sleep disorder with severe insomnia (in adulthood) ---
r_associated #0: 20 -->
en:retardation
n1=en:sleep disorder with severe insomnia (in adulthood) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:sleep disturbances ---
r_associated #0: 20 -->
en:retardation
n1=en:sleep disturbances | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:sleep disturbances (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:sleep disturbances (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:sleep disturbances common ---
r_associated #0: 20 -->
en:retardation
n1=en:sleep disturbances common | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:sleep impairment, progressive ---
r_associated #0: 20 -->
en:retardation
n1=en:sleep impairment, progressive | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:sleep paralysis at beginning or end of sleep period (in 60% of patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:sleep paralysis at beginning or end of sleep period (in 60% of patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:sleep pattern disturbance ---
r_associated #0: 20 -->
en:retardation
n1=en:sleep pattern disturbance | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:sleep talking ---
r_associated #0: 20 -->
en:retardation
n1=en:sleep talking | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:sleep wake disorders ---
r_associated #0: 20 -->
en:retardation
n1=en:sleep wake disorders | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:sleep-onset rem ---
r_associated #0: 20 -->
en:retardation
n1=en:sleep-onset rem | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:sleep-wake cycle disturbance ---
r_associated #0: 20 -->
en:retardation
n1=en:sleep-wake cycle disturbance | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:sleepiness ---
r_associated #0: 20 -->
en:retardation
n1=en:sleepiness | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:slow gait ---
r_associated #0: 20 -->
en:retardation
n1=en:slow gait | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:slow gross motor activity ---
r_associated #0: 20 -->
en:retardation
n1=en:slow gross motor activity | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:slow paraparetic gait ---
r_associated #0: 20 -->
en:retardation
n1=en:slow paraparetic gait | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:slow reactions ---
r_associated #0: 20 -->
en:retardation
n1=en:slow reactions | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:slow speech ---
r_associated #0: 20 -->
en:retardation
n1=en:slow speech | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:slow spike-wave discharges ---
r_associated #0: 20 -->
en:retardation
n1=en:slow spike-wave discharges | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:slow, broad-based gait ---
r_associated #0: 20 -->
en:retardation
n1=en:slow, broad-based gait | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:slowed background activity ---
r_associated #0: 20 -->
en:retardation
n1=en:slowed background activity | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:slowing mental development by 1.5 to 3 years ---
r_associated #0: 20 -->
en:retardation
n1=en:slowing mental development by 1.5 to 3 years | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:slowing mental development by 1.5 to 3 years of age ---
r_associated #0: 20 -->
en:retardation
n1=en:slowing mental development by 1.5 to 3 years of age | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:slowly progressive neurologic deterioration ---
r_associated #0: 20 -->
en:retardation
n1=en:slowly progressive neurologic deterioration | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:slurred speech ---
r_associated #0: 20 -->
en:retardation
n1=en:slurred speech | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:slurred speech, episodic ---
r_associated #0: 20 -->
en:retardation
n1=en:slurred speech, episodic | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:sly syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:sly syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:small and medium-sized leptomeningeal arteries show luminal narrowing or obliteration ---
r_associated #0: 20 -->
en:retardation
n1=en:small and medium-sized leptomeningeal arteries show luminal narrowing or obliteration | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:small anterior commissure ---
r_associated #0: 20 -->
en:retardation
n1=en:small anterior commissure | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:small brain ---
r_associated #0: 20 -->
en:retardation
n1=en:small brain | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:small brain size (some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:small brain size (some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:small brain with no other malformation see on mri ---
r_associated #0: 20 -->
en:retardation
n1=en:small brain with no other malformation see on mri | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:small but structurally normal cerebral cortex ---
r_associated #0: 20 -->
en:retardation
n1=en:small but structurally normal cerebral cortex | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:small caudate ---
r_associated #0: 20 -->
en:retardation
n1=en:small caudate | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:small cavum septum ---
r_associated #0: 20 -->
en:retardation
n1=en:small cavum septum | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:small cerebellum ---
r_associated #0: 20 -->
en:retardation
n1=en:small cerebellum | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:small cerebellum (especially vermis) ---
r_associated #0: 20 -->
en:retardation
n1=en:small cerebellum (especially vermis) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:small cerebral cortex ---
r_associated #0: 20 -->
en:retardation
n1=en:small cerebral cortex | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:small frontal lobes (in one patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:small frontal lobes (in one patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:small hippocampi (1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:small hippocampi (1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:small midbrain ---
r_associated #0: 20 -->
en:retardation
n1=en:small midbrain | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:small pituitary gland (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:small pituitary gland (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:small rotary component may be present ---
r_associated #0: 20 -->
en:retardation
n1=en:small rotary component may be present | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:small sella ---
r_associated #0: 20 -->
en:retardation
n1=en:small sella | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:small shrunken brain ---
r_associated #0: 20 -->
en:retardation
n1=en:small shrunken brain | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:small size of the left hippocampus gyri ---
r_associated #0: 20 -->
en:retardation
n1=en:small size of the left hippocampus gyri | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:small thalami ---
r_associated #0: 20 -->
en:retardation
n1=en:small thalami | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:small, smooth cerebellum ---
r_associated #0: 20 -->
en:retardation
n1=en:small, smooth cerebellum | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:small, thin cerebellum ---
r_associated #0: 20 -->
en:retardation
n1=en:small, thin cerebellum | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:smith-lemli-opitz syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:smith-lemli-opitz syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:smith-magenis syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:smith-magenis syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:smooth brain surface ---
r_associated #0: 20 -->
en:retardation
n1=en:smooth brain surface | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:smooth, thin cortical mantle (wws) ---
r_associated #0: 20 -->
en:retardation
n1=en:smooth, thin cortical mantle (wws) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:social and occupational deterioration ---
r_associated #0: 20 -->
en:retardation
n1=en:social and occupational deterioration | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:social communication disorder ---
r_associated #0: 20 -->
en:retardation
n1=en:social communication disorder | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:socialized behavior disorder ---
r_associated #0: 20 -->
en:retardation
n1=en:socialized behavior disorder | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:socialized conduct disorder ---
r_associated #0: 20 -->
en:retardation
n1=en:socialized conduct disorder | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:somatic symptom and related disorders ---
r_associated #0: 20 -->
en:retardation
n1=en:somatic symptom and related disorders | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:somatoform disorder ---
r_associated #0: 20 -->
en:retardation
n1=en:somatoform disorder | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:somatosensory evoked potentials show prolonged latency ---
r_associated #0: 20 -->
en:retardation
n1=en:somatosensory evoked potentials show prolonged latency | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:some may not achieve ambulation ---
r_associated #0: 20 -->
en:retardation
n1=en:some may not achieve ambulation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:some patients do not achieve ability to walk ---
r_associated #0: 20 -->
en:retardation
n1=en:some patients do not achieve ability to walk | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:some patients have neurologic involvement ---
r_associated #0: 20 -->
en:retardation
n1=en:some patients have neurologic involvement | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:some patients have no structural brain abnormalities ---
r_associated #0: 20 -->
en:retardation
n1=en:some patients have no structural brain abnormalities | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:some patients have periodic wave complexes on eeg ---
r_associated #0: 20 -->
en:retardation
n1=en:some patients have periodic wave complexes on eeg | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:some patients may develop afebrile seizures later in life ---
r_associated #0: 20 -->
en:retardation
n1=en:some patients may develop afebrile seizures later in life | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:some patients may show normal early development ---
r_associated #0: 20 -->
en:retardation
n1=en:some patients may show normal early development | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:some patients never achieve independent ambulation ---
r_associated #0: 20 -->
en:retardation
n1=en:some patients never achieve independent ambulation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:some patients only achieve sitting ---
r_associated #0: 20 -->
en:retardation
n1=en:some patients only achieve sitting | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:somnolence ---
r_associated #0: 20 -->
en:retardation
n1=en:somnolence | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:sparing of central white matter structures ---
r_associated #0: 20 -->
en:retardation
n1=en:sparing of central white matter structures | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:sparing of optic tracts ---
r_associated #0: 20 -->
en:retardation
n1=en:sparing of optic tracts | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:sparing of the inferior olives ---
r_associated #0: 20 -->
en:retardation
n1=en:sparing of the inferior olives | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spasmodic dysphonia ---
r_associated #0: 20 -->
en:retardation
n1=en:spasmodic dysphonia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spasmodic torticollis ---
r_associated #0: 20 -->
en:retardation
n1=en:spasmodic torticollis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spastic ataxia ---
r_associated #0: 20 -->
en:retardation
n1=en:spastic ataxia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spastic cerebral palsy ---
r_associated #0: 20 -->
en:retardation
n1=en:spastic cerebral palsy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spastic diplegia ---
r_associated #0: 20 -->
en:retardation
n1=en:spastic diplegia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spastic diplegia (1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:spastic diplegia (1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spastic diplegia (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:spastic diplegia (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spastic diplegia, progressive ---
r_associated #0: 20 -->
en:retardation
n1=en:spastic diplegia, progressive | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spastic diplegia, symmetric ---
r_associated #0: 20 -->
en:retardation
n1=en:spastic diplegia, symmetric | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spastic dystonia ---
r_associated #0: 20 -->
en:retardation
n1=en:spastic dystonia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spastic gait ---
r_associated #0: 20 -->
en:retardation
n1=en:spastic gait | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spastic paralysis ---
r_associated #0: 20 -->
en:retardation
n1=en:spastic paralysis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spastic paraparesis (1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:spastic paraparesis (1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spastic paraparesis (rare) ---
r_associated #0: 20 -->
en:retardation
n1=en:spastic paraparesis (rare) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spastic paraplegia ---
r_associated #0: 20 -->
en:retardation
n1=en:spastic paraplegia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spastic paraplegia (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:spastic paraplegia (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spastic paraplegia 15, autosomal recessive ---
r_associated #0: 20 -->
en:retardation
n1=en:spastic paraplegia 15, autosomal recessive | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spastic paraplegia 16, x-linked (disorder) ---
r_associated #0: 20 -->
en:retardation
n1=en:spastic paraplegia 16, x-linked (disorder) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spastic paraplegia 2, x-linked (disorder) ---
r_associated #0: 20 -->
en:retardation
n1=en:spastic paraplegia 2, x-linked (disorder) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spastic paraplegia 54, autosomal recessive ---
r_associated #0: 20 -->
en:retardation
n1=en:spastic paraplegia 54, autosomal recessive | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spastic paraplegia, ataxia, and mental retardation ---
r_associated #0: 20 -->
en:retardation
n1=en:spastic paraplegia, ataxia, and mental retardation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spastic paraplegia, later onset (in one patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:spastic paraplegia, later onset (in one patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spastic paraplegia, pure ---
r_associated #0: 20 -->
en:retardation
n1=en:spastic paraplegia, pure | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spastic paraplegia, severe ---
r_associated #0: 20 -->
en:retardation
n1=en:spastic paraplegia, severe | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spastic paraplegia, slowly progressive ---
r_associated #0: 20 -->
en:retardation
n1=en:spastic paraplegia, slowly progressive | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spastic quadriplegia ---
r_associated #0: 20 -->
en:retardation
n1=en:spastic quadriplegia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spastic quadriplegia (in one patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:spastic quadriplegia (in one patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spastic quadriplegia, residual mild-to-severe (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:spastic quadriplegia, residual mild-to-severe (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spastic quadriplegia, severe ---
r_associated #0: 20 -->
en:retardation
n1=en:spastic quadriplegia, severe | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spastic tetraparesis ---
r_associated #0: 20 -->
en:retardation
n1=en:spastic tetraparesis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spastic tetraparesis (in severe cases) ---
r_associated #0: 20 -->
en:retardation
n1=en:spastic tetraparesis (in severe cases) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spastic tetraplegia (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:spastic tetraplegia (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spastic tetraplegia (onset in the second decade) ---
r_associated #0: 20 -->
en:retardation
n1=en:spastic tetraplegia (onset in the second decade) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spastic-ataxic gait ---
r_associated #0: 20 -->
en:retardation
n1=en:spastic-ataxic gait | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spastic-ataxic tetraparesis ---
r_associated #0: 20 -->
en:retardation
n1=en:spastic-ataxic tetraparesis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spasticity ---
r_associated #0: 20 -->
en:retardation
n1=en:spasticity | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spasticity (1 family) ---
r_associated #0: 20 -->
en:retardation
n1=en:spasticity (1 family) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spasticity (1 of 4 patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:spasticity (1 of 4 patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spasticity (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:spasticity (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spasticity (in some) ---
r_associated #0: 20 -->
en:retardation
n1=en:spasticity (in some) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spasticity (later onset) ---
r_associated #0: 20 -->
en:retardation
n1=en:spasticity (later onset) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spasticity (later) ---
r_associated #0: 20 -->
en:retardation
n1=en:spasticity (later) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spasticity (less common) ---
r_associated #0: 20 -->
en:retardation
n1=en:spasticity (less common) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spasticity (patient a) ---
r_associated #0: 20 -->
en:retardation
n1=en:spasticity (patient a) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spasticity (rare) ---
r_associated #0: 20 -->
en:retardation
n1=en:spasticity (rare) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spasticity (reported in 1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:spasticity (reported in 1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spasticity (type ii) ---
r_associated #0: 20 -->
en:retardation
n1=en:spasticity (type ii) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spasticity in infancy (1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:spasticity in infancy (1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spasticity may be present ---
r_associated #0: 20 -->
en:retardation
n1=en:spasticity may be present | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spasticity may occur ---
r_associated #0: 20 -->
en:retardation
n1=en:spasticity may occur | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spasticity of facial muscles ---
r_associated #0: 20 -->
en:retardation
n1=en:spasticity of facial muscles | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spasticity of lower and upper limbs ---
r_associated #0: 20 -->
en:retardation
n1=en:spasticity of lower and upper limbs | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spasticity of pharyngeal muscles ---
r_associated #0: 20 -->
en:retardation
n1=en:spasticity of pharyngeal muscles | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spasticity, distal ---
r_associated #0: 20 -->
en:retardation
n1=en:spasticity, distal | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spasticity, hyperreflexia ---
r_associated #0: 20 -->
en:retardation
n1=en:spasticity, hyperreflexia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spasticity, lower limbs greater than upper limbs ---
r_associated #0: 20 -->
en:retardation
n1=en:spasticity, lower limbs greater than upper limbs | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spasticity, mainly in the lower limbs ---
r_associated #0: 20 -->
en:retardation
n1=en:spasticity, mainly in the lower limbs | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spasticity, mild (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:spasticity, mild (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spasticity, more apparent in the lower limbs ---
r_associated #0: 20 -->
en:retardation
n1=en:spasticity, more apparent in the lower limbs | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spasticity, primarily lower limbs, but upper limbs may be involved ---
r_associated #0: 20 -->
en:retardation
n1=en:spasticity, primarily lower limbs, but upper limbs may be involved | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spasticity, progressive, develops in childhood ---
r_associated #0: 20 -->
en:retardation
n1=en:spasticity, progressive, develops in childhood | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spasticity, severe ---
r_associated #0: 20 -->
en:retardation
n1=en:spasticity, severe | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spasticity, severe, affecting lower limbs ---
r_associated #0: 20 -->
en:retardation
n1=en:spasticity, severe, affecting lower limbs | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spasticity, usually of the lower limbs ---
r_associated #0: 20 -->
en:retardation
n1=en:spasticity, usually of the lower limbs | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spasticity/paresis (rare) ---
r_associated #0: 20 -->
en:retardation
n1=en:spasticity/paresis (rare) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:special symptoms or syndromes, nec in mdr18_1 ---
r_associated #0: 20 -->
en:retardation
n1=en:special symptoms or syndromes, nec in mdr18_1 | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:specific developmental disorder ---
r_associated #0: 20 -->
en:retardation
n1=en:specific developmental disorder | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:specific developmental disorders of scholastic skills ---
r_associated #0: 20 -->
en:retardation
n1=en:specific developmental disorders of scholastic skills | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:specific learning problems ---
r_associated #0: 20 -->
en:retardation
n1=en:specific learning problems | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:specific nonpsychotic mental disorders following organic brain damage ---
r_associated #0: 20 -->
en:retardation
n1=en:specific nonpsychotic mental disorders following organic brain damage | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:specific visual spatial processing defect ---
r_associated #0: 20 -->
en:retardation
n1=en:specific visual spatial processing defect | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spect scan may show hypermetabolism of the temporal lobe ---
r_associated #0: 20 -->
en:retardation
n1=en:spect scan may show hypermetabolism of the temporal lobe | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:speech abnormalities (palilalia) ---
r_associated #0: 20 -->
en:retardation
n1=en:speech abnormalities (palilalia) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:speech absent or delayed ---
r_associated #0: 20 -->
en:retardation
n1=en:speech absent or delayed | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:speech and language delay (rare) ---
r_associated #0: 20 -->
en:retardation
n1=en:speech and language delay (rare) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:speech and language delay, severe ---
r_associated #0: 20 -->
en:retardation
n1=en:speech and language delay, severe | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:speech and language disorder ---
r_associated #0: 20 -->
en:retardation
n1=en:speech and language disorder | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:speech and language regression ---
r_associated #0: 20 -->
en:retardation
n1=en:speech and language regression | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:speech articulation defects ---
r_associated #0: 20 -->
en:retardation
n1=en:speech articulation defects | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:speech articulation problems ---
r_associated #0: 20 -->
en:retardation
