'en:adrenocortical hypofunction, chronic primary congenital'
(id=6806749 ; fe=en:adrenocortical hypofunction, chronic primary congenital ; type=1 ; niveau=200 ; luminosité=25 ; somme entrante=18790 creation date=2017-06-25 touchdate=2025-10-12 16:13:03.000)

≈ 351 relations sortantes en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 43 / 1 -> en:congenital malalignment of the toenails n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital malalignment of the toenails | rel=r_associated | relid=0 | w=43 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 42 / 0.977 -> en:congenital cardiovascular disorders during pregnancy, childbirth and the puerperium n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital cardiovascular disorders during pregnancy, childbirth and the puerperium | rel=r_associated | relid=0 | w=42 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 42 / 0.977 -> en:congenital palato-esophageal incoordination n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital palato-esophageal incoordination | rel=r_associated | relid=0 | w=42 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 42 / 0.977 -> en:microvillus inclusion disease n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=42 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 41 / 0.953 -> en:drug-induced adrenocortical insufficiency n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:drug-induced adrenocortical insufficiency | rel=r_associated | relid=0 | w=41 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 40 / 0.93 -> en:congenital fecaliths n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital fecaliths | rel=r_associated | relid=0 | w=40 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 40 / 0.93 -> en:congenital obstruction of large intestine n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital obstruction of large intestine | rel=r_associated | relid=0 | w=40 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 40 / 0.93 -> en:generalized myotonia of thomsen n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:generalized myotonia of thomsen | rel=r_associated | relid=0 | w=40 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 40 / 0.93 -> en:vitamin d-dependent rickets, type 1 n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:vitamin d-dependent rickets, type 1 | rel=r_associated | relid=0 | w=40 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 39 / 0.907 -> en:basal ganglia disease, biotin-responsive n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:basal ganglia disease, biotin-responsive | rel=r_associated | relid=0 | w=39 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 39 / 0.907 -> en:congenital abnormality n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital abnormality | rel=r_associated | relid=0 | w=39 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 39 / 0.907 -> en:stomach in central position n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:stomach in central position | rel=r_associated | relid=0 | w=39 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 38 / 0.884 -> en:chromosome disorder n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:chromosome disorder | rel=r_associated | relid=0 | w=38 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 37 / 0.86 -> en:adrenoleukodystrophy n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:adrenoleukodystrophy | rel=r_associated | relid=0 | w=37 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 36 / 0.837 -> en:congenital cardiovascular disorder n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital cardiovascular disorder | rel=r_associated | relid=0 | w=36 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 36 / 0.837 -> en:congenital exophthalmos n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital exophthalmos | rel=r_associated | relid=0 | w=36 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 36 / 0.837 -> en:congenital oral/facial/cranial defect n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital oral/facial/cranial defect | rel=r_associated | relid=0 | w=36 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 36 / 0.837 -> en:tricuspid valve primary chords absent n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:tricuspid valve primary chords absent | rel=r_associated | relid=0 | w=36 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 35 / 0.814 -> en:benign congenital myopathy n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:benign congenital myopathy | rel=r_associated | relid=0 | w=35 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 35 / 0.814 -> en:congenital achalasia of esophagus n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital achalasia of esophagus | rel=r_associated | relid=0 | w=35 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 35 / 0.814 -> en:congenital arcus juvenilis n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital arcus juvenilis | rel=r_associated | relid=0 | w=35 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 35 / 0.814 -> en:congenital contracture of gastrocnemius muscle n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital contracture of gastrocnemius muscle | rel=r_associated | relid=0 | w=35 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 35 / 0.814 -> en:congenital cyst of vulva n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital cyst of vulva | rel=r_associated | relid=0 | w=35 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 35 / 0.814 -> en:congenital disease of brain n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital disease of brain | rel=r_associated | relid=0 | w=35 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 35 / 0.814 -> en:congenital esotropia n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital esotropia | rel=r_associated | relid=0 | w=35 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 35 / 0.814 -> en:congenital hearing disorder n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital hearing disorder | rel=r_associated | relid=0 | w=35 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 35 / 0.814 -> en:congenital hypothyroidism n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital hypothyroidism | rel=r_associated | relid=0 | w=35 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 35 / 0.814 -> en:congenital male infertility n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital male infertility | rel=r_associated | relid=0 | w=35 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 35 / 0.814 -> en:congenital myasthenic syndrome n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital myasthenic syndrome | rel=r_associated | relid=0 | w=35 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 35 / 0.814 -> en:congenital obstruction of bladder neck n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital obstruction of bladder neck | rel=r_associated | relid=0 | w=35 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 35 / 0.814 -> en:congenital occlusion of anus n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital occlusion of anus | rel=r_associated | relid=0 | w=35 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 35 / 0.814 -> en:congenital respiratory disorder n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital respiratory disorder | rel=r_associated | relid=0 | w=35 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 35 / 0.814 -> en:congenital scoliosis due to bony malformation n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital scoliosis due to bony malformation | rel=r_associated | relid=0 | w=35 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 35 / 0.814 -> en:congenital spastic foot n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital spastic foot | rel=r_associated | relid=0 | w=35 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 35 / 0.814 -> en:congenital/genetic syndrome with poikiloderma n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital/genetic syndrome with poikiloderma | rel=r_associated | relid=0 | w=35 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 35 / 0.814 -> en:cortisol deficiency n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:cortisol deficiency | rel=r_associated | relid=0 | w=35 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 35 / 0.814 -> en:digeorge syndrome n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:digeorge syndrome | rel=r_associated | relid=0 | w=35 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 35 / 0.814 -> en:double orifice of right atrioventricular valve in double inlet ventricle n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:double orifice of right atrioventricular valve in double inlet ventricle | rel=r_associated | relid=0 | w=35 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 35 / 0.814 -> en:keratitis, hereditary n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:keratitis, hereditary | rel=r_associated | relid=0 | w=35 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 35 / 0.814 -> en:longitudinal deficiency of part of limb n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:longitudinal deficiency of part of limb | rel=r_associated | relid=0 | w=35 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 35 / 0.814 -> en:myostatin-related muscle hypertrophy n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:myostatin-related muscle hypertrophy | rel=r_associated | relid=0 | w=35 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 35 / 0.814 -> en:nonfenestrated interatrial communication within oval fossa n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:nonfenestrated interatrial communication within oval fossa | rel=r_associated | relid=0 | w=35 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 35 / 0.814 -> en:obstructed interchordal space of tricuspid chordae tendinae n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:obstructed interchordal space of tricuspid chordae tendinae | rel=r_associated | relid=0 | w=35 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 35 / 0.814 -> 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:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 35 / 0.814 -> en:post-adrenalectomy adrenal insufficiency n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:post-adrenalectomy adrenal insufficiency | rel=r_associated | relid=0 | w=35 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 35 / 0.814 -> en:secondary adrenal insufficiency n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:secondary adrenal insufficiency | rel=r_associated | relid=0 | w=35 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 35 / 0.814 -> en:testicular hypofunction due to defect in adrenocortical hormone synthesis n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:testicular hypofunction due to defect in adrenocortical hormone synthesis | rel=r_associated | relid=0 | w=35 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 35 / 0.814 -> en:vocal cord dysfunction familial n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:vocal cord dysfunction familial | rel=r_associated | relid=0 | w=35 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 35 / 0.814 -> hypofonctionnement corticosurrénalien primaire congénital n1=en:adrenocortical hypofunction, chronic primary congenital | n2=hypofonctionnement corticosurrénalien primaire congénital | rel=r_associated | relid=0 | w=35 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 34 / 0.791 -> en:addison's disease n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:addison's disease | rel=r_associated | relid=0 | w=34 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 34 / 0.791 -> en:adrenal crisis