'en:pericellular fibrosis of congenital syphilis'
(id=6746200 ; fe=en:pericellular fibrosis of congenital syphilis ; type=1 ; niveau=200 ;
luminosité=25 ;
somme entrante=11250 creation date=2017-06-22 touchdate=2025-12-24 01:13:59.000) ≈ 187 relations sortantes
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 41 / 1 ->
en:congenital complete atrioventricular block
n1=en:pericellular fibrosis of congenital syphilis | n2=en:congenital complete atrioventricular block | rel=r_associated | relid=0 | w=41
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 36 / 0.878 ->
en:fetal disorder
n1=en:pericellular fibrosis of congenital syphilis | n2=en:fetal disorder | rel=r_associated | relid=0 | w=36
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 35 / 0.854 ->
en:abnormal root proximity between adjacent teeth
n1=en:pericellular fibrosis of congenital syphilis | n2=en:abnormal root proximity between adjacent teeth | rel=r_associated | relid=0 | w=35
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 35 / 0.854 ->
en:congenital arcus juvenilis
n1=en:pericellular fibrosis of congenital syphilis | n2=en:congenital arcus juvenilis | rel=r_associated | relid=0 | w=35
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 35 / 0.854 ->
en:congenital cardiac failure
n1=en:pericellular fibrosis of congenital syphilis | n2=en:congenital cardiac failure | rel=r_associated | relid=0 | w=35
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 35 / 0.854 ->
en:prader-willi syndrome
n1=en:pericellular fibrosis of congenital syphilis | n2=en:prader-willi syndrome | rel=r_associated | relid=0 | w=35
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 34 / 0.829 ->
en:congenital accessory skin tag
n1=en:pericellular fibrosis of congenital syphilis | n2=en:congenital accessory skin tag | rel=r_associated | relid=0 | w=34
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 34 / 0.829 ->
en:congenital anal fissure
n1=en:pericellular fibrosis of congenital syphilis | n2=en:congenital anal fissure | rel=r_associated | relid=0 | w=34
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 34 / 0.829 ->
en:congenital axial myopia
n1=en:pericellular fibrosis of congenital syphilis | n2=en:congenital axial myopia | rel=r_associated | relid=0 | w=34
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 34 / 0.829 ->
en:congenital cutaneous angiomatosis
n1=en:pericellular fibrosis of congenital syphilis | n2=en:congenital cutaneous angiomatosis | rel=r_associated | relid=0 | w=34
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 34 / 0.829 ->
en:congenital dysarthria
n1=en:pericellular fibrosis of congenital syphilis | n2=en:congenital dysarthria | rel=r_associated | relid=0 | w=34
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 34 / 0.829 ->
en:congenital fibrinogen abnormality
n1=en:pericellular fibrosis of congenital syphilis | n2=en:congenital fibrinogen abnormality | rel=r_associated | relid=0 | w=34
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 34 / 0.829 ->
en:congenital functional disorders of the small intestine
n1=en:pericellular fibrosis of congenital syphilis | n2=en:congenital functional disorders of the small intestine | rel=r_associated | relid=0 | w=34
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 34 / 0.829 ->
en:congenital hepatic fibrosis
n1=en:pericellular fibrosis of congenital syphilis | n2=en:congenital hepatic fibrosis | rel=r_associated | relid=0 | w=34
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 34 / 0.829 ->
en:congenital hepatic porphyria
n1=en:pericellular fibrosis of congenital syphilis | n2=en:congenital hepatic porphyria | rel=r_associated | relid=0 | w=34
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 34 / 0.829 ->
en:periportal fibrosis
n1=en:pericellular fibrosis of congenital syphilis | n2=en:periportal fibrosis | rel=r_associated | relid=0 | w=34
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 32 / 0.78 ->
en:congenital alpha-2-antiplasmin deficiency
n1=en:pericellular fibrosis of congenital syphilis | n2=en:congenital alpha-2-antiplasmin deficiency | rel=r_associated | relid=0 | w=32
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 32 / 0.78 ->
en:congenital anemia
n1=en:pericellular fibrosis of congenital syphilis | n2=en:congenital anemia | rel=r_associated | relid=0 | w=32
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 32 / 0.78 ->
en:congenital blepharophimosis of lower eyelid
n1=en:pericellular fibrosis of congenital syphilis | n2=en:congenital blepharophimosis of lower eyelid | rel=r_associated | relid=0 | w=32
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 32 / 0.78 ->
en:congenital respiratory disorder
n1=en:pericellular fibrosis of congenital syphilis | n2=en:congenital respiratory disorder | rel=r_associated | relid=0 | w=32
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 32 / 0.78 ->
en:tooth malformation
n1=en:pericellular fibrosis of congenital syphilis | n2=en:tooth malformation | rel=r_associated | relid=0 | w=32
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 31 / 0.756 ->
en:congenital blood disorder
n1=en:pericellular fibrosis of congenital syphilis | n2=en:congenital blood disorder | rel=r_associated | relid=0 | w=31
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 31 / 0.756 ->
en:congenital constriction of pylorus
n1=en:pericellular fibrosis of congenital syphilis | n2=en:congenital constriction of pylorus | rel=r_associated | relid=0 | w=31
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 31 / 0.756 ->
en:congenital facial asymmetry
n1=en:pericellular fibrosis of congenital syphilis | n2=en:congenital facial asymmetry | rel=r_associated | relid=0 | w=31
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 31 / 0.756 ->
en:congenital muscle disorder
n1=en:pericellular fibrosis of congenital syphilis | n2=en:congenital muscle disorder | rel=r_associated | relid=0 | w=31
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 30 / 0.732 ->
en:cirrhosis
n1=en:pericellular fibrosis of congenital syphilis | n2=en:cirrhosis | rel=r_associated | relid=0 | w=30
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 30 / 0.732 ->
en:congenital atrophy of thyroid
n1=en:pericellular fibrosis of congenital syphilis | n2=en:congenital atrophy of thyroid | rel=r_associated | relid=0 | w=30
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 30 / 0.732 ->
en:congenital bundle of his tachycardia
n1=en:pericellular fibrosis of congenital syphilis | n2=en:congenital bundle of his tachycardia | rel=r_associated | relid=0 | w=30
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 30 / 0.732 ->
en:congenital celiac disease
n1=en:pericellular fibrosis of congenital syphilis | n2=en:congenital celiac disease | rel=r_associated | relid=0 | w=30
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 30 / 0.732 ->
en:congenital cyst of vulva
n1=en:pericellular fibrosis of congenital syphilis | n2=en:congenital cyst of vulva | rel=r_associated | relid=0 | w=30
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 30 / 0.732 ->
en:congenital functional disorders of the colon
n1=en:pericellular fibrosis of congenital syphilis | n2=en:congenital functional disorders of the colon | rel=r_associated | relid=0 | w=30
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 30 / 0.732 ->
en:congenital infectious disease
n1=en:pericellular fibrosis of congenital syphilis | n2=en:congenital infectious disease | rel=r_associated | relid=0 | w=30
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 30 / 0.732 ->
en:congenital pneumonia
n1=en:pericellular fibrosis of congenital syphilis | n2=en:congenital pneumonia | rel=r_associated | relid=0 | w=30
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 30 / 0.732 ->
en:congenital/genetic syndrome with poikiloderma
n1=en:pericellular fibrosis of congenital syphilis | n2=en:congenital/genetic syndrome with poikiloderma | rel=r_associated | relid=0 | w=30
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 30 / 0.732 ->
en:right atrial appendage absent
n1=en:pericellular fibrosis of congenital syphilis | n2=en:right atrial appendage absent | rel=r_associated | relid=0 | w=30
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 30 / 0.732 ->
en:truncal valve overriding ventricular septum
n1=en:pericellular fibrosis of congenital syphilis | n2=en:truncal valve overriding ventricular septum | rel=r_associated | relid=0 | w=30
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 29 / 0.707 ->
en:cap myopathy
n1=en:pericellular fibrosis of congenital syphilis | n2=en:cap myopathy | rel=r_associated | relid=0 | w=29
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 29 / 0.707 ->
en:congenital brain damage
n1=en:pericellular fibrosis of congenital syphilis | n2=en:congenital brain damage | rel=r_associated | relid=0 | w=29
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 29 / 0.707 ->
en:congenital choroidal fold
n1=en:pericellular fibrosis of congenital syphilis | n2=en:congenital choroidal fold | rel=r_associated | relid=0 | w=29
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 29 / 0.707 ->
en:congenital ear disorder
n1=en:pericellular fibrosis of congenital syphilis | n2=en:congenital ear disorder | rel=r_associated | relid=0 | w=29
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 29 / 0.707 ->
en:congenital fecaliths
n1=en:pericellular fibrosis of congenital syphilis | n2=en:congenital fecaliths | rel=r_associated | relid=0 | w=29
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 29 / 0.707 ->
en:congenital flat foot
n1=en:pericellular fibrosis of congenital syphilis | n2=en:congenital flat foot | rel=r_associated | relid=0 | w=29
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 29 / 0.707 ->
en:congenital skin disorder
n1=en:pericellular fibrosis of congenital syphilis | n2=en:congenital skin disorder | rel=r_associated | relid=0 | w=29
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 29 / 0.707 ->
en:extensive congenital erosions, vesicles and reticulate scarring
n1=en:pericellular fibrosis of congenital syphilis | n2=en:extensive congenital erosions, vesicles and reticulate scarring | rel=r_associated | relid=0 | w=29
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 29 / 0.707 ->
en:fordyce's disease
n1=en:pericellular fibrosis of congenital syphilis | n2=en:fordyce's disease | rel=r_associated | relid=0 | w=29
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 29 / 0.707 ->
en:north american indian childhood cirrhosis
n1=en:pericellular fibrosis of congenital syphilis | n2=en:north american indian childhood cirrhosis | rel=r_associated | relid=0 | w=29
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 29 / 0.707 ->
en:vitamin d-dependent rickets, type 2
n1=en:pericellular fibrosis of congenital syphilis | n2=en:vitamin d-dependent rickets, type 2 | rel=r_associated | relid=0 | w=29
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 28 / 0.683 ->
en:alcoholic fibrosis and sclerosis of liver
n1=en:pericellular fibrosis of congenital syphilis | n2=en:alcoholic fibrosis and sclerosis of liver | rel=r_associated | relid=0 | w=28