n1=en:speech articulation problems | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:speech deficits ---
r_associated #0: 20 -->
en:retardation
n1=en:speech deficits | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:speech delay ---
r_associated #0: 20 -->
en:retardation
n1=en:speech delay | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:speech delay (1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:speech delay (1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:speech delay (10%) ---
r_associated #0: 20 -->
en:retardation
n1=en:speech delay (10%) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:speech delay (59%) ---
r_associated #0: 20 -->
en:retardation
n1=en:speech delay (59%) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:speech delay (in all patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:speech delay (in all patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:speech delay (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:speech delay (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:speech deterioration ---
r_associated #0: 20 -->
en:retardation
n1=en:speech deterioration | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:speech development delayed (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:speech development delayed (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:speech difficulties (48%) ---
r_associated #0: 20 -->
en:retardation
n1=en:speech difficulties (48%) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:speech difficulties due to hypoglossia ---
r_associated #0: 20 -->
en:retardation
n1=en:speech difficulties due to hypoglossia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:speech disability ---
r_associated #0: 20 -->
en:retardation
n1=en:speech disability | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:speech disorder ---
r_associated #0: 20 -->
en:retardation
n1=en:speech disorder | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:speech disorder (in 1 of 6 patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:speech disorder (in 1 of 6 patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:speech disorders (rare) ---
r_associated #0: 20 -->
en:retardation
n1=en:speech disorders (rare) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:speech hesitancy ---
r_associated #0: 20 -->
en:retardation
n1=en:speech hesitancy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:speech impairment ---
r_associated #0: 20 -->
en:retardation
n1=en:speech impairment | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:speech limited ---
r_associated #0: 20 -->
en:retardation
n1=en:speech limited | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:speech limited to single word or no words ---
r_associated #0: 20 -->
en:retardation
n1=en:speech limited to single word or no words | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:speech never acquired ---
r_associated #0: 20 -->
en:retardation
n1=en:speech never acquired | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:speech severely limited or absent ---
r_associated #0: 20 -->
en:retardation
n1=en:speech severely limited or absent | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:speech, limited or nonverbal ---
r_associated #0: 20 -->
en:retardation
n1=en:speech, limited or nonverbal | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spheroids contain neurofilaments ---
r_associated #0: 20 -->
en:retardation
n1=en:spheroids contain neurofilaments | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spina bifida ---
r_associated #0: 20 -->
en:retardation
n1=en:spina bifida | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spina bifida (less common) ---
r_associated #0: 20 -->
en:retardation
n1=en:spina bifida (less common) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spina bifida occulta ---
r_associated #0: 20 -->
en:retardation
n1=en:spina bifida occulta | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spinal arteriovenous malformation ---
r_associated #0: 20 -->
en:retardation
n1=en:spinal arteriovenous malformation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spinal cord atrophy (1 family) ---
r_associated #0: 20 -->
en:retardation
n1=en:spinal cord atrophy (1 family) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spinal cord atrophy (rare) ---
r_associated #0: 20 -->
en:retardation
n1=en:spinal cord atrophy (rare) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spinal cord compression ---
r_associated #0: 20 -->
en:retardation
n1=en:spinal cord compression | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spinal cord compression by tumor infiltration ---
r_associated #0: 20 -->
en:retardation
n1=en:spinal cord compression by tumor infiltration | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spinal cord disorder ---
r_associated #0: 20 -->
en:retardation
n1=en:spinal cord disorder | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spinal cord glial hyperplasia ---
r_associated #0: 20 -->
en:retardation
n1=en:spinal cord glial hyperplasia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spinal cord paresis ---
r_associated #0: 20 -->
en:retardation
n1=en:spinal cord paresis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spinal cord syrinx (in 2 patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:spinal cord syrinx (in 2 patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spinal cysts (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:spinal cysts (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spinal muscular atrophy ---
r_associated #0: 20 -->
en:retardation
n1=en:spinal muscular atrophy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spinal neurofibromas (64%) ---
r_associated #0: 20 -->
en:retardation
n1=en:spinal neurofibromas (64%) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spinal neuropathy ---
r_associated #0: 20 -->
en:retardation
n1=en:spinal neuropathy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spinal stenosis ---
r_associated #0: 20 -->
en:retardation
n1=en:spinal stenosis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spinal tract degeneration ---
r_associated #0: 20 -->
en:retardation
n1=en:spinal tract degeneration | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spinocerebellar ataxia ---
r_associated #0: 20 -->
en:retardation
n1=en:spinocerebellar ataxia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spinocerebellar ataxia (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:spinocerebellar ataxia (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spinocerebellar ataxia (upper and lower limb involvement) ---
r_associated #0: 20 -->
en:retardation
n1=en:spinocerebellar ataxia (upper and lower limb involvement) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spinocerebellar ataxia 21 ---
r_associated #0: 20 -->
en:retardation
n1=en:spinocerebellar ataxia 21 | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spinocerebellar ataxia, autosomal recessive 12 ---
r_associated #0: 20 -->
en:retardation
n1=en:spinocerebellar ataxia, autosomal recessive 12 | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spinocerebellar degeneration ---
r_associated #0: 20 -->
en:retardation
n1=en:spinocerebellar degeneration | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spinocerebellar tract degeneration ---
r_associated #0: 20 -->
en:retardation
n1=en:spinocerebellar tract degeneration | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spinocerebellar tract disease in lower limbs (in adulthood) ---
r_associated #0: 20 -->
en:retardation
n1=en:spinocerebellar tract disease in lower limbs (in adulthood) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:splenic rupture ---
r_associated #0: 20 -->
en:retardation
n1=en:splenic rupture | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:splenomegaly ---
r_associated #0: 20 -->
en:retardation
n1=en:splenomegaly | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spondyloepimetaphyseal dysplasia, genevieve type ---
r_associated #0: 20 -->
en:retardation
n1=en:spondyloepimetaphyseal dysplasia, genevieve type | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spongiform changes are mild or may not be present ---
r_associated #0: 20 -->
en:retardation
n1=en:spongiform changes are mild or may not be present | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spongiform degeneration ---
r_associated #0: 20 -->
en:retardation
n1=en:spongiform degeneration | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spongiform encephalomyelopathy ---
r_associated #0: 20 -->
en:retardation
n1=en:spongiform encephalomyelopathy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spongiosis, mild ---
r_associated #0: 20 -->
en:retardation
n1=en:spongiosis, mild | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spongy degeneration ---
r_associated #0: 20 -->
en:retardation
n1=en:spongy degeneration | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spongy gliosis ---
r_associated #0: 20 -->
en:retardation
n1=en:spongy gliosis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:spontaneous abortion ---
r_associated #0: 20 -->
en:retardation
n1=en:spontaneous abortion | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:sprain and strain of ankle ---
r_associated #0: 20 -->
en:retardation
n1=en:sprain and strain of ankle | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:stammering/stuttering/tics ---
r_associated #0: 20 -->
en:retardation
n1=en:stammering/stuttering/tics | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:stance ataxia ---
r_associated #0: 20 -->
en:retardation
n1=en:stance ataxia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:stargardt macular degeneration absent or hypoplastic corpus callosum mental retardation and dysmorphic features ---
r_associated #0: 20 -->
en:retardation
n1=en:stargardt macular degeneration absent or hypoplastic corpus callosum mental retardation and dysmorphic features | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:staring ---
r_associated #0: 20 -->
en:retardation
n1=en:staring | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:staring episodes during seizures ---
r_associated #0: 20 -->
en:retardation
n1=en:staring episodes during seizures | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:staring spells ---
r_associated #0: 20 -->
en:retardation
n1=en:staring spells | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:start with tonic posturing ---
r_associated #0: 20 -->
en:retardation
n1=en:start with tonic posturing | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:startle myoclonus ---
r_associated #0: 20 -->
en:retardation
n1=en:startle myoclonus | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:status dystonicus ---
r_associated #0: 20 -->
en:retardation
n1=en:status dystonicus | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:status epilepticus ---
r_associated #0: 20 -->
en:retardation
n1=en:status epilepticus | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:status epilepticus (in 1 of 6 patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:status epilepticus (in 1 of 6 patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:status epilepticus (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:status epilepticus (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:status epilepticus (in some) ---
r_associated #0: 20 -->
en:retardation
n1=en:status epilepticus (in some) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:status epilepticus may occur ---
r_associated #0: 20 -->
en:retardation
n1=en:status epilepticus may occur | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:status epilepticus rarely occurs ---
r_associated #0: 20 -->
en:retardation
n1=en:status epilepticus rarely occurs | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:stenosis of the aqueduct of sylvius (rare) ---
r_associated #0: 20 -->
en:retardation
n1=en:stenosis of the aqueduct of sylvius (rare) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:stenosis of the jugular foramen ---
r_associated #0: 20 -->
en:retardation
n1=en:stenosis of the jugular foramen | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:stereotypic movements ---
r_associated #0: 20 -->
en:retardation
n1=en:stereotypic movements | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:stevenson-carey syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:stevenson-carey syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:stiff gait ---
r_associated #0: 20 -->
en:retardation
n1=en:stiff gait | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:stiff limbs ---
r_associated #0: 20 -->
en:retardation
n1=en:stiff limbs | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:stiffness ---
r_associated #0: 20 -->
en:retardation
n1=en:stiffness | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:stiffness of the lower limbs ---
r_associated #0: 20 -->
en:retardation
n1=en:stiffness of the lower limbs | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:stiffness while walking ---
r_associated #0: 20 -->
en:retardation
n1=en:stiffness while walking | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:stimulation sensitive generalized myoclonus (stage 3) ---
r_associated #0: 20 -->
en:retardation
n1=en:stimulation sensitive generalized myoclonus (stage 3) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:stimulation sensitive segmental myoclonus (stage 2) ---
r_associated #0: 20 -->
en:retardation
n1=en:stimulation sensitive segmental myoclonus (stage 2) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:stoke-like lesions ---
r_associated #0: 20 -->
en:retardation
n1=en:stoke-like lesions | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:stomach function disorder ---
r_associated #0: 20 -->
en:retardation
n1=en:stomach function disorder | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:stomatognathic system abnormalities ---
r_associated #0: 20 -->
en:retardation
n1=en:stomatognathic system abnormalities | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:strabismus ---
r_associated #0: 20 -->
en:retardation
n1=en:strabismus | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:strep throat/scarlet fever ---
r_associated #0: 20 -->
en:retardation
n1=en:strep throat/scarlet fever | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:stretched cerebellar peduncles ---
r_associated #0: 20 -->
en:retardation
n1=en:stretched cerebellar peduncles | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:striatal atrophy ---
r_associated #0: 20 -->
en:retardation
n1=en:striatal atrophy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:striatal lesions ---
r_associated #0: 20 -->
en:retardation
n1=en:striatal lesions | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:striatal necrosis ---
r_associated #0: 20 -->
en:retardation
n1=en:striatal necrosis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:striatonigral degeneration, infantile (disorder) ---
r_associated #0: 20 -->
en:retardation
n1=en:striatonigral degeneration, infantile (disorder) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:stroke (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:stroke (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:stroke (rare) ---
r_associated #0: 20 -->
en:retardation
n1=en:stroke (rare) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:stroke (uncommon) ---
r_associated #0: 20 -->
en:retardation
n1=en:stroke (uncommon) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:stroke-like episodes ---
r_associated #0: 20 -->
en:retardation
n1=en:stroke-like episodes | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:stroke-like episodes (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:stroke-like episodes (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:stroke-like symptoms ---
r_associated #0: 20 -->
en:retardation
n1=en:stroke-like symptoms | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:strokes due to coagulopathy ---
r_associated #0: 20 -->
en:retardation
n1=en:strokes due to coagulopathy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:structural abnormalities in the basal ganglia (especially caudate) ---
r_associated #0: 20 -->
en:retardation
n1=en:structural abnormalities in the basal ganglia (especially caudate) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:structural abnormalities of cerebellum ---
r_associated #0: 20 -->
en:retardation
n1=en:structural abnormalities of cerebellum | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:structural brain abnormalities ---
r_associated #0: 20 -->
en:retardation
n1=en:structural brain abnormalities | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:structural brain anomalies ---
r_associated #0: 20 -->
en:retardation
n1=en:structural brain anomalies | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:structural changes in the temporal lobe ---
r_associated #0: 20 -->
en:retardation
n1=en:structural changes in the temporal lobe | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:structure of central auditory system ---
r_associated #0: 20 -->
en:retardation
n1=en:structure of central auditory system | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:structure of central sensory visual system ---
r_associated #0: 20 -->
en:retardation
n1=en:structure of central sensory visual system | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:structure of decussation of superior cerebellar peduncles ---
r_associated #0: 20 -->
en:retardation
n1=en:structure of decussation of superior cerebellar peduncles | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:stt3a-cdg and stt3b-cdg ---
r_associated #0: 20 -->
en:retardation
n1=en:stt3a-cdg and stt3b-cdg | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:sturge-weber syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:sturge-weber syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:subacute neurologic deterioration ---
r_associated #0: 20 -->
en:retardation
n1=en:subacute neurologic deterioration | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:subarachnoid cyst ---
r_associated #0: 20 -->
en:retardation
n1=en:subarachnoid cyst | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:subarachnoid hemorrhage ---
r_associated #0: 20 -->
en:retardation
n1=en:subarachnoid hemorrhage | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:subarachnoid hemorrhage (rare) ---
r_associated #0: 20 -->
en:retardation
n1=en:subarachnoid hemorrhage (rare) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:subclinical absence seizures ---
r_associated #0: 20 -->
en:retardation
n1=en:subclinical absence seizures | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:subcortical and periventricular white matter abnormalities seen on mri (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:subcortical and periventricular white matter abnormalities seen on mri (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:subcortical atrophy (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:subcortical atrophy (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:subcortical band or laminar heterotopia (in female carriers) ---
r_associated #0: 20 -->
en:retardation
n1=en:subcortical band or laminar heterotopia (in female carriers) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:subcortical cysts in frontal and temporal lobes ---
r_associated #0: 20 -->
en:retardation
n1=en:subcortical cysts in frontal and temporal lobes | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:subcortical cysts may occur elsewhere ---
r_associated #0: 20 -->
en:retardation
n1=en:subcortical cysts may occur elsewhere | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:subcortical cysts temporal lobe ---
r_associated #0: 20 -->
en:retardation
n1=en:subcortical cysts temporal lobe | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:subcortical dementia, progressive (6% of patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:subcortical dementia, progressive (6% of patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:subcortical focal lacunae ---
r_associated #0: 20 -->
en:retardation
n1=en:subcortical focal lacunae | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:subcortical gliosis ---
r_associated #0: 20 -->
en:retardation
n1=en:subcortical gliosis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:subcortical heterotopia ---
r_associated #0: 20 -->
en:retardation
n1=en:subcortical heterotopia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:subcortical hypomyelination ---
r_associated #0: 20 -->
en:retardation
n1=en:subcortical hypomyelination | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:subcortical lacunar lesions seen early in disease ---
r_associated #0: 20 -->
en:retardation
n1=en:subcortical lacunar lesions seen early in disease | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:subcortical lesions ---
r_associated #0: 20 -->
en:retardation
n1=en:subcortical lesions | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:subcortical lesions with edema ---
r_associated #0: 20 -->
en:retardation
n1=en:subcortical lesions with edema | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:subcortical leukodystrophy ---
r_associated #0: 20 -->
en:retardation
n1=en:subcortical leukodystrophy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:subcortical nodular grey matter heterotopia ---
r_associated #0: 20 -->
en:retardation
n1=en:subcortical nodular grey matter heterotopia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:subcortical nodular lesions in perivascular white matter ---
r_associated #0: 20 -->
en:retardation
n1=en:subcortical nodular lesions in perivascular white matter | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:subcortical origin of the myoclonus based on neurophysiologic studies ---
r_associated #0: 20 -->
en:retardation
n1=en:subcortical origin of the myoclonus based on neurophysiologic studies | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:subcortical temporal white matter disease, moderate ---
r_associated #0: 20 -->
en:retardation
n1=en:subcortical temporal white matter disease, moderate | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:subcortical white matter abnormalities (rare) ---
r_associated #0: 20 -->
en:retardation
n1=en:subcortical white matter abnormalities (rare) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:subcortical white matter abnormalities seen on mri ---
r_associated #0: 20 -->
en:retardation
n1=en:subcortical white matter abnormalities seen on mri | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:subcortical white matter calcifications ---
r_associated #0: 20 -->
en:retardation
n1=en:subcortical white matter calcifications | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:subcortical white matter lesions in the temporal lobes seen on brain mri ---
r_associated #0: 20 -->
en:retardation
n1=en:subcortical white matter lesions in the temporal lobes seen on brain mri | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:subependymal calcifications ---
r_associated #0: 20 -->
en:retardation
n1=en:subependymal calcifications | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:subependymal hemorrhage ---
r_associated #0: 20 -->
en:retardation
n1=en:subependymal hemorrhage | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:subependymal heterotopias ---
r_associated #0: 20 -->
en:retardation
n1=en:subependymal heterotopias | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:subependymal heterotopic nodules ---
r_associated #0: 20 -->
en:retardation
n1=en:subependymal heterotopic nodules | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:subependymal nodules ---
r_associated #0: 20 -->
en:retardation
n1=en:subependymal nodules | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:subependymal pseudocyst ---
r_associated #0: 20 -->
en:retardation
n1=en:subependymal pseudocyst | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:subnormal cognition ---
r_associated #0: 20 -->
en:retardation
n1=en:subnormal cognition | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:subnormal intelligence (62%) ---
r_associated #0: 20 -->
en:retardation
n1=en:subnormal intelligence (62%) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:substance abuse related disorder ---
r_associated #0: 20 -->
en:retardation
n1=en:substance abuse related disorder | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:substance withdrawal syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:substance withdrawal syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:substance-related disorder ---
r_associated #0: 20 -->
en:retardation
n1=en:substance-related disorder | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:substantia nigra gliosis ---
r_associated #0: 20 -->
en:retardation