n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:adrenal crisis | rel=r_associated | relid=0 | w=34 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 34 / 0.791 -> en:alpha-fetoprotein deficiency n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:alpha-fetoprotein deficiency | rel=r_associated | relid=0 | w=34 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 34 / 0.791 -> en:congenital anterior subcapsular polar cataract n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital anterior subcapsular polar cataract | rel=r_associated | relid=0 | w=34 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 34 / 0.791 -> en:congenital blepharophimosis n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital blepharophimosis | rel=r_associated | relid=0 | w=34 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 34 / 0.791 -> en:congenital brain damage n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital brain damage | rel=r_associated | relid=0 | w=34 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 34 / 0.791 -> en:congenital cerebellar cortical atrophy n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital cerebellar cortical atrophy | rel=r_associated | relid=0 | w=34 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 34 / 0.791 -> en:congenital factor ix deficiency with inhibitor n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital factor ix deficiency with inhibitor | rel=r_associated | relid=0 | w=34 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 34 / 0.791 -> en:congenital hypertonia n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital hypertonia | rel=r_associated | relid=0 | w=34 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 34 / 0.791 -> en:congenital leptin deficiency n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital leptin deficiency | rel=r_associated | relid=0 | w=34 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 34 / 0.791 -> en:congenital malignant melanoma n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital malignant melanoma | rel=r_associated | relid=0 | w=34 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 34 / 0.791 -> en:congenital methemoglobinemia n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital methemoglobinemia | rel=r_associated | relid=0 | w=34 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 34 / 0.791 -> en:congenital nystagmus n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital nystagmus | rel=r_associated | relid=0 | w=34 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 34 / 0.791 -> en:congenital pericardial effusion n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital pericardial effusion | rel=r_associated | relid=0 | w=34 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 34 / 0.791 -> en:congenital pterygium of nail n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital pterygium of nail | rel=r_associated | relid=0 | w=34 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 34 / 0.791 -> en:congenital skeletal disorder n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital skeletal disorder | rel=r_associated | relid=0 | w=34 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 34 / 0.791 -> en:congenital uremia n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital uremia | rel=r_associated | relid=0 | w=34 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 34 / 0.791 -> en:extensive congenital erosions, vesicles and reticulate scarring n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:extensive congenital erosions, vesicles and reticulate scarring | rel=r_associated | relid=0 | w=34 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 34 / 0.791 -> en:fetal congenital tumor causing disproportion n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:fetal congenital tumor causing disproportion | rel=r_associated | relid=0 | w=34 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 34 / 0.791 -> en:fetal disorder n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:fetal disorder | rel=r_associated | relid=0 | w=34 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 34 / 0.791 -> en:infant metachromatic leukodystrophies n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:infant metachromatic leukodystrophies | rel=r_associated | relid=0 | w=34 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 34 / 0.791 -> en:infantile myofibromatosis n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:infantile myofibromatosis | rel=r_associated | relid=0 | w=34 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 34 / 0.791 -> en:left atrioventricular valve bifoliate with fused left sided superior and inferior bridging leaflet n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:left atrioventricular valve bifoliate with fused left sided superior and inferior bridging leaflet | rel=r_associated | relid=0 | w=34 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 34 / 0.791 -> en:patent foramen ovale n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:patent foramen ovale | rel=r_associated | relid=0 | w=34 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 34 / 0.791 -> en:precocious exfoliation of teeth related to idiopathic root resorption n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:precocious exfoliation of teeth related to idiopathic root resorption | rel=r_associated | relid=0 | w=34 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 34 / 0.791 -> en:pulmonary valve overriding ventricular septum n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:pulmonary valve overriding ventricular septum | rel=r_associated | relid=0 | w=34 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 34 / 0.791 -> en:secondary megacolon - congenital n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:secondary megacolon - congenital | rel=r_associated | relid=0 | w=34 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 34 / 0.791 -> en:spinal hydromeningocele n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:spinal hydromeningocele | rel=r_associated | relid=0 | w=34 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 34 / 0.791 -> en:tripartite right ventricle n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:tripartite right ventricle | rel=r_associated | relid=0 | w=34 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 32 / 0.744 -> en:becker generalized myotonia n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:becker generalized myotonia | rel=r_associated | relid=0 | w=32 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 32 / 0.744 -> en:congenital anemia n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital anemia | rel=r_associated | relid=0 | w=32 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 32 / 0.744 -> en:congenital calcium pyrophosphate dihydrate crystal deposition disease n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital calcium pyrophosphate dihydrate crystal deposition disease | rel=r_associated | relid=0 | w=32 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 32 / 0.744 -> en:congenital celiac disease n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital celiac disease | rel=r_associated | relid=0 | w=32 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 32 / 0.744 -> en:congenital constriction of pylorus n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital constriction of pylorus | rel=r_associated | relid=0 | w=32 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 32 / 0.744 -> en:congenital cyst of fallopian tube n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital cyst of fallopian tube | rel=r_associated | relid=0 | w=32 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 32 / 0.744 -> en:congenital infectious disease n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital infectious disease | rel=r_associated | relid=0 | w=32 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 32 / 0.744 -> en:congenital nephritis n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital nephritis | rel=r_associated | relid=0 | w=32 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 32 / 0.744 -> en:congenital nephrotic syndrome n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital nephrotic syndrome | rel=r_associated | relid=0 | w=32 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 32 / 0.744 -> en:congenital pseudobulbar palsy n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital pseudobulbar palsy | rel=r_associated | relid=0 | w=32 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 32 / 0.744 -> en:congenital single renal cyst n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital single renal cyst | rel=r_associated | relid=0 | w=32 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 32 / 0.744 -> en:megophthalmos n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:megophthalmos | rel=r_associated | relid=0 | w=32 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 32 / 0.744 -> en:mineralocorticoid deficiency n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:mineralocorticoid deficiency | rel=r_associated | relid=0 | w=32 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 32 / 0.744 -> en:prominent valve of inferior vena cava n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:prominent valve of inferior vena cava | rel=r_associated | relid=0 | w=32 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 32 / 0.744 -> en:right inferior caval vein connecting to left atrium and right atrium n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:right inferior caval vein connecting to left atrium and right atrium | rel=r_associated | relid=0 | w=32 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 32 / 0.744 -> en:upper esophageal web n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:upper esophageal web | rel=r_associated | relid=0 | w=32 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 31 / 0.721 -> en:adrenal insufficiency neonatal n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:adrenal insufficiency neonatal | rel=r_associated | relid=0 | w=31 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 31 / 0.721 -> en:arthrogryposis n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:arthrogryposis | rel=r_associated | relid=0 | w=31 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 31 / 0.721 -> en:cap myopathy n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:cap myopathy | rel=r_associated | relid=0 | w=31 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 31 / 0.721 -> en:chronic diarrhea due to glucoamylase deficiency n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:chronic diarrhea due to glucoamylase deficiency | rel=r_associated | relid=0 | w=31 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 31 / 0.721 -> en:combined pituitary hormone deficiency genetic form n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:combined pituitary hormone deficiency genetic form | rel=r_associated | relid=0 | w=31 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 31 / 0.721 -> en:congenital amegakaryocytic thrombocytopenia n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital amegakaryocytic thrombocytopenia | rel=r_associated | relid=0 | w=31 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 31 / 0.721 -> en:congenital atrophy of left lobe of liver n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital atrophy of left lobe of liver | rel=r_associated | relid=0 | w=31 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 31 / 0.721 -> en:congenital axial myopia n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital axial myopia | rel=r_associated | relid=0 | w=31 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 