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 28 / 0.683 ->
en:arthrogryposis
n1=en:pericellular fibrosis of congenital syphilis | n2=en:arthrogryposis | rel=r_associated | relid=0 | w=28
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 28 / 0.683 ->
en:becker generalized myotonia
n1=en:pericellular fibrosis of congenital syphilis | n2=en:becker generalized myotonia | rel=r_associated | relid=0 | w=28
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 28 / 0.683 ->
en:congenital disorder of facial nerve
n1=en:pericellular fibrosis of congenital syphilis | n2=en:congenital disorder of facial nerve | rel=r_associated | relid=0 | w=28
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 28 / 0.683 ->
en:congenital palato-esophageal incoordination
n1=en:pericellular fibrosis of congenital syphilis | n2=en:congenital palato-esophageal incoordination | rel=r_associated | relid=0 | w=28
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 28 / 0.683 ->
en:congenital plasminogen activator inhibitor deficiency type 1
n1=en:pericellular fibrosis of congenital syphilis | n2=en:congenital plasminogen activator inhibitor deficiency type 1 | rel=r_associated | relid=0 | w=28
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 28 / 0.683 ->
en:congenital retinoschisis
n1=en:pericellular fibrosis of congenital syphilis | n2=en:congenital retinoschisis | rel=r_associated | relid=0 | w=28
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 28 / 0.683 ->
en:congenital uremia
n1=en:pericellular fibrosis of congenital syphilis | n2=en:congenital uremia | rel=r_associated | relid=0 | w=28
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 28 / 0.683 ->
en:parachute malformation of left atrioventricular valve
n1=en:pericellular fibrosis of congenital syphilis | n2=en:parachute malformation of left atrioventricular valve | rel=r_associated | relid=0 | w=28
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 27 / 0.659 ->
en:chronic diarrhea due to glucoamylase deficiency
n1=en:pericellular fibrosis of congenital syphilis | n2=en:chronic diarrhea due to glucoamylase deficiency | rel=r_associated | relid=0 | w=27
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 27 / 0.659 ->
en:congenital blepharophimosis of upper eyelid
n1=en:pericellular fibrosis of congenital syphilis | n2=en:congenital blepharophimosis of upper eyelid | rel=r_associated | relid=0 | w=27
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 27 / 0.659 ->
en:congenital cardiovascular disorder
n1=en:pericellular fibrosis of congenital syphilis | n2=en:congenital cardiovascular disorder | rel=r_associated | relid=0 | w=27
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 27 / 0.659 ->
en:congenital claw toe
n1=en:pericellular fibrosis of congenital syphilis | n2=en:congenital claw toe | rel=r_associated | relid=0 | w=27
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 27 / 0.659 ->
en:congenital elephantiasis
n1=en:pericellular fibrosis of congenital syphilis | n2=en:congenital elephantiasis | rel=r_associated | relid=0 | w=27
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 27 / 0.659 ->
en:congenital factor ix deficiency variant
n1=en:pericellular fibrosis of congenital syphilis | n2=en:congenital factor ix deficiency variant | rel=r_associated | relid=0 | w=27
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 27 / 0.659 ->
en:congenital hydrocele
n1=en:pericellular fibrosis of congenital syphilis | n2=en:congenital hydrocele | rel=r_associated | relid=0 | w=27
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 27 / 0.659 ->
en:congenital reproductive system disorder
n1=en:pericellular fibrosis of congenital syphilis | n2=en:congenital reproductive system disorder | rel=r_associated | relid=0 | w=27
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 27 / 0.659 ->
en:pipestem portal cirrhosis
n1=en:pericellular fibrosis of congenital syphilis | n2=en:pipestem portal cirrhosis | rel=r_associated | relid=0 | w=27
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 27 / 0.659 ->
en:right atrial appendage - left - juxtaposition
n1=en:pericellular fibrosis of congenital syphilis | n2=en:right atrial appendage - left - juxtaposition | rel=r_associated | relid=0 | w=27
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 26 / 0.634 ->
en:chromosome disorder
n1=en:pericellular fibrosis of congenital syphilis | n2=en:chromosome disorder | rel=r_associated | relid=0 | w=26
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 26 / 0.634 ->
en:congenital auditory imperception
n1=en:pericellular fibrosis of congenital syphilis | n2=en:congenital auditory imperception | rel=r_associated | relid=0 | w=26
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 26 / 0.634 ->
en:congenital blocked tear duct
n1=en:pericellular fibrosis of congenital syphilis | n2=en:congenital blocked tear duct | rel=r_associated | relid=0 | w=26
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 26 / 0.634 ->
en:congenital debility of fetus
n1=en:pericellular fibrosis of congenital syphilis | n2=en:congenital debility of fetus | rel=r_associated | relid=0 | w=26
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 26 / 0.634 ->
en:congenital digestive system disorder
n1=en:pericellular fibrosis of congenital syphilis | n2=en:congenital digestive system disorder | rel=r_associated | relid=0 | w=26
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 26 / 0.634 ->
en:congenital esotropia
n1=en:pericellular fibrosis of congenital syphilis | n2=en:congenital esotropia | rel=r_associated | relid=0 | w=26
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 26 / 0.634 ->
en:congenital factor ix deficiency without inhibitor
n1=en:pericellular fibrosis of congenital syphilis | n2=en:congenital factor ix deficiency without inhibitor | rel=r_associated | relid=0 | w=26
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 26 / 0.634 ->
en:congenital hernia of bladder
n1=en:pericellular fibrosis of congenital syphilis | n2=en:congenital hernia of bladder | rel=r_associated | relid=0 | w=26
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 26 / 0.634 ->
en:congenital oral/facial/cranial defect
n1=en:pericellular fibrosis of congenital syphilis | n2=en:congenital oral/facial/cranial defect | rel=r_associated | relid=0 | w=26
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 26 / 0.634 ->
en:congenital pancreatic cyst
n1=en:pericellular fibrosis of congenital syphilis | n2=en:congenital pancreatic cyst | rel=r_associated | relid=0 | w=26
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 26 / 0.634 ->
en:congenital skeletal disorder
n1=en:pericellular fibrosis of congenital syphilis | n2=en:congenital skeletal disorder | rel=r_associated | relid=0 | w=26
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 26 / 0.634 ->
en:congenital skin contracture
n1=en:pericellular fibrosis of congenital syphilis | n2=en:congenital skin contracture | rel=r_associated | relid=0 | w=26
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 26 / 0.634 ->
en:congenital stenosis
n1=en:pericellular fibrosis of congenital syphilis | n2=en:congenital stenosis | rel=r_associated | relid=0 | w=26
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 26 / 0.634 ->
en:infant metachromatic leukodystrophies
n1=en:pericellular fibrosis of congenital syphilis | n2=en:infant metachromatic leukodystrophies | rel=r_associated | relid=0 | w=26
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 25 / 0.61 ->
en:congenital abnormality
n1=en:pericellular fibrosis of congenital syphilis | n2=en:congenital abnormality | rel=r_associated | relid=0 | w=25
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 25 / 0.61 ->
en:congenital connective tissue disorder
n1=en:pericellular fibrosis of congenital syphilis | n2=en:congenital connective tissue disorder | rel=r_associated | relid=0 | w=25
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 25 / 0.61 ->
en:congenital dysphasia
n1=en:pericellular fibrosis of congenital syphilis | n2=en:congenital dysphasia | rel=r_associated | relid=0 | w=25
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 25 / 0.61 ->
en:congenital end-plate acetylcholinesterase deficiency
n1=en:pericellular fibrosis of congenital syphilis | n2=en:congenital end-plate acetylcholinesterase deficiency | rel=r_associated | relid=0 | w=25
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 25 / 0.61 ->
en:congenital hearing disorder
n1=en:pericellular fibrosis of congenital syphilis | n2=en:congenital hearing disorder | rel=r_associated | relid=0 | w=25
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 25 / 0.61 ->
en:congenital immunodeficiency disease
n1=en:pericellular fibrosis of congenital syphilis | n2=en:congenital immunodeficiency disease | rel=r_associated | relid=0 | w=25
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 25 / 0.61 ->
en:congenital leptin deficiency
n1=en:pericellular fibrosis of congenital syphilis | n2=en:congenital leptin deficiency | rel=r_associated | relid=0 | w=25
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 25 / 0.61 ->
en:congenital malignant melanoma
n1=en:pericellular fibrosis of congenital syphilis | n2=en:congenital malignant melanoma | rel=r_associated | relid=0 | w=25
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 25 / 0.61 ->
en:digeorge syndrome
n1=en:pericellular fibrosis of congenital syphilis | n2=en:digeorge syndrome | rel=r_associated | relid=0 | w=25
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 25 / 0.61 ->
en:parachute malformation of right atrioventricular valve
n1=en:pericellular fibrosis of congenital syphilis | n2=en:parachute malformation of right atrioventricular valve | rel=r_associated | relid=0 | w=25
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 25 / 0.61 ->
en:regional congenital anomaly
n1=en:pericellular fibrosis of congenital syphilis | n2=en:regional congenital anomaly | rel=r_associated | relid=0 | w=25
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 24 / 0.585 ->
en:congenital
n1=en:pericellular fibrosis of congenital syphilis | n2=en:congenital | rel=r_associated | relid=0 | w=24
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 24 / 0.585 ->
en:congenital and developmental myasthenia
n1=en:pericellular fibrosis of congenital syphilis | n2=en:congenital and developmental myasthenia | rel=r_associated | relid=0 | w=24
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 24 / 0.585 ->
en:congenital eye disorder
n1=en:pericellular fibrosis of congenital syphilis | n2=en:congenital eye disorder | rel=r_associated | relid=0 | w=24
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 24 / 0.585 ->
en:congenital neutrophil actin dysfunction
n1=en:pericellular fibrosis of congenital syphilis | n2=en:congenital neutrophil actin dysfunction | rel=r_associated | relid=0 | w=24
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 24 / 0.585 ->
en:dental arch length loss secondary to congenitally missing teeth
n1=en:pericellular fibrosis of congenital syphilis | n2=en:dental arch length loss secondary to congenitally missing teeth | rel=r_associated | relid=0 | w=24