n1=en:substantia nigra gliosis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:succinic semialdehyde dehydrogenase deficiency ---
r_associated #0: 20 -->
en:retardation
n1=en:succinic semialdehyde dehydrogenase deficiency | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:sudden arousal from slow-wave sleep with screaming, autonomic, and behavioral manifestations of intense fear (sleep terrors) ---
r_associated #0: 20 -->
en:retardation
n1=en:sudden arousal from slow-wave sleep with screaming, autonomic, and behavioral manifestations of intense fear (sleep terrors) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:sudden awakening ---
r_associated #0: 20 -->
en:retardation
n1=en:sudden awakening | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:sudden onset of neuropsychiatric symptoms ---
r_associated #0: 20 -->
en:retardation
n1=en:sudden onset of neuropsychiatric symptoms | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:suicidal and self-injurious behaviours nec ---
r_associated #0: 20 -->
en:retardation
n1=en:suicidal and self-injurious behaviours nec | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:suicide and intentional self-inflicted injury ---
r_associated #0: 20 -->
en:retardation
n1=en:suicide and intentional self-inflicted injury | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:suicide attempt ---
r_associated #0: 20 -->
en:retardation
n1=en:suicide attempt | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:superficial injury of ear ---
r_associated #0: 20 -->
en:retardation
n1=en:superficial injury of ear | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:superficial laminar spongiosis ---
r_associated #0: 20 -->
en:retardation
n1=en:superficial laminar spongiosis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:supernumerary structure ---
r_associated #0: 20 -->
en:retardation
n1=en:supernumerary structure | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:suppression-burst pattern ---
r_associated #0: 20 -->
en:retardation
n1=en:suppression-burst pattern | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:suppression-burst pattern see on eeg ---
r_associated #0: 20 -->
en:retardation
n1=en:suppression-burst pattern see on eeg | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:supranuclear gaze palsy ---
r_associated #0: 20 -->
en:retardation
n1=en:supranuclear gaze palsy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:supratentorial structures unformed or regressed ---
r_associated #0: 20 -->
en:retardation
n1=en:supratentorial structures unformed or regressed | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:swallowed foreign body in digestive system ---
r_associated #0: 20 -->
en:retardation
n1=en:swallowed foreign body in digestive system | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:sweating problem ---
r_associated #0: 20 -->
en:retardation
n1=en:sweating problem | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:swelling of the cerebral white matter ---
r_associated #0: 20 -->
en:retardation
n1=en:swelling of the cerebral white matter | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:swelling of the deep white matter seen on mri ---
r_associated #0: 20 -->
en:retardation
n1=en:swelling of the deep white matter seen on mri | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:swollen achromatic cells (pick cells) ---
r_associated #0: 20 -->
en:retardation
n1=en:swollen achromatic cells (pick cells) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:symmetric lesions in the basal ganglia consistent with leigh syndrome (256000), in a subset of patients ---
r_associated #0: 20 -->
en:retardation
n1=en:symmetric lesions in the basal ganglia consistent with leigh syndrome (256000), in a subset of patients | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:symmetric spinal nerve root neurofibromas ---
r_associated #0: 20 -->
en:retardation
n1=en:symmetric spinal nerve root neurofibromas | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:symmetric ventriculomegaly ---
r_associated #0: 20 -->
en:retardation
n1=en:symmetric ventriculomegaly | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:symmetrical progressive demyelination ---
r_associated #0: 20 -->
en:retardation
n1=en:symmetrical progressive demyelination | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:symptoms are exacerbated during pregnancy ---
r_associated #0: 20 -->
en:retardation
n1=en:symptoms are exacerbated during pregnancy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:symptoms occur at rest ---
r_associated #0: 20 -->
en:retardation
n1=en:symptoms occur at rest | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:symptoms of hypothalamic disturbances (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:symptoms of hypothalamic disturbances (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:symptoms stabilize within 4 weeks ---
r_associated #0: 20 -->
en:retardation
n1=en:symptoms stabilize within 4 weeks | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:syncope ---
r_associated #0: 20 -->
en:retardation
n1=en:syncope | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:syndactyly ---
r_associated #0: 20 -->
en:retardation
n1=en:syndactyly | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:syndrome screaming ---
r_associated #0: 20 -->
en:retardation
n1=en:syndrome screaming | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:syndromes of cervical spine ---
r_associated #0: 20 -->
en:retardation
n1=en:syndromes of cervical spine | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:synkinesia (rare) ---
r_associated #0: 20 -->
en:retardation
n1=en:synkinesia (rare) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:synkinesis ---
r_associated #0: 20 -->
en:retardation
n1=en:synkinesis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:syphilis female ---
r_associated #0: 20 -->
en:retardation
n1=en:syphilis female | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:syphilis male ---
r_associated #0: 20 -->
en:retardation
n1=en:syphilis male | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:syringomyelia ---
r_associated #0: 20 -->
en:retardation
n1=en:syringomyelia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:syringomyelia (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:syringomyelia (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:syringomyelia, noncommunicating (80% of cases) ---
r_associated #0: 20 -->
en:retardation
n1=en:syringomyelia, noncommunicating (80% of cases) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:t1-weighted hyperintensity surrounding a central band of hypointensity in the substantia nigra ---
r_associated #0: 20 -->
en:retardation
n1=en:t1-weighted hyperintensity surrounding a central band of hypointensity in the substantia nigra | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:t2-weighted hyperintense lesions in the thalamus, basal ganglia, and brainstem ---
r_associated #0: 20 -->
en:retardation
n1=en:t2-weighted hyperintense lesions in the thalamus, basal ganglia, and brainstem | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:t2-weighted hyperintensities in deep brain regions ---
r_associated #0: 20 -->
en:retardation
n1=en:t2-weighted hyperintensities in deep brain regions | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:t2-weighted hyperintensities in deep cerebral white matter, brainstem, and cerebellar white matter with sparing of the periventricular rim ---
r_associated #0: 20 -->
en:retardation
n1=en:t2-weighted hyperintensities in deep cerebral white matter, brainstem, and cerebellar white matter with sparing of the periventricular rim | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:t2-weighted hyperintensities in subcortical brain regions seen on mri ---
r_associated #0: 20 -->
en:retardation
n1=en:t2-weighted hyperintensities in subcortical brain regions seen on mri | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:t2-weighted hyperintensities in the basal ganglia ---
r_associated #0: 20 -->
en:retardation
n1=en:t2-weighted hyperintensities in the basal ganglia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:t2-weighted hyperintensities in the basal ganglia, corpus callosum, and brainstem seen on mri ---
r_associated #0: 20 -->
en:retardation
n1=en:t2-weighted hyperintensities in the basal ganglia, corpus callosum, and brainstem seen on mri | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:t2-weighted hyperintensities in the corticospinal tracts and posterior arms of the internal capsule in older patients seen on mri ---
r_associated #0: 20 -->
en:retardation
n1=en:t2-weighted hyperintensities in the corticospinal tracts and posterior arms of the internal capsule in older patients seen on mri | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:t2-weighted hyperintensities in the periventricular and deep subcortical white matter ---
r_associated #0: 20 -->
en:retardation
n1=en:t2-weighted hyperintensities in the periventricular and deep subcortical white matter | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:t2-weighted hyperintensities in the putamen and caudate nuclei ---
r_associated #0: 20 -->
en:retardation
n1=en:t2-weighted hyperintensities in the putamen and caudate nuclei | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:t2-weighted hyperintensities in the supratentorial white matter seen on brain mri ---
r_associated #0: 20 -->
en:retardation
n1=en:t2-weighted hyperintensities in the supratentorial white matter seen on brain mri | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:t2-weighted hypodensities in the basal ganglia ---
r_associated #0: 20 -->
en:retardation
n1=en:t2-weighted hypodensities in the basal ganglia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:t2-weighted mri shows hyperintensities in the thalamus, basal ganglia, and brainstem during acute illness (may later resolve) ---
r_associated #0: 20 -->
en:retardation
n1=en:t2-weighted mri shows hyperintensities in the thalamus, basal ganglia, and brainstem during acute illness (may later resolve) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:t2-weighted signal abnormalities in the deep white matter ---
r_associated #0: 20 -->
en:retardation
n1=en:t2-weighted signal abnormalities in the deep white matter | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:tachycardia, paroxysmal ---
r_associated #0: 20 -->
en:retardation
n1=en:tachycardia, paroxysmal | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:tardive dyskinesia ---
r_associated #0: 20 -->
en:retardation
n1=en:tardive dyskinesia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:tau immunreactivity ---
r_associated #0: 20 -->
en:retardation
n1=en:tau immunreactivity | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:tau inclusions are 'flame-shaped' or 'tuft-like' ---
r_associated #0: 20 -->
en:retardation
n1=en:tau inclusions are 'flame-shaped' or 'tuft-like' | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:tau-containing inclusions ---
r_associated #0: 20 -->
en:retardation
n1=en:tau-containing inclusions | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:tau-immunoreactive inclusions in neurons and astrocytes ---
r_associated #0: 20 -->
en:retardation
n1=en:tau-immunoreactive inclusions in neurons and astrocytes | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:tau-positive inclusions may be found ---
r_associated #0: 20 -->
en:retardation
n1=en:tau-positive inclusions may be found | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:tbp- and 1c2-immunoreactive neuronal inclusions ---
r_associated #0: 20 -->
en:retardation
n1=en:tbp- and 1c2-immunoreactive neuronal inclusions | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:tdp43-positive inclusions ---
r_associated #0: 20 -->
en:retardation
n1=en:tdp43-positive inclusions | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:tdp43-positive neuronal and glial cytoplasmic inclusions ---
r_associated #0: 20 -->
en:retardation
n1=en:tdp43-positive neuronal and glial cytoplasmic inclusions | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:tdp43-positive neuronal inclusions ---
r_associated #0: 20 -->
en:retardation
n1=en:tdp43-positive neuronal inclusions | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:tectal enlargement ---
r_associated #0: 20 -->
en:retardation
n1=en:tectal enlargement | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:temporal epileptiform discharges seen on eeg ---
r_associated #0: 20 -->
en:retardation
n1=en:temporal epileptiform discharges seen on eeg | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:temporal lobe ---
r_associated #0: 20 -->
en:retardation
n1=en:temporal lobe | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:temporal lobe epilepsy (1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:temporal lobe epilepsy (1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:temporal lobe heterotopias ---
r_associated #0: 20 -->
en:retardation
n1=en:temporal lobe heterotopias | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:temporal lobe infarct (rare) ---
r_associated #0: 20 -->
en:retardation
n1=en:temporal lobe infarct (rare) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:temporal lobe seizures (in 1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:temporal lobe seizures (in 1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:temtamy syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:temtamy syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:tendency to walk on toes ---
r_associated #0: 20 -->
en:retardation
n1=en:tendency to walk on toes | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:testicular hydrocele ---
r_associated #0: 20 -->
en:retardation
n1=en:testicular hydrocele | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:tetanus ---
r_associated #0: 20 -->
en:retardation
n1=en:tetanus | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:tetany ---
r_associated #0: 20 -->
en:retardation
n1=en:tetany | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:tetany, hypocalcemic (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:tetany, hypocalcemic (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:tetany, hypocalcemic, episodic ---
r_associated #0: 20 -->
en:retardation
n1=en:tetany, hypocalcemic, episodic | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:tethered cord (rare) ---
r_associated #0: 20 -->
en:retardation
n1=en:tethered cord (rare) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:tethered cord (uncommon) ---
r_associated #0: 20 -->
en:retardation
n1=en:tethered cord (uncommon) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:tethered spinal cord ---
r_associated #0: 20 -->
en:retardation
n1=en:tethered spinal cord | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:tethered spinal cord syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:tethered spinal cord syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:tetralogy of fallot ---
r_associated #0: 20 -->
en:retardation
n1=en:tetralogy of fallot | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:tetraplegic spasticity ---
r_associated #0: 20 -->
en:retardation
n1=en:tetraplegic spasticity | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:tfg- and tdp43-positive intraneuronal inclusions in some sensory and motor spinal cord neurons ---
r_associated #0: 20 -->
en:retardation
n1=en:tfg- and tdp43-positive intraneuronal inclusions in some sensory and motor spinal cord neurons | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:thalamic hypoplasia ---
r_associated #0: 20 -->
en:retardation
n1=en:thalamic hypoplasia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:thalamic lesions ---
r_associated #0: 20 -->
en:retardation
n1=en:thalamic lesions | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:thalamic neuronal loss, especially in the medial dorsal nucleus ---
r_associated #0: 20 -->
en:retardation
n1=en:thalamic neuronal loss, especially in the medial dorsal nucleus | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:thenar muscle atrophy ---
r_associated #0: 20 -->
en:retardation
n1=en:thenar muscle atrophy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:thenar muscle weakness ---
r_associated #0: 20 -->
en:retardation
n1=en:thenar muscle weakness | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:thiamin-responsive maple syrup urine disease ---
r_associated #0: 20 -->
en:retardation
n1=en:thiamin-responsive maple syrup urine disease | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:thick and elongated superior cerebellar peduncles ---
r_associated #0: 20 -->
en:retardation
n1=en:thick and elongated superior cerebellar peduncles | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:thick corpus callosum ---
r_associated #0: 20 -->
en:retardation
n1=en:thick corpus callosum | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:thick cortex ---
r_associated #0: 20 -->
en:retardation
n1=en:thick cortex | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:thick, maloriented superior cerebellar peduncles ---
r_associated #0: 20 -->
en:retardation
n1=en:thick, maloriented superior cerebellar peduncles | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:thick, short corpus callosum ---
r_associated #0: 20 -->
en:retardation
n1=en:thick, short corpus callosum | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:thickened cortices ---
r_associated #0: 20 -->
en:retardation
n1=en:thickened cortices | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:thickened frontal cortex ---
r_associated #0: 20 -->
en:retardation
n1=en:thickened frontal cortex | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:thickened optic nerve sheath ---
r_associated #0: 20 -->
en:retardation
n1=en:thickened optic nerve sheath | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:thickening of the skull (less common) ---
r_associated #0: 20 -->
en:retardation
n1=en:thickening of the skull (less common) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:thin bony cortex ---
r_associated #0: 20 -->
en:retardation
n1=en:thin bony cortex | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:thin brainstem ---
r_associated #0: 20 -->
en:retardation
n1=en:thin brainstem | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:thin cerebral cortex ---
r_associated #0: 20 -->
en:retardation
n1=en:thin cerebral cortex | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:thin corpus callosum (1 family) ---
r_associated #0: 20 -->
en:retardation
n1=en:thin corpus callosum (1 family) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:thin corpus callosum (1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:thin corpus callosum (1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:thin corpus callosum (1/4 patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:thin corpus callosum (1/4 patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:thin corpus callosum (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:thin corpus callosum (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:thin corpus callosum enlarged ventricles ---
r_associated #0: 20 -->
en:retardation
n1=en:thin corpus callosum enlarged ventricles | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:thin cortical mantle (wws) ---
r_associated #0: 20 -->
en:retardation
n1=en:thin cortical mantle (wws) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:thin optic chiasm ---
r_associated #0: 20 -->
en:retardation
n1=en:thin optic chiasm | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:thin pituitary stalk ---
r_associated #0: 20 -->
en:retardation
n1=en:thin pituitary stalk | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:thinning of the cerebellopontine tracts ---
r_associated #0: 20 -->
en:retardation
n1=en:thinning of the cerebellopontine tracts | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:third ventricle subependymal focal gliosis ---
r_associated #0: 20 -->
en:retardation
n1=en:third ventricle subependymal focal gliosis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:thoracogastroschisis ---
r_associated #0: 20 -->
en:retardation
n1=en:thoracogastroschisis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:thoracoschisis ---
r_associated #0: 20 -->
en:retardation
n1=en:thoracoschisis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:thrombosis of cerebral veins ---
r_associated #0: 20 -->
en:retardation
n1=en:thrombosis of cerebral veins | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:thumb in palm deformity ---
r_associated #0: 20 -->
en:retardation
n1=en:thumb in palm deformity | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:thyroglossal duct cyst ---
r_associated #0: 20 -->
en:retardation
n1=en:thyroglossal duct cyst | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:thyroid dysgenesis ---
r_associated #0: 20 -->
en:retardation
n1=en:thyroid dysgenesis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:thyroid gland malformation ---
r_associated #0: 20 -->
en:retardation
n1=en:thyroid gland malformation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:thyrotoxicosis [hyperthyroidism] ---
r_associated #0: 20 -->
en:retardation
n1=en:thyrotoxicosis [hyperthyroidism] | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:tip-toe gait ---
r_associated #0: 20 -->
en:retardation
n1=en:tip-toe gait | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:tobacco use disorder ---
r_associated #0: 20 -->
en:retardation
n1=en:tobacco use disorder | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:toe-walking gait ---
r_associated #0: 20 -->
en:retardation
n1=en:toe-walking gait | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:toe-walking in early childhood ---
r_associated #0: 20 -->
en:retardation
n1=en:toe-walking in early childhood | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:tongue movements, protrusions ---
r_associated #0: 20 -->
en:retardation
n1=en:tongue movements, protrusions | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:tonic clonic seizures, infrequent (in one patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:tonic clonic seizures, infrequent (in one patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:tonic convulsion ---
r_associated #0: 20 -->
en:retardation
n1=en:tonic convulsion | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:tonic head extension ---
r_associated #0: 20 -->
en:retardation
n1=en:tonic head extension | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:tonic posturing ---
r_associated #0: 20 -->
en:retardation
n1=en:tonic posturing | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:tonic seizures, refractory ---
r_associated #0: 20 -->
en:retardation
n1=en:tonic seizures, refractory | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:tonic spasms ---
r_associated #0: 20 -->
en:retardation
n1=en:tonic spasms | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:tonic-clonic seizures (less common) ---
r_associated #0: 20 -->
en:retardation
n1=en:tonic-clonic seizures (less common) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:tonus dysregulation ---
r_associated #0: 20 -->
en:retardation
n1=en:tonus dysregulation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:tooth development and eruption disorder ---
r_associated #0: 20 -->
en:retardation
n1=en:tooth development and eruption disorder | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:torsion dystonia (involuntary sustained muscle contractions, twisting and repetitive movements, abnormal posturing) ---
r_associated #0: 20 -->
en:retardation
n1=en:torsion dystonia (involuntary sustained muscle contractions, twisting and repetitive movements, abnormal posturing) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:torticollis ---
r_associated #0: 20 -->
en:retardation
n1=en:torticollis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:total body paralysis, paroxysmal ---
r_associated #0: 20 -->
en:retardation
n1=en:total body paralysis, paroxysmal | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:touch, vibration, and limb position may or may not be affected ---
r_associated #0: 20 -->
en:retardation
n1=en:touch, vibration, and limb position may or may not be affected | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:tow-walking ---
r_associated #0: 20 -->
en:retardation
n1=en:tow-walking | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:toxemia of pregnancy ---
r_associated #0: 20 -->
en:retardation
n1=en:toxemia of pregnancy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:toxic effect of other and unspecified substances ---
r_associated #0: 20 -->
en:retardation
n1=en:toxic effect of other and unspecified substances | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:toxic nodular goiter ---