31 / 0.721 -> en:congenital blocked tear duct n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital blocked tear duct | rel=r_associated | relid=0 | w=31 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 31 / 0.721 -> en:congenital bundle of his tachycardia n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital bundle of his tachycardia | rel=r_associated | relid=0 | w=31 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 31 / 0.721 -> en:congenital complete atrioventricular block n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital complete atrioventricular block | rel=r_associated | relid=0 | w=31 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 31 / 0.721 -> en:congenital elephantiasis n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital elephantiasis | rel=r_associated | relid=0 | w=31 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 31 / 0.721 -> en:congenital factor ix deficiency without inhibitor n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital factor ix deficiency without inhibitor | rel=r_associated | relid=0 | w=31 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 31 / 0.721 -> en:congenital functional disorders of the small intestine n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital functional disorders of the small intestine | rel=r_associated | relid=0 | w=31 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 31 / 0.721 -> en:congenital metabolic disorder n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital metabolic disorder | rel=r_associated | relid=0 | w=31 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 31 / 0.721 -> en:congenital monosaccharide malabsorption n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital monosaccharide malabsorption | rel=r_associated | relid=0 | w=31 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 31 / 0.721 -> en:congenital nervous system disorder n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital nervous system disorder | rel=r_associated | relid=0 | w=31 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 31 / 0.721 -> en:congenital obstruction of aqueduct of sylvius n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital obstruction of aqueduct of sylvius | rel=r_associated | relid=0 | w=31 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 31 / 0.721 -> en:congenital peripheral aneurysm n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital peripheral aneurysm | rel=r_associated | relid=0 | w=31 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 31 / 0.721 -> en:congenital skin disorder n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital skin disorder | rel=r_associated | relid=0 | w=31 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 31 / 0.721 -> en:congenital velopharyngeal dysfunction n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital velopharyngeal dysfunction | rel=r_associated | relid=0 | w=31 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 31 / 0.721 -> en:congenital viral hepatitis n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital viral hepatitis | rel=r_associated | relid=0 | w=31 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 31 / 0.721 -> en:congenital vocal cord palsy n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital vocal cord palsy | rel=r_associated | relid=0 | w=31 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 31 / 0.721 -> en:congenital volvulus of stomach n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital volvulus of stomach | rel=r_associated | relid=0 | w=31 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 31 / 0.721 -> en:genetic diseases, inborn n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=31 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 31 / 0.721 -> en:glucocorticoid deficiency n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:glucocorticoid deficiency | rel=r_associated | relid=0 | w=31 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 31 / 0.721 -> en:intestinal epithelial dysplasia n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:intestinal epithelial dysplasia | rel=r_associated | relid=0 | w=31 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 31 / 0.721 -> en:mottled teeth, congenital n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:mottled teeth, congenital | rel=r_associated | relid=0 | w=31 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 31 / 0.721 -> en:mydriasis, congenital n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:mydriasis, congenital | rel=r_associated | relid=0 | w=31 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 31 / 0.721 -> en:palmoplantar porokeratosis n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:palmoplantar porokeratosis | rel=r_associated | relid=0 | w=31 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 31 / 0.721 -> en:parachute malformation of left atrioventricular valve n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:parachute malformation of left atrioventricular valve | rel=r_associated | relid=0 | w=31 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 30 / 0.698 -> en:adrenal insufficiency due to adrenal metastasis n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:adrenal insufficiency due to adrenal metastasis | rel=r_associated | relid=0 | w=30 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 30 / 0.698 -> en:adrenocortical insufficiency neonatal n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:adrenocortical insufficiency neonatal | rel=r_associated | relid=0 | w=30 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 30 / 0.698 -> en:adrenogenital syndrome n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:adrenogenital syndrome | rel=r_associated | relid=0 | w=30 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 30 / 0.698 -> en:congenital atrophy of thyroid n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital atrophy of thyroid | rel=r_associated | relid=0 | w=30 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 30 / 0.698 -> en:congenital auditory imperception n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital auditory imperception | rel=r_associated | relid=0 | w=30 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 30 / 0.698 -> en:congenital cardiac failure n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital cardiac failure | rel=r_associated | relid=0 | w=30 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 30 / 0.698 -> en:congenital disorder of facial nerve n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital disorder of facial nerve | rel=r_associated | relid=0 | w=30 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 30 / 0.698 -> en:congenital end-plate acetylcholinesterase deficiency n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital end-plate acetylcholinesterase deficiency | rel=r_associated | relid=0 | w=30 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 30 / 0.698 -> en:congenital kidney disorder n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital kidney disorder | rel=r_associated | relid=0 | w=30 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 30 / 0.698 -> en:congenital kyphosis n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital kyphosis | rel=r_associated | relid=0 | w=30 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 30 / 0.698 -> en:congenital myotonic dystrophy n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital myotonic dystrophy | rel=r_associated | relid=0 | w=30 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 30 / 0.698 -> en:congenital pseudostrabismus n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital pseudostrabismus | rel=r_associated | relid=0 | w=30 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 30 / 0.698 -> en:congenital quadriplegia n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital quadriplegia | rel=r_associated | relid=0 | w=30 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 30 / 0.698 -> en:congenital skin contracture n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital skin contracture | rel=r_associated | relid=0 | w=30 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 30 / 0.698 -> en:cushing syndrome n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:cushing syndrome | rel=r_associated | relid=0 | w=30 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 30 / 0.698 -> en:gelatinous atrioventricular valve leaflet in atrioventricular septal defect n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:gelatinous atrioventricular valve leaflet in atrioventricular septal defect | rel=r_associated | relid=0 | w=30 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 30 / 0.698 -> en:multiple supernumerary teeth unrelated to systemic condition n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:multiple supernumerary teeth unrelated to systemic condition | rel=r_associated | relid=0 | w=30 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 30 / 0.698 -> en:regional congenital anomaly n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:regional congenital anomaly | rel=r_associated | relid=0 | w=30 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 30 / 0.698 -> en:right atrial endocardial fibroelastosis n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:right atrial endocardial fibroelastosis | rel=r_associated | relid=0 | w=30 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 30 / 0.698 -> en:williams syndrome n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:williams syndrome | rel=r_associated | relid=0 | w=30 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 29 / 0.674 -> en:abnormal root proximity between adjacent teeth n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:abnormal root proximity between adjacent teeth | rel=r_associated | relid=0 | w=29 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 29 / 0.674 -> en:adrenal androgen deficiency n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:adrenal androgen deficiency | rel=r_associated | relid=0 | w=29 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 29 / 0.674 -> en:congenital and developmental myasthenia n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital and developmental myasthenia | rel=r_associated | relid=0 | w=29 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 29 / 0.674 -> en:congenital biliary tract disorder n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital biliary tract disorder | rel=r_associated | relid=0 | w=29 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 29 / 0.674 -> en:congenital blepharophimosis of lower eyelid n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital blepharophimosis of lower eyelid | rel=r_associated | relid=0 | w=29 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 29 / 0.674 -> en:congenital choroidal fold n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital choroidal fold | rel=r_associated | relid=0 | w=29 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 29 / 0.674 -> en:congenital digestive system disorder n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital digestive system disorder | rel=r_associated | relid=0 | w=29 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 29 / 0.674 -> en:congenital dysarthria n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital dysarthria | rel=r_associated | relid=0 | w=29 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 29 / 0.674 -> en:congenital ear disorder n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital ear disorder | rel=r_associated | relid=0 | w=29 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 29 / 0.674 -> en:congenital fissure of