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 24 / 0.585 ->
en:hutch diverticulum
n1=en:pericellular fibrosis of congenital syphilis | n2=en:hutch diverticulum | rel=r_associated | relid=0 | w=24
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 23 / 0.561 ->
en:congenital factor ix deficiency with inhibitor
n1=en:pericellular fibrosis of congenital syphilis | n2=en:congenital factor ix deficiency with inhibitor | rel=r_associated | relid=0 | w=23
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 23 / 0.561 ->
en:congenital methemoglobinemia
n1=en:pericellular fibrosis of congenital syphilis | n2=en:congenital methemoglobinemia | rel=r_associated | relid=0 | w=23
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 23 / 0.561 ->
en:prominent valve of inferior vena cava
n1=en:pericellular fibrosis of congenital syphilis | n2=en:prominent valve of inferior vena cava | rel=r_associated | relid=0 | w=23
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 23 / 0.561 ->
en:rotation of tooth
n1=en:pericellular fibrosis of congenital syphilis | n2=en:rotation of tooth | rel=r_associated | relid=0 | w=23
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 23 / 0.561 ->
en:true cleft of common atrioventricular valve leaflet
n1=en:pericellular fibrosis of congenital syphilis | n2=en:true cleft of common atrioventricular valve leaflet | rel=r_associated | relid=0 | w=23
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 22 / 0.537 ->
anomalie congénitale
n1=en:pericellular fibrosis of congenital syphilis | n2=anomalie congénitale | rel=r_associated | relid=0 | w=22
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 22 / 0.537 ->
en:congenital amegakaryocytic thrombocytopenia
n1=en:pericellular fibrosis of congenital syphilis | n2=en:congenital amegakaryocytic thrombocytopenia | rel=r_associated | relid=0 | w=22
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 22 / 0.537 ->
en:congenital hypertonia
n1=en:pericellular fibrosis of congenital syphilis | n2=en:congenital hypertonia | rel=r_associated | relid=0 | w=22
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 22 / 0.537 ->
en:congenital inguinal hernia
n1=en:pericellular fibrosis of congenital syphilis | n2=en:congenital inguinal hernia | rel=r_associated | relid=0 | w=22
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 22 / 0.537 ->
en:congenital monosaccharide malabsorption
n1=en:pericellular fibrosis of congenital syphilis | n2=en:congenital monosaccharide malabsorption | rel=r_associated | relid=0 | w=22
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 22 / 0.537 ->
en:congenital pancreatic trypsin deficiency
n1=en:pericellular fibrosis of congenital syphilis | n2=en:congenital pancreatic trypsin deficiency | rel=r_associated | relid=0 | w=22
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 22 / 0.537 ->
en:congenital vascular disorder
n1=en:pericellular fibrosis of congenital syphilis | n2=en:congenital vascular disorder | rel=r_associated | relid=0 | w=22
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 22 / 0.537 ->
en:congenital velopharyngeal dysfunction
n1=en:pericellular fibrosis of congenital syphilis | n2=en:congenital velopharyngeal dysfunction | rel=r_associated | relid=0 | w=22
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 22 / 0.537 ->
en:rudimentary left ventricle
n1=en:pericellular fibrosis of congenital syphilis | n2=en:rudimentary left ventricle | rel=r_associated | relid=0 | w=22
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 22 / 0.537 ->
en:symmer's pipe-stem fibrosis
n1=en:pericellular fibrosis of congenital syphilis | n2=en:symmer's pipe-stem fibrosis | rel=r_associated | relid=0 | w=22
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 21 / 0.512 ->
en:adrenocortical hypofunction, chronic primary congenital
n1=en:pericellular fibrosis of congenital syphilis | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=21
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 21 / 0.512 ->
en:congenital atrophy of left lobe of liver
n1=en:pericellular fibrosis of congenital syphilis | n2=en:congenital atrophy of left lobe of liver | rel=r_associated | relid=0 | w=21
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 21 / 0.512 ->
en:congenital exophthalmos
n1=en:pericellular fibrosis of congenital syphilis | n2=en:congenital exophthalmos | rel=r_associated | relid=0 | w=21
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 21 / 0.512 ->
en:congenital melanocytic nevus of trunk
n1=en:pericellular fibrosis of congenital syphilis | n2=en:congenital melanocytic nevus of trunk | rel=r_associated | relid=0 | w=21
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 21 / 0.512 ->
en:congenital posterior subcapsular polar cataract
n1=en:pericellular fibrosis of congenital syphilis | n2=en:congenital posterior subcapsular polar cataract | rel=r_associated | relid=0 | w=21
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 21 / 0.512 ->
en:fetal congenital tumor causing disproportion
n1=en:pericellular fibrosis of congenital syphilis | n2=en:fetal congenital tumor causing disproportion | rel=r_associated | relid=0 | w=21
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 21 / 0.512 ->
en:parachute malformation of common atrioventricular valve
n1=en:pericellular fibrosis of congenital syphilis | n2=en:parachute malformation of common atrioventricular valve | rel=r_associated | relid=0 | w=21
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 21 / 0.512 ->
en:right atrial endocardial fibroelastosis
n1=en:pericellular fibrosis of congenital syphilis | n2=en:right atrial endocardial fibroelastosis | rel=r_associated | relid=0 | w=21
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 21 / 0.512 ->
en:shortened trunk
n1=en:pericellular fibrosis of congenital syphilis | n2=en:shortened trunk | rel=r_associated | relid=0 | w=21
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 20 / 0.488 ->
affection oculaire congénitale
n1=en:pericellular fibrosis of congenital syphilis | n2=affection oculaire congénitale | rel=r_associated | relid=0 | w=20
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 20 / 0.488 ->
anomalie chromosomique
n1=en:pericellular fibrosis of congenital syphilis | n2=anomalie chromosomique | rel=r_associated | relid=0 | w=20
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 20 / 0.488 ->
anomalie congénitale de l'oeil
n1=en:pericellular fibrosis of congenital syphilis | n2=anomalie congénitale de l'oeil | rel=r_associated | relid=0 | w=20
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 20 / 0.488 ->
anomalie cytogénétique
n1=en:pericellular fibrosis of congenital syphilis | n2=anomalie cytogénétique | rel=r_associated | relid=0 | w=20
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 20 / 0.488 ->
anomalie du développement
n1=en:pericellular fibrosis of congenital syphilis | n2=anomalie du développement | rel=r_associated | relid=0 | w=20
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 20 / 0.488 ->
anormalité des chromosomes
n1=en:pericellular fibrosis of congenital syphilis | n2=anormalité des chromosomes | rel=r_associated | relid=0 | w=20
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 20 / 0.488 ->
arthrogrypose
n1=en:pericellular fibrosis of congenital syphilis | n2=arthrogrypose | rel=r_associated | relid=0 | w=20
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 20 / 0.488 ->
congénital
n1=en:pericellular fibrosis of congenital syphilis | n2=congénital | rel=r_associated | relid=0 | w=20
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 20 / 0.488 ->
congenital
n1=en:pericellular fibrosis of congenital syphilis | n2=congenital | rel=r_associated | relid=0 | w=20
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 20 / 0.488 ->
congénitale
n1=en:pericellular fibrosis of congenital syphilis | n2=congénitale | rel=r_associated | relid=0 | w=20
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 20 / 0.488 ->
débilité congénitale du foetus
n1=en:pericellular fibrosis of congenital syphilis | n2=débilité congénitale du foetus | rel=r_associated | relid=0 | w=20
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 20 / 0.488 ->
débilité congénitale foetale
n1=en:pericellular fibrosis of congenital syphilis | n2=débilité congénitale foetale | rel=r_associated | relid=0 | w=20
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 20 / 0.488 ->
déficience congénitale
n1=en:pericellular fibrosis of congenital syphilis | n2=déficience congénitale | rel=r_associated | relid=0 | w=20
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 20 / 0.488 ->
déformation congénitale
n1=en:pericellular fibrosis of congenital syphilis | n2=déformation congénitale | rel=r_associated | relid=0 | w=20
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 20 / 0.488 ->
difformité congénitale
n1=en:pericellular fibrosis of congenital syphilis | n2=difformité congénitale | rel=r_associated | relid=0 | w=20
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 20 / 0.488 ->
en:birth defect
n1=en:pericellular fibrosis of congenital syphilis | n2=en:birth defect | rel=r_associated | relid=0 | w=20
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 20 / 0.488 ->
en:buphthalmia
n1=en:pericellular fibrosis of congenital syphilis | n2=en:buphthalmia | rel=r_associated | relid=0 | w=20
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 20 / 0.488 ->
en:chromosomal aberration
n1=en:pericellular fibrosis of congenital syphilis | n2=en:chromosomal aberration | rel=r_associated | relid=0 | w=20
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 20 / 0.488 ->
en:chromosomal abnormality
n1=en:pericellular fibrosis of congenital syphilis | n2=en:chromosomal abnormality | rel=r_associated | relid=0 | w=20
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 20 / 0.488 ->
en:congenital analbuminemia
n1=en:pericellular fibrosis of congenital syphilis | n2=en:congenital analbuminemia | rel=r_associated | relid=0 | w=20
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 20 / 0.488 ->
en:congenital anomaly
n1=en:pericellular fibrosis of congenital syphilis | n2=en:congenital anomaly | rel=r_associated | relid=0 | w=20
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 20 / 0.488 ->
en:congenital cyst of aryepiglottic fold
n1=en:pericellular fibrosis of congenital syphilis | n2=en:congenital cyst of aryepiglottic fold | rel=r_associated | relid=0 | w=20
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 20 / 0.488 ->
en:congenital defect
n1=en:pericellular fibrosis of congenital syphilis | n2=en:congenital defect | rel=r_associated | relid=0 | w=20
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 20 / 0.488 ->
en:congenital kyphosis
n1=en:pericellular fibrosis of congenital syphilis | n2=en:congenital kyphosis | rel=r_associated | relid=0 | w=20
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 20 / 0.488 ->
en:congenital laryngeal cyst
n1=en:pericellular fibrosis of congenital syphilis | n2=en:congenital laryngeal cyst | rel=r_associated | relid=0 | w=20
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 20 / 0.488 ->
en:congenital malformation