r_associated #0: 20 -->
en:retardation
n1=en:toxic nodular goiter | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:toxoplasmosis ---
r_associated #0: 20 -->
en:retardation
n1=en:toxoplasmosis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:trachoma ---
r_associated #0: 20 -->
en:retardation
n1=en:trachoma | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:transient ataxia ---
r_associated #0: 20 -->
en:retardation
n1=en:transient ataxia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:transient cerebral ischemia ---
r_associated #0: 20 -->
en:retardation
n1=en:transient cerebral ischemia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:transient ischemic attack ---
r_associated #0: 20 -->
en:retardation
n1=en:transient ischemic attack | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:transient mild dystonia may precede abrupt onset of disorder by several years ---
r_associated #0: 20 -->
en:retardation
n1=en:transient mild dystonia may precede abrupt onset of disorder by several years | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:transient, reversible neurologic deficits ---
r_associated #0: 20 -->
en:retardation
n1=en:transient, reversible neurologic deficits | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:transitional facial palsy (15%) ---
r_associated #0: 20 -->
en:retardation
n1=en:transitional facial palsy (15%) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:transposition of great vessels ---
r_associated #0: 20 -->
en:retardation
n1=en:transposition of great vessels | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:trauma and stressor related disorders ---
r_associated #0: 20 -->
en:retardation
n1=en:trauma and stressor related disorders | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:trauma/injury problem ---
r_associated #0: 20 -->
en:retardation
n1=en:trauma/injury problem | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:tremor (1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:tremor (1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:tremor (3 patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:tremor (3 patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:tremor (30%) ---
r_associated #0: 20 -->
en:retardation
n1=en:tremor (30%) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:tremor (57% of patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:tremor (57% of patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:tremor (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:tremor (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:tremor (later-onset) ---
r_associated #0: 20 -->
en:retardation
n1=en:tremor (later-onset) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:tremor (less common) ---
r_associated #0: 20 -->
en:retardation
n1=en:tremor (less common) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:tremor (rare) ---
r_associated #0: 20 -->
en:retardation
n1=en:tremor (rare) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:tremor adverse event ---
r_associated #0: 20 -->
en:retardation
n1=en:tremor adverse event | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:tremor due to hyperthyroidism ---
r_associated #0: 20 -->
en:retardation
n1=en:tremor due to hyperthyroidism | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:tremor is exacerbated by stress and exercise ---
r_associated #0: 20 -->
en:retardation
n1=en:tremor is exacerbated by stress and exercise | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:tremor of hands ---
r_associated #0: 20 -->
en:retardation
n1=en:tremor of hands | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:tremor of palate ---
r_associated #0: 20 -->
en:retardation
n1=en:tremor of palate | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:tremor of the upper limb ---
r_associated #0: 20 -->
en:retardation
n1=en:tremor of the upper limb | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:tremor with febrile episodes (rare) ---
r_associated #0: 20 -->
en:retardation
n1=en:tremor with febrile episodes (rare) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:tremor, action (arms, tongue, head, legs and trunk) ---
r_associated #0: 20 -->
en:retardation
n1=en:tremor, action (arms, tongue, head, legs and trunk) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:tremor, action, progressive ---
r_associated #0: 20 -->
en:retardation
n1=en:tremor, action, progressive | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:tremor, mild ---
r_associated #0: 20 -->
en:retardation
n1=en:tremor, mild | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:tremor, postural (arms, tongue, head, legs and trunk) ---
r_associated #0: 20 -->
en:retardation
n1=en:tremor, postural (arms, tongue, head, legs and trunk) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:tremor, postural, upper limb, onset in fourth decade (reported in 1 family) ---
r_associated #0: 20 -->
en:retardation
n1=en:tremor, postural, upper limb, onset in fourth decade (reported in 1 family) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:tremor, small-amplitude, high-frequency, restricted to the hands ---
r_associated #0: 20 -->
en:retardation
n1=en:tremor, small-amplitude, high-frequency, restricted to the hands | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:tremor, static ---
r_associated #0: 20 -->
en:retardation
n1=en:tremor, static | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:tremor, variable ---
r_associated #0: 20 -->
en:retardation
n1=en:tremor, variable | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:tremors, action ---
r_associated #0: 20 -->
en:retardation
n1=en:tremors, action | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:tremors, limb ---
r_associated #0: 20 -->
en:retardation
n1=en:tremors, limb | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:trichorhinophalangeal syndrome type ii ---
r_associated #0: 20 -->
en:retardation
n1=en:trichorhinophalangeal syndrome type ii | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:trigeminal anesthesia ---
r_associated #0: 20 -->
en:retardation
n1=en:trigeminal anesthesia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:trigeminal neuralgia ---
r_associated #0: 20 -->
en:retardation
n1=en:trigeminal neuralgia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:triglyceride storage disease with ichthyosis ---
r_associated #0: 20 -->
en:retardation
n1=en:triglyceride storage disease with ichthyosis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:trismus ---
r_associated #0: 20 -->
en:retardation
n1=en:trismus | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:trismus (rare) ---
r_associated #0: 20 -->
en:retardation
n1=en:trismus (rare) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:trisomy 14 ---
r_associated #0: 20 -->
en:retardation
n1=en:trisomy 14 | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:trisomy 17 ---
r_associated #0: 20 -->
en:retardation
n1=en:trisomy 17 | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:trisomy 22 ---
r_associated #0: 20 -->
en:retardation
n1=en:trisomy 22 | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:truncal arching ---
r_associated #0: 20 -->
en:retardation
n1=en:truncal arching | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:truncal ataxia, mild ---
r_associated #0: 20 -->
en:retardation
n1=en:truncal ataxia, mild | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:truncal ataxia, severe ---
r_associated #0: 20 -->
en:retardation
n1=en:truncal ataxia, severe | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:truncal instability ---
r_associated #0: 20 -->
en:retardation
n1=en:truncal instability | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:truncal titubation ---
r_associated #0: 20 -->
en:retardation
n1=en:truncal titubation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:tuberous sclerosis ---
r_associated #0: 20 -->
en:retardation
n1=en:tuberous sclerosis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:tussive syncopes ---
r_associated #0: 20 -->
en:retardation
n1=en:tussive syncopes | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:twin-twin transfusion syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:twin-twin transfusion syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:twitching of the fingers and toes ---
r_associated #0: 20 -->
en:retardation
n1=en:twitching of the fingers and toes | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:tympanic membrane perforation ---
r_associated #0: 20 -->
en:retardation
n1=en:tympanic membrane perforation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:type i arnold chiari malformation ---
r_associated #0: 20 -->
en:retardation
n1=en:type i arnold chiari malformation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:type i eeg response is occipital spikes ---
r_associated #0: 20 -->
en:retardation
n1=en:type i eeg response is occipital spikes | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:type ii acrocephalopolysyndactyly ---
r_associated #0: 20 -->
en:retardation
n1=en:type ii acrocephalopolysyndactyly | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:type ii eeg response is parietooccipital spikes followed by biphasic slow waves ---
r_associated #0: 20 -->
en:retardation
n1=en:type ii eeg response is parietooccipital spikes followed by biphasic slow waves | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:type iii eeg response is parietooccipital spikes followed by biphasic slow waves and spreading to the frontal region ---
r_associated #0: 20 -->
en:retardation
n1=en:type iii eeg response is parietooccipital spikes followed by biphasic slow waves and spreading to the frontal region | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:type iv eeg response is generalized spike-wave discharges ---
r_associated #0: 20 -->
en:retardation
n1=en:type iv eeg response is generalized spike-wave discharges | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ubiquitin-positive cytoplasmic and intranuclear neuronal inclusions ---
r_associated #0: 20 -->
en:retardation
n1=en:ubiquitin-positive cytoplasmic and intranuclear neuronal inclusions | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ubiquitin-positive inclusions ---
r_associated #0: 20 -->
en:retardation
n1=en:ubiquitin-positive inclusions | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ubiquitin-positive intranuclear neuronal inclusions ---
r_associated #0: 20 -->
en:retardation
n1=en:ubiquitin-positive intranuclear neuronal inclusions | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ubqln2- and tdp43-immunopositive inclusions in spinal motor, brainstem, and hippocampal neurons ---
r_associated #0: 20 -->
en:retardation
n1=en:ubqln2- and tdp43-immunopositive inclusions in spinal motor, brainstem, and hippocampal neurons | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:udpglucose 4-epimerase deficiency disease ---
r_associated #0: 20 -->
en:retardation
n1=en:udpglucose 4-epimerase deficiency disease | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:unable to grasp objects ---
r_associated #0: 20 -->
en:retardation
n1=en:unable to grasp objects | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:unable to sit unsupported ---
r_associated #0: 20 -->
en:retardation
n1=en:unable to sit unsupported | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:unable to stand ---
r_associated #0: 20 -->
en:retardation
n1=en:unable to stand | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:unable to talk ---
r_associated #0: 20 -->
en:retardation
n1=en:unable to talk | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:unable to walk ---
r_associated #0: 20 -->
en:retardation
n1=en:unable to walk | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:uncomplicated hypertension ---
r_associated #0: 20 -->
en:retardation
n1=en:uncomplicated hypertension | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:uncoordinated movements ---
r_associated #0: 20 -->
en:retardation
n1=en:uncoordinated movements | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:underdeveloped corpus callosum (3 patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:underdeveloped corpus callosum (3 patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:undersulcation of the frontal lobes ---
r_associated #0: 20 -->
en:retardation
n1=en:undersulcation of the frontal lobes | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:undescended testes ---
r_associated #0: 20 -->
en:retardation
n1=en:undescended testes | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:unexplained abnormal blood test ---
r_associated #0: 20 -->
en:retardation
n1=en:unexplained abnormal blood test | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:unidentified bright objects on brain mri ---
r_associated #0: 20 -->
en:retardation
n1=en:unidentified bright objects on brain mri | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:unilateral cerebellar hypoplasia ---
r_associated #0: 20 -->
en:retardation
n1=en:unilateral cerebellar hypoplasia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:unilateral headache location ---
r_associated #0: 20 -->
en:retardation
n1=en:unilateral headache location | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:unintelligible speech, vocalizations, grunting ---
r_associated #0: 20 -->
en:retardation
n1=en:unintelligible speech, vocalizations, grunting | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:unresponsive to stimuli ---
r_associated #0: 20 -->
en:retardation
n1=en:unresponsive to stimuli | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:unresponsiveness ---
r_associated #0: 20 -->
en:retardation
n1=en:unresponsiveness | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:unspecified behavioural and emotional disorders with onset usually occurring in childhood and adolescence ---
r_associated #0: 20 -->
en:retardation
n1=en:unspecified behavioural and emotional disorders with onset usually occurring in childhood and adolescence | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:unspecified disorder of adult personality and behaviour ---
r_associated #0: 20 -->
en:retardation
n1=en:unspecified disorder of adult personality and behaviour | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:unspecified drug-induced mental disorder ---
r_associated #0: 20 -->
en:retardation
n1=en:unspecified drug-induced mental disorder | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:unspecified intellectual disabilities ---
r_associated #0: 20 -->
en:retardation
n1=en:unspecified intellectual disabilities | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:unspecified mental retardation; other impairments of behaviour ---
r_associated #0: 20 -->
en:retardation
n1=en:unspecified mental retardation; other impairments of behaviour | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:unspecified mental retardation; significant impairment of behaviour requiring attention or treatment ---
r_associated #0: 20 -->
en:retardation
n1=en:unspecified mental retardation; significant impairment of behaviour requiring attention or treatment | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:unspecified mental retardation; with the statement of no, or minimal, impairment of behaviour ---
r_associated #0: 20 -->
en:retardation
n1=en:unspecified mental retardation; with the statement of no, or minimal, impairment of behaviour | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:unspecified mental retardation; without mention of impairment of behaviour ---
r_associated #0: 20 -->
en:retardation
n1=en:unspecified mental retardation; without mention of impairment of behaviour | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:unspecified neoplasms ---
r_associated #0: 20 -->
en:retardation
n1=en:unspecified neoplasms | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:unspecified psychophysiological malfunction ---
r_associated #0: 20 -->
en:retardation
n1=en:unspecified psychophysiological malfunction | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:unstable, ataxic gait ---
r_associated #0: 20 -->
en:retardation
n1=en:unstable, ataxic gait | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:unsteadiness, episodic ---
r_associated #0: 20 -->
en:retardation
n1=en:unsteadiness, episodic | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:unsteady gait due to muscle weakness ---
r_associated #0: 20 -->
en:retardation
n1=en:unsteady gait due to muscle weakness | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:unsteady standing ---
r_associated #0: 20 -->
en:retardation
n1=en:unsteady standing | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:unusual aura symptoms include alien limb phenomenon, diplopia, apraxia, dysarthria, impaired hearing, vertigo ---
r_associated #0: 20 -->
en:retardation
n1=en:unusual aura symptoms include alien limb phenomenon, diplopia, apraxia, dysarthria, impaired hearing, vertigo | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:unwanted pregnancy confirmed ---
r_associated #0: 20 -->
en:retardation
n1=en:unwanted pregnancy confirmed | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:upbeat central vestibular nystagmus ---
r_associated #0: 20 -->
en:retardation
n1=en:upbeat central vestibular nystagmus | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:upper and lower motor neuron degeneration ---
r_associated #0: 20 -->
en:retardation
n1=en:upper and lower motor neuron degeneration | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:upper and lower motor neuron disease ---
r_associated #0: 20 -->
en:retardation
n1=en:upper and lower motor neuron disease | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:upper and lower neuron manifestations ---
r_associated #0: 20 -->
en:retardation
n1=en:upper and lower neuron manifestations | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:upper body involvement ---
r_associated #0: 20 -->
en:retardation
n1=en:upper body involvement | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:upper extremities may be involved ---
r_associated #0: 20 -->
en:retardation
n1=en:upper extremities may be involved | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:upper extremity action tremor ---
r_associated #0: 20 -->
en:retardation
n1=en:upper extremity action tremor | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:upper limb ataxia ---
r_associated #0: 20 -->
en:retardation
n1=en:upper limb ataxia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:upper limb dysmetria ---
r_associated #0: 20 -->
en:retardation
n1=en:upper limb dysmetria | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:upper limb dystonia ---
r_associated #0: 20 -->
en:retardation
n1=en:upper limb dystonia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:upper limb hyperreflexia (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:upper limb hyperreflexia (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:upper limb hyperreflexia (some) ---
r_associated #0: 20 -->
en:retardation
n1=en:upper limb hyperreflexia (some) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:upper limb involvement ---
r_associated #0: 20 -->
en:retardation
n1=en:upper limb involvement | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:upper limb involvement (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:upper limb involvement (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:upper limb involvement (onset in the first decade) ---
r_associated #0: 20 -->
en:retardation
n1=en:upper limb involvement (onset in the first decade) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:upper limb involvement may occur ---
r_associated #0: 20 -->
en:retardation
n1=en:upper limb involvement may occur | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:upper limb spasticity ---
r_associated #0: 20 -->
en:retardation
n1=en:upper limb spasticity | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:upper limb spasticity (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:upper limb spasticity (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:upper limb spasticity (some) ---
r_associated #0: 20 -->
en:retardation
n1=en:upper limb spasticity (some) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:upper limb spasticity, mild ---
r_associated #0: 20 -->
en:retardation
n1=en:upper limb spasticity, mild | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:upper limb weakness ---
r_associated #0: 20 -->
en:retardation
n1=en:upper limb weakness | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:upper limb weakness may occur later ---
r_associated #0: 20 -->
en:retardation
n1=en:upper limb weakness may occur later | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:upper limbs affected ---
r_associated #0: 20 -->
en:retardation
n1=en:upper limbs affected | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:upper limbs may be affected ---
r_associated #0: 20 -->
en:retardation
n1=en:upper limbs may be affected | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:upper limbs may show hyperreflexia ---
r_associated #0: 20 -->
en:retardation
n1=en:upper limbs may show hyperreflexia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:upper limbs may show mild involvement ---
r_associated #0: 20 -->
en:retardation
n1=en:upper limbs may show mild involvement | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:upper limbs more often affected than lower limbs ---
r_associated #0: 20 -->
en:retardation
n1=en:upper limbs more often affected than lower limbs | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:upper motor involvement (some patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:upper motor involvement (some patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:upper motor neuron degeneration ---
r_associated #0: 20 -->
en:retardation
n1=en:upper motor neuron degeneration | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:upper motor neuron dysfunction ---
r_associated #0: 20 -->
en:retardation
n1=en:upper motor neuron dysfunction | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:upper motor neuron signs ---
r_associated #0: 20 -->
en:retardation
n1=en:upper motor neuron signs | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:upper motor neuron signs (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:upper motor neuron signs (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:upper motor neuron signs, early ---
r_associated #0: 20 -->
en:retardation
n1=en:upper motor neuron signs, early | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:upper motor signs ---
r_associated #0: 20 -->
en:retardation
n1=en:upper motor signs | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:upper motor signs (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:upper motor signs (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:uremic coma ---
r_associated #0: 20 -->
en:retardation
n1=en:uremic coma | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ureterocele ---
r_associated #0: 20 -->
en:retardation
n1=en:ureterocele | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:urinary stone ---
r_associated #0: 20 -->
en:retardation
n1=en:urinary stone | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:urinary system neoplasm ---
r_associated #0: 20 -->
en:retardation
n1=en:urinary system neoplasm | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:urocanase deficiency ---
r_associated #0: 20 -->
en:retardation
n1=en:urocanase deficiency | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:urogenital trichomoniasis proven ---
r_associated #0: 20 -->
en:retardation
n1=en:urogenital trichomoniasis proven | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:urologic injuries ---
r_associated #0: 20 -->
en:retardation
n1=en:urologic injuries | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:urticaria ---
r_associated #0: 20 -->
en:retardation
n1=en:urticaria | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:usually occurs at night ---
r_associated #0: 20 -->
en:retardation
n1=en:usually occurs at night | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:uterine anomalies ---
r_associated #0: 20 -->
en:retardation
n1=en:uterine anomalies | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:uterovaginal prolapse ---
r_associated #0: 20 -->
en:retardation
n1=en:uterovaginal prolapse | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:vacuolated neurons ---
r_associated #0: 20 -->
en:retardation
n1=en:vacuolated neurons | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:vacuolization (patient a) ---
r_associated #0: 20 -->
en:retardation
n1=en:vacuolization (patient a) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:vacuolizing myelinopathy ---