tongue n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital fissure of tongue | rel=r_associated | relid=0 | w=29 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 29 / 0.674 -> en:congenital flat foot n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital flat foot | rel=r_associated | relid=0 | w=29 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 29 / 0.674 -> en:congenital functional disorders of the colon n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital functional disorders of the colon | rel=r_associated | relid=0 | w=29 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 29 / 0.674 -> en:congenital mass of mitral leaflet n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital mass of mitral leaflet | rel=r_associated | relid=0 | w=29 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 29 / 0.674 -> en:congenital muscle disorder n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital muscle disorder | rel=r_associated | relid=0 | w=29 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 29 / 0.674 -> en:congenital onychatrophy n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital onychatrophy | rel=r_associated | relid=0 | w=29 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 29 / 0.674 -> en:congenital pancreatic cyst n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital pancreatic cyst | rel=r_associated | relid=0 | w=29 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 29 / 0.674 -> en:congenital pancreatic trypsin deficiency n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital pancreatic trypsin deficiency | rel=r_associated | relid=0 | w=29 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 29 / 0.674 -> en:congenital paraplegia n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital paraplegia | rel=r_associated | relid=0 | w=29 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 29 / 0.674 -> en:congenital posterior subcapsular polar cataract n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital posterior subcapsular polar cataract | rel=r_associated | relid=0 | w=29 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 29 / 0.674 -> en:congenital sequelae of disorders n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital sequelae of disorders | rel=r_associated | relid=0 | w=29 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 29 / 0.674 -> en:congenital stenosis n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital stenosis | rel=r_associated | relid=0 | w=29 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 29 / 0.674 -> en:congenital von willebrand's disease n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital von willebrand's disease | rel=r_associated | relid=0 | w=29 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 29 / 0.674 -> en:dental midlines coincident and incorrect n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:dental midlines coincident and incorrect | rel=r_associated | relid=0 | w=29 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 29 / 0.674 -> en:generalized intestinal dysmotility n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:generalized intestinal dysmotility | rel=r_associated | relid=0 | w=29 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 29 / 0.674 -> en:hutch diverticulum n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:hutch diverticulum | rel=r_associated | relid=0 | w=29 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 29 / 0.674 -> en:hypoaldosteronemia n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:hypoaldosteronemia | rel=r_associated | relid=0 | w=29 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 29 / 0.674 -> en:iatrogenic adrenal insufficiency n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:iatrogenic adrenal insufficiency | rel=r_associated | relid=0 | w=29 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 29 / 0.674 -> en:night blindness, congenital stationary n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:night blindness, congenital stationary | rel=r_associated | relid=0 | w=29 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 29 / 0.674 -> en:pseudomonas pyocyaneus congenital infection n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:pseudomonas pyocyaneus congenital infection | rel=r_associated | relid=0 | w=29 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 29 / 0.674 -> en:redundant prepuce n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:redundant prepuce | rel=r_associated | relid=0 | w=29 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 29 / 0.674 -> en:right ventricular myocardial sinusoids n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:right ventricular myocardial sinusoids | rel=r_associated | relid=0 | w=29 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 29 / 0.674 -> en:stomach in right sided position n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:stomach in right sided position | rel=r_associated | relid=0 | w=29 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 29 / 0.674 -> en:tooth malformation n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:tooth malformation | rel=r_associated | relid=0 | w=29 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 28 / 0.651 -> en:congenital adrenal gland hypoplasia n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital adrenal gland hypoplasia | rel=r_associated | relid=0 | w=28 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 28 / 0.651 -> en:congenital anal fissure n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital anal fissure | rel=r_associated | relid=0 | w=28 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 28 / 0.651 -> en:congenital connective tissue disorder n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital connective tissue disorder | rel=r_associated | relid=0 | w=28 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 28 / 0.651 -> en:congenital facial asymmetry n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital facial asymmetry | rel=r_associated | relid=0 | w=28 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 28 / 0.651 -> en:congenital factor ix deficiency variant n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital factor ix deficiency variant | rel=r_associated | relid=0 | w=28 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 28 / 0.651 -> en:congenital fecaliths causing obstruction n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital fecaliths causing obstruction | rel=r_associated | relid=0 | w=28 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 28 / 0.651 -> en:congenital ischemic atrophy of central nervous system structure n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital ischemic atrophy of central nervous system structure | rel=r_associated | relid=0 | w=28 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 28 / 0.651 -> en:congenital melanocytic nevus of trunk n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital melanocytic nevus of trunk | rel=r_associated | relid=0 | w=28 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 28 / 0.651 -> en:congenital nasolacrimal duct obstruction n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital nasolacrimal duct obstruction | rel=r_associated | relid=0 | w=28 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 28 / 0.651 -> en:congenital obstruction of bile duct n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital obstruction of bile duct | rel=r_associated | relid=0 | w=28 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 28 / 0.651 -> en:congenital plasminogen activator inhibitor deficiency type 1 n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital plasminogen activator inhibitor deficiency type 1 | rel=r_associated | relid=0 | w=28 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 28 / 0.651 -> en:congenital thrombocytopenic purpura n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital thrombocytopenic purpura | rel=r_associated | relid=0 | w=28 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 28 / 0.651 -> en:congenital vascular disorder n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital vascular disorder | rel=r_associated | relid=0 | w=28 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 28 / 0.651 -> en:dental arch length loss secondary to congenitally missing teeth n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:dental arch length loss secondary to congenitally missing teeth | rel=r_associated | relid=0 | w=28 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 28 / 0.651 -> en:ear dimple n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:ear dimple | rel=r_associated | relid=0 | w=28 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 28 / 0.651 -> en:ectopic bone tissue congenital n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:ectopic bone tissue congenital | rel=r_associated | relid=0 | w=28 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 28 / 0.651 -> en:fascial dystrophy, congenital n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:fascial dystrophy, congenital | rel=r_associated | relid=0 | w=28 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 28 / 0.651 -> en:foxg1 syndrome n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:foxg1 syndrome | rel=r_associated | relid=0 | w=28 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 28 / 0.651 -> en:lactase deficiency, congenital n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:lactase deficiency, congenital | rel=r_associated | relid=0 | w=28 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 28 / 0.651 -> en:prader-willi syndrome n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:prader-willi syndrome | rel=r_associated | relid=0 | w=28 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 28 / 0.651 -> en:precocious exfoliation of teeth related to root resorption associated with trauma n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:precocious exfoliation of teeth related to root resorption associated with trauma | rel=r_associated | relid=0 | w=28 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 28 / 0.651 -> en:systemic venovenous collateral vein n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:systemic venovenous collateral vein | rel=r_associated | relid=0 | w=28 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 28 / 0.651 -> en:tricuspid but functionally bicuspid aortic valve n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:tricuspid but functionally bicuspid aortic valve | rel=r_associated | relid=0 | w=28 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 27 / 0.628 -> en:adrenal atrophy n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:adrenal atrophy | rel=r_associated | relid=0 | w=27 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 27 / 0.628 -> en:adrenocortical insufficiency n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:adrenocortical insufficiency | rel=r_associated | relid=0 | w=27 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 27 / 0.628 -> en:congenital chylothorax n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital chylothorax | rel=r_associated | relid=0 | w=27 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 27 / 0.628 -> en:congenital claw toe n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital claw toe | rel=r_associated | relid=0 | w=27 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 27 / 0.628 -> en:congenital color blindness n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital color blindness | rel=r_associated | relid=0 | w=27 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 27 / 0.628 -> en:congenital disorder of gallbladder