n1=en:pericellular fibrosis of congenital syphilis | n2=en:congenital malformation | rel=r_associated | relid=0 | w=20
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 20 / 0.488 ->
en:congenital megaprepuce
n1=en:pericellular fibrosis of congenital syphilis | n2=en:congenital megaprepuce | rel=r_associated | relid=0 | w=20
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 20 / 0.488 ->
en:congenital metabolic disorder
n1=en:pericellular fibrosis of congenital syphilis | n2=en:congenital metabolic disorder | rel=r_associated | relid=0 | w=20
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 20 / 0.488 ->
en:congenital nervous system disorder
n1=en:pericellular fibrosis of congenital syphilis | n2=en:congenital nervous system disorder | rel=r_associated | relid=0 | w=20
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 20 / 0.488 ->
en:congenital pain insensitivity
n1=en:pericellular fibrosis of congenital syphilis | n2=en:congenital pain insensitivity | rel=r_associated | relid=0 | w=20
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 20 / 0.488 ->
en:congenital porphyria
n1=en:pericellular fibrosis of congenital syphilis | n2=en:congenital porphyria | rel=r_associated | relid=0 | w=20
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 20 / 0.488 ->
en:congenital quadriplegia
n1=en:pericellular fibrosis of congenital syphilis | n2=en:congenital quadriplegia | rel=r_associated | relid=0 | w=20
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 20 / 0.488 ->
en:developmental anomaly
n1=en:pericellular fibrosis of congenital syphilis | n2=en:developmental anomaly | rel=r_associated | relid=0 | w=20
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 20 / 0.488 ->
en:developmental fault
n1=en:pericellular fibrosis of congenital syphilis | n2=en:developmental fault | rel=r_associated | relid=0 | w=20
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 20 / 0.488 ->
en:erythropoietic porphyria
n1=en:pericellular fibrosis of congenital syphilis | n2=en:erythropoietic porphyria | rel=r_associated | relid=0 | w=20
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 20 / 0.488 ->
en:erythropoietic uroporphyria
n1=en:pericellular fibrosis of congenital syphilis | n2=en:erythropoietic uroporphyria | rel=r_associated | relid=0 | w=20
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 20 / 0.488 ->
en:Fordyce's disease
n1=en:pericellular fibrosis of congenital syphilis | n2=en:Fordyce's disease | rel=r_associated | relid=0 | w=20
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 20 / 0.488 ->
en:Günther's disease
n1=en:pericellular fibrosis of congenital syphilis | n2=en:Günther's disease | rel=r_associated | relid=0 | w=20
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 20 / 0.488 ->
en:hepatic bridging fibrosis
n1=en:pericellular fibrosis of congenital syphilis | n2=en:hepatic bridging fibrosis | rel=r_associated | relid=0 | w=20
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 20 / 0.488 ->
en:infantile myofibromatosis
n1=en:pericellular fibrosis of congenital syphilis | n2=en:infantile myofibromatosis | rel=r_associated | relid=0 | w=20
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 20 / 0.488 ->
en:major physical defect
n1=en:pericellular fibrosis of congenital syphilis | n2=en:major physical defect | rel=r_associated | relid=0 | w=20
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 20 / 0.488 ->
en:megophthalmos
n1=en:pericellular fibrosis of congenital syphilis | n2=en:megophthalmos | rel=r_associated | relid=0 | w=20
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 20 / 0.488 ->
en:mottled teeth, congenital
n1=en:pericellular fibrosis of congenital syphilis | n2=en:mottled teeth, congenital | rel=r_associated | relid=0 | w=20
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 20 / 0.488 ->
en:palmoplantar porokeratosis
n1=en:pericellular fibrosis of congenital syphilis | n2=en:palmoplantar porokeratosis | rel=r_associated | relid=0 | w=20
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 20 / 0.488 ->
en:patent foramen ovale
n1=en:pericellular fibrosis of congenital syphilis | n2=en:patent foramen ovale | rel=r_associated | relid=0 | w=20
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 20 / 0.488 ->
en:physical defect
n1=en:pericellular fibrosis of congenital syphilis | n2=en:physical defect | rel=r_associated | relid=0 | w=20
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 20 / 0.488 ->
en:pigmented paravenous chorioretinal atrophy
n1=en:pericellular fibrosis of congenital syphilis | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 20 / 0.488 ->
en:Prader-Willi syndrome
n1=en:pericellular fibrosis of congenital syphilis | n2=en:Prader-Willi syndrome | rel=r_associated | relid=0 | w=20
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 20 / 0.488 ->
en:teratosis
n1=en:pericellular fibrosis of congenital syphilis | n2=en:teratosis | rel=r_associated | relid=0 | w=20
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 20 / 0.488 ->
en:williams syndrome
n1=en:pericellular fibrosis of congenital syphilis | n2=en:williams syndrome | rel=r_associated | relid=0 | w=20
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 20 / 0.488 ->
en:Williams syndrome
n1=en:pericellular fibrosis of congenital syphilis | n2=en:Williams syndrome | rel=r_associated | relid=0 | w=20
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 20 / 0.488 ->
foramen ovale perméable
n1=en:pericellular fibrosis of congenital syphilis | n2=foramen ovale perméable | rel=r_associated | relid=0 | w=20
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 20 / 0.488 ->
maladie congénitale
n1=en:pericellular fibrosis of congenital syphilis | n2=maladie congénitale | rel=r_associated | relid=0 | w=20
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 20 / 0.488 ->
malformation
n1=en:pericellular fibrosis of congenital syphilis | n2=malformation | rel=r_associated | relid=0 | w=20
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 20 / 0.488 ->
malformation congénitale
n1=en:pericellular fibrosis of congenital syphilis | n2=malformation congénitale | rel=r_associated | relid=0 | w=20
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 20 / 0.488 ->
méthémoglobinémie congénitale
n1=en:pericellular fibrosis of congenital syphilis | n2=méthémoglobinémie congénitale | rel=r_associated | relid=0 | w=20
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 20 / 0.488 ->
méthémoglobinémie héréditaire
n1=en:pericellular fibrosis of congenital syphilis | n2=méthémoglobinémie héréditaire | rel=r_associated | relid=0 | w=20
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 20 / 0.488 ->
myofibromatose infantile
n1=en:pericellular fibrosis of congenital syphilis | n2=myofibromatose infantile | rel=r_associated | relid=0 | w=20
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 20 / 0.488 ->
nystagmus congénital isolé
n1=en:pericellular fibrosis of congenital syphilis | n2=nystagmus congénital isolé | rel=r_associated | relid=0 | w=20
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 20 / 0.488 ->
pathologie congénitale
n1=en:pericellular fibrosis of congenital syphilis | n2=pathologie congénitale | rel=r_associated | relid=0 | w=20
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 20 / 0.488 ->
persistance du foramen ovale
n1=en:pericellular fibrosis of congenital syphilis | n2=persistance du foramen ovale | rel=r_associated | relid=0 | w=20
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 20 / 0.488 ->
porphyrie érythropoïétique
n1=en:pericellular fibrosis of congenital syphilis | n2=porphyrie érythropoïétique | rel=r_associated | relid=0 | w=20
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 20 / 0.488 ->
rétinite pigmentaire paraveineuse
n1=en:pericellular fibrosis of congenital syphilis | n2=rétinite pigmentaire paraveineuse | rel=r_associated | relid=0 | w=20
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 20 / 0.488 ->
tare congénitale
n1=en:pericellular fibrosis of congenital syphilis | n2=tare congénitale | rel=r_associated | relid=0 | w=20
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 20 / 0.488 ->
trouble chromosomique
n1=en:pericellular fibrosis of congenital syphilis | n2=trouble chromosomique | rel=r_associated | relid=0 | w=20
- en:pericellular fibrosis of congenital syphilis --
r_associated #0: 20 / 0.488 ->
vice de conformation
n1=en:pericellular fibrosis of congenital syphilis | n2=vice de conformation | rel=r_associated | relid=0 | w=20
| ≈ 237 relations entrantes
- anomalie congénitale ---
r_associated #0: 334 -->
en:pericellular fibrosis of congenital syphilis
n1=anomalie congénitale | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=334
- en:congenital abnormality ---
r_associated #0: 333 -->
en:pericellular fibrosis of congenital syphilis
n1=en:congenital abnormality | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=333
- anormalité des chromosomes ---
r_associated #0: 322 -->
en:pericellular fibrosis of congenital syphilis
n1=anormalité des chromosomes | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=322
- en:chromosome disorder ---
r_associated #0: 320 -->
en:pericellular fibrosis of congenital syphilis
n1=en:chromosome disorder | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=320
- malformation congénitale ---
r_associated #0: 311 -->
en:pericellular fibrosis of congenital syphilis
n1=malformation congénitale | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=311
- en:congenital defect ---
r_associated #0: 310 -->
en:pericellular fibrosis of congenital syphilis
n1=en:congenital defect | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=310
- en:congenital anomaly ---
r_associated #0: 309 -->
en:pericellular fibrosis of congenital syphilis
n1=en:congenital anomaly | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=309
- déformation congénitale ---
r_associated #0: 296 -->
en:pericellular fibrosis of congenital syphilis
n1=déformation congénitale | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=296
- déficience congénitale ---
r_associated #0: 295 -->
en:pericellular fibrosis of congenital syphilis
n1=déficience congénitale | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=295
- trouble chromosomique ---
r_associated #0: 250 -->
en:pericellular fibrosis of congenital syphilis
n1=trouble chromosomique | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=250
- anomalie chromosomique ---
r_associated #0: 242 -->
en:pericellular fibrosis of congenital syphilis
n1=anomalie chromosomique | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=242
- anomalie congénitale de l'oeil ---
r_associated #0: 209 -->
en:pericellular fibrosis of congenital syphilis
n1=anomalie congénitale de l'oeil | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=209
- difformité congénitale ---
r_associated #0: 205 -->
en:pericellular fibrosis of congenital syphilis
n1=difformité congénitale | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=205
- en:congenital eye disorder ---
r_associated #0: 205 -->
en:pericellular fibrosis of congenital syphilis
n1=en:congenital eye disorder | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=205