r_associated #0: 20 -->
en:retardation
n1=en:vacuolizing myelinopathy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:vaginitis/vulvitis nos ---
r_associated #0: 20 -->
en:retardation
n1=en:vaginitis/vulvitis nos | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:van maldergem syndrome 2 ---
r_associated #0: 20 -->
en:retardation
n1=en:van maldergem syndrome 2 | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:van maldergem wetzburger verloes syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:van maldergem wetzburger verloes syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:variable delay (iq range 52-104) ---
r_associated #0: 20 -->
en:retardation
n1=en:variable delay (iq range 52-104) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:variable intracranial abnormalities ---
r_associated #0: 20 -->
en:retardation
n1=en:variable intracranial abnormalities | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:variable mental retardation ---
r_associated #0: 20 -->
en:retardation
n1=en:variable mental retardation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:variable mental retardation (40%) ---
r_associated #0: 20 -->
en:retardation
n1=en:variable mental retardation (40%) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:variable mental retardation ranging from severe neurodegeneration to mild mental retardation ---
r_associated #0: 20 -->
en:retardation
n1=en:variable mental retardation ranging from severe neurodegeneration to mild mental retardation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:variable neurologic deterioration (likely result of hemophagocytic syndrome) ---
r_associated #0: 20 -->
en:retardation
n1=en:variable neurologic deterioration (likely result of hemophagocytic syndrome) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:variable outcome after acute illness ---
r_associated #0: 20 -->
en:retardation
n1=en:variable outcome after acute illness | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:varicose vein of lower extremities ---
r_associated #0: 20 -->
en:retardation
n1=en:varicose vein of lower extremities | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:varying degree of mental retardation ---
r_associated #0: 20 -->
en:retardation
n1=en:varying degree of mental retardation | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:vasculopathy of the small arteries penetrating the white matter ---
r_associated #0: 20 -->
en:retardation
n1=en:vasculopathy of the small arteries penetrating the white matter | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:vasovagal syncope ---
r_associated #0: 20 -->
en:retardation
n1=en:vasovagal syncope | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:vcp-positive inclusions ---
r_associated #0: 20 -->
en:retardation
n1=en:vcp-positive inclusions | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ventricles slightly enlarged ---
r_associated #0: 20 -->
en:retardation
n1=en:ventricles slightly enlarged | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ventricular anomalies ---
r_associated #0: 20 -->
en:retardation
n1=en:ventricular anomalies | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ventricular asymmetry ---
r_associated #0: 20 -->
en:retardation
n1=en:ventricular asymmetry | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ventricular dilatation (29%) ---
r_associated #0: 20 -->
en:retardation
n1=en:ventricular dilatation (29%) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ventricular dilatation (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:ventricular dilatation (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ventricular dilatation (rare) ---
r_associated #0: 20 -->
en:retardation
n1=en:ventricular dilatation (rare) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ventricular enlargement ---
r_associated #0: 20 -->
en:retardation
n1=en:ventricular enlargement | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ventricular enlargement, mild ---
r_associated #0: 20 -->
en:retardation
n1=en:ventricular enlargement, mild | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ventricular septal defect ---
r_associated #0: 20 -->
en:retardation
n1=en:ventricular septal defect | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ventriculomegaly (38%) ---
r_associated #0: 20 -->
en:retardation
n1=en:ventriculomegaly (38%) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ventriculomegaly (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:ventriculomegaly (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ventriculomegaly (variable) ---
r_associated #0: 20 -->
en:retardation
n1=en:ventriculomegaly (variable) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ventriculomegaly, mild (rare) ---
r_associated #0: 20 -->
en:retardation
n1=en:ventriculomegaly, mild (rare) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:ventriculomeglia ---
r_associated #0: 20 -->
en:retardation
n1=en:ventriculomeglia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:verbal delay (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:verbal delay (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:vermian hypoplasia ---
r_associated #0: 20 -->
en:retardation
n1=en:vermian hypoplasia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:vertical orientation of hippocampus ---
r_associated #0: 20 -->
en:retardation
n1=en:vertical orientation of hippocampus | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:vertiginous syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:vertiginous syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:vertigo ---
r_associated #0: 20 -->
en:retardation
n1=en:vertigo | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:vertigo, episodic (onset in second or third decade) ---
r_associated #0: 20 -->
en:retardation
n1=en:vertigo, episodic (onset in second or third decade) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:vertigo, mild ---
r_associated #0: 20 -->
en:retardation
n1=en:vertigo, mild | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:very poor expressive speech ---
r_associated #0: 20 -->
en:retardation
n1=en:very poor expressive speech | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:vestibular anomalies (less common) ---
r_associated #0: 20 -->
en:retardation
n1=en:vestibular anomalies (less common) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:vestibular diseases ---
r_associated #0: 20 -->
en:retardation
n1=en:vestibular diseases | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:vestibular dysfunction ---
r_associated #0: 20 -->
en:retardation
n1=en:vestibular dysfunction | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:vestibular dysfunction, mild ---
r_associated #0: 20 -->
en:retardation
n1=en:vestibular dysfunction, mild | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:vestibulopathy, bilateral, progressive (onset in fourth or fifth decade) ---
r_associated #0: 20 -->
en:retardation
n1=en:vestibulopathy, bilateral, progressive (onset in fourth or fifth decade) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:viral hepatitis ---
r_associated #0: 20 -->
en:retardation
n1=en:viral hepatitis | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:virtual absence of pyramidal tracts (wws) ---
r_associated #0: 20 -->
en:retardation
n1=en:virtual absence of pyramidal tracts (wws) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:visceroautonomic dysfunction ---
r_associated #0: 20 -->
en:retardation
n1=en:visceroautonomic dysfunction | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:visual acuity is normal ---
r_associated #0: 20 -->
en:retardation
n1=en:visual acuity is normal | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:visual auras ---
r_associated #0: 20 -->
en:retardation
n1=en:visual auras | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:visual blackouts (stage 1) ---
r_associated #0: 20 -->
en:retardation
n1=en:visual blackouts (stage 1) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:visual changes ---
r_associated #0: 20 -->
en:retardation
n1=en:visual changes | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:visual hallucination ---
r_associated #0: 20 -->
en:retardation
n1=en:visual hallucination | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:visual hallucinations may occur ---
r_associated #0: 20 -->
en:retardation
n1=en:visual hallucinations may occur | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:visual impairment ---
r_associated #0: 20 -->
en:retardation
n1=en:visual impairment | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:visual inattention ---
r_associated #0: 20 -->
en:retardation
n1=en:visual inattention | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:visual symptoms (in 60% of patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:visual symptoms (in 60% of patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:visuospatial agnosia (in a subset of patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:visuospatial agnosia (in a subset of patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:vitamin deficiency/other nutritional/disease ---
r_associated #0: 20 -->
en:retardation
n1=en:vitamin deficiency/other nutritional/disease | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:vocalization (finding) ---
r_associated #0: 20 -->
en:retardation
n1=en:vocalization (finding) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:waardenburg syndrome, type iie ---
r_associated #0: 20 -->
en:retardation
n1=en:waardenburg syndrome, type iie | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:waddling gait ---
r_associated #0: 20 -->
en:retardation
n1=en:waddling gait | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:waisman syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:waisman syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:walking delay ---
r_associated #0: 20 -->
en:retardation
n1=en:walking delay | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:walking disability ---
r_associated #0: 20 -->
en:retardation
n1=en:walking disability | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:walking during slow-wave sleep (sleepwalking) ---
r_associated #0: 20 -->
en:retardation
n1=en:walking during slow-wave sleep (sleepwalking) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:walking impairment due to myoclonus late in disease ---
r_associated #0: 20 -->
en:retardation
n1=en:walking impairment due to myoclonus late in disease | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:walking independently at 2.5 years to 4 years of age ---
r_associated #0: 20 -->
en:retardation
n1=en:walking independently at 2.5 years to 4 years of age | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:warburg sjo fledelius syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:warburg sjo fledelius syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:warsaw breakage syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:warsaw breakage syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:weak or absent tendon reflexes of knees and ankles (in some patients) ---
r_associated #0: 20 -->
en:retardation
n1=en:weak or absent tendon reflexes of knees and ankles (in some patients) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:weakness of hip and ankle flexion ---
r_associated #0: 20 -->
en:retardation
n1=en:weakness of hip and ankle flexion | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:weaver syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:weaver syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:west syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:west syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:white blood cell abnormality ---
r_associated #0: 20 -->
en:retardation
n1=en:white blood cell abnormality | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:white mater abnormalities in the posterior periventricular region ---
r_associated #0: 20 -->
en:retardation
n1=en:white mater abnormalities in the posterior periventricular region | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:white matter ---
r_associated #0: 20 -->
en:retardation
n1=en:white matter | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:white matter abnormalities (1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:white matter abnormalities (1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:white matter abnormalities (in some) ---
r_associated #0: 20 -->
en:retardation
n1=en:white matter abnormalities (in some) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:white matter abnormalities (rare) ---
r_associated #0: 20 -->
en:retardation
n1=en:white matter abnormalities (rare) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:white matter abnormalities (uncommon) ---
r_associated #0: 20 -->
en:retardation
n1=en:white matter abnormalities (uncommon) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:white matter abnormalities in the periventricular regions (1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:white matter abnormalities in the periventricular regions (1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:white matter abnormalities on mri ---
r_associated #0: 20 -->
en:retardation
n1=en:white matter abnormalities on mri | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:white matter abnormalities seen on mri ---
r_associated #0: 20 -->
en:retardation
n1=en:white matter abnormalities seen on mri | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:white matter abnormalities seen on mri which resolve over time ---
r_associated #0: 20 -->
en:retardation
n1=en:white matter abnormalities seen on mri which resolve over time | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:white matter alterations (in one family) ---
r_associated #0: 20 -->
en:retardation
n1=en:white matter alterations (in one family) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:white matter changes ---
r_associated #0: 20 -->
en:retardation
n1=en:white matter changes | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:white matter changes may occur (in adulthood) ---
r_associated #0: 20 -->
en:retardation
n1=en:white matter changes may occur (in adulthood) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:white matter changes on brain imaging (less common) ---
r_associated #0: 20 -->
en:retardation
n1=en:white matter changes on brain imaging (less common) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:white matter degeneration ---
r_associated #0: 20 -->
en:retardation
n1=en:white matter degeneration | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:white matter dysmyelination/demyelination (71%) ---
r_associated #0: 20 -->
en:retardation
n1=en:white matter dysmyelination/demyelination (71%) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:white matter hyperintensities ---
r_associated #0: 20 -->
en:retardation
n1=en:white matter hyperintensities | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:white matter hyperintensities (mri, t2 images) suggestive of old infarcts ---
r_associated #0: 20 -->
en:retardation
n1=en:white matter hyperintensities (mri, t2 images) suggestive of old infarcts | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:white matter hyperintensities in t2 imaging ---
r_associated #0: 20 -->
en:retardation
n1=en:white matter hyperintensities in t2 imaging | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:white matter hyperintensities in various brain regions ---
r_associated #0: 20 -->
en:retardation
n1=en:white matter hyperintensities in various brain regions | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:white matter hypodensities on brain imaging ---
r_associated #0: 20 -->
en:retardation
n1=en:white matter hypodensities on brain imaging | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:white matter hypodensities seen on mri ---
r_associated #0: 20 -->
en:retardation
n1=en:white matter hypodensities seen on mri | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:white matter immaturity ---
r_associated #0: 20 -->
en:retardation
n1=en:white matter immaturity | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:white matter lacks axons and myelin ---
r_associated #0: 20 -->
en:retardation
n1=en:white matter lacks axons and myelin | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:white matter lesion ---
r_associated #0: 20 -->
en:retardation
n1=en:white matter lesion | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:white matter lesions (1 patient) ---
r_associated #0: 20 -->
en:retardation
n1=en:white matter lesions (1 patient) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:white matter lesions in the basal ganglia ---
r_associated #0: 20 -->
en:retardation
n1=en:white matter lesions in the basal ganglia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:white matter lesions in the brainstem may occur ---
r_associated #0: 20 -->
en:retardation
n1=en:white matter lesions in the brainstem may occur | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:white matter lesions in the supratentorial white matter, brainstem, cerebellum, and spinal cord ---
r_associated #0: 20 -->
en:retardation
n1=en:white matter lesions in the supratentorial white matter, brainstem, cerebellum, and spinal cord | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:white matter lesions may occur in the thalami, basal ganglia, and periventricular white matter (see leigh syndrome, 256000) ---
r_associated #0: 20 -->
en:retardation
n1=en:white matter lesions may occur in the thalami, basal ganglia, and periventricular white matter (see leigh syndrome, 256000) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:white matter lesions seen on brain imaging ---
r_associated #0: 20 -->
en:retardation
n1=en:white matter lesions seen on brain imaging | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:white matter neuronal heterotopia ---
r_associated #0: 20 -->
en:retardation
n1=en:white matter neuronal heterotopia | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:white matter rarefaction and cystic degeneration ---
r_associated #0: 20 -->
en:retardation
n1=en:white matter rarefaction and cystic degeneration | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:white matter signal abnormalities in the deep white matter and periventricular regions ---
r_associated #0: 20 -->
en:retardation
n1=en:white matter signal abnormalities in the deep white matter and periventricular regions | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:white matter signal abnormalities in various brain regions ---
r_associated #0: 20 -->
en:retardation
n1=en:white matter signal abnormalities in various brain regions | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:white matter streaks ---
r_associated #0: 20 -->
en:retardation
n1=en:white matter streaks | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:white matter vacuolization ---
r_associated #0: 20 -->
en:retardation
n1=en:white matter vacuolization | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:whooping cough due to unspecified organism ---
r_associated #0: 20 -->
en:retardation
n1=en:whooping cough due to unspecified organism | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:wide subarachnoid spaces ---
r_associated #0: 20 -->
en:retardation
n1=en:wide subarachnoid spaces | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:wide sylvian fissures ---
r_associated #0: 20 -->
en:retardation
n1=en:wide sylvian fissures | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:wide sylvian fissures with incomplete opercularization ---
r_associated #0: 20 -->
en:retardation
n1=en:wide sylvian fissures with incomplete opercularization | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:widened lateral ventricles ---
r_associated #0: 20 -->
en:retardation
n1=en:widened lateral ventricles | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:widened subarachnoid spaces ---
r_associated #0: 20 -->
en:retardation
n1=en:widened subarachnoid spaces | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:widening of cortical sulci ---
r_associated #0: 20 -->
en:retardation
n1=en:widening of cortical sulci | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:widening of the operculum ---
r_associated #0: 20 -->
en:retardation
n1=en:widening of the operculum | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:widening of the spinal canal ---
r_associated #0: 20 -->
en:retardation
n1=en:widening of the spinal canal | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:widening of the ventricles ---
r_associated #0: 20 -->
en:retardation
n1=en:widening of the ventricles | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:widespread brain atrophy ---
r_associated #0: 20 -->
en:retardation
n1=en:widespread brain atrophy | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:widespread brain calcifications ---
r_associated #0: 20 -->
en:retardation
n1=en:widespread brain calcifications | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:widespread neuronal loss ---
r_associated #0: 20 -->
en:retardation
n1=en:widespread neuronal loss | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:widespread tau (mapt)-positive glial and neuronal inclusions ---
r_associated #0: 20 -->
en:retardation
n1=en:widespread tau (mapt)-positive glial and neuronal inclusions | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:wieacker-wolff syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:wieacker-wolff syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:williams syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:williams syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:wilms tumor-aniridia-genitourinary anomalies-mental retardation syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:wilms tumor-aniridia-genitourinary anomalies-mental retardation syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:wolf-hirschhorn syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:wolf-hirschhorn syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:woodhouse sakati syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:woodhouse sakati syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:word finding difficulty (disorder) ---
r_associated #0: 20 -->
en:retardation
n1=en:word finding difficulty (disorder) | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:writing fatigability ---
r_associated #0: 20 -->
en:retardation
n1=en:writing fatigability | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:x-linked creatine transporter deficiency ---
r_associated #0: 20 -->
en:retardation
n1=en:x-linked creatine transporter deficiency | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:x-linked hydrocephalus syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:x-linked hydrocephalus syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:x-linked lissencephaly ---
r_associated #0: 20 -->
en:retardation
n1=en:x-linked lissencephaly | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:xeroderma pigmentosum, complementation group b ---
r_associated #0: 20 -->
en:retardation
n1=en:xeroderma pigmentosum, complementation group b | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:xia-gibbs syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:xia-gibbs syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:zechi-ceide syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:zechi-ceide syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- en:zunich neuroectodermal syndrome ---
r_associated #0: 20 -->
en:retardation
n1=en:zunich neuroectodermal syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=20
- endocriniens ---
r_associated #0: 20 -->
en:retardation
n1=endocriniens | n2=en:retardation | rel=r_associated | relid=0 | w=20
- enfance ---
r_associated #0: 20 -->
en:retardation
n1=enfance | n2=en:retardation | rel=r_associated | relid=0 | w=20
- faible développement mental ---
r_associated #0: 20 -->
en:retardation
n1=faible développement mental | n2=en:retardation | rel=r_associated | relid=0 | w=20
- faiblesse ---
r_associated #0: 20 -->
en:retardation
n1=faiblesse | n2=en:retardation | rel=r_associated | relid=0 | w=20
- handicap ---
r_associated #0: 20 -->
en:retardation
n1=handicap | n2=en:retardation | rel=r_associated | relid=0 | w=20
- handicap intellectuel ---
r_associated #0: 20 -->
en:retardation
n1=handicap intellectuel | n2=en:retardation | rel=r_associated | relid=0 | w=20
- handicap psychique ---
r_associated #0: 20 -->
en:retardation
n1=handicap psychique | n2=en:retardation | rel=r_associated | relid=0 | w=20
- handicaps moteurs ---
r_associated #0: 20 -->
en:retardation
n1=handicaps moteurs | n2=en:retardation | rel=r_associated | relid=0 | w=20
- handicapé mental ---
r_associated #0: 20 -->