and biliary tract n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital disorder of gallbladder and biliary tract | rel=r_associated | relid=0 | w=27 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 27 / 0.628 -> en:congenital hepatic fibrosis n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital hepatic fibrosis | rel=r_associated | relid=0 | w=27 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 27 / 0.628 -> en:congenital hepatomegaly n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital hepatomegaly | rel=r_associated | relid=0 | w=27 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 27 / 0.628 -> en:congenital hydrosalpinx n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital hydrosalpinx | rel=r_associated | relid=0 | w=27 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 27 / 0.628 -> en:congenital laryngeal adductor palsy n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital laryngeal adductor palsy | rel=r_associated | relid=0 | w=27 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 27 / 0.628 -> en:congenital leptomeningeal angiomatosis n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital leptomeningeal angiomatosis | rel=r_associated | relid=0 | w=27 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 27 / 0.628 -> en:congenital neurogenic ileus syndrome n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital neurogenic ileus syndrome | rel=r_associated | relid=0 | w=27 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 27 / 0.628 -> en:congenital neutrophil actin dysfunction n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital neutrophil actin dysfunction | rel=r_associated | relid=0 | w=27 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 27 / 0.628 -> en:congenital occlusion of ureter n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital occlusion of ureter | rel=r_associated | relid=0 | w=27 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 27 / 0.628 -> en:congenital reproductive system disorder n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital reproductive system disorder | rel=r_associated | relid=0 | w=27 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 27 / 0.628 -> en:congenital retinoschisis n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital retinoschisis | rel=r_associated | relid=0 | w=27 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 27 / 0.628 -> en:congenital secretory diarrhea n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital secretory diarrhea | rel=r_associated | relid=0 | w=27 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 27 / 0.628 -> en:erythropoietic porphyria n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:erythropoietic porphyria | rel=r_associated | relid=0 | w=27 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 27 / 0.628 -> en:fordyce's disease n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:fordyce's disease | rel=r_associated | relid=0 | w=27 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 27 / 0.628 -> en:impervious urethra n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:impervious urethra | rel=r_associated | relid=0 | w=27 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 27 / 0.628 -> en:longitudinal deficiency of limb n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:longitudinal deficiency of limb | rel=r_associated | relid=0 | w=27 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 27 / 0.628 -> en:parachute malformation of common atrioventricular valve n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:parachute malformation of common atrioventricular valve | rel=r_associated | relid=0 | w=27 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 27 / 0.628 -> en:parachute malformation of right atrioventricular valve n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:parachute malformation of right atrioventricular valve | rel=r_associated | relid=0 | w=27 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 27 / 0.628 -> en:primary left ventricular endocardial fibroelastosis n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:primary left ventricular endocardial fibroelastosis | rel=r_associated | relid=0 | w=27 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 27 / 0.628 -> en:right-sided pulmonary arterial trunk n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:right-sided pulmonary arterial trunk | rel=r_associated | relid=0 | w=27 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 27 / 0.628 -> en:rudimentary left ventricle n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:rudimentary left ventricle | rel=r_associated | relid=0 | w=27 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 27 / 0.628 -> en:smith-lemli-opitz syndrome n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:smith-lemli-opitz syndrome | rel=r_associated | relid=0 | w=27 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 27 / 0.628 -> en:truncal valve overriding ventricular septum n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:truncal valve overriding ventricular septum | rel=r_associated | relid=0 | w=27 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 27 / 0.628 -> en:vitamin d-dependent rickets, type 2 n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:vitamin d-dependent rickets, type 2 | rel=r_associated | relid=0 | w=27 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 26 / 0.605 -> en:allgrove syndrome n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:allgrove syndrome | rel=r_associated | relid=0 | w=26 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 26 / 0.605 -> en:congenital n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital | rel=r_associated | relid=0 | w=26 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 26 / 0.605 -> en:congenital accessory skin tag n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital accessory skin tag | rel=r_associated | relid=0 | w=26 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 26 / 0.605 -> en:congenital alpha-2-antiplasmin deficiency n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital alpha-2-antiplasmin deficiency | rel=r_associated | relid=0 | w=26 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 26 / 0.605 -> en:congenital blepharophimosis of upper eyelid n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital blepharophimosis of upper eyelid | rel=r_associated | relid=0 | w=26 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 26 / 0.605 -> en:congenital blood disorder n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital blood disorder | rel=r_associated | relid=0 | w=26 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 26 / 0.605 -> en:congenital cutaneous angiomatosis n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital cutaneous angiomatosis | rel=r_associated | relid=0 | w=26 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 26 / 0.605 -> en:congenital debility of fetus n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital debility of fetus | rel=r_associated | relid=0 | w=26 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 26 / 0.605 -> en:congenital dysphasia n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital dysphasia | rel=r_associated | relid=0 | w=26 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 26 / 0.605 -> en:congenital eye disorder n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital eye disorder | rel=r_associated | relid=0 | w=26 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 26 / 0.605 -> en:congenital fibrinogen abnormality n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital fibrinogen abnormality | rel=r_associated | relid=0 | w=26 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 26 / 0.605 -> en:congenital hepatic porphyria n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital hepatic porphyria | rel=r_associated | relid=0 | w=26 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 26 / 0.605 -> en:congenital hernia of bladder n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital hernia of bladder | rel=r_associated | relid=0 | w=26 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 26 / 0.605 -> en:congenital hydrocele n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital hydrocele | rel=r_associated | relid=0 | w=26 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 26 / 0.605 -> en:congenital immunodeficiency disease n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital immunodeficiency disease | rel=r_associated | relid=0 | w=26 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 26 / 0.605 -> en:congenital incomplete atrioventricular heart block n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital incomplete atrioventricular heart block | rel=r_associated | relid=0 | w=26 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 26 / 0.605 -> en:congenital inguinal hernia n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital inguinal hernia | rel=r_associated | relid=0 | w=26 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 26 / 0.605 -> en:congenital long qt syndrome n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital long qt syndrome | rel=r_associated | relid=0 | w=26 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 26 / 0.605 -> en:congenital obstruction of small intestine n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital obstruction of small intestine | rel=r_associated | relid=0 | w=26 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 26 / 0.605 -> en:congenital pain insensitivity n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital pain insensitivity | rel=r_associated | relid=0 | w=26 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 26 / 0.605 -> en:congenital pneumonia n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital pneumonia | rel=r_associated | relid=0 | w=26 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 26 / 0.605 -> en:congenital pseudoporencephaly n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital pseudoporencephaly | rel=r_associated | relid=0 | w=26 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 26 / 0.605 -> en:congenital rectal fissure n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital rectal fissure | rel=r_associated | relid=0 | w=26 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 26 / 0.605 -> en:congenital renal atrophy n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital renal atrophy | rel=r_associated | relid=0 | w=26 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 26 / 0.605 -> en:congenital sixth nerve palsy n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital sixth nerve palsy | rel=r_associated | relid=0 | w=26 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 26 / 0.605 -> en:familial adrenocortical hypoplasia n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:familial adrenocortical hypoplasia | rel=r_associated | relid=0 | w=26 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 26 / 0.605 -> en:fenestrated interatrial communication within oval fossa n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:fenestrated interatrial communication within oval fossa | rel=r_associated | relid=0 | w=26 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 26 / 0.605 -> en:hereditary adrenal unresponsiveness to corticotropin n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:hereditary adrenal unresponsiveness to corticotropin | rel=r_associated | relid=0 | w=26 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 26 / 0.605 -> en:kallmann syndrome n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:kallmann syndrome | rel=r_associated | relid=0 | w=26 