- maladie congénitale ---
r_associated #0: 203 -->
en:pericellular fibrosis of congenital syphilis
n1=maladie congénitale | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=203
- affection oculaire congénitale ---
r_associated #0: 200 -->
en:pericellular fibrosis of congenital syphilis
n1=affection oculaire congénitale | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=200
- pathologie congénitale ---
r_associated #0: 195 -->
en:pericellular fibrosis of congenital syphilis
n1=pathologie congénitale | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=195
- en:chromosomal abnormality ---
r_associated #0: 175 -->
en:pericellular fibrosis of congenital syphilis
n1=en:chromosomal abnormality | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=175
- en:congenital malformation ---
r_associated #0: 130 -->
en:pericellular fibrosis of congenital syphilis
n1=en:congenital malformation | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=130
- en:congenital methemoglobinemia ---
r_associated #0: 122 -->
en:pericellular fibrosis of congenital syphilis
n1=en:congenital methemoglobinemia | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=122
- en:birth defect ---
r_associated #0: 120 -->
en:pericellular fibrosis of congenital syphilis
n1=en:birth defect | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=120
- méthémoglobinémie congénitale ---
r_associated #0: 120 -->
en:pericellular fibrosis of congenital syphilis
n1=méthémoglobinémie congénitale | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=120
- tare congénitale ---
r_associated #0: 85 -->
en:pericellular fibrosis of congenital syphilis
n1=tare congénitale | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=85
- congenital ---
r_associated #0: 74 -->
en:pericellular fibrosis of congenital syphilis
n1=congenital | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=74
- en:congenital ---
r_associated #0: 71 -->
en:pericellular fibrosis of congenital syphilis
n1=en:congenital | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=71
- congénitale ---
r_associated #0: 64 -->
en:pericellular fibrosis of congenital syphilis
n1=congénitale | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=64
- persistance du foramen ovale ---
r_associated #0: 61 -->
en:pericellular fibrosis of congenital syphilis
n1=persistance du foramen ovale | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=61
- anomalie cytogénétique ---
r_associated #0: 60 -->
en:pericellular fibrosis of congenital syphilis
n1=anomalie cytogénétique | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=60
- congénital ---
r_associated #0: 59 -->
en:pericellular fibrosis of congenital syphilis
n1=congénital | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=59
- en:patent foramen ovale ---
r_associated #0: 58 -->
en:pericellular fibrosis of congenital syphilis
n1=en:patent foramen ovale | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=58
- vice de conformation ---
r_associated #0: 55 -->
en:pericellular fibrosis of congenital syphilis
n1=vice de conformation | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=55
- foramen ovale perméable ---
r_associated #0: 49 -->
en:pericellular fibrosis of congenital syphilis
n1=foramen ovale perméable | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=49
- en:teratosis ---
r_associated #0: 48 -->
en:pericellular fibrosis of congenital syphilis
n1=en:teratosis | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=48
- en:major physical defect ---
r_associated #0: 47 -->
en:pericellular fibrosis of congenital syphilis
n1=en:major physical defect | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=47
- en:prader-willi syndrome ---
r_associated #0: 47 -->
en:pericellular fibrosis of congenital syphilis
n1=en:prader-willi syndrome | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=47
- en:Prader-Willi syndrome ---
r_associated #0: 45 -->
en:pericellular fibrosis of congenital syphilis
n1=en:Prader-Willi syndrome | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=45
- anomalie du développement ---
r_associated #0: 44 -->
en:pericellular fibrosis of congenital syphilis
n1=anomalie du développement | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=44
- en:physical defect ---
r_associated #0: 44 -->
en:pericellular fibrosis of congenital syphilis
n1=en:physical defect | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=44
- en:congenital kyphosis ---
r_associated #0: 43 -->
en:pericellular fibrosis of congenital syphilis
n1=en:congenital kyphosis | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=43
- en:rotation of tooth ---
r_associated #0: 43 -->
en:pericellular fibrosis of congenital syphilis
n1=en:rotation of tooth | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=43
- en:congenital auditory imperception ---
r_associated #0: 42 -->
en:pericellular fibrosis of congenital syphilis
n1=en:congenital auditory imperception | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=42
- en:congenital leptin deficiency ---
r_associated #0: 42 -->
en:pericellular fibrosis of congenital syphilis
n1=en:congenital leptin deficiency | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=42
- en:tooth malformation ---
r_associated #0: 42 -->
en:pericellular fibrosis of congenital syphilis
n1=en:tooth malformation | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=42
- rétinite pigmentaire paraveineuse ---
r_associated #0: 42 -->
en:pericellular fibrosis of congenital syphilis
n1=rétinite pigmentaire paraveineuse | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=42
- en:congenital digestive system disorder ---
r_associated #0: 41 -->
en:pericellular fibrosis of congenital syphilis
n1=en:congenital digestive system disorder | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=41
- en:williams syndrome ---
r_associated #0: 41 -->
en:pericellular fibrosis of congenital syphilis
n1=en:williams syndrome | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=41
- porphyrie érythropoïétique ---
r_associated #0: 41 -->
en:pericellular fibrosis of congenital syphilis
n1=porphyrie érythropoïétique | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=41
- en:Williams syndrome ---
r_associated #0: 40 -->
en:pericellular fibrosis of congenital syphilis
n1=en:Williams syndrome | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=40
- en:pigmented paravenous chorioretinal atrophy ---
r_associated #0: 40 -->
en:pericellular fibrosis of congenital syphilis
n1=en:pigmented paravenous chorioretinal atrophy | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=40
- en:congenital cardiovascular disorder ---
r_associated #0: 37 -->
en:pericellular fibrosis of congenital syphilis
n1=en:congenital cardiovascular disorder | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=37
- en:erythropoietic porphyria ---
r_associated #0: 37 -->
en:pericellular fibrosis of congenital syphilis
n1=en:erythropoietic porphyria | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=37
- en:congenital fecaliths ---
r_associated #0: 36 -->
en:pericellular fibrosis of congenital syphilis
n1=en:congenital fecaliths | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=36
- myofibromatose infantile ---
r_associated #0: 36 -->
en:pericellular fibrosis of congenital syphilis
n1=myofibromatose infantile | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=36
- arthrogrypose ---
r_associated #0: 35 -->
en:pericellular fibrosis of congenital syphilis
n1=arthrogrypose | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=35
- en:adrenocortical hypofunction, chronic primary congenital ---
r_associated #0: 35 -->
en:pericellular fibrosis of congenital syphilis
n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=35
- en:arthrogryposis ---
r_associated #0: 35 -->
en:pericellular fibrosis of congenital syphilis
n1=en:arthrogryposis | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=35
- en:congenital complete atrioventricular block ---
r_associated #0: 35 -->
en:pericellular fibrosis of congenital syphilis
n1=en:congenital complete atrioventricular block | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=35
- en:congenital end-plate acetylcholinesterase deficiency ---
r_associated #0: 35 -->
en:pericellular fibrosis of congenital syphilis
n1=en:congenital end-plate acetylcholinesterase deficiency | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=35
- en:congenital factor ix deficiency with inhibitor ---
r_associated #0: 35 -->
en:pericellular fibrosis of congenital syphilis
n1=en:congenital factor ix deficiency with inhibitor | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=35
- en:congenital oral/facial/cranial defect ---
r_associated #0: 35 -->
en:pericellular fibrosis of congenital syphilis
n1=en:congenital oral/facial/cranial defect | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=35
- en:congenital pain insensitivity ---
r_associated #0: 35 -->
en:pericellular fibrosis of congenital syphilis
n1=en:congenital pain insensitivity | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=35
- en:congenital vascular disorder ---
r_associated #0: 35 -->
en:pericellular fibrosis of congenital syphilis
n1=en:congenital vascular disorder | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=35
- en:congenital/genetic syndrome with poikiloderma ---
r_associated #0: 35 -->
en:pericellular fibrosis of congenital syphilis
n1=en:congenital/genetic syndrome with poikiloderma | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=35
- en:nystagmus ---
r_associated #0: 35 -->
en:pericellular fibrosis of congenital syphilis
n1=en:nystagmus | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=35
- en:truncal valve overriding ventricular septum ---
r_associated #0: 35 -->
en:pericellular fibrosis of congenital syphilis
n1=en:truncal valve overriding ventricular septum | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=35
- en:congenital accessory skin tag ---
r_associated #0: 34 -->
en:pericellular fibrosis of congenital syphilis
n1=en:congenital accessory skin tag | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=34
- en:congenital inguinal hernia ---
r_associated #0: 34 -->
en:pericellular fibrosis of congenital syphilis
n1=en:congenital inguinal hernia | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=34
- en:congenital metabolic disorder ---
r_associated #0: 34 -->
en:pericellular fibrosis of congenital syphilis
n1=en:congenital metabolic disorder | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=34
- en:congenital skeletal disorder ---
r_associated #0: 34 -->
en:pericellular fibrosis of congenital syphilis
n1=en:congenital skeletal disorder | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=34
- en:parachute malformation of left atrioventricular valve ---
r_associated #0: 34 -->
en:pericellular fibrosis of congenital syphilis
n1=en:parachute malformation of left atrioventricular valve | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=34
- en:pipestem portal cirrhosis ---
r_associated #0: 34 -->
en:pericellular fibrosis of congenital syphilis