en:retardation
n1=handicapé mental | n2=en:retardation | rel=r_associated | relid=0 | w=20
- hyperphénylalaninémie ---
r_associated #0: 20 -->
en:retardation
n1=hyperphénylalaninémie | n2=en:retardation | rel=r_associated | relid=0 | w=20
- idiotie ---
r_associated #0: 20 -->
en:retardation
n1=idiotie | n2=en:retardation | rel=r_associated | relid=0 | w=20
- imbécilité ---
r_associated #0: 20 -->
en:retardation
n1=imbécilité | n2=en:retardation | rel=r_associated | relid=0 | w=20
- imbécillité ---
r_associated #0: 20 -->
en:retardation
n1=imbécillité | n2=en:retardation | rel=r_associated | relid=0 | w=20
- incapacité intellectuelle ---
r_associated #0: 20 -->
en:retardation
n1=incapacité intellectuelle | n2=en:retardation | rel=r_associated | relid=0 | w=20
- infirmité ---
r_associated #0: 20 -->
en:retardation
n1=infirmité | n2=en:retardation | rel=r_associated | relid=0 | w=20
- insomnie ---
r_associated #0: 20 -->
en:retardation
n1=insomnie | n2=en:retardation | rel=r_associated | relid=0 | w=20
- intellectuel ---
r_associated #0: 20 -->
en:retardation
n1=intellectuel | n2=en:retardation | rel=r_associated | relid=0 | w=20
- intellectuelle ---
r_associated #0: 20 -->
en:retardation
n1=intellectuelle | n2=en:retardation | rel=r_associated | relid=0 | w=20
- intelligence ---
r_associated #0: 20 -->
en:retardation
n1=intelligence | n2=en:retardation | rel=r_associated | relid=0 | w=20
- maladie ---
r_associated #0: 20 -->
en:retardation
n1=maladie | n2=en:retardation | rel=r_associated | relid=0 | w=20
- mental ---
r_associated #0: 20 -->
en:retardation
n1=mental | n2=en:retardation | rel=r_associated | relid=0 | w=20
- mutisme électif ---
r_associated #0: 20 -->
en:retardation
n1=mutisme électif | n2=en:retardation | rel=r_associated | relid=0 | w=20
- médecine ---
r_associated #0: 20 -->
en:retardation
n1=médecine | n2=en:retardation | rel=r_associated | relid=0 | w=20
- méninge ---
r_associated #0: 20 -->
en:retardation
n1=méninge | n2=en:retardation | rel=r_associated | relid=0 | w=20
- méninges ---
r_associated #0: 20 -->
en:retardation
n1=méninges | n2=en:retardation | rel=r_associated | relid=0 | w=20
- nymphomanie ---
r_associated #0: 20 -->
en:retardation
n1=nymphomanie | n2=en:retardation | rel=r_associated | relid=0 | w=20
- processus pathologique ---
r_associated #0: 20 -->
en:retardation
n1=processus pathologique | n2=en:retardation | rel=r_associated | relid=0 | w=20
- profonde ---
r_associated #0: 20 -->
en:retardation
n1=profonde | n2=en:retardation | rel=r_associated | relid=0 | w=20
- psychiatrie ---
r_associated #0: 20 -->
en:retardation
n1=psychiatrie | n2=en:retardation | rel=r_associated | relid=0 | w=20
- quotient intellectuel ---
r_associated #0: 20 -->
en:retardation
n1=quotient intellectuel | n2=en:retardation | rel=r_associated | relid=0 | w=20
- retard de l'acquisition du langage secondaire à une perte de l'audition ---
r_associated #0: 20 -->
en:retardation
n1=retard de l'acquisition du langage secondaire à une perte de l'audition | n2=en:retardation | rel=r_associated | relid=0 | w=20
- retard mental avec atrophie optique, surdité et épilepsie ---
r_associated #0: 20 -->
en:retardation
n1=retard mental avec atrophie optique, surdité et épilepsie | n2=en:retardation | rel=r_associated | relid=0 | w=20
- retard mental de Jugberg-Marsidi ---
r_associated #0: 20 -->
en:retardation
n1=retard mental de Jugberg-Marsidi | n2=en:retardation | rel=r_associated | relid=0 | w=20
- retard mental de type Mietens-Weber ---
r_associated #0: 20 -->
en:retardation
n1=retard mental de type Mietens-Weber | n2=en:retardation | rel=r_associated | relid=0 | w=20
- retard mental lié au chromosome X fragile ---
r_associated #0: 20 -->
en:retardation
n1=retard mental lié au chromosome X fragile | n2=en:retardation | rel=r_associated | relid=0 | w=20
- retard mental lié à l'X ---
r_associated #0: 20 -->
en:retardation
n1=retard mental lié à l'X | n2=en:retardation | rel=r_associated | relid=0 | w=20
- retard mental psychosocial ---
r_associated #0: 20 -->
en:retardation
n1=retard mental psychosocial | n2=en:retardation | rel=r_associated | relid=0 | w=20
- retard mental, pouce et gros orteil larges ---
r_associated #0: 20 -->
en:retardation
n1=retard mental, pouce et gros orteil larges | n2=en:retardation | rel=r_associated | relid=0 | w=20
- retard mental, sévérité non spécifiée ---
r_associated #0: 20 -->
en:retardation
n1=retard mental, sévérité non spécifiée | n2=en:retardation | rel=r_associated | relid=0 | w=20
- retard mental-psychosocial ---
r_associated #0: 20 -->
en:retardation
n1=retard mental-psychosocial | n2=en:retardation | rel=r_associated | relid=0 | w=20
- retardation mentale non précisée ---
r_associated #0: 20 -->
en:retardation
n1=retardation mentale non précisée | n2=en:retardation | rel=r_associated | relid=0 | w=20
- retards mentaux ---
r_associated #0: 20 -->
en:retardation
n1=retards mentaux | n2=en:retardation | rel=r_associated | relid=0 | w=20
- retards mentaux psychosociaux ---
r_associated #0: 20 -->
en:retardation
n1=retards mentaux psychosociaux | n2=en:retardation | rel=r_associated | relid=0 | w=20
- retardé ---
r_associated #0: 20 -->
en:retardation
n1=retardé | n2=en:retardation | rel=r_associated | relid=0 | w=20
- sottise ---
r_associated #0: 20 -->
en:retardation
n1=sottise | n2=en:retardation | rel=r_associated | relid=0 | w=20
- surdité verbale ---
r_associated #0: 20 -->
en:retardation
n1=surdité verbale | n2=en:retardation | rel=r_associated | relid=0 | w=20
- tronc cérébral ---
r_associated #0: 20 -->
en:retardation
n1=tronc cérébral | n2=en:retardation | rel=r_associated | relid=0 | w=20
- trouble ---
r_associated #0: 20 -->
en:retardation
n1=trouble | n2=en:retardation | rel=r_associated | relid=0 | w=20
- trouble mental ---
r_associated #0: 20 -->
en:retardation
n1=trouble mental | n2=en:retardation | rel=r_associated | relid=0 | w=20
- trouble psychiatrique ---
r_associated #0: 20 -->
en:retardation
n1=trouble psychiatrique | n2=en:retardation | rel=r_associated | relid=0 | w=20
- trouble psychique ---
r_associated #0: 20 -->
en:retardation
n1=trouble psychique | n2=en:retardation | rel=r_associated | relid=0 | w=20
- trouble réceptif auditif congénital ---
r_associated #0: 20 -->
en:retardation
n1=trouble réceptif auditif congénital | n2=en:retardation | rel=r_associated | relid=0 | w=20
- troubles endocriniens ---
r_associated #0: 20 -->
en:retardation
n1=troubles endocriniens | n2=en:retardation | rel=r_associated | relid=0 | w=20
- visuels ---
r_associated #0: 20 -->
en:retardation
n1=visuels | n2=en:retardation | rel=r_associated | relid=0 | w=20
- état mental altéré ---
r_associated #0: 20 -->
en:retardation
n1=état mental altéré | n2=en:retardation | rel=r_associated | relid=0 | w=20
- être bouché ---
r_associated #0: 20 -->
en:retardation
n1=être bouché | n2=en:retardation | rel=r_associated | relid=0 | w=20
- Arrhenius (loi d') ---
r_associated #0: 15 -->
en:retardation
n1=Arrhenius (loi d') | n2=en:retardation | rel=r_associated | relid=0 | w=15
- Handicap intellectuel ---
r_associated #0: 15 -->
en:retardation
n1=Handicap intellectuel | n2=en:retardation | rel=r_associated | relid=0 | w=15
- Retard mental ---
r_associated #0: 15 -->
en:retardation
n1=Retard mental | n2=en:retardation | rel=r_associated | relid=0 | w=15
- apoplexie cérébrale ---
r_associated #0: 15 -->
en:retardation
n1=apoplexie cérébrale | n2=en:retardation | rel=r_associated | relid=0 | w=15
- cancer col ---
r_associated #0: 15 -->
en:retardation
n1=cancer col | n2=en:retardation | rel=r_associated | relid=0 | w=15
- chorée héréditaire ---
r_associated #0: 15 -->
en:retardation
n1=chorée héréditaire | n2=en:retardation | rel=r_associated | relid=0 | w=15
- coma hépatique ---
r_associated #0: 15 -->
en:retardation
n1=coma hépatique | n2=en:retardation | rel=r_associated | relid=0 | w=15
- dysrythmie cardiaque ---
r_associated #0: 15 -->
en:retardation
n1=dysrythmie cardiaque | n2=en:retardation | rel=r_associated | relid=0 | w=15
- déficit en céto-acide décarboxylase ---
r_associated #0: 15 -->
en:retardation
n1=déficit en céto-acide décarboxylase | n2=en:retardation | rel=r_associated | relid=0 | w=15
- encéphalopathie hépato-cérébrale ---
r_associated #0: 15 -->
en:retardation
n1=encéphalopathie hépato-cérébrale | n2=en:retardation | rel=r_associated | relid=0 | w=15
- encéphalopathie porto-cave ---
r_associated #0: 15 -->
en:retardation
n1=encéphalopathie porto-cave | n2=en:retardation | rel=r_associated | relid=0 | w=15
- glucosurie rénale ---
r_associated #0: 15 -->
en:retardation
n1=glucosurie rénale | n2=en:retardation | rel=r_associated | relid=0 | w=15
- gonflement axonal des racines nerveuses spinales et des nerfs crâniens ---
r_associated #0: 15 -->
en:retardation
n1=gonflement axonal des racines nerveuses spinales et des nerfs crâniens | n2=en:retardation | rel=r_associated | relid=0 | w=15
- ictus apoplectique ---
r_associated #0: 15 -->
en:retardation
n1=ictus apoplectique | n2=en:retardation | rel=r_associated | relid=0 | w=15
- ictus cérébral ---
r_associated #0: 15 -->
en:retardation
n1=ictus cérébral | n2=en:retardation | rel=r_associated | relid=0 | w=15
- kyste du canal thyroglossal ---
r_associated #0: 15 -->
en:retardation
n1=kyste du canal thyroglossal | n2=en:retardation | rel=r_associated | relid=0 | w=15
- maladie cérébrovasculaire aiguë mal définie ---
r_associated #0: 15 -->
en:retardation
n1=maladie cérébrovasculaire aiguë mal définie | n2=en:retardation | rel=r_associated | relid=0 | w=15
- malformation artérioveineuse cérébrovasculaire ---
r_associated #0: 15 -->
en:retardation
n1=malformation artérioveineuse cérébrovasculaire | n2=en:retardation | rel=r_associated | relid=0 | w=15
- malformation d'Arnold-Chiari ---
r_associated #0: 15 -->
en:retardation
n1=malformation d'Arnold-Chiari | n2=en:retardation | rel=r_associated | relid=0 | w=15
- parésie musculaire ---
r_associated #0: 15 -->
en:retardation
n1=parésie musculaire | n2=en:retardation | rel=r_associated | relid=0 | w=15
- perturbation du développement psychomoteur ---
r_associated #0: 15 -->
en:retardation
n1=perturbation du développement psychomoteur | n2=en:retardation | rel=r_associated | relid=0 | w=15
- retard mental ---
r_associated #0: 15 -->
en:retardation
n1=retard mental | n2=en:retardation | rel=r_associated | relid=0 | w=15
- réaction schizophrénique ---
r_associated #0: 15 -->
en:retardation
n1=réaction schizophrénique | n2=en:retardation | rel=r_associated | relid=0 | w=15
- trouble somatoforme ---
r_associated #0: 15 -->
en:retardation
n1=trouble somatoforme | n2=en:retardation | rel=r_associated | relid=0 | w=15
- Épilepsie partielle ---
r_associated #0: 15 -->
en:retardation
n1=Épilepsie partielle | n2=en:retardation | rel=r_associated | relid=0 | w=15
- épilepsie partielle ---
r_associated #0: 15 -->
en:retardation
n1=épilepsie partielle | n2=en:retardation | rel=r_associated | relid=0 | w=15
- Déficience mentale ---
r_associated #0: 10 -->
en:retardation
n1=Déficience mentale | n2=en:retardation | rel=r_associated | relid=0 | w=10
- Fothergill ---
r_associated #0: 10 -->
en:retardation
n1=Fothergill | n2=en:retardation | rel=r_associated | relid=0 | w=10
- Intellectuelle ---
r_associated #0: 10 -->
en:retardation
n1=Intellectuelle | n2=en:retardation | rel=r_associated | relid=0 | w=10
- Völker-Dieben (atrophie optique liée au sexe de) ---
r_associated #0: 10 -->
en:retardation
n1=Völker-Dieben (atrophie optique liée au sexe de) | n2=en:retardation | rel=r_associated | relid=0 | w=10
- Went (atrophie optique liée au sexe de) ---
r_associated #0: 10 -->
en:retardation
n1=Went (atrophie optique liée au sexe de) | n2=en:retardation | rel=r_associated | relid=0 | w=10
- abcès du cerveau ---
r_associated #0: 10 -->
en:retardation
n1=abcès du cerveau | n2=en:retardation | rel=r_associated | relid=0 | w=10
- accident cérébro-vasculaire ---
r_associated #0: 10 -->
en:retardation
n1=accident cérébro-vasculaire | n2=en:retardation | rel=r_associated | relid=0 | w=10
- accident ischémique cérébral ---
r_associated #0: 10 -->
en:retardation
n1=accident ischémique cérébral | n2=en:retardation | rel=r_associated | relid=0 | w=10
- accidents vasculaires cérébraux ---
r_associated #0: 10 -->
en:retardation
n1=accidents vasculaires cérébraux | n2=en:retardation | rel=r_associated | relid=0 | w=10
- addiction à l'alcool ---
r_associated #0: 10 -->
en:retardation
n1=addiction à l'alcool | n2=en:retardation | rel=r_associated | relid=0 | w=10
- affection cardiaque ---
r_associated #0: 10 -->
en:retardation
n1=affection cardiaque | n2=en:retardation | rel=r_associated | relid=0 | w=10
- affection du système nerveux périphérique ---
r_associated #0: 10 -->
en:retardation
n1=affection du système nerveux périphérique | n2=en:retardation | rel=r_associated | relid=0 | w=10
- affection extrapyramidale ---
r_associated #0: 10 -->
en:retardation
n1=affection extrapyramidale | n2=en:retardation | rel=r_associated | relid=0 | w=10
- agrypnie ---
r_associated #0: 10 -->
en:retardation
n1=agrypnie | n2=en:retardation | rel=r_associated | relid=0 | w=10
- albinisme ---
r_associated #0: 10 -->
en:retardation
n1=albinisme | n2=en:retardation | rel=r_associated | relid=0 | w=10
- algie rachidienne ---
r_associated #0: 10 -->
en:retardation
n1=algie rachidienne | n2=en:retardation | rel=r_associated | relid=0 | w=10
- algie vasculaire de la face ---
r_associated #0: 10 -->
en:retardation
n1=algie vasculaire de la face | n2=en:retardation | rel=r_associated | relid=0 | w=10
- altération du développement psychomoteur ---
r_associated #0: 10 -->
en:retardation
n1=altération du développement psychomoteur | n2=en:retardation | rel=r_associated | relid=0 | w=10
- amyotrophie ---
r_associated #0: 10 -->
en:retardation
n1=amyotrophie | n2=en:retardation | rel=r_associated | relid=0 | w=10
- anencéphalie ---
r_associated #0: 10 -->
en:retardation
n1=anencéphalie | n2=en:retardation | rel=r_associated | relid=0 | w=10
- anomalie cardiaque ---
r_associated #0: 10 -->
en:retardation
n1=anomalie cardiaque | n2=en:retardation | rel=r_associated | relid=0 | w=10
- anomalie chromosomique ---
r_associated #0: 10 -->
en:retardation
n1=anomalie chromosomique | n2=en:retardation | rel=r_associated | relid=0 | w=10
- anomalie congénitale de l'oeil ---
r_associated #0: 10 -->
en:retardation
n1=anomalie congénitale de l'oeil | n2=en:retardation | rel=r_associated | relid=0 | w=10
- anomalie du coeur ---
r_associated #0: 10 -->
en:retardation
n1=anomalie du coeur | n2=en:retardation | rel=r_associated | relid=0 | w=10
- anormalité des chromosomes ---
r_associated #0: 10 -->
en:retardation
n1=anormalité des chromosomes | n2=en:retardation | rel=r_associated | relid=0 | w=10
- anosmie ---
r_associated #0: 10 -->
en:retardation
n1=anosmie | n2=en:retardation | rel=r_associated | relid=0 | w=10
- aphasie ---
r_associated #0: 10 -->
en:retardation
n1=aphasie | n2=en:retardation | rel=r_associated | relid=0 | w=10
- arythmie cardiaque ---
r_associated #0: 10 -->
en:retardation
n1=arythmie cardiaque | n2=en:retardation | rel=r_associated | relid=0 | w=10
- asthme ---
r_associated #0: 10 -->
en:retardation
n1=asthme | n2=en:retardation | rel=r_associated | relid=0 | w=10
- astroglie ---
r_associated #0: 10 -->
en:retardation
n1=astroglie | n2=en:retardation | rel=r_associated | relid=0 | w=10
- atrophie des muscles ---
r_associated #0: 10 -->
en:retardation
n1=atrophie des muscles | n2=en:retardation | rel=r_associated | relid=0 | w=10
- atrophie musculaire ---
r_associated #0: 10 -->
en:retardation
n1=atrophie musculaire | n2=en:retardation | rel=r_associated | relid=0 | w=10
- attaque apoplectique ---
r_associated #0: 10 -->
en:retardation
n1=attaque apoplectique | n2=en:retardation | rel=r_associated | relid=0 | w=10
- attaque d'apoplexie ---
r_associated #0: 10 -->
en:retardation
n1=attaque d'apoplexie | n2=en:retardation | rel=r_associated | relid=0 | w=10
- balanitis ---
r_associated #0: 10 -->
en:retardation
n1=balanitis | n2=en:retardation | rel=r_associated | relid=0 | w=10
- bruxisme ---
r_associated #0: 10 -->
en:retardation
n1=bruxisme | n2=en:retardation | rel=r_associated | relid=0 | w=10
- cancer de l'estomac ---
r_associated #0: 10 -->
en:retardation
n1=cancer de l'estomac | n2=en:retardation | rel=r_associated | relid=0 | w=10
- cancer de la prostate ---
r_associated #0: 10 -->
en:retardation
n1=cancer de la prostate | n2=en:retardation | rel=r_associated | relid=0 | w=10
- cancer prostatique ---
r_associated #0: 10 -->
en:retardation
n1=cancer prostatique | n2=en:retardation | rel=r_associated | relid=0 | w=10
- cas cliniques d'oreillons ---
r_associated #0: 10 -->
en:retardation
n1=cas cliniques d'oreillons | n2=en:retardation | rel=r_associated | relid=0 | w=10
- cataplexie ---
r_associated #0: 10 -->
en:retardation
n1=cataplexie | n2=en:retardation | rel=r_associated | relid=0 | w=10
- cheilognathopalatoschisis ---
r_associated #0: 10 -->
en:retardation
n1=cheilognathopalatoschisis | n2=en:retardation | rel=r_associated | relid=0 | w=10
- chorée de Huntington ---
r_associated #0: 10 -->
en:retardation
n1=chorée de Huntington | n2=en:retardation | rel=r_associated | relid=0 | w=10
- clonus ---
r_associated #0: 10 -->
en:retardation
n1=clonus | n2=en:retardation | rel=r_associated | relid=0 | w=10
- coarctation ---
r_associated #0: 10 -->
en:retardation
n1=coarctation | n2=en:retardation | rel=r_associated | relid=0 | w=10
- colpocéphalie ---
r_associated #0: 10 -->
en:retardation
n1=colpocéphalie | n2=en:retardation | rel=r_associated | relid=0 | w=10
- coma urémique ---
r_associated #0: 10 -->
en:retardation
n1=coma urémique | n2=en:retardation | rel=r_associated | relid=0 | w=10
- congenital ---
r_associated #0: 10 -->
en:retardation
n1=congenital | n2=en:retardation | rel=r_associated | relid=0 | w=10
- convulsions fébriles ---
r_associated #0: 10 -->
en:retardation
n1=convulsions fébriles | n2=en:retardation | rel=r_associated | relid=0 | w=10
- crâniosténose ---
r_associated #0: 10 -->
en:retardation
n1=crâniosténose | n2=en:retardation | rel=r_associated | relid=0 | w=10
- crâniosynostose ---
r_associated #0: 10 -->
en:retardation
n1=crâniosynostose | n2=en:retardation | rel=r_associated | relid=0 | w=10
- cyclopia ---
r_associated #0: 10 -->
en:retardation
n1=cyclopia | n2=en:retardation | rel=r_associated | relid=0 | w=10
- demence ---
r_associated #0: 10 -->
en:retardation
n1=demence | n2=en:retardation | rel=r_associated | relid=0 | w=10
- douleur de la face ---
r_associated #0: 10 -->
en:retardation
n1=douleur de la face | n2=en:retardation | rel=r_associated | relid=0 | w=10
- drop attack ---
r_associated #0: 10 -->
en:retardation
n1=drop attack | n2=en:retardation | rel=r_associated | relid=0 | w=10
- dysostose fronto-nasale acromélique ---
r_associated #0: 10 -->
en:retardation
n1=dysostose fronto-nasale acromélique | n2=en:retardation | rel=r_associated | relid=0 | w=10
- dysphasie ---
r_associated #0: 10 -->
en:retardation
n1=dysphasie | n2=en:retardation | rel=r_associated | relid=0 | w=10
- dystonie ---
r_associated #0: 10 -->
en:retardation
n1=dystonie | n2=en:retardation | rel=r_associated | relid=0 | w=10
- déficience congénitale ---
r_associated #0: 10 -->
en:retardation
n1=déficience congénitale | n2=en:retardation | rel=r_associated | relid=0 | w=10
- déficit en cytochrome oxydase ---
r_associated #0: 10 -->
en:retardation
n1=déficit en cytochrome oxydase | n2=en:retardation | rel=r_associated | relid=0 | w=10
- déficit intellectuel ---
r_associated #0: 10 -->
en:retardation
n1=déficit intellectuel | n2=en:retardation | rel=r_associated | relid=0 | w=10
- déformation congénitale ---
r_associated #0: 10 -->
en:retardation
n1=déformation congénitale | n2=en:retardation | rel=r_associated | relid=0 | w=10
- dégénérescence granulovacuolaire ---
r_associated #0: 10 -->
en:retardation
n1=dégénérescence granulovacuolaire | n2=en:retardation | rel=r_associated | relid=0 | w=10
- détérioration mentale ---
r_associated #0: 10 -->
en:retardation
n1=détérioration mentale | n2=en:retardation | rel=r_associated | relid=0 | w=10
- ectopia cordis ---
r_associated #0: 10 -->
en:retardation
n1=ectopia cordis | n2=en:retardation | rel=r_associated | relid=0 | w=10
- en:Arrhenius'law ---
r_associated #0: 10 -->
en:retardation
n1=en:Arrhenius'law | n2=en:retardation | rel=r_associated | relid=0 | w=10
- en:and growth retardation ---
r_associated #0: 10 -->
en:retardation
n1=en:and growth retardation | n2=en:retardation | rel=r_associated | relid=0 | w=10
- en:cerebral ventriculomegaly ---
r_associated #0: 10 -->
en:retardation
n1=en:cerebral ventriculomegaly | n2=en:retardation | rel=r_associated | relid=0 | w=10
- en:deficiency ---
r_associated #0: 10 -->
en:retardation
n1=en:deficiency | n2=en:retardation | rel=r_associated | relid=0 | w=10
- en:endocrine disorder ---
r_associated #0: 10 -->
en:retardation
n1=en:endocrine disorder | n2=en:retardation | rel=r_associated | relid=0 | w=10
- en:eye abnormality ---
r_associated #0: 10 -->
en:retardation
n1=en:eye abnormality | n2=en:retardation | rel=r_associated | relid=0 | w=10
- en:failure ---
r_associated #0: 10 -->
en:retardation
n1=en:failure | n2=en:retardation | rel=r_associated | relid=0 | w=10
- en:febrile convulsions ---
r_associated #0: 10 -->
en:retardation
n1=en:febrile convulsions | n2=en:retardation | rel=r_associated | relid=0 | w=10
- en:imperfection ---
r_associated #0: 10 -->
en:retardation
n1=en:imperfection | n2=en:retardation | rel=r_associated | relid=0 | w=10
- en:malignant neoplasm of stomach ---
r_associated #0: 10 -->
en:retardation
n1=en:malignant neoplasm of stomach | n2=en:retardation | rel=r_associated | relid=0 | w=10
- en:mumps without complication ---
r_associated #0: 10 -->
en:retardation
n1=en:mumps without complication | n2=en:retardation | rel=r_associated | relid=0 | w=10
- en:muscular fasciculation ---
r_associated #0: 10 -->
en:retardation
n1=en:muscular fasciculation | n2=en:retardation | rel=r_associated | relid=0 | w=10
- en:paresis ---
r_associated #0: 10 -->
en:retardation
n1=en:paresis | n2=en:retardation | rel=r_associated | relid=0 | w=10
- en:unusual facies ---
r_associated #0: 10 -->
en:retardation
n1=en:unusual facies | n2=en:retardation | rel=r_associated | relid=0 | w=10
- en:white substance ---
r_associated #0: 10 -->
en:retardation
n1=en:white substance | n2=en:retardation | rel=r_associated | relid=0 | w=10
- encéphalocèle ---
r_associated #0: 10 -->
en:retardation
n1=encéphalocèle | n2=en:retardation | rel=r_associated | relid=0 | w=10
- encéphalopathie ---
r_associated #0: 10 -->
en:retardation
n1=encéphalopathie | n2=en:retardation | rel=r_associated | relid=0 | w=10
- encéphalopathie hépatique ---
r_associated #0: 10 -->
en:retardation
n1=encéphalopathie hépatique | n2=en:retardation | rel=r_associated | relid=0 | w=10
- epilepsie ---
r_associated #0: 10 -->
en:retardation
n1=epilepsie | n2=en:retardation | rel=r_associated | relid=0 | w=10
- exencéphalie ---
r_associated #0: 10 -->
en:retardation
n1=exencéphalie | n2=en:retardation | rel=r_associated | relid=0 | w=10
- exstrophie ---
r_associated #0: 10 -->
en:retardation
n1=exstrophie | n2=en:retardation | rel=r_associated | relid=0 | w=10
- faciale (paralysie du nouveau-né) ---
r_associated #0: 10 -->
en:retardation
n1=faciale (paralysie du nouveau-né) | n2=en:retardation | rel=r_associated | relid=0 | w=10
- faiblesse de muscle ---
r_associated #0: 10 -->
en:retardation
n1=faiblesse de muscle | n2=en:retardation | rel=r_associated | relid=0 | w=10
- faiblesse du muscle ---
r_associated #0: 10 -->
en:retardation
n1=faiblesse du muscle | n2=en:retardation | rel=r_associated | relid=0 | w=10
- faiblesse du visage ---
r_associated #0: 10 -->
en:retardation
n1=faiblesse du visage | n2=en:retardation | rel=r_associated | relid=0 | w=10
- faiblesse musculaire ---
r_associated #0: 10 -->
en:retardation
n1=faiblesse musculaire | n2=en:retardation | rel=r_associated | relid=0 | w=10
- fente laryngée ---
r_associated #0: 10 -->
en:retardation
n1=fente laryngée | n2=en:retardation | rel=r_associated | relid=0 | w=10
- fonte musculaire ---
r_associated #0: 10 -->
en:retardation
n1=fonte musculaire | n2=en:retardation | rel=r_associated | relid=0 | w=10
- gastroschisis ---
r_associated #0: 10 -->
en:retardation
n1=gastroschisis | n2=en:retardation | rel=r_associated | relid=0 | w=10
- glycosurie rénale ---
r_associated #0: 10 -->
en:retardation
n1=glycosurie rénale | n2=en:retardation | rel=r_associated | relid=0 | w=10
- grimaces ---
r_associated #0: 10 -->
en:retardation
n1=grimaces | n2=en:retardation | rel=r_associated | relid=0 | w=10
- hamartoma ---
r_associated #0: 10 -->
en:retardation
n1=hamartoma | n2=en:retardation | rel=r_associated | relid=0 | w=10
- herpès zoster ---