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 26 / 0.605 -> en:leber congenital amaurosis n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:leber congenital amaurosis | rel=r_associated | relid=0 | w=26 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 26 / 0.605 -> en:myelocele n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:myelocele | rel=r_associated | relid=0 | w=26 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 26 / 0.605 -> en:pseudohypoaldosteronism type 1 n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:pseudohypoaldosteronism type 1 | rel=r_associated | relid=0 | w=26 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 26 / 0.605 -> en:right atrial appendage absent n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:right atrial appendage absent | rel=r_associated | relid=0 | w=26 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 26 / 0.605 -> en:rotation of tooth n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:rotation of tooth | rel=r_associated | relid=0 | w=26 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 26 / 0.605 -> en:steroid withdrawal syndrome n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:steroid withdrawal syndrome | rel=r_associated | relid=0 | w=26 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 25 / 0.581 -> en:adrenocortical n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:adrenocortical | rel=r_associated | relid=0 | w=25 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 25 / 0.581 -> en:shortened trunk n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:shortened trunk | rel=r_associated | relid=0 | w=25 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 25 / 0.581 -> en:true cleft of common atrioventricular valve leaflet n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:true cleft of common atrioventricular valve leaflet | rel=r_associated | relid=0 | w=25 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 24 / 0.558 -> anomalie congénitale n1=en:adrenocortical hypofunction, chronic primary congenital | n2=anomalie congénitale | rel=r_associated | relid=0 | w=24 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 23 / 0.535 -> adréno-leucodystrophie n1=en:adrenocortical hypofunction, chronic primary congenital | n2=adréno-leucodystrophie | rel=r_associated | relid=0 | w=23 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 23 / 0.535 -> adrénoleucodystrophie n1=en:adrenocortical hypofunction, chronic primary congenital | n2=adrénoleucodystrophie | rel=r_associated | relid=0 | w=23 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 23 / 0.535 -> en:right atrial appendage - left - juxtaposition n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:right atrial appendage - left - juxtaposition | rel=r_associated | relid=0 | w=23 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 23 / 0.535 -> en:urachal cyst n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:urachal cyst | rel=r_associated | relid=0 | w=23 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 22 / 0.512 -> en:obstructed pulmonary venous connection at coronary sinus orifice n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:obstructed pulmonary venous connection at coronary sinus orifice | rel=r_associated | relid=0 | w=22 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 22 / 0.512 -> en:posterior deviation of infundibular septum of obstructive aortic arch type n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:posterior deviation of infundibular septum of obstructive aortic arch type | rel=r_associated | relid=0 | w=22 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 21 / 0.488 -> en:trifoliate left atrioventricular valve n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:trifoliate left atrioventricular valve | rel=r_associated | relid=0 | w=21 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 20 / 0.465 -> adrénoleucodystrophie de l?enfant n1=en:adrenocortical hypofunction, chronic primary congenital | n2=adrénoleucodystrophie de l?enfant | rel=r_associated | relid=0 | w=20 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 20 / 0.465 -> adrénoleucodystrophie liée à l'X n1=en:adrenocortical hypofunction, chronic primary congenital | n2=adrénoleucodystrophie liée à l'X | rel=r_associated | relid=0 | w=20 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 20 / 0.465 -> adrénoleucodystrophie néonatale récessive n1=en:adrenocortical hypofunction, chronic primary congenital | n2=adrénoleucodystrophie néonatale récessive | rel=r_associated | relid=0 | w=20 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 20 / 0.465 -> affection oculaire congénitale n1=en:adrenocortical hypofunction, chronic primary congenital | n2=affection oculaire congénitale | rel=r_associated | relid=0 | w=20 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 20 / 0.465 -> amn n1=en:adrenocortical hypofunction, chronic primary congenital | n2=amn | rel=r_associated | relid=0 | w=20 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 20 / 0.465 -> anomalie chromosomique n1=en:adrenocortical hypofunction, chronic primary congenital | n2=anomalie chromosomique | rel=r_associated | relid=0 | w=20 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 20 / 0.465 -> anomalie congénitale de l'oeil n1=en:adrenocortical hypofunction, chronic primary congenital | n2=anomalie congénitale de l'oeil | rel=r_associated | relid=0 | w=20 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 20 / 0.465 -> anomalie cytogénétique n1=en:adrenocortical hypofunction, chronic primary congenital | n2=anomalie cytogénétique | rel=r_associated | relid=0 | w=20 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 20 / 0.465 -> anomalie du développement n1=en:adrenocortical hypofunction, chronic primary congenital | n2=anomalie du développement | rel=r_associated | relid=0 | w=20 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 20 / 0.465 -> anormalité des chromosomes n1=en:adrenocortical hypofunction, chronic primary congenital | n2=anormalité des chromosomes | rel=r_associated | relid=0 | w=20 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 20 / 0.465 -> arthrogrypose n1=en:adrenocortical hypofunction, chronic primary congenital | n2=arthrogrypose | rel=r_associated | relid=0 | w=20 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 20 / 0.465 -> atrophie congénitale de la thyroïde n1=en:adrenocortical hypofunction, chronic primary congenital | n2=atrophie congénitale de la thyroïde | rel=r_associated | relid=0 | w=20 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 20 / 0.465 -> congénital n1=en:adrenocortical hypofunction, chronic primary congenital | n2=congénital | rel=r_associated | relid=0 | w=20 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 20 / 0.465 -> congenital n1=en:adrenocortical hypofunction, chronic primary congenital | n2=congenital | rel=r_associated | relid=0 | w=20 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 20 / 0.465 -> congénitale n1=en:adrenocortical hypofunction, chronic primary congenital | n2=congénitale | rel=r_associated | relid=0 | w=20 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 20 / 0.465 -> contractures congénitales et arachnodactylie n1=en:adrenocortical hypofunction, chronic primary congenital | n2=contractures congénitales et arachnodactylie | rel=r_associated | relid=0 | w=20 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 20 / 0.465 -> crétinismes n1=en:adrenocortical hypofunction, chronic primary congenital | n2=crétinismes | rel=r_associated | relid=0 | w=20 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 20 / 0.465 -> débilité congénitale du foetus n1=en:adrenocortical hypofunction, chronic primary congenital | n2=débilité congénitale du foetus | rel=r_associated | relid=0 | w=20 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 20 / 0.465 -> débilité congénitale foetale n1=en:adrenocortical hypofunction, chronic primary congenital | n2=débilité congénitale foetale | rel=r_associated | relid=0 | w=20 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 20 / 0.465 -> déficience congénitale n1=en:adrenocortical hypofunction, chronic primary congenital | n2=déficience congénitale | rel=r_associated | relid=0 | w=20 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 20 / 0.465 -> déformation congénitale n1=en:adrenocortical hypofunction, chronic primary congenital | n2=déformation congénitale | rel=r_associated | relid=0 | w=20 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 20 / 0.465 -> difformité congénitale n1=en:adrenocortical hypofunction, chronic primary congenital | n2=difformité congénitale | rel=r_associated | relid=0 | w=20 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 20 / 0.465 -> en:addison disease n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:addison disease | rel=r_associated | relid=0 | w=20 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 20 / 0.465 -> en:Addison disease n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:Addison disease | rel=r_associated | relid=0 | w=20 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 20 / 0.465 -> en:Addison's disease n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:Addison's disease | rel=r_associated | relid=0 | w=20 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 20 / 0.465 -> en:amyoplasia congenita n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:amyoplasia congenita | rel=r_associated | relid=0 | w=20 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 20 / 0.465 -> en:birth defect n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:birth defect | rel=r_associated | relid=0 | w=20 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 20 / 0.465 -> en:chromosomal abnormality n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:chromosomal abnormality | rel=r_associated | relid=0 | w=20 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 20 / 0.465 -> en:congenital analbuminemia n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital analbuminemia | rel=r_associated | relid=0 | w=20 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 20 / 0.465 -> en:congenital anomaly n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital anomaly | rel=r_associated | relid=0 | w=20 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 20 / 0.465 -> en:congenital cyst of aryepiglottic fold n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital cyst of aryepiglottic fold | rel=r_associated | relid=0 | w=20 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 20 / 0.465 -> en:congenital defect n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital defect | rel=r_associated | relid=0 | w=20 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 20 / 0.465 -> en:congenital goiter n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital goiter | rel=r_associated | relid=0 | w=20 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 20 / 0.465 -> en:congenital laryngeal cyst n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital laryngeal cyst | rel=r_associated | relid=0 | w=20 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 20 / 0.465 -> en:congenital malformation n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital malformation | rel=r_associated | relid=0 | w=20 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 20 / 0.465 -> en:congenital megaprepuce n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:congenital megaprepuce | rel=r_associated | relid=0 | w=20 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 20 / 0.465 -> en:developmental fault n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:developmental fault | rel=r_associated | relid=0 | w=20 