n1=en:pipestem portal cirrhosis | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=34
- en:true cleft of common atrioventricular valve leaflet ---
r_associated #0: 34 -->
en:pericellular fibrosis of congenital syphilis
n1=en:true cleft of common atrioventricular valve leaflet | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=34
- en:infantile myofibromatosis ---
r_associated #0: 33 -->
en:pericellular fibrosis of congenital syphilis
n1=en:infantile myofibromatosis | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=33
- en:cap myopathy ---
r_associated #0: 32 -->
en:pericellular fibrosis of congenital syphilis
n1=en:cap myopathy | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=32
- en:congenital functional disorders of the colon ---
r_associated #0: 32 -->
en:pericellular fibrosis of congenital syphilis
n1=en:congenital functional disorders of the colon | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=32
- en:congenital hearing disorder ---
r_associated #0: 32 -->
en:pericellular fibrosis of congenital syphilis
n1=en:congenital hearing disorder | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=32
- en:congenital hepatic porphyria ---
r_associated #0: 32 -->
en:pericellular fibrosis of congenital syphilis
n1=en:congenital hepatic porphyria | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=32
- en:congenital megaprepuce ---
r_associated #0: 32 -->
en:pericellular fibrosis of congenital syphilis
n1=en:congenital megaprepuce | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=32
- en:congenital neutrophil actin dysfunction ---
r_associated #0: 32 -->
en:pericellular fibrosis of congenital syphilis
n1=en:congenital neutrophil actin dysfunction | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=32
- en:congenital pneumonia ---
r_associated #0: 32 -->
en:pericellular fibrosis of congenital syphilis
n1=en:congenital pneumonia | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=32
- en:congenital quadriplegia ---
r_associated #0: 32 -->
en:pericellular fibrosis of congenital syphilis
n1=en:congenital quadriplegia | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=32
- en:congenital velopharyngeal dysfunction ---
r_associated #0: 32 -->
en:pericellular fibrosis of congenital syphilis
n1=en:congenital velopharyngeal dysfunction | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=32
- en:dental arch length loss secondary to congenitally missing teeth ---
r_associated #0: 32 -->
en:pericellular fibrosis of congenital syphilis
n1=en:dental arch length loss secondary to congenitally missing teeth | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=32
- en:extensive congenital erosions, vesicles and reticulate scarring ---
r_associated #0: 32 -->
en:pericellular fibrosis of congenital syphilis
n1=en:extensive congenital erosions, vesicles and reticulate scarring | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=32
- en:congenital amegakaryocytic thrombocytopenia ---
r_associated #0: 31 -->
en:pericellular fibrosis of congenital syphilis
n1=en:congenital amegakaryocytic thrombocytopenia | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=31
- en:congenital exophthalmos ---
r_associated #0: 31 -->
en:pericellular fibrosis of congenital syphilis
n1=en:congenital exophthalmos | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=31
- en:congenital factor ix deficiency variant ---
r_associated #0: 31 -->
en:pericellular fibrosis of congenital syphilis
n1=en:congenital factor ix deficiency variant | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=31
- en:congenital laryngeal cyst ---
r_associated #0: 31 -->
en:pericellular fibrosis of congenital syphilis
n1=en:congenital laryngeal cyst | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=31
- en:congenital nervous system disorder ---
r_associated #0: 31 -->
en:pericellular fibrosis of congenital syphilis
n1=en:congenital nervous system disorder | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=31
- en:congenital pancreatic cyst ---
r_associated #0: 31 -->
en:pericellular fibrosis of congenital syphilis
n1=en:congenital pancreatic cyst | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=31
- en:hutch diverticulum ---
r_associated #0: 31 -->
en:pericellular fibrosis of congenital syphilis
n1=en:hutch diverticulum | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=31
- en:right atrial appendage - left - juxtaposition ---
r_associated #0: 31 -->
en:pericellular fibrosis of congenital syphilis
n1=en:right atrial appendage - left - juxtaposition | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=31
- en:shortened trunk ---
r_associated #0: 31 -->
en:pericellular fibrosis of congenital syphilis
n1=en:shortened trunk | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=31
- en:symmer's pipe-stem fibrosis ---
r_associated #0: 31 -->
en:pericellular fibrosis of congenital syphilis
n1=en:symmer's pipe-stem fibrosis | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=31
- nystagmus congénital isolé ---
r_associated #0: 31 -->
en:pericellular fibrosis of congenital syphilis
n1=nystagmus congénital isolé | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=31
- débilité congénitale du foetus ---
r_associated #0: 30 -->
en:pericellular fibrosis of congenital syphilis
n1=débilité congénitale du foetus | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=30
- débilité congénitale foetale ---
r_associated #0: 30 -->
en:pericellular fibrosis of congenital syphilis
n1=débilité congénitale foetale | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=30
- en:congenital blepharophimosis of upper eyelid ---
r_associated #0: 30 -->
en:pericellular fibrosis of congenital syphilis
n1=en:congenital blepharophimosis of upper eyelid | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=30
- en:congenital debility of fetus ---
r_associated #0: 30 -->
en:pericellular fibrosis of congenital syphilis
n1=en:congenital debility of fetus | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=30
- en:congenital dysarthria ---
r_associated #0: 30 -->
en:pericellular fibrosis of congenital syphilis
n1=en:congenital dysarthria | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=30
- en:congenital reproductive system disorder ---
r_associated #0: 30 -->
en:pericellular fibrosis of congenital syphilis
n1=en:congenital reproductive system disorder | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=30
- en:congenital respiratory disorder ---
r_associated #0: 30 -->
en:pericellular fibrosis of congenital syphilis
n1=en:congenital respiratory disorder | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=30
- en:congenital stenosis ---
r_associated #0: 30 -->
en:pericellular fibrosis of congenital syphilis
n1=en:congenital stenosis | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=30
- en:developmental fault ---
r_associated #0: 30 -->
en:pericellular fibrosis of congenital syphilis
n1=en:developmental fault | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=30
- en:erythropoietic uroporphyria ---
r_associated #0: 30 -->
en:pericellular fibrosis of congenital syphilis
n1=en:erythropoietic uroporphyria | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=30
- en:megophthalmos ---
r_associated #0: 30 -->
en:pericellular fibrosis of congenital syphilis
n1=en:megophthalmos | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=30
- en:north american indian childhood cirrhosis ---
r_associated #0: 30 -->
en:pericellular fibrosis of congenital syphilis
n1=en:north american indian childhood cirrhosis | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=30
- en:prominent valve of inferior vena cava ---
r_associated #0: 30 -->
en:pericellular fibrosis of congenital syphilis
n1=en:prominent valve of inferior vena cava | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=30
- en:vitamin d-dependent rickets, type 2 ---
r_associated #0: 30 -->
en:pericellular fibrosis of congenital syphilis
n1=en:vitamin d-dependent rickets, type 2 | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=30
- méthémoglobinémie héréditaire ---
r_associated #0: 30 -->
en:pericellular fibrosis of congenital syphilis
n1=méthémoglobinémie héréditaire | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=30
- nystagmus ---
r_associated #0: 30 -->
en:pericellular fibrosis of congenital syphilis
n1=nystagmus | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=30
- en:buphthalmia ---
r_associated #0: 29 -->
en:pericellular fibrosis of congenital syphilis
n1=en:buphthalmia | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=29
- en:congenital analbuminemia ---
r_associated #0: 29 -->
en:pericellular fibrosis of congenital syphilis
n1=en:congenital analbuminemia | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=29
- en:congenital axial myopia ---
r_associated #0: 29 -->
en:pericellular fibrosis of congenital syphilis
n1=en:congenital axial myopia | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=29
- en:congenital connective tissue disorder ---
r_associated #0: 29 -->
en:pericellular fibrosis of congenital syphilis
n1=en:congenital connective tissue disorder | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=29
- en:congenital fibrinogen abnormality ---
r_associated #0: 29 -->
en:pericellular fibrosis of congenital syphilis
n1=en:congenital fibrinogen abnormality | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=29
- en:congenital malignant melanoma ---
r_associated #0: 29 -->
en:pericellular fibrosis of congenital syphilis
n1=en:congenital malignant melanoma | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=29
- en:congenital plasminogen activator inhibitor deficiency type 1 ---
r_associated #0: 29 -->
en:pericellular fibrosis of congenital syphilis
n1=en:congenital plasminogen activator inhibitor deficiency type 1 | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=29
- en:congenital posterior subcapsular polar cataract ---
r_associated #0: 29 -->
en:pericellular fibrosis of congenital syphilis
n1=en:congenital posterior subcapsular polar cataract | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=29
- en:congenital skin contracture ---
r_associated #0: 29 -->
en:pericellular fibrosis of congenital syphilis
n1=en:congenital skin contracture | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=29
- en:right atrial appendage absent ---
r_associated #0: 29 -->
en:pericellular fibrosis of congenital syphilis
n1=en:right atrial appendage absent | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=29
- en:Günther's disease ---
r_associated #0: 28 -->
en:pericellular fibrosis of congenital syphilis
n1=en:Günther's disease | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=28
- en:chromosomal aberration ---
r_associated #0: 28 -->
en:pericellular fibrosis of congenital syphilis
n1=en:chromosomal aberration | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=28
- en:chronic diarrhea due to glucoamylase deficiency ---
r_associated #0: 28 -->
en:pericellular fibrosis of congenital syphilis
n1=en:chronic diarrhea due to glucoamylase deficiency | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=28
- en:congenital and developmental myasthenia ---
r_associated #0: 28 -->