r_associated #0: 10 -->
en:retardation
n1=herpès zoster | n2=en:retardation | rel=r_associated | relid=0 | w=10
- holoprosencéphalie ---
r_associated #0: 10 -->
en:retardation
n1=holoprosencéphalie | n2=en:retardation | rel=r_associated | relid=0 | w=10
- hydranencéphalie ---
r_associated #0: 10 -->
en:retardation
n1=hydranencéphalie | n2=en:retardation | rel=r_associated | relid=0 | w=10
- hydrocèle ---
r_associated #0: 10 -->
en:retardation
n1=hydrocèle | n2=en:retardation | rel=r_associated | relid=0 | w=10
- hydrocèle testiculaire ---
r_associated #0: 10 -->
en:retardation
n1=hydrocèle testiculaire | n2=en:retardation | rel=r_associated | relid=0 | w=10
- hydrocèle vaginal ---
r_associated #0: 10 -->
en:retardation
n1=hydrocèle vaginal | n2=en:retardation | rel=r_associated | relid=0 | w=10
- hypertélorisme ---
r_associated #0: 10 -->
en:retardation
n1=hypertélorisme | n2=en:retardation | rel=r_associated | relid=0 | w=10
- hypoplasie du nerf optique ---
r_associated #0: 10 -->
en:retardation
n1=hypoplasie du nerf optique | n2=en:retardation | rel=r_associated | relid=0 | w=10
- hémihypertrophie ---
r_associated #0: 10 -->
en:retardation
n1=hémihypertrophie | n2=en:retardation | rel=r_associated | relid=0 | w=10
- hémimégalencéphalie ---
r_associated #0: 10 -->
en:retardation
n1=hémimégalencéphalie | n2=en:retardation | rel=r_associated | relid=0 | w=10
- hémorragie intracranienne ---
r_associated #0: 10 -->
en:retardation
n1=hémorragie intracranienne | n2=en:retardation | rel=r_associated | relid=0 | w=10
- hémorragie intracrânienne ---
r_associated #0: 10 -->
en:retardation
n1=hémorragie intracrânienne | n2=en:retardation | rel=r_associated | relid=0 | w=10
- hémorrhoïde ---
r_associated #0: 10 -->
en:retardation
n1=hémorrhoïde | n2=en:retardation | rel=r_associated | relid=0 | w=10
- hépatomégalie ---
r_associated #0: 10 -->
en:retardation
n1=hépatomégalie | n2=en:retardation | rel=r_associated | relid=0 | w=10
- immobilité ---
r_associated #0: 10 -->
en:retardation
n1=immobilité | n2=en:retardation | rel=r_associated | relid=0 | w=10
- impétigo ---
r_associated #0: 10 -->
en:retardation
n1=impétigo | n2=en:retardation | rel=r_associated | relid=0 | w=10
- je-m'en-fichisme ---
r_associated #0: 10 -->
en:retardation
n1=je-m'en-fichisme | n2=en:retardation | rel=r_associated | relid=0 | w=10
- kyste du canal thyréoglosse ---
r_associated #0: 10 -->
en:retardation
n1=kyste du canal thyréoglosse | n2=en:retardation | rel=r_associated | relid=0 | w=10
- kyste du tractus thyréoglosse ---
r_associated #0: 10 -->
en:retardation
n1=kyste du tractus thyréoglosse | n2=en:retardation | rel=r_associated | relid=0 | w=10
- kyste sébacé ---
r_associated #0: 10 -->
en:retardation
n1=kyste sébacé | n2=en:retardation | rel=r_associated | relid=0 | w=10
- kyste thyréoglosse ---
r_associated #0: 10 -->
en:retardation
n1=kyste thyréoglosse | n2=en:retardation | rel=r_associated | relid=0 | w=10
- laparoschisis ---
r_associated #0: 10 -->
en:retardation
n1=laparoschisis | n2=en:retardation | rel=r_associated | relid=0 | w=10
- laryngocèle ---
r_associated #0: 10 -->
en:retardation
n1=laryngocèle | n2=en:retardation | rel=r_associated | relid=0 | w=10
- lissencéphalie ---
r_associated #0: 10 -->
en:retardation
n1=lissencéphalie | n2=en:retardation | rel=r_associated | relid=0 | w=10
- maladie de Huntington ---
r_associated #0: 10 -->
en:retardation
n1=maladie de Huntington | n2=en:retardation | rel=r_associated | relid=0 | w=10
- maladie des urines à l'odeur de sirop d'érable ---
r_associated #0: 10 -->
en:retardation
n1=maladie des urines à l'odeur de sirop d'érable | n2=en:retardation | rel=r_associated | relid=0 | w=10
- maladie du sirop d'érable ---
r_associated #0: 10 -->
en:retardation
n1=maladie du sirop d'érable | n2=en:retardation | rel=r_associated | relid=0 | w=10
- maladie du système nerveux périphérique ---
r_associated #0: 10 -->
en:retardation
n1=maladie du système nerveux périphérique | n2=en:retardation | rel=r_associated | relid=0 | w=10
- malaise vagal ---
r_associated #0: 10 -->
en:retardation
n1=malaise vagal | n2=en:retardation | rel=r_associated | relid=0 | w=10
- malformation artérioveineuse intracrânienne ---
r_associated #0: 10 -->
en:retardation
n1=malformation artérioveineuse intracrânienne | n2=en:retardation | rel=r_associated | relid=0 | w=10
- malformation cardiaque ---
r_associated #0: 10 -->
en:retardation
n1=malformation cardiaque | n2=en:retardation | rel=r_associated | relid=0 | w=10
- manque de sommeil ---
r_associated #0: 10 -->
en:retardation
n1=manque de sommeil | n2=en:retardation | rel=r_associated | relid=0 | w=10
- matière blanche ---
r_associated #0: 10 -->
en:retardation
n1=matière blanche | n2=en:retardation | rel=r_associated | relid=0 | w=10
- matière grise ---
r_associated #0: 10 -->
en:retardation
n1=matière grise | n2=en:retardation | rel=r_associated | relid=0 | w=10
- mevalonic aciduria ---
r_associated #0: 10 -->
en:retardation
n1=mevalonic aciduria | n2=en:retardation | rel=r_associated | relid=0 | w=10
- migraine avec aura ---
r_associated #0: 10 -->
en:retardation
n1=migraine avec aura | n2=en:retardation | rel=r_associated | relid=0 | w=10
- molluscum contagiosum ---
r_associated #0: 10 -->
en:retardation
n1=molluscum contagiosum | n2=en:retardation | rel=r_associated | relid=0 | w=10
- myopathie ---
r_associated #0: 10 -->
en:retardation
n1=myopathie | n2=en:retardation | rel=r_associated | relid=0 | w=10
- myotonia ---
r_associated #0: 10 -->
en:retardation
n1=myotonia | n2=en:retardation | rel=r_associated | relid=0 | w=10
- myéloméningocèle ---
r_associated #0: 10 -->
en:retardation
n1=myéloméningocèle | n2=en:retardation | rel=r_associated | relid=0 | w=10
- méningiome ---
r_associated #0: 10 -->
en:retardation
n1=méningiome | n2=en:retardation | rel=r_associated | relid=0 | w=10
- nanisme ---
r_associated #0: 10 -->
en:retardation
n1=nanisme | n2=en:retardation | rel=r_associated | relid=0 | w=10
- narcolepsie ---
r_associated #0: 10 -->
en:retardation
n1=narcolepsie | n2=en:retardation | rel=r_associated | relid=0 | w=10
- non précisée, hydrocèle ---
r_associated #0: 10 -->
en:retardation
n1=non précisée, hydrocèle | n2=en:retardation | rel=r_associated | relid=0 | w=10
- non précisée, tumeur maligne du col de l'utérus ---
r_associated #0: 10 -->
en:retardation
n1=non précisée, tumeur maligne du col de l'utérus | n2=en:retardation | rel=r_associated | relid=0 | w=10
- névralgie du trijumeau ---
r_associated #0: 10 -->
en:retardation
n1=névralgie du trijumeau | n2=en:retardation | rel=r_associated | relid=0 | w=10
- névralgie essentielle du trijumeau ---
r_associated #0: 10 -->
en:retardation
n1=névralgie essentielle du trijumeau | n2=en:retardation | rel=r_associated | relid=0 | w=10
- névralgie faciale ---
r_associated #0: 10 -->
en:retardation
n1=névralgie faciale | n2=en:retardation | rel=r_associated | relid=0 | w=10
- névralgie trigéminale ---
r_associated #0: 10 -->
en:retardation
n1=névralgie trigéminale | n2=en:retardation | rel=r_associated | relid=0 | w=10
- névrose ---
r_associated #0: 10 -->
en:retardation
n1=névrose | n2=en:retardation | rel=r_associated | relid=0 | w=10
- oedème cytotoxique cortical ---
r_associated #0: 10 -->
en:retardation
n1=oedème cytotoxique cortical | n2=en:retardation | rel=r_associated | relid=0 | w=10
- omphalocèle ---
r_associated #0: 10 -->
en:retardation
n1=omphalocèle | n2=en:retardation | rel=r_associated | relid=0 | w=10
- opsoclonus ---
r_associated #0: 10 -->
en:retardation
n1=opsoclonus | n2=en:retardation | rel=r_associated | relid=0 | w=10
- oreillons ---
r_associated #0: 10 -->
en:retardation
n1=oreillons | n2=en:retardation | rel=r_associated | relid=0 | w=10
- oreillons sans complication ---
r_associated #0: 10 -->
en:retardation
n1=oreillons sans complication | n2=en:retardation | rel=r_associated | relid=0 | w=10
- oreillons sans mention de complications ---
r_associated #0: 10 -->
en:retardation
n1=oreillons sans mention de complications | n2=en:retardation | rel=r_associated | relid=0 | w=10
- ostéoporose ---
r_associated #0: 10 -->
en:retardation
n1=ostéoporose | n2=en:retardation | rel=r_associated | relid=0 | w=10
- otite séromuqueuse ---
r_associated #0: 10 -->
en:retardation
n1=otite séromuqueuse | n2=en:retardation | rel=r_associated | relid=0 | w=10
- otocéphalie ---
r_associated #0: 10 -->
en:retardation
n1=otocéphalie | n2=en:retardation | rel=r_associated | relid=0 | w=10
- palud
(paludisme) ---
r_associated #0: 10 -->
en:retardation
n1=palud (paludisme) | n2=en:retardation | rel=r_associated | relid=0 | w=10
- paralysie générale ---
r_associated #0: 10 -->
en:retardation
n1=paralysie générale | n2=en:retardation | rel=r_associated | relid=0 | w=10
- parkinsonisme ---
r_associated #0: 10 -->
en:retardation
n1=parkinsonisme | n2=en:retardation | rel=r_associated | relid=0 | w=10
- parotidite infectieuse ---
r_associated #0: 10 -->
en:retardation
n1=parotidite infectieuse | n2=en:retardation | rel=r_associated | relid=0 | w=10
- parotidite ourlienne ---
r_associated #0: 10 -->
en:retardation
n1=parotidite ourlienne | n2=en:retardation | rel=r_associated | relid=0 | w=10
- parotidite épidémique ---
r_associated #0: 10 -->
en:retardation
n1=parotidite épidémique | n2=en:retardation | rel=r_associated | relid=0 | w=10
- parésie ---
r_associated #0: 10 -->
en:retardation
n1=parésie | n2=en:retardation | rel=r_associated | relid=0 | w=10
- parésie faciale ---
r_associated #0: 10 -->
en:retardation
n1=parésie faciale | n2=en:retardation | rel=r_associated | relid=0 | w=10
- polyneuropathie ---
r_associated #0: 10 -->
en:retardation
n1=polyneuropathie | n2=en:retardation | rel=r_associated | relid=0 | w=10
- polysyndactylie ---
r_associated #0: 10 -->
en:retardation
n1=polysyndactylie | n2=en:retardation | rel=r_associated | relid=0 | w=10
- pseudo-tumeur ---
r_associated #0: 10 -->
en:retardation
n1=pseudo-tumeur | n2=en:retardation | rel=r_associated | relid=0 | w=10
- pterygium colli ---
r_associated #0: 10 -->
en:retardation
n1=pterygium colli | n2=en:retardation | rel=r_associated | relid=0 | w=10
- ptérygium colli ---
r_associated #0: 10 -->
en:retardation
n1=ptérygium colli | n2=en:retardation | rel=r_associated | relid=0 | w=10
- retard de croissance staturo-pondérale ---
r_associated #0: 10 -->
en:retardation
n1=retard de croissance staturo-pondérale | n2=en:retardation | rel=r_associated | relid=0 | w=10
- réaction schizophrène ---
r_associated #0: 10 -->
en:retardation
n1=réaction schizophrène | n2=en:retardation | rel=r_associated | relid=0 | w=10
- rétinite pigmentaire, surdité, retard mental, et hypogonadisme ---
r_associated #0: 10 -->
en:retardation
n1=rétinite pigmentaire, surdité, retard mental, et hypogonadisme | n2=en:retardation | rel=r_associated | relid=0 | w=10
- schizencéphalie ---
r_associated #0: 10 -->
en:retardation
n1=schizencéphalie | n2=en:retardation | rel=r_associated | relid=0 | w=10
- situs inversus ---
r_associated #0: 10 -->
en:retardation
n1=situs inversus | n2=en:retardation | rel=r_associated | relid=0 | w=10
- spina bifida ---
r_associated #0: 10 -->
en:retardation
n1=spina bifida | n2=en:retardation | rel=r_associated | relid=0 | w=10
- spina bifida occulta ---
r_associated #0: 10 -->
en:retardation
n1=spina bifida occulta | n2=en:retardation | rel=r_associated | relid=0 | w=10
- splénomégalie ---
r_associated #0: 10 -->
en:retardation
n1=splénomégalie | n2=en:retardation | rel=r_associated | relid=0 | w=10
- strabisme ---
r_associated #0: 10 -->
en:retardation
n1=strabisme | n2=en:retardation | rel=r_associated | relid=0 | w=10
- sténose du pylore ---
r_associated #0: 10 -->
en:retardation
n1=sténose du pylore | n2=en:retardation | rel=r_associated | relid=0 | w=10
- surdité ---
r_associated #0: 10 -->
en:retardation
n1=surdité | n2=en:retardation | rel=r_associated | relid=0 | w=10
- syndrome cataracte-ataxie-surdité et retard mental ---
r_associated #0: 10 -->
en:retardation
n1=syndrome cataracte-ataxie-surdité et retard mental | n2=en:retardation | rel=r_associated | relid=0 | w=10
- syndrome de Rett ---
r_associated #0: 10 -->
en:retardation
n1=syndrome de Rett | n2=en:retardation | rel=r_associated | relid=0 | w=10
- syndrome de Treft-Sanborn-Carey ---
r_associated #0: 10 -->
en:retardation
n1=syndrome de Treft-Sanborn-Carey | n2=en:retardation | rel=r_associated | relid=0 | w=10
- syndrome de la selle turcique vide ---
r_associated #0: 10 -->
en:retardation
n1=syndrome de la selle turcique vide | n2=en:retardation | rel=r_associated | relid=0 | w=10
- thrombose d'un sinus sagittal ---
r_associated #0: 10 -->
en:retardation
n1=thrombose d'un sinus sagittal | n2=en:retardation | rel=r_associated | relid=0 | w=10
- thrombose de l'artère cérébrale ---
r_associated #0: 10 -->
en:retardation
n1=thrombose de l'artère cérébrale | n2=en:retardation | rel=r_associated | relid=0 | w=10
- thrombose de sinus sagittaux ---
r_associated #0: 10 -->
en:retardation
n1=thrombose de sinus sagittaux | n2=en:retardation | rel=r_associated | relid=0 | w=10
- thrombose des sinus sagittaux ---
r_associated #0: 10 -->
en:retardation
n1=thrombose des sinus sagittaux | n2=en:retardation | rel=r_associated | relid=0 | w=10
- thrombose du sinus sagittal ---
r_associated #0: 10 -->
en:retardation
n1=thrombose du sinus sagittal | n2=en:retardation | rel=r_associated | relid=0 | w=10
- tic douloureux ---
r_associated #0: 10 -->
en:retardation
n1=tic douloureux | n2=en:retardation | rel=r_associated | relid=0 | w=10
- tic douloureux de la face ---
r_associated #0: 10 -->
en:retardation
n1=tic douloureux de la face | n2=en:retardation | rel=r_associated | relid=0 | w=10
- toxoplasmose ---
r_associated #0: 10 -->
en:retardation
n1=toxoplasmose | n2=en:retardation | rel=r_associated | relid=0 | w=10
- trachome ---
r_associated #0: 10 -->
en:retardation
n1=trachome | n2=en:retardation | rel=r_associated | relid=0 | w=10
- trichomégalie avec retard mental, nanisme, et dégénérescence pigmentée de la rétine ---
r_associated #0: 10 -->
en:retardation
n1=trichomégalie avec retard mental, nanisme, et dégénérescence pigmentée de la rétine | n2=en:retardation | rel=r_associated | relid=0 | w=10
- trouble alimentaire ---
r_associated #0: 10 -->
en:retardation
n1=trouble alimentaire | n2=en:retardation | rel=r_associated | relid=0 | w=10
- trouble anxieux ---
r_associated #0: 10 -->
en:retardation
n1=trouble anxieux | n2=en:retardation | rel=r_associated | relid=0 | w=10
- trouble de la conduction du coeur ---
r_associated #0: 10 -->
en:retardation
n1=trouble de la conduction du coeur | n2=en:retardation | rel=r_associated | relid=0 | w=10
- trouble du rythme cardiaque ---
r_associated #0: 10 -->
en:retardation
n1=trouble du rythme cardiaque | n2=en:retardation | rel=r_associated | relid=0 | w=10
- trouble neurologique du développement ---
r_associated #0: 10 -->
en:retardation
n1=trouble neurologique du développement | n2=en:retardation | rel=r_associated | relid=0 | w=10
- troubles comportementaux ---
r_associated #0: 10 -->
en:retardation
n1=troubles comportementaux | n2=en:retardation | rel=r_associated | relid=0 | w=10
- troubles du comportement ---
r_associated #0: 10 -->
en:retardation
n1=troubles du comportement | n2=en:retardation | rel=r_associated | relid=0 | w=10
- tumeur de la prostate ---
r_associated #0: 10 -->
en:retardation
n1=tumeur de la prostate | n2=en:retardation | rel=r_associated | relid=0 | w=10
- tumeur du système nerveux central ---
r_associated #0: 10 -->
en:retardation
n1=tumeur du système nerveux central | n2=en:retardation | rel=r_associated | relid=0 | w=10
- tumeur maligne de la peau ---
r_associated #0: 10 -->
en:retardation
n1=tumeur maligne de la peau | n2=en:retardation | rel=r_associated | relid=0 | w=10
- tumeur maligne du col de l'utérus ---
r_associated #0: 10 -->
en:retardation
n1=tumeur maligne du col de l'utérus | n2=en:retardation | rel=r_associated | relid=0 | w=10
- tumeur maligne du col utérin ---
r_associated #0: 10 -->
en:retardation
n1=tumeur maligne du col utérin | n2=en:retardation | rel=r_associated | relid=0 | w=10
- tumeur maligne gastrique ---
r_associated #0: 10 -->
en:retardation
n1=tumeur maligne gastrique | n2=en:retardation | rel=r_associated | relid=0 | w=10
- tétanie ---
r_associated #0: 10 -->
en:retardation
n1=tétanie | n2=en:retardation | rel=r_associated | relid=0 | w=10
- urticaire-surdité-amylose rénale ---
r_associated #0: 10 -->
en:retardation
n1=urticaire-surdité-amylose rénale | n2=en:retardation | rel=r_associated | relid=0 | w=10
- urétérocèle ---
r_associated #0: 10 -->
en:retardation
n1=urétérocèle | n2=en:retardation | rel=r_associated | relid=0 | w=10
- ventriculomégalie cérébrale ---
r_associated #0: 10 -->
en:retardation
n1=ventriculomégalie cérébrale | n2=en:retardation | rel=r_associated | relid=0 | w=10
- Épilepsie ---
r_associated #0: 10 -->
en:retardation
n1=Épilepsie | n2=en:retardation | rel=r_associated | relid=0 | w=10
- épanchement pleural ---
r_associated #0: 10 -->
en:retardation
n1=épanchement pleural | n2=en:retardation | rel=r_associated | relid=0 | w=10
- épilepsie ---
r_associated #0: 10 -->
en:retardation
n1=épilepsie | n2=en:retardation | rel=r_associated | relid=0 | w=10
- érythème fessier du nourrisson ---
r_associated #0: 10 -->
en:retardation
n1=érythème fessier du nourrisson | n2=en:retardation | rel=r_associated | relid=0 | w=10
- état de mal épileptique ---
r_associated #0: 10 -->
en:retardation
n1=état de mal épileptique | n2=en:retardation | rel=r_associated | relid=0 | w=10
- arriération mentale légère ---
r_associated #0: 6 -->
en:retardation
n1=arriération mentale légère | n2=en:retardation | rel=r_associated | relid=0 | w=6
- arriération mentale moyenne ---
r_associated #0: 6 -->
en:retardation
n1=arriération mentale moyenne | n2=en:retardation | rel=r_associated | relid=0 | w=6
- ARRX ---
r_associated #0: 5 -->
en:retardation
n1=ARRX | n2=en:retardation | rel=r_associated | relid=0 | w=5
- Effet cytopathique ---
r_associated #0: 5 -->
en:retardation
n1=Effet cytopathique | n2=en:retardation | rel=r_associated | relid=0 | w=5
- Endocriniens ---
r_associated #0: 5 -->
en:retardation
n1=Endocriniens | n2=en:retardation | rel=r_associated | relid=0 | w=5
- Handicap mental ---
r_associated #0: 5 -->
en:retardation
n1=Handicap mental | n2=en:retardation | rel=r_associated | relid=0 | w=5
- Handicap psychique ---
r_associated #0: 5 -->
en:retardation
n1=Handicap psychique | n2=en:retardation | rel=r_associated | relid=0 | w=5
- Quotient intellectuel ---
r_associated #0: 5 -->
en:retardation
n1=Quotient intellectuel | n2=en:retardation | rel=r_associated | relid=0 | w=5
- Tronc cérébral ---
r_associated #0: 5 -->
en:retardation
n1=Tronc cérébral | n2=en:retardation | rel=r_associated | relid=0 | w=5
- Trouble psychiatrique ---
r_associated #0: 5 -->
en:retardation
n1=Trouble psychiatrique | n2=en:retardation | rel=r_associated | relid=0 | w=5
- Trouble psychique ---
r_associated #0: 5 -->
en:retardation
n1=Trouble psychique | n2=en:retardation | rel=r_associated | relid=0 | w=5
- Trouble somatoforme ---
r_associated #0: 5 -->
en:retardation
n1=Trouble somatoforme | n2=en:retardation | rel=r_associated | relid=0 | w=5
- aVf ---
r_associated #0: 5 -->
en:retardation
n1=aVf | n2=en:retardation | rel=r_associated | relid=0 | w=5
- abcès cérébral ---
r_associated #0: 5 -->
en:retardation
n1=abcès cérébral | n2=en:retardation | rel=r_associated | relid=0 | w=5
- absence de croissance ---
r_associated #0: 5 -->
en:retardation
n1=absence de croissance | n2=en:retardation | rel=r_associated | relid=0 | w=5
- accident cérébrovasculaire ---
r_associated #0: 5 -->
en:retardation
n1=accident cérébrovasculaire | n2=en:retardation | rel=r_associated | relid=0 | w=5
- accident vasculaire cérébral ---
r_associated #0: 5 -->
en:retardation
n1=accident vasculaire cérébral | n2=en:retardation | rel=r_associated | relid=0 | w=5
- accès fébriles ---
r_associated #0: 5 -->
en:retardation
n1=accès fébriles | n2=en:retardation | rel=r_associated | relid=0 | w=5
- affection nerveuse périphérique ---
r_associated #0: 5 -->
en:retardation
n1=affection nerveuse périphérique | n2=en:retardation | rel=r_associated | relid=0 | w=5
- altération de la conscience ---
r_associated #0: 5 -->
en:retardation
n1=altération de la conscience | n2=en:retardation | rel=r_associated | relid=0 | w=5
- altération mentale ---
r_associated #0: 5 -->
en:retardation
n1=altération mentale | n2=en:retardation | rel=r_associated | relid=0 | w=5
- anomalie congénitale ---
r_associated #0: 5 -->
en:retardation
n1=anomalie congénitale | n2=en:retardation | rel=r_associated | relid=0 | w=5
- arrière-pied ---
r_associated #0: 5 -->
en:retardation
n1=arrière-pied | n2=en:retardation | rel=r_associated | relid=0 | w=5
- arriération mentale de sévérité non précisée ---
r_associated #0: 5 -->
en:retardation
n1=arriération mentale de sévérité non précisée | n2=en:retardation | rel=r_associated | relid=0 | w=5
- arriération mentale modérée ---
r_associated #0: 5 -->
en:retardation
n1=arriération mentale modérée | n2=en:retardation | rel=r_associated | relid=0 | w=5
- arriération mentale profonde ---
r_associated #0: 5 -->
en:retardation
n1=arriération mentale profonde | n2=en:retardation | rel=r_associated | relid=0 | w=5
- arriération mentale sévère ---
r_associated #0: 5 -->
en:retardation
n1=arriération mentale sévère | n2=en:retardation | rel=r_associated | relid=0 | w=5
- arythmie ---
r_associated #0: 5 -->
en:retardation
n1=arythmie | n2=en:retardation | rel=r_associated | relid=0 | w=5
- astrocyte ---
r_associated #0: 5 -->
en:retardation
n1=astrocyte | n2=en:retardation | rel=r_associated | relid=0 | w=5
- atteinte extrapyramidale ---
r_associated #0: 5 -->
en:retardation
n1=atteinte extrapyramidale | n2=en:retardation | rel=r_associated | relid=0 | w=5
- blindness ---
r_associated #0: 5 -->
en:retardation
n1=blindness | n2=en:retardation | rel=r_associated | relid=0 | w=5
- cancer cutané ---
r_associated #0: 5 -->
en:retardation
n1=cancer cutané | n2=en:retardation | rel=r_associated | relid=0 | w=5
- cancer de la peau ---
r_associated #0: 5 -->
en:retardation
n1=cancer de la peau | n2=en:retardation | rel=r_associated | relid=0 | w=5
- cancer gastrique ---
r_associated #0: 5 -->
en:retardation
n1=cancer gastrique | n2=en:retardation | rel=r_associated | relid=0 | w=5
- carcinome gastrique ---
r_associated #0: 5 -->
en:retardation
n1=carcinome gastrique | n2=en:retardation | rel=r_associated | relid=0 | w=5
- contraction clonique ---
r_associated #0: 5 -->
en:retardation
n1=contraction clonique | n2=en:retardation | rel=r_associated | relid=0 | w=5
- coupant avec des ciseaux ---
r_associated #0: 5 -->
en:retardation
n1=coupant avec des ciseaux | n2=en:retardation | rel=r_associated | relid=0 | w=5
- craniosynostose ---
r_associated #0: 5 -->
en:retardation
n1=craniosynostose | n2=en:retardation | rel=r_associated | relid=0 | w=5
- crises fébriles ---
r_associated #0: 5 -->
en:retardation
n1=crises fébriles | n2=en:retardation | rel=r_associated | relid=0 | w=5
- crânio-sténose ---
r_associated #0: 5 -->
en:retardation
n1=crânio-sténose | n2=en:retardation | rel=r_associated | relid=0 | w=5
- difficulté d'apprentissage de la lecture ---
r_associated #0: 5 -->
en:retardation
n1=difficulté d'apprentissage de la lecture | n2=en:retardation | rel=r_associated | relid=0 | w=5
- dysphagia ---
r_associated #0: 5 -->
en:retardation
n1=dysphagia | n2=en:retardation | rel=r_associated | relid=0 | w=5
- dysrythmie cardiaque non précisée ---
r_associated #0: 5 -->
en:retardation
n1=dysrythmie cardiaque non précisée | n2=en:retardation | rel=r_associated | relid=0 | w=5
- décalage de la tête ---
r_associated #0: 5 -->
en:retardation
n1=décalage de la tête | n2=en:retardation | rel=r_associated | relid=0 | w=5
- défaut articulatoire ---
r_associated #0: 5 -->
en:retardation
n1=défaut articulatoire | n2=en:retardation | rel=r_associated | relid=0 | w=5
- déficit du développement psychomoteur ---
r_associated #0: 5 -->
en:retardation
n1=déficit du développement psychomoteur | n2=en:retardation | rel=r_associated | relid=0 | w=5
- dégénérescence cytopathique ---
r_associated #0: 5 -->
en:retardation
n1=dégénérescence cytopathique | n2=en:retardation | rel=r_associated | relid=0 | w=5
- dégénérescence des ganglions de la base ---
r_associated #0: 5 -->
en:retardation
n1=dégénérescence des ganglions de la base | n2=en:retardation | rel=r_associated | relid=0 | w=5
- dégénérescence spongieuse ---
r_associated #0: 5 -->
en:retardation
n1=dégénérescence spongieuse | n2=en:retardation | rel=r_associated | relid=0 | w=5
- détérioration intellectuelle ---
r_associated #0: 5 -->
en:retardation
n1=détérioration intellectuelle | n2=en:retardation | rel=r_associated | relid=0 | w=5
- ectopia ---
r_associated #0: 5 -->