en:pericellular fibrosis of congenital syphilis
n1=en:congenital and developmental myasthenia | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=28
- en:congenital atrophy of left lobe of liver ---
r_associated #0: 28 -->
en:pericellular fibrosis of congenital syphilis
n1=en:congenital atrophy of left lobe of liver | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=28
- en:congenital blocked tear duct ---
r_associated #0: 28 -->
en:pericellular fibrosis of congenital syphilis
n1=en:congenital blocked tear duct | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=28
- en:congenital blood disorder ---
r_associated #0: 28 -->
en:pericellular fibrosis of congenital syphilis
n1=en:congenital blood disorder | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=28
- en:congenital claw toe ---
r_associated #0: 28 -->
en:pericellular fibrosis of congenital syphilis
n1=en:congenital claw toe | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=28
- en:congenital ear disorder ---
r_associated #0: 28 -->
en:pericellular fibrosis of congenital syphilis
n1=en:congenital ear disorder | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=28
- en:congenital hydrocele ---
r_associated #0: 28 -->
en:pericellular fibrosis of congenital syphilis
n1=en:congenital hydrocele | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=28
- en:congenital hypertonia ---
r_associated #0: 28 -->
en:pericellular fibrosis of congenital syphilis
n1=en:congenital hypertonia | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=28
- en:congenital palato-esophageal incoordination ---
r_associated #0: 28 -->
en:pericellular fibrosis of congenital syphilis
n1=en:congenital palato-esophageal incoordination | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=28
- en:congenital uremia ---
r_associated #0: 28 -->
en:pericellular fibrosis of congenital syphilis
n1=en:congenital uremia | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=28
- en:developmental anomaly ---
r_associated #0: 28 -->
en:pericellular fibrosis of congenital syphilis
n1=en:developmental anomaly | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=28
- en:digeorge syndrome ---
r_associated #0: 28 -->
en:pericellular fibrosis of congenital syphilis
n1=en:digeorge syndrome | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=28
- en:fetal disorder ---
r_associated #0: 28 -->
en:pericellular fibrosis of congenital syphilis
n1=en:fetal disorder | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=28
- en:rudimentary left ventricle ---
r_associated #0: 28 -->
en:pericellular fibrosis of congenital syphilis
n1=en:rudimentary left ventricle | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=28
- Maladie congénitale ---
r_associated #0: 27 -->
en:pericellular fibrosis of congenital syphilis
n1=Maladie congénitale | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=27
- en:congenital blepharophimosis of lower eyelid ---
r_associated #0: 27 -->
en:pericellular fibrosis of congenital syphilis
n1=en:congenital blepharophimosis of lower eyelid | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=27
- en:congenital celiac disease ---
r_associated #0: 27 -->
en:pericellular fibrosis of congenital syphilis
n1=en:congenital celiac disease | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=27
- en:congenital choroidal fold ---
r_associated #0: 27 -->
en:pericellular fibrosis of congenital syphilis
n1=en:congenital choroidal fold | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=27
- en:congenital constriction of pylorus ---
r_associated #0: 27 -->
en:pericellular fibrosis of congenital syphilis
n1=en:congenital constriction of pylorus | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=27
- en:congenital dysphasia ---
r_associated #0: 27 -->
en:pericellular fibrosis of congenital syphilis
n1=en:congenital dysphasia | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=27
- en:congenital elephantiasis ---
r_associated #0: 27 -->
en:pericellular fibrosis of congenital syphilis
n1=en:congenital elephantiasis | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=27
- en:congenital facial asymmetry ---
r_associated #0: 27 -->
en:pericellular fibrosis of congenital syphilis
n1=en:congenital facial asymmetry | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=27
- en:congenital immunodeficiency disease ---
r_associated #0: 27 -->
en:pericellular fibrosis of congenital syphilis
n1=en:congenital immunodeficiency disease | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=27
- en:congenital infectious disease ---
r_associated #0: 27 -->
en:pericellular fibrosis of congenital syphilis
n1=en:congenital infectious disease | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=27
- en:congenital porphyria ---
r_associated #0: 27 -->
en:pericellular fibrosis of congenital syphilis
n1=en:congenital porphyria | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=27
- en:congenital retinoschisis ---
r_associated #0: 27 -->
en:pericellular fibrosis of congenital syphilis
n1=en:congenital retinoschisis | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=27
- en:hepatic bridging fibrosis ---
r_associated #0: 27 -->
en:pericellular fibrosis of congenital syphilis
n1=en:hepatic bridging fibrosis | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=27
- en:infant metachromatic leukodystrophies ---
r_associated #0: 27 -->
en:pericellular fibrosis of congenital syphilis
n1=en:infant metachromatic leukodystrophies | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=27
- en:mottled teeth, congenital ---
r_associated #0: 27 -->
en:pericellular fibrosis of congenital syphilis
n1=en:mottled teeth, congenital | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=27
- en:palmoplantar porokeratosis ---
r_associated #0: 27 -->
en:pericellular fibrosis of congenital syphilis
n1=en:palmoplantar porokeratosis | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=27
- en:parachute malformation of right atrioventricular valve ---
r_associated #0: 27 -->
en:pericellular fibrosis of congenital syphilis
n1=en:parachute malformation of right atrioventricular valve | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=27
- en:Fordyce's disease ---
r_associated #0: 26 -->
en:pericellular fibrosis of congenital syphilis
n1=en:Fordyce's disease | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=26
- en:alcoholic fibrosis and sclerosis of liver ---
r_associated #0: 26 -->
en:pericellular fibrosis of congenital syphilis
n1=en:alcoholic fibrosis and sclerosis of liver | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=26
- en:congenital brain damage ---
r_associated #0: 26 -->
en:pericellular fibrosis of congenital syphilis
n1=en:congenital brain damage | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=26
- en:congenital bundle of his tachycardia ---
r_associated #0: 26 -->
en:pericellular fibrosis of congenital syphilis
n1=en:congenital bundle of his tachycardia | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=26
- en:congenital cyst of aryepiglottic fold ---
r_associated #0: 26 -->
en:pericellular fibrosis of congenital syphilis
n1=en:congenital cyst of aryepiglottic fold | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=26
- en:congenital factor ix deficiency without inhibitor ---
r_associated #0: 26 -->
en:pericellular fibrosis of congenital syphilis
n1=en:congenital factor ix deficiency without inhibitor | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=26
- en:congenital melanocytic nevus of trunk ---
r_associated #0: 26 -->
en:pericellular fibrosis of congenital syphilis
n1=en:congenital melanocytic nevus of trunk | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=26
- en:congenital monosaccharide malabsorption ---
r_associated #0: 26 -->
en:pericellular fibrosis of congenital syphilis
n1=en:congenital monosaccharide malabsorption | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=26
- en:congenital muscle disorder ---
r_associated #0: 26 -->
en:pericellular fibrosis of congenital syphilis
n1=en:congenital muscle disorder | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=26
- en:congenital pancreatic trypsin deficiency ---
r_associated #0: 26 -->
en:pericellular fibrosis of congenital syphilis
n1=en:congenital pancreatic trypsin deficiency | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=26
- en:fetal congenital tumor causing disproportion ---
r_associated #0: 26 -->
en:pericellular fibrosis of congenital syphilis
n1=en:fetal congenital tumor causing disproportion | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=26
- en:fordyce's disease ---
r_associated #0: 26 -->
en:pericellular fibrosis of congenital syphilis
n1=en:fordyce's disease | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=26
- en:parachute malformation of common atrioventricular valve ---
r_associated #0: 26 -->
en:pericellular fibrosis of congenital syphilis
n1=en:parachute malformation of common atrioventricular valve | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=26
- en:regional congenital anomaly ---
r_associated #0: 26 -->
en:pericellular fibrosis of congenital syphilis
n1=en:regional congenital anomaly | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=26
- en:right atrial endocardial fibroelastosis ---
r_associated #0: 26 -->
en:pericellular fibrosis of congenital syphilis
n1=en:right atrial endocardial fibroelastosis | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=26
- malformation ---
r_associated #0: 26 -->
en:pericellular fibrosis of congenital syphilis
n1=malformation | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=26
- Malformation ---
r_associated #0: 25 -->
en:pericellular fibrosis of congenital syphilis
n1=Malformation | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=25
- contractures congénitales et arachnodactylie ---
r_associated #0: 25 -->
en:pericellular fibrosis of congenital syphilis
n1=contractures congénitales et arachnodactylie | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=25
- en:congenital cardiac failure ---
r_associated #0: 25 -->
en:pericellular fibrosis of congenital syphilis
n1=en:congenital cardiac failure | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=25
- en:congenital disorder of facial nerve ---
r_associated #0: 25 -->
en:pericellular fibrosis of congenital syphilis
n1=en:congenital disorder of facial nerve | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=25
- en:congenital hernia of bladder ---
r_associated #0: 25 -->
en:pericellular fibrosis of congenital syphilis
n1=en:congenital hernia of bladder | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=25
- en:amyoplasia congenita ---
r_associated #0: 24 -->
en:pericellular fibrosis of congenital syphilis
n1=en:amyoplasia congenita | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=24
- en:congenital anemia ---
r_associated #0: 24 -->
en:pericellular fibrosis of congenital syphilis
n1=en:congenital anemia | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=24
- en:congenital cutaneous angiomatosis ---
r_associated #0: 24 -->
en:pericellular fibrosis of congenital syphilis
n1=en:congenital cutaneous angiomatosis | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=24
- en:congenital esotropia ---
r_associated #0: 24 -->
en:pericellular fibrosis of congenital syphilis
n1=en:congenital esotropia | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=24
- en:congenital skin disorder ---
r_associated #0: 24 -->
en:pericellular fibrosis of congenital syphilis
n1=en:congenital skin disorder | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=24
- déficit congénital en mégacaryocytes ---
r_associated #0: 23 -->
en:pericellular fibrosis of congenital syphilis
n1=déficit congénital en mégacaryocytes | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=23
- en:abnormal root proximity between adjacent teeth ---
r_associated #0: 23 -->
en:pericellular fibrosis of congenital syphilis
n1=en:abnormal root proximity between adjacent teeth | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=23
- en:becker generalized myotonia ---
r_associated #0: 23 -->
en:pericellular fibrosis of congenital syphilis
n1=en:becker generalized myotonia | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=23
- en:congenital alpha-2-antiplasmin deficiency ---
r_associated #0: 23 -->
en:pericellular fibrosis of congenital syphilis
n1=en:congenital alpha-2-antiplasmin deficiency | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=23
- en:congenital arcus juvenilis ---
r_associated #0: 23 -->
en:pericellular fibrosis of congenital syphilis
n1=en:congenital arcus juvenilis | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=23
- en:congenital atrophy of thyroid ---
r_associated #0: 23 -->
en:pericellular fibrosis of congenital syphilis
n1=en:congenital atrophy of thyroid | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=23
- en:congenital flat foot ---
r_associated #0: 23 -->
en:pericellular fibrosis of congenital syphilis
n1=en:congenital flat foot | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=23
- en:periportal fibrosis ---
r_associated #0: 23 -->
en:pericellular fibrosis of congenital syphilis
n1=en:periportal fibrosis | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=23
- ARTHROGRYPOSE ---
r_associated #0: 22 -->
en:pericellular fibrosis of congenital syphilis
n1=ARTHROGRYPOSE | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=22
- en:congenital functional disorders of the small intestine ---
r_associated #0: 22 -->
en:pericellular fibrosis of congenital syphilis
n1=en:congenital functional disorders of the small intestine | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=22
- une anomalie congénitale ---
r_associated #0: 22 -->
en:pericellular fibrosis of congenital syphilis
n1=une anomalie congénitale | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=22
- buphtalmie ---
r_associated #0: 21 -->
en:pericellular fibrosis of congenital syphilis
n1=buphtalmie | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=21
- en:cirrhosis ---
r_associated #0: 21 -->
en:pericellular fibrosis of congenital syphilis
n1=en:cirrhosis | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=21
- en:congenital anal fissure ---
r_associated #0: 21 -->
en:pericellular fibrosis of congenital syphilis
n1=en:congenital anal fissure | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=21
- en:congenital cyst of vulva ---
r_associated #0: 21 -->
en:pericellular fibrosis of congenital syphilis
n1=en:congenital cyst of vulva | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=21
- en:congenital hepatic fibrosis ---
r_associated #0: 21 -->
en:pericellular fibrosis of congenital syphilis
n1=en:congenital hepatic fibrosis | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=21
- syndrome de Prader-Willi ---
r_associated #0: 21 -->
en:pericellular fibrosis of congenital syphilis
n1=syndrome de Prader-Willi | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=21
- syndrome de Williams ---
r_associated #0: 21 -->
en:pericellular fibrosis of congenital syphilis
n1=syndrome de Williams | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=21
- Anomalie chromosomique ---
r_associated #0: 20 -->
en:pericellular fibrosis of congenital syphilis
n1=Anomalie chromosomique | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=20
- Malformation congénitale ---
r_associated #0: 20 -->
en:pericellular fibrosis of congenital syphilis
n1=Malformation congénitale | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=20
- Arthrogrypose ---
r_associated #0: 15 -->
en:pericellular fibrosis of congenital syphilis
n1=Arthrogrypose | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=15
- BNV ---
r_associated #0: 15 -->
en:pericellular fibrosis of congenital syphilis
n1=BNV | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=15
- malentendant (enfant) ---
r_associated #0: 15 -->
en:pericellular fibrosis of congenital syphilis
n1=malentendant (enfant) | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=15
- CONGENITAL ---
r_associated #0: 10 -->
en:pericellular fibrosis of congenital syphilis
n1=CONGENITAL | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=10
- CONGÉNITALE ---
r_associated #0: 10 -->
en:pericellular fibrosis of congenital syphilis
n1=CONGÉNITALE | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=10
- Congenital ---
r_associated #0: 10 -->
en:pericellular fibrosis of congenital syphilis
n1=Congenital | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=10
- Syndrome de Prader-Willi ---
r_associated #0: 10 -->
en:pericellular fibrosis of congenital syphilis
n1=Syndrome de Prader-Willi | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=10
- aberration chromosomique ---
r_associated #0: 10 -->
en:pericellular fibrosis of congenital syphilis
n1=aberration chromosomique | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=10
- en:PWS ---
r_associated #0: 10 -->
en:pericellular fibrosis of congenital syphilis
n1=en:PWS | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=10
- en:WBS ---
r_associated #0: 10 -->
en:pericellular fibrosis of congenital syphilis
n1=en:WBS | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=10
- en:Williams' syndrome ---
r_associated #0: 10 -->
en:pericellular fibrosis of congenital syphilis
n1=en:Williams' syndrome | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=10
- en:Williams-Beuren syndrome ---
r_associated #0: 10 -->
en:pericellular fibrosis of congenital syphilis
n1=en:Williams-Beuren syndrome | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=10
- en:buphtalmia ---
r_associated #0: 10 -->
en:pericellular fibrosis of congenital syphilis
n1=en:buphtalmia | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=10
- en:buphthalmos ---
r_associated #0: 10 -->
en:pericellular fibrosis of congenital syphilis
n1=en:buphthalmos | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=10
- en:buphthalmus ---
r_associated #0: 10 -->
en:pericellular fibrosis of congenital syphilis
n1=en:buphthalmus | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=10
- en:cacomorphosis ---
r_associated #0: 10 -->
en:pericellular fibrosis of congenital syphilis
n1=en:cacomorphosis | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=10
- en:chromosomal disorder ---
r_associated #0: 10 -->
en:pericellular fibrosis of congenital syphilis
n1=en:chromosomal disorder | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=10
- en:contractural arachnodactyly ---
r_associated #0: 10 -->
en:pericellular fibrosis of congenital syphilis
n1=en:contractural arachnodactyly | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=10
- en:hypoacousic child ---
r_associated #0: 10 -->
en:pericellular fibrosis of congenital syphilis
n1=en:hypoacousic child | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=10
- nystagmus héréditaire vertical ---
r_associated #0: 10 -->
en:pericellular fibrosis of congenital syphilis
n1=nystagmus héréditaire vertical | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=10
- nystagmus lié au sexe ---
r_associated #0: 10 -->
en:pericellular fibrosis of congenital syphilis
n1=nystagmus lié au sexe | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=10
- nystagmus myoclonies ---
r_associated #0: 10 -->
en:pericellular fibrosis of congenital syphilis
n1=nystagmus myoclonies | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=10
- porphyrie (anesthésie chez un patient atteint de) ---
r_associated #0: 10 -->
en:pericellular fibrosis of congenital syphilis
n1=porphyrie (anesthésie chez un patient atteint de) | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=10
- rétinite pigmentaire liée à la périphérine (pro219leu) ---
r_associated #0: 10 -->
en:pericellular fibrosis of congenital syphilis
n1=rétinite pigmentaire liée à la périphérine (pro219leu) | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=10
- Williams (syndrome de) ---
r_associated #0: 5 -->
en:pericellular fibrosis of congenital syphilis
n1=Williams (syndrome de) | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=5
- malf ormation dysraphique ---
r_associated #0: 5 -->
en:pericellular fibrosis of congenital syphilis
n1=malf ormation dysraphique | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=5
- malformation kystique adénomatoïde du poumon ---
r_associated #0: 5 -->
en:pericellular fibrosis of congenital syphilis
n1=malformation kystique adénomatoïde du poumon | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=5
- malformation luxante de la hanche ---
r_associated #0: 5 -->
en:pericellular fibrosis of congenital syphilis
n1=malformation luxante de la hanche | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=5
- malformation mamelonnaire ---
r_associated #0: 5 -->
en:pericellular fibrosis of congenital syphilis
n1=malformation mamelonnaire | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=5
- malformation mammaire ---
r_associated #0: 5 -->
en:pericellular fibrosis of congenital syphilis
n1=malformation mammaire | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=5
- malformation ombilicale ---
r_associated #0: 5 -->
en:pericellular fibrosis of congenital syphilis
n1=malformation ombilicale | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=5
- malformation utérine ---
r_associated #0: 5 -->
en:pericellular fibrosis of congenital syphilis
n1=malformation utérine | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=5
- malformation vaginale ---
r_associated #0: 5 -->
en:pericellular fibrosis of congenital syphilis
n1=malformation vaginale | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=5
- malformation vasculaire cérébrale du nourrisson ---
r_associated #0: 5 -->
en:pericellular fibrosis of congenital syphilis
n1=malformation vasculaire cérébrale du nourrisson | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=5
- malformations de la charnière occipitocervicale ---
r_associated #0: 5 -->
en:pericellular fibrosis of congenital syphilis
n1=malformations de la charnière occipitocervicale | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=5
- nystagmus (zone de moindre) ---
r_associated #0: 5 -->
en:pericellular fibrosis of congenital syphilis
n1=nystagmus (zone de moindre) | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=5
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