en:retardation
n1=ectopia | n2=en:retardation | rel=r_associated | relid=0 | w=5
- effet cytopathique ---
r_associated #0: 5 -->
en:retardation
n1=effet cytopathique | n2=en:retardation | rel=r_associated | relid=0 | w=5
- effusion pleurale ---
r_associated #0: 5 -->
en:retardation
n1=effusion pleurale | n2=en:retardation | rel=r_associated | relid=0 | w=5
- embole pulmonaire ---
r_associated #0: 5 -->
en:retardation
n1=embole pulmonaire | n2=en:retardation | rel=r_associated | relid=0 | w=5
- embolie du poumon ---
r_associated #0: 5 -->
en:retardation
n1=embolie du poumon | n2=en:retardation | rel=r_associated | relid=0 | w=5
- embolie pulmonaire ---
r_associated #0: 5 -->
en:retardation
n1=embolie pulmonaire | n2=en:retardation | rel=r_associated | relid=0 | w=5
- emphysème du poumon ---
r_associated #0: 5 -->
en:retardation
n1=emphysème du poumon | n2=en:retardation | rel=r_associated | relid=0 | w=5
- emphysème pulmonaire ---
r_associated #0: 5 -->
en:retardation
n1=emphysème pulmonaire | n2=en:retardation | rel=r_associated | relid=0 | w=5
- en:Seckel syndrome ---
r_associated #0: 5 -->
en:retardation
n1=en:Seckel syndrome | n2=en:retardation | rel=r_associated | relid=0 | w=5
- en:backwardness ---
r_associated #0: 5 -->
en:retardation
n1=en:backwardness | n2=en:retardation | rel=r_associated | relid=0 | w=5
- en:brains ---
r_associated #0: 5 -->
en:retardation
n1=en:brains | n2=en:retardation | rel=r_associated | relid=0 | w=5
- en:brainstem ---
r_associated #0: 5 -->
en:retardation
n1=en:brainstem | n2=en:retardation | rel=r_associated | relid=0 | w=5
- en:congenital anomaly ---
r_associated #0: 5 -->
en:retardation
n1=en:congenital anomaly | n2=en:retardation | rel=r_associated | relid=0 | w=5
- en:deceleration ---
r_associated #0: 5 -->
en:retardation
n1=en:deceleration | n2=en:retardation | rel=r_associated | relid=0 | w=5
- en:lag ---
r_associated #0: 5 -->
en:retardation
n1=en:lag | n2=en:retardation | rel=r_associated | relid=0 | w=5
- en:malignant neoplasm of skin ---
r_associated #0: 5 -->
en:retardation
n1=en:malignant neoplasm of skin | n2=en:retardation | rel=r_associated | relid=0 | w=5
- en:malignant tumor of cervix ---
r_associated #0: 5 -->
en:retardation
n1=en:malignant tumor of cervix | n2=en:retardation | rel=r_associated | relid=0 | w=5
- en:meninx ---
r_associated #0: 5 -->
en:retardation
n1=en:meninx | n2=en:retardation | rel=r_associated | relid=0 | w=5
- en:muscle twitch ---
r_associated #0: 5 -->
en:retardation
n1=en:muscle twitch | n2=en:retardation | rel=r_associated | relid=0 | w=5
- en:peripheral neuropathy ---
r_associated #0: 5 -->
en:retardation
n1=en:peripheral neuropathy | n2=en:retardation | rel=r_associated | relid=0 | w=5
- en:serous otitis media ---
r_associated #0: 5 -->
en:retardation
n1=en:serous otitis media | n2=en:retardation | rel=r_associated | relid=0 | w=5
- en:slowdown ---
r_associated #0: 5 -->
en:retardation
n1=en:slowdown | n2=en:retardation | rel=r_associated | relid=0 | w=5
- en:slowness ---
r_associated #0: 5 -->
en:retardation
n1=en:slowness | n2=en:retardation | rel=r_associated | relid=0 | w=5
- en:subnormality ---
r_associated #0: 5 -->
en:retardation
n1=en:subnormality | n2=en:retardation | rel=r_associated | relid=0 | w=5
- en:twitching ---
r_associated #0: 5 -->
en:retardation
n1=en:twitching | n2=en:retardation | rel=r_associated | relid=0 | w=5
- encoprésie ---
r_associated #0: 5 -->
en:retardation
n1=encoprésie | n2=en:retardation | rel=r_associated | relid=0 | w=5
- epilepsy ---
r_associated #0: 5 -->
en:retardation
n1=epilepsy | n2=en:retardation | rel=r_associated | relid=0 | w=5
- erreur de réfraction ---
r_associated #0: 5 -->
en:retardation
n1=erreur de réfraction | n2=en:retardation | rel=r_associated | relid=0 | w=5
- faiblesse musculaire du visage ---
r_associated #0: 5 -->
en:retardation
n1=faiblesse musculaire du visage | n2=en:retardation | rel=r_associated | relid=0 | w=5
- fasciculation d'un muscle squelettique ---
r_associated #0: 5 -->
en:retardation
n1=fasciculation d'un muscle squelettique | n2=en:retardation | rel=r_associated | relid=0 | w=5
- fibrillation et flutter auriculaires ---
r_associated #0: 5 -->
en:retardation
n1=fibrillation et flutter auriculaires | n2=en:retardation | rel=r_associated | relid=0 | w=5
- fracture du fémur ---
r_associated #0: 5 -->
en:retardation
n1=fracture du fémur | n2=en:retardation | rel=r_associated | relid=0 | w=5
- hamartome ---
r_associated #0: 5 -->
en:retardation
n1=hamartome | n2=en:retardation | rel=r_associated | relid=0 | w=5
- hydrocéphalie ---
r_associated #0: 5 -->
en:retardation
n1=hydrocéphalie | n2=en:retardation | rel=r_associated | relid=0 | w=5
- hypotonie du nouveau-né ---
r_associated #0: 5 -->
en:retardation
n1=hypotonie du nouveau-né | n2=en:retardation | rel=r_associated | relid=0 | w=5
- insuffisance hépatique transitoire ---
r_associated #0: 5 -->
en:retardation
n1=insuffisance hépatique transitoire | n2=en:retardation | rel=r_associated | relid=0 | w=5
- intelligence moyenne ---
r_associated #0: 5 -->
en:retardation
n1=intelligence moyenne | n2=en:retardation | rel=r_associated | relid=0 | w=5
- leuco-encéphalopathie ---
r_associated #0: 5 -->
en:retardation
n1=leuco-encéphalopathie | n2=en:retardation | rel=r_associated | relid=0 | w=5
- leucoencéphalopathie ---
r_associated #0: 5 -->
en:retardation
n1=leucoencéphalopathie | n2=en:retardation | rel=r_associated | relid=0 | w=5
- lipome ---
r_associated #0: 5 -->
en:retardation
n1=lipome | n2=en:retardation | rel=r_associated | relid=0 | w=5
- maladie des urines avec odeur de sirop erable ---
r_associated #0: 5 -->
en:retardation
n1=maladie des urines avec odeur de sirop erable | n2=en:retardation | rel=r_associated | relid=0 | w=5
- malformation artérioveineuse cérébrale ---
r_associated #0: 5 -->
en:retardation
n1=malformation artérioveineuse cérébrale | n2=en:retardation | rel=r_associated | relid=0 | w=5
- malformation congénitale ---
r_associated #0: 5 -->
en:retardation
n1=malformation congénitale | n2=en:retardation | rel=r_associated | relid=0 | w=5
- malformation rachidienne congénitale ---
r_associated #0: 5 -->
en:retardation
n1=malformation rachidienne congénitale | n2=en:retardation | rel=r_associated | relid=0 | w=5
- myatrophie ---
r_associated #0: 5 -->
en:retardation
n1=myatrophie | n2=en:retardation | rel=r_associated | relid=0 | w=5
- méningiome angiomateux ---
r_associated #0: 5 -->
en:retardation
n1=méningiome angiomateux | n2=en:retardation | rel=r_associated | relid=0 | w=5
- neuropathie périphérique ---
r_associated #0: 5 -->
en:retardation
n1=neuropathie périphérique | n2=en:retardation | rel=r_associated | relid=0 | w=5
- névralgie du nerf trijumeau ---
r_associated #0: 5 -->
en:retardation
n1=névralgie du nerf trijumeau | n2=en:retardation | rel=r_associated | relid=0 | w=5
- oreillons sans mention de complication ---
r_associated #0: 5 -->
en:retardation
n1=oreillons sans mention de complication | n2=en:retardation | rel=r_associated | relid=0 | w=5
- paralysie cérébrale ---
r_associated #0: 5 -->
en:retardation
n1=paralysie cérébrale | n2=en:retardation | rel=r_associated | relid=0 | w=5
- poliomyélite aiguë ---
r_associated #0: 5 -->
en:retardation
n1=poliomyélite aiguë | n2=en:retardation | rel=r_associated | relid=0 | w=5
- pseudotumeur ---
r_associated #0: 5 -->
en:retardation
n1=pseudotumeur | n2=en:retardation | rel=r_associated | relid=0 | w=5
- quotient intellectuel moyen ---
r_associated #0: 5 -->
en:retardation
n1=quotient intellectuel moyen | n2=en:retardation | rel=r_associated | relid=0 | w=5
- réaction schizoïde ---
r_associated #0: 5 -->
en:retardation
n1=réaction schizoïde | n2=en:retardation | rel=r_associated | relid=0 | w=5
- secousse musculaire ---
r_associated #0: 5 -->
en:retardation
n1=secousse musculaire | n2=en:retardation | rel=r_associated | relid=0 | w=5
- sommeil paradoxal (REM) anormal ---
r_associated #0: 5 -->
en:retardation
n1=sommeil paradoxal (REM) anormal | n2=en:retardation | rel=r_associated | relid=0 | w=5
- sténose pylorique ---
r_associated #0: 5 -->
en:retardation
n1=sténose pylorique | n2=en:retardation | rel=r_associated | relid=0 | w=5
- syndrome de Reye ---
r_associated #0: 5 -->
en:retardation
n1=syndrome de Reye | n2=en:retardation | rel=r_associated | relid=0 | w=5
- syndrome du retard de développement ---
r_associated #0: 5 -->
en:retardation
n1=syndrome du retard de développement | n2=en:retardation | rel=r_associated | relid=0 | w=5
- syndrome tumeur de Wilms-aniridie-anomalies génito-urinaires-retard mental ---
r_associated #0: 5 -->
en:retardation
n1=syndrome tumeur de Wilms-aniridie-anomalies génito-urinaires-retard mental | n2=en:retardation | rel=r_associated | relid=0 | w=5
- thrombose artérielle cérébrale ---
r_associated #0: 5 -->
en:retardation
n1=thrombose artérielle cérébrale | n2=en:retardation | rel=r_associated | relid=0 | w=5
- trouble chromosomique ---
r_associated #0: 5 -->
en:retardation
n1=trouble chromosomique | n2=en:retardation | rel=r_associated | relid=0 | w=5
- trouble d'acquisition de la lecture ---
r_associated #0: 5 -->
en:retardation
n1=trouble d'acquisition de la lecture | n2=en:retardation | rel=r_associated | relid=0 | w=5
- trouble de comportement en société ---
r_associated #0: 5 -->
en:retardation
n1=trouble de comportement en société | n2=en:retardation | rel=r_associated | relid=0 | w=5
- trouble extrapyramidal ---
r_associated #0: 5 -->
en:retardation
n1=trouble extrapyramidal | n2=en:retardation | rel=r_associated | relid=0 | w=5
- trouble mental dans l'enfance ---
r_associated #0: 5 -->
en:retardation
n1=trouble mental dans l'enfance | n2=en:retardation | rel=r_associated | relid=0 | w=5
- trouble mental diagnostique dans l'enfance ---
r_associated #0: 5 -->
en:retardation
n1=trouble mental diagnostique dans l'enfance | n2=en:retardation | rel=r_associated | relid=0 | w=5
- trouble mental organique ---
r_associated #0: 5 -->
en:retardation
n1=trouble mental organique | n2=en:retardation | rel=r_associated | relid=0 | w=5
- trouble nerveux périphérique ---
r_associated #0: 5 -->
en:retardation
n1=trouble nerveux périphérique | n2=en:retardation | rel=r_associated | relid=0 | w=5
- troubles mentaux dans l'enfance ---
r_associated #0: 5 -->
en:retardation
n1=troubles mentaux dans l'enfance | n2=en:retardation | rel=r_associated | relid=0 | w=5
- tumeur bénigne des organes urinaires ---
r_associated #0: 5 -->
en:retardation
n1=tumeur bénigne des organes urinaires | n2=en:retardation | rel=r_associated | relid=0 | w=5
- tumeur maligne de l'estomac ---
r_associated #0: 5 -->
en:retardation
n1=tumeur maligne de l'estomac | n2=en:retardation | rel=r_associated | relid=0 | w=5
- tumeur maligne de la prostate ---
r_associated #0: 5 -->
en:retardation
n1=tumeur maligne de la prostate | n2=en:retardation | rel=r_associated | relid=0 | w=5
- tumeur maligne prostatique ---
r_associated #0: 5 -->
en:retardation
n1=tumeur maligne prostatique | n2=en:retardation | rel=r_associated | relid=0 | w=5
- écholalie ---
r_associated #0: 5 -->
en:retardation
n1=écholalie | n2=en:retardation | rel=r_associated | relid=0 | w=5
- épanchement pleural liquidien ---
r_associated #0: 5 -->
en:retardation
n1=épanchement pleural liquidien | n2=en:retardation | rel=r_associated | relid=0 | w=5
- évolution chronique-progressive avec épisodes de détérioration rapide après fièvre ou traumatisme crânien ---
r_associated #0: 5 -->
en:retardation
n1=évolution chronique-progressive avec épisodes de détérioration rapide après fièvre ou traumatisme crânien | n2=en:retardation | rel=r_associated | relid=0 | w=5
- en:chains ---
r_associated #0: 3 -->
en:retardation
n1=en:chains | n2=en:retardation | rel=r_associated | relid=0 | w=3
- en:mildly ---
r_associated #0: 3 -->
en:retardation
n1=en:mildly | n2=en:retardation | rel=r_associated | relid=0 | w=3
- en:abusing ---
r_associated #0: 2 -->
en:retardation
n1=en:abusing | n2=en:retardation | rel=r_associated | relid=0 | w=2
- en:agitation ---
r_associated #0: 2 -->
en:retardation
n1=en:agitation | n2=en:retardation | rel=r_associated | relid=0 | w=2
- en:childhood ---
r_associated #0: 2 -->
en:retardation
n1=en:childhood | n2=en:retardation | rel=r_associated | relid=0 | w=2
- en:coma ---
r_associated #0: 2 -->
en:retardation
n1=en:coma | n2=en:retardation | rel=r_associated | relid=0 | w=2
- en:furthering ---
r_associated #0: 2 -->
en:retardation
n1=en:furthering | n2=en:retardation | rel=r_associated | relid=0 | w=2
- en:inventing ---
r_associated #0: 2 -->
en:retardation
n1=en:inventing | n2=en:retardation | rel=r_associated | relid=0 | w=2
- en:malformed ---
r_associated #0: 2 -->
en:retardation
n1=en:malformed | n2=en:retardation | rel=r_associated | relid=0 | w=2
- en:palate ---
r_associated #0: 2 -->
en:retardation
n1=en:palate | n2=en:retardation | rel=r_associated | relid=0 | w=2
- en:respite ---
r_associated #0: 2 -->
en:retardation
n1=en:respite | n2=en:retardation | rel=r_associated | relid=0 | w=2
- en:seizure ---
r_associated #0: 2 -->
en:retardation
n1=en:seizure | n2=en:retardation | rel=r_associated | relid=0 | w=2
- en:untreated ---
r_associated #0: 2 -->
en:retardation
n1=en:untreated | n2=en:retardation | rel=r_associated | relid=0 | w=2
- en:weakness ---
r_associated #0: 2 -->
en:retardation
n1=en:weakness | n2=en:retardation | rel=r_associated | relid=0 | w=2
- en:abnormally ---
r_associated #0: 1 -->
en:retardation
n1=en:abnormally | n2=en:retardation | rel=r_associated | relid=0 | w=1
- en:abruption ---
r_associated #0: 1 -->
en:retardation
n1=en:abruption | n2=en:retardation | rel=r_associated | relid=0 | w=1
- en:absence ---
r_associated #0: 1 -->
en:retardation
n1=en:absence | n2=en:retardation | rel=r_associated | relid=0 | w=1
- en:abuse ---
r_associated #0: 1 -->
en:retardation
n1=en:abuse | n2=en:retardation | rel=r_associated | relid=0 | w=1
- en:abused ---
r_associated #0: 1 -->
en:retardation
n1=en:abused | n2=en:retardation | rel=r_associated | relid=0 | w=1
- en:adducting ---
r_associated #0: 1 -->
en:retardation
n1=en:adducting | n2=en:retardation | rel=r_associated | relid=0 | w=1
- en:adolescence ---
r_associated #0: 1 -->
en:retardation
n1=en:adolescence | n2=en:retardation | rel=r_associated | relid=0 | w=1
- en:aging ---
r_associated #0: 1 -->
en:retardation
n1=en:aging | n2=en:retardation | rel=r_associated | relid=0 | w=1
- en:assessments ---
r_associated #0: 1 -->
en:retardation
n1=en:assessments | n2=en:retardation | rel=r_associated | relid=0 | w=1
- en:associates ---
r_associated #0: 1 -->
en:retardation
n1=en:associates | n2=en:retardation | rel=r_associated | relid=0 | w=1
- en:associating ---
r_associated #0: 1 -->
en:retardation
n1=en:associating | n2=en:retardation | rel=r_associated | relid=0 | w=1
- en:beaked ---
r_associated #0: 1 -->
en:retardation
n1=en:beaked | n2=en:retardation | rel=r_associated | relid=0 | w=1
- en:birth ---
r_associated #0: 1 -->
en:retardation
n1=en:birth | n2=en:retardation | rel=r_associated | relid=0 | w=1
- en:birthing ---
r_associated #0: 1 -->
en:retardation
n1=en:birthing | n2=en:retardation | rel=r_associated | relid=0 | w=1
- en:causing ---
r_associated #0: 1 -->
en:retardation
n1=en:causing | n2=en:retardation | rel=r_associated | relid=0 | w=1
- en:cere ---
r_associated #0: 1 -->
en:retardation
n1=en:cere | n2=en:retardation | rel=r_associated | relid=0 | w=1
- en:cerebellar ---
r_associated #0: 1 -->
en:retardation
n1=en:cerebellar | n2=en:retardation | rel=r_associated | relid=0 | w=1
- en:ceres ---
r_associated #0: 1 -->
en:retardation
n1=en:ceres | n2=en:retardation | rel=r_associated | relid=0 | w=1
- en:chained ---
r_associated #0: 1 -->
en:retardation
n1=en:chained | n2=en:retardation | rel=r_associated | relid=0 | w=1
- en:chaining ---
r_associated #0: 1 -->
en:retardation
n1=en:chaining | n2=en:retardation | rel=r_associated | relid=0 | w=1
- en:characteristic ---
r_associated #0: 1 -->
en:retardation
n1=en:characteristic | n2=en:retardation | rel=r_associated | relid=0 | w=1
- en:characterizing ---
r_associated #0: 1 -->
en:retardation
n1=en:characterizing | n2=en:retardation | rel=r_associated | relid=0 | w=1
- en:compensator ---
r_associated #0: 1 -->
en:retardation
n1=en:compensator | n2=en:retardation | rel=r_associated | relid=0 | w=1
- en:competency ---
r_associated #0: 1 -->
en:retardation
n1=en:competency | n2=en:retardation | rel=r_associated | relid=0 | w=1
- en:cretinism ---
r_associated #0: 1 -->
en:retardation
n1=en:cretinism | n2=en:retardation | rel=r_associated | relid=0 | w=1
- en:cst ---
r_associated #0: 1 -->
en:retardation
n1=en:cst | n2=en:retardation | rel=r_associated | relid=0 | w=1
- en:cushing ---
r_associated #0: 1 -->
en:retardation
n1=en:cushing | n2=en:retardation | rel=r_associated | relid=0 | w=1
- en:decisional ---
r_associated #0: 1 -->
en:retardation
n1=en:decisional | n2=en:retardation | rel=r_associated | relid=0 | w=1
- en:defect ---
r_associated #0: 1 -->
en:retardation
n1=en:defect | n2=en:retardation | rel=r_associated | relid=0 | w=1
- en:defecting ---
r_associated #0: 1 -->
en:retardation
n1=en:defecting | n2=en:retardation | rel=r_associated | relid=0 | w=1
- en:defiant ---
r_associated #0: 1 -->
en:retardation
n1=en:defiant | n2=en:retardation | rel=r_associated | relid=0 | w=1
- en:delay ---
r_associated #0: 1 -->
en:retardation
n1=en:delay | n2=en:retardation | rel=r_associated | relid=0 | w=1
- en:delayed ---
r_associated #0: 1 -->
en:retardation
n1=en:delayed | n2=en:retardation | rel=r_associated | relid=0 | w=1
- en:diagnoses ---
r_associated #0: 1 -->
en:retardation
n1=en:diagnoses | n2=en:retardation | rel=r_associated | relid=0 | w=1
- en:diagnosing ---
r_associated #0: 1 -->
en:retardation
n1=en:diagnosing | n2=en:retardation | rel=r_associated | relid=0 | w=1
- en:disabling ---
r_associated #0: 1 -->
en:retardation
n1=en:disabling | n2=en:retardation | rel=r_associated | relid=0 | w=1
- en:dislocated ---
r_associated #0: 1 -->
en:retardation
n1=en:dislocated | n2=en:retardation | rel=r_associated | relid=0 | w=1
- en:dislocating ---
r_associated #0: 1 -->
en:retardation
n1=en:dislocating | n2=en:retardation | rel=r_associated | relid=0 | w=1
- en:dissociative ---
r_associated #0: 1 -->
en:retardation
n1=en:dissociative | n2=en:retardation | rel=r_associated | relid=0 | w=1
- en:dysgenesis ---
r_associated #0: 1 -->
en:retardation
n1=en:dysgenesis | n2=en:retardation | rel=r_associated | relid=0 | w=1
- en:electrophoretic ---
r_associated #0: 1 -->
en:retardation
n1=en:electrophoretic | n2=en:retardation | rel=r_associated | relid=0 | w=1
- en:fetal ---
r_associated #0: 1 -->
en:retardation
n1=en:fetal | n2=en:retardation | rel=r_associated | relid=0 | w=1
- en:folic ---
r_associated #0: 1 -->
en:retardation
n1=en:folic | n2=en:retardation | rel=r_associated | relid=0 | w=1
- en:foundational ---
r_associated #0: 1 -->
en:retardation
n1=en:foundational | n2=en:retardation | rel=r_associated | relid=0 | w=1
- en:gale ---
r_associated #0: 1 -->
en:retardation
n1=en:gale | n2=en:retardation | rel=r_associated | relid=0 | w=1
- en:handicapping ---
r_associated #0: 1 -->
en:retardation
n1=en:handicapping | n2=en:retardation | rel=r_associated | relid=0 | w=1
- en:huntington ---
r_associated #0: 1 -->
en:retardation
n1=en:huntington | n2=en:retardation | rel=r_associated | relid=0 | w=1
- en:hydrocephaluses ---
r_associated #0: 1 -->
en:retardation
n1=en:hydrocephaluses | n2=en:retardation | rel=r_associated | relid=0 | w=1
- en:hypo ---
r_associated #0: 1 -->
en:retardation
n1=en:hypo | n2=en:retardation | rel=r_associated | relid=0 | w=1
- en:identifying ---
r_associated #0: 1 -->
en:retardation
n1=en:identifying | n2=en:retardation | rel=r_associated | relid=0 | w=1
- en:impairing ---
r_associated #0: 1 -->
en:retardation
n1=en:impairing | n2=en:retardation | rel=r_associated | relid=0 | w=1
- en:impairment ---
r_associated #0: 1 -->
en:retardation
n1=en:impairment | n2=en:retardation | rel=r_associated | relid=0 | w=1
- en:individualizing ---
r_associated #0: 1 -->
en:retardation
n1=en:individualizing | n2=en:retardation | rel=r_associated | relid=0 | w=1
- en:infancy ---
r_associated #0: 1 -->
en:retardation
n1=en:infancy | n2=en:retardation | rel=r_associated | relid=0 | w=1
- en:intermittent ---
r_associated #0: 1 -->
en:retardation
n1=en:intermittent | n2=en:retardation | rel=r_associated | relid=0 | w=1
- en:invented ---
r_associated #0: 1 -->
en:retardation
n1=en:invented | n2=en:retardation | rel=r_associated | relid=0 | w=1
- en:iq ---
r_associated #0: 1 -->
en:retardation
n1=en:iq | n2=en:retardation | rel=r_associated | relid=0 | w=1
- en:iud ---
r_associated #0: 1 -->
en:retardation
n1=en:iud | n2=en:retardation | rel=r_associated | relid=0 | w=1
- en:learnt ---
r_associated #0: 1 -->
en:retardation
n1=en:learnt | n2=en:retardation | rel=r_associated | relid=0 | w=1
- en:linked ---
r_associated #0: 1 -->
en:retardation
n1=en:linked | n2=en:retardation | rel=r_associated | relid=0 | w=1
- en:malformation ---
r_associated #0: 1 -->
en:retardation
n1=en:malformation | n2=en:retardation | rel=r_associated | relid=0 | w=1
- en:mendelian ---
r_associated #0: 1 -->
en:retardation
n1=en:mendelian | n2=en:retardation | rel=r_associated | relid=0 | w=1
- en:mental defectiveness ---
r_associated #0: 1 -->
en:retardation
n1=en:mental defectiveness | n2=en:retardation | rel=r_associated | relid=0 | w=1
- en:mitigated ---
r_associated #0: 1 -->
en:retardation
n1=en:mitigated | n2=en:retardation | rel=r_associated | relid=0 | w=1
- en:moderating ---
r_associated #0: 1 -->
en:retardation
n1=en:moderating | n2=en:retardation | rel=r_associated | relid=0 | w=1
- en:modulator ---
r_associated #0: 1 -->
en:retardation
n1=en:modulator | n2=en:retardation | rel=r_associated | relid=0 | w=1
- en:mps ---
r_associated #0: 1 -->
en:retardation
n1=en:mps | n2=en:retardation | rel=r_associated | relid=0 | w=1
- en:ness ---
r_associated #0: 1 -->
en:retardation
n1=en:ness | n2=en:retardation | rel=r_associated | relid=0 | w=1
- en:neuroleptics ---
r_associated #0: 1 -->
en:retardation
n1=en:neuroleptics | n2=en:retardation | rel=r_associated | relid=0 | w=1
- en:neuropsychological ---
r_associated #0: 1 -->
en:retardation
n1=en:neuropsychological | n2=en:retardation | rel=r_associated | relid=0 | w=1
- en:newborn ---
r_associated #0: 1 -->
en:retardation
n1=en:newborn | n2=en:retardation | rel=r_associated | relid=0 | w=1
- en:palpebral ---
r_associated #0: 1 -->
en:retardation
n1=en:palpebral | n2=en:retardation | rel=r_associated | relid=0 | w=1
- en:pituitary ---
r_associated #0: 1 -->
en:retardation
n1=en:pituitary | n2=en:retardation | rel=r_associated | relid=0 | w=1
- en:prescreening ---
r_associated #0: 1 -->
en:retardation
n1=en:prescreening | n2=en:retardation | rel=r_associated | relid=0 | w=1
- en:preterm ---
r_associated #0: 1 -->
en:retardation
n1=en:preterm | n2=en:retardation | rel=r_associated | relid=0 | w=1
- en:psychomotor ---
r_associated #0: 1 -->
en:retardation
n1=en:psychomotor | n2=en:retardation | rel=r_associated | relid=0 | w=1
- en:rf ---
r_associated #0: 1 -->
en:retardation
n1=en:rf | n2=en:retardation | rel=r_associated | relid=0 | w=1
- en:savant ---
r_associated #0: 1 -->
en:retardation
n1=en:savant | n2=en:retardation | rel=r_associated | relid=0 | w=1
- en:seckel ---
r_associated #0: 1 -->
en:retardation
n1=en:seckel | n2=en:retardation | rel=r_associated | relid=0 | w=1
- en:sequelae ---
r_associated #0: 1 -->
en:retardation
n1=en:sequelae | n2=en:retardation | rel=r_associated | relid=0 | w=1
- en:severity ---
r_associated #0: 1 -->
en:retardation
n1=en:severity | n2=en:retardation | rel=r_associated | relid=0 | w=1
- en:slower ---
r_associated #0: 1 -->
en:retardation
n1=en:slower | n2=en:retardation | rel=r_associated | relid=0 | w=1
- en:sociocultural ---
r_associated #0: 1 -->
en:retardation
n1=en:sociocultural | n2=en:retardation | rel=r_associated | relid=0 | w=1
- en:socioeconomic ---
r_associated #0: 1 -->
en:retardation
n1=en:socioeconomic | n2=en:retardation | rel=r_associated | relid=0 | w=1
- en:sparse ---
r_associated #0: 1 -->
en:retardation
n1=en:sparse | n2=en:retardation | rel=r_associated | relid=0 | w=1
- en:stereotypic ---
r_associated #0: 1 -->
en:retardation
n1=en:stereotypic | n2=en:retardation | rel=r_associated | relid=0 | w=1
- en:thrive ---
r_associated #0: 1 -->
en:retardation
n1=en:thrive | n2=en:retardation | rel=r_associated | relid=0 | w=1
- en:thriven ---
r_associated #0: 1 -->
en:retardation
n1=en:thriven | n2=en:retardation | rel=r_associated | relid=0 | w=1
- en:throve ---
r_associated #0: 1 -->
en:retardation
n1=en:throve | n2=en:retardation | rel=r_associated | relid=0 | w=1
- en:tremor ---
r_associated #0: 1 -->
en:retardation
n1=en:tremor | n2=en:retardation | rel=r_associated | relid=0 | w=1
|