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 20 / 0.465 -> en:Günther's disease n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:Günther's disease | rel=r_associated | relid=0 | w=20 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 20 / 0.465 -> en:hypoaldosteronism n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:hypoaldosteronism | rel=r_associated | relid=0 | w=20 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 20 / 0.465 -> en:major physical defect n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:major physical defect | rel=r_associated | relid=0 | w=20 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 20 / 0.465 -> en:neonatal hypothyroidism n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:neonatal hypothyroidism | rel=r_associated | relid=0 | w=20 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 20 / 0.465 -> en:nystagmus n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:nystagmus | rel=r_associated | relid=0 | w=20 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 20 / 0.465 -> en:physical defect n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:physical defect | rel=r_associated | relid=0 | w=20 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 20 / 0.465 -> en:pigmented paravenous chorioretinal atrophy n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 20 / 0.465 -> en:Prader-Willi syndrome n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:Prader-Willi syndrome | rel=r_associated | relid=0 | w=20 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 20 / 0.465 -> en:teratosis n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:teratosis | rel=r_associated | relid=0 | w=20 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 20 / 0.465 -> en:Williams syndrome n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:Williams syndrome | rel=r_associated | relid=0 | w=20 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 20 / 0.465 -> foramen ovale perméable n1=en:adrenocortical hypofunction, chronic primary congenital | n2=foramen ovale perméable | rel=r_associated | relid=0 | w=20 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 20 / 0.465 -> goitre congénital n1=en:adrenocortical hypofunction, chronic primary congenital | n2=goitre congénital | rel=r_associated | relid=0 | w=20 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 20 / 0.465 -> hypo-aldostéronisme n1=en:adrenocortical hypofunction, chronic primary congenital | n2=hypo-aldostéronisme | rel=r_associated | relid=0 | w=20 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 20 / 0.465 -> hypoaldostéronisme n1=en:adrenocortical hypofunction, chronic primary congenital | n2=hypoaldostéronisme | rel=r_associated | relid=0 | w=20 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 20 / 0.465 -> hypothyroïdie congénitale n1=en:adrenocortical hypofunction, chronic primary congenital | n2=hypothyroïdie congénitale | rel=r_associated | relid=0 | w=20 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 20 / 0.465 -> hypothyroïdisme congénital n1=en:adrenocortical hypofunction, chronic primary congenital | n2=hypothyroïdisme congénital | rel=r_associated | relid=0 | w=20 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 20 / 0.465 -> infantilisme type brissaud n1=en:adrenocortical hypofunction, chronic primary congenital | n2=infantilisme type brissaud | rel=r_associated | relid=0 | w=20 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 20 / 0.465 -> insuffisance surrénale n1=en:adrenocortical hypofunction, chronic primary congenital | n2=insuffisance surrénale | rel=r_associated | relid=0 | w=20 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 20 / 0.465 -> insuffisance surrénalienne chronique primaire n1=en:adrenocortical hypofunction, chronic primary congenital | n2=insuffisance surrénalienne chronique primaire | rel=r_associated | relid=0 | w=20 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 20 / 0.465 -> Maladie congénitale n1=en:adrenocortical hypofunction, chronic primary congenital | n2=Maladie congénitale | rel=r_associated | relid=0 | w=20 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 20 / 0.465 -> maladie congénitale n1=en:adrenocortical hypofunction, chronic primary congenital | n2=maladie congénitale | rel=r_associated | relid=0 | w=20 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 20 / 0.465 -> maladie d'Addison n1=en:adrenocortical hypofunction, chronic primary congenital | n2=maladie d'Addison | rel=r_associated | relid=0 | w=20 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 20 / 0.465 -> maladie d'addison n1=en:adrenocortical hypofunction, chronic primary congenital | n2=maladie d'addison | rel=r_associated | relid=0 | w=20 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 20 / 0.465 -> malformation congénitale n1=en:adrenocortical hypofunction, chronic primary congenital | n2=malformation congénitale | rel=r_associated | relid=0 | w=20 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 20 / 0.465 -> méthémoglobinémie congénitale n1=en:adrenocortical hypofunction, chronic primary congenital | n2=méthémoglobinémie congénitale | rel=r_associated | relid=0 | w=20 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 20 / 0.465 -> myofibromatose infantile n1=en:adrenocortical hypofunction, chronic primary congenital | n2=myofibromatose infantile | rel=r_associated | relid=0 | w=20 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 20 / 0.465 -> nanisme hypothyroïdien n1=en:adrenocortical hypofunction, chronic primary congenital | n2=nanisme hypothyroïdien | rel=r_associated | relid=0 | w=20 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 20 / 0.465 -> nystagmus congénital isolé n1=en:adrenocortical hypofunction, chronic primary congenital | n2=nystagmus congénital isolé | rel=r_associated | relid=0 | w=20 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 20 / 0.465 -> ouraque (kyste de l') n1=en:adrenocortical hypofunction, chronic primary congenital | n2=ouraque (kyste de l') | rel=r_associated | relid=0 | w=20 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 20 / 0.465 -> pathologie congénitale n1=en:adrenocortical hypofunction, chronic primary congenital | n2=pathologie congénitale | rel=r_associated | relid=0 | w=20 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 20 / 0.465 -> persistance du foramen ovale n1=en:adrenocortical hypofunction, chronic primary congenital | n2=persistance du foramen ovale | rel=r_associated | relid=0 | w=20 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 20 / 0.465 -> porphyrie érythropoïétique n1=en:adrenocortical hypofunction, chronic primary congenital | n2=porphyrie érythropoïétique | rel=r_associated | relid=0 | w=20 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 20 / 0.465 -> rétinite pigmentaire paraveineuse n1=en:adrenocortical hypofunction, chronic primary congenital | n2=rétinite pigmentaire paraveineuse | rel=r_associated | relid=0 | w=20 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 20 / 0.465 -> syndrome d'insuffisance thyroïdienne congénitale n1=en:adrenocortical hypofunction, chronic primary congenital | n2=syndrome d'insuffisance thyroïdienne congénitale | rel=r_associated | relid=0 | w=20 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 20 / 0.465 -> tare congénitale n1=en:adrenocortical hypofunction, chronic primary congenital | n2=tare congénitale | rel=r_associated | relid=0 | w=20 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 20 / 0.465 -> trouble chromosomique n1=en:adrenocortical hypofunction, chronic primary congenital | n2=trouble chromosomique | rel=r_associated | relid=0 | w=20 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 20 / 0.465 -> une anomalie congénitale n1=en:adrenocortical hypofunction, chronic primary congenital | n2=une anomalie congénitale | rel=r_associated | relid=0 | w=20 en:adrenocortical hypofunction, chronic primary congenital -- r_associated #0: 20 / 0.465 -> vice de conformation n1=en:adrenocortical hypofunction, chronic primary congenital | n2=vice de conformation | rel=r_associated | relid=0 | w=20

≈ 440 relations entrantes anomalie congénitale --- r_associated #0: 424 --> en:adrenocortical hypofunction, chronic primary congenital n1=anomalie congénitale | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=424 en:congenital abnormality --- r_associated #0: 423 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital abnormality | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=423 malformation congénitale --- r_associated #0: 351 --> en:adrenocortical hypofunction, chronic primary congenital n1=malformation congénitale | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=351 en:congenital anomaly --- r_associated #0: 346 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital anomaly | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=346 en:congenital defect --- r_associated #0: 310 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital defect | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=310 déformation congénitale --- r_associated #0: 296 --> en:adrenocortical hypofunction, chronic primary congenital n1=déformation congénitale | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=296 déficience congénitale --- r_associated #0: 295 --> en:adrenocortical hypofunction, chronic primary congenital n1=déficience congénitale | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=295 adréno-leucodystrophie --- r_associated #0: 213 --> en:adrenocortical hypofunction, chronic primary congenital n1=adréno-leucodystrophie | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=213 en:adrenoleukodystrophy --- r_associated #0: 210 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:adrenoleukodystrophy | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=210 anomalie congénitale de l'oeil --- r_associated #0: 206 --> en:adrenocortical hypofunction, chronic primary congenital n1=anomalie congénitale de l'oeil | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=206 difformité congénitale --- r_associated #0: 205 --> en:adrenocortical hypofunction, chronic primary congenital n1=difformité congénitale | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=205 en:congenital eye disorder --- r_associated #0: 205 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital eye disorder | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=205 maladie congénitale --- r_associated #0: 201 --> en:adrenocortical hypofunction, chronic primary congenital n1=maladie congénitale | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=201 pathologie congénitale --- r_associated #0: 195 --> en:adrenocortical hypofunction, chronic primary congenital n1=pathologie congénitale | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=195 hypothyroïdie congénitale --- r_associated #0: 190 --> en:adrenocortical hypofunction, chronic primary congenital n1=hypothyroïdie congénitale | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=190 infantilisme type brissaud --- r_associated #0: 190 --> en:adrenocortical hypofunction, chronic primary congenital n1=infantilisme type brissaud | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=190 en:congenital goiter --- r_associated #0: 189 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital goiter | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=189 nanisme hypothyroïdien --- r_associated #0: 185 --> en:adrenocortical hypofunction, chronic primary congenital n1=nanisme hypothyroïdien | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=185 affection oculaire congénitale --- r_associated #0: 180 --> en:adrenocortical hypofunction, chronic primary congenital n1=affection oculaire congénitale | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=180 syndrome d'insuffisance thyroïdienne congénitale --- r_associated #0: 180 --> en:adrenocortical hypofunction, chronic primary congenital n1=syndrome d'insuffisance thyroïdienne congénitale | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=180 goitre congénital --- r_associated #0: 175 --> en:adrenocortical hypofunction, chronic primary congenital n1=goitre congénital | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=175 hypothyroïdisme congénital --- r_associated #0: 175 --> en:adrenocortical hypofunction, chronic primary congenital n1=hypothyroïdisme congénital | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=175 en:congenital atrophy of thyroid --- r_associated #0: 171 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital atrophy of thyroid | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=171 atrophie congénitale de la thyroïde --- r_associated #0: 170 --> en:adrenocortical hypofunction, chronic primary congenital n1=atrophie congénitale de la thyroïde | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=170 crétinismes --- r_associated #0: 165 --> en:adrenocortical hypofunction, chronic primary congenital n1=crétinismes | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=165 en:congenital hypothyroidism --- r_associated #0: 165 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital hypothyroidism | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=165 en:arthrogryposis --- r_associated #0: 163 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:arthrogryposis | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=163 arthrogrypose --- r_associated #0: 160 --> en:adrenocortical hypofunction, chronic primary congenital n1=arthrogrypose | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=160 hypo-aldostéronisme --- r_associated #0: 147 --> en:adrenocortical hypofunction, chronic primary congenital n1=hypo-aldostéronisme | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=147 hypoaldostéronisme --- r_associated #0: 145 --> en:adrenocortical hypofunction, chronic primary congenital n1=hypoaldostéronisme | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=145 adrénoleucodystrophie --- r_associated #0: 144 --> en:adrenocortical hypofunction, chronic primary congenital n1=adrénoleucodystrophie | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=144 en:hypoaldosteronemia --- r_associated #0: 143 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:hypoaldosteronemia | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=143 en:hypoaldosteronism --- r_associated #0: 140 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:hypoaldosteronism | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=140 débilité congénitale du foetus --- r_associated #0: 135 --> en:adrenocortical hypofunction, chronic primary congenital n1=débilité congénitale du foetus | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=135 en:congenital debility of fetus --- r_associated #0: 134 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital debility of fetus | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=134 en:congenital malformation --- r_associated #0: 130 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital malformation | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=130 en:congenital methemoglobinemia --- r_associated #0: 124 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital methemoglobinemia | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=124 débilité congénitale foetale --- r_associated #0: 120 --> en:adrenocortical hypofunction, chronic primary congenital n1=débilité congénitale foetale | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=120 en:birth defect --- r_associated #0: 120 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:birth defect | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=120 méthémoglobinémie congénitale --- r_associated #0: 120 --> en:adrenocortical hypofunction, chronic primary congenital n1=méthémoglobinémie congénitale | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=120 tare congénitale --- r_associated #0: 85 --> en:adrenocortical hypofunction, chronic primary congenital n1=tare congénitale | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=85 en:congenital --- r_associated #0: 69 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=69 congenital --- r_associated #0: 67 --> en:adrenocortical hypofunction, chronic primary congenital n1=congenital | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=67 congénitale --- r_associated #0: 61 --> en:adrenocortical hypofunction, chronic primary congenital n1=congénitale | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=61 en:addison disease --- r_associated #0: 59 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:addison disease | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=59 congénital --- r_associated #0: 58 --> en:adrenocortical hypofunction, chronic primary congenital n1=congénital | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=58 persistance du foramen ovale --- r_associated #0: 56 --> en:adrenocortical hypofunction, chronic primary congenital n1=persistance du foramen ovale | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=56 vice de conformation --- r_associated #0: 56 --> en:adrenocortical hypofunction, chronic primary congenital n1=vice de conformation | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=56 maladie d'Addison --- r_associated #0: 55 --> en:adrenocortical hypofunction, chronic primary congenital n1=maladie d'Addison | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=55 maladie d'addison --- r_associated #0: 55 --> en:adrenocortical hypofunction, chronic primary congenital n1=maladie d'addison | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=55 en:patent foramen ovale --- r_associated #0: 53 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:patent foramen ovale | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=53 foramen ovale perméable --- r_associated #0: 52 --> en:adrenocortical hypofunction, chronic primary congenital n1=foramen ovale perméable | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=52 en:Addison's disease --- r_associated #0: 51 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:Addison's disease | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=51 en:addison's disease --- r_associated #0: 50 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:addison's disease | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=50 anomalie du développement --- r_associated #0: 49 --> en:adrenocortical hypofunction, chronic primary congenital n1=anomalie du développement | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=49 en:teratosis --- r_associated #0: 49 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:teratosis | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=49 insuffisance surrénalienne chronique primaire --- r_associated #0: 45 --> en:adrenocortical hypofunction, chronic primary congenital n1=insuffisance surrénalienne chronique primaire | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=45 en:williams syndrome --- r_associated #0: 44 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:williams syndrome | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=44 amn --- r_associated #0: 43 --> en:adrenocortical hypofunction, chronic primary congenital n1=amn | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=43 en:Williams syndrome --- r_associated #0: 43 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:Williams syndrome | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=43 en:congenital/genetic syndrome with poikiloderma --- r_associated #0: 43 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital/genetic syndrome with poikiloderma | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=43 en:tricuspid but functionally bicuspid aortic valve --- r_associated #0: 43 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:tricuspid but functionally bicuspid aortic valve | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=43 en:congenital anal fissure --- r_associated #0: 42 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital anal fissure | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=42 en:congenital anterior subcapsular polar cataract --- r_associated #0: 42 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital anterior subcapsular polar cataract | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=42 en:major physical defect --- r_associated #0: 42 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:major physical defect | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=42 en:spinal hydromeningocele --- r_associated #0: 42 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:spinal hydromeningocele | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=42 rétinite pigmentaire paraveineuse --- r_associated #0: 42 --> en:adrenocortical hypofunction, chronic primary congenital n1=rétinite pigmentaire paraveineuse | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=42 en:congenital ear disorder --- r_associated #0: 41 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital ear disorder | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=41 en:congenital leptin deficiency --- r_associated #0: 41 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital leptin deficiency | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=41 en:mottled teeth, congenital --- r_associated #0: 41 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:mottled teeth, congenital | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=41 en:physical defect --- r_associated #0: 41 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:physical defect | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=41 dysplasie olfacto-génitale --- r_associated #0: 40 --> en:adrenocortical hypofunction, chronic primary congenital n1=dysplasie olfacto-génitale | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=40 en:congenital incomplete atrioventricular heart block --- r_associated #0: 39 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital incomplete atrioventricular heart block | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=39 en:congenital obstruction of large intestine --- r_associated #0: 39 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital obstruction of large intestine | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=39 en:neonatal hypothyroidism --- r_associated #0: 39 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:neonatal hypothyroidism | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=39 en:pigmented paravenous chorioretinal atrophy --- r_associated #0: 39 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:pigmented paravenous chorioretinal atrophy | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=39 ouraque (kyste de l') --- r_associated #0: 39 --> en:adrenocortical hypofunction, chronic primary congenital n1=ouraque (kyste de l') | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=39 en:congenital claw toe --- r_associated #0: 38 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital claw toe | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=38 en:congenital connective tissue disorder --- r_associated #0: 37 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital connective tissue disorder | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=37 en:congenital functional disorders of the small intestine --- r_associated #0: 37 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital functional disorders of the small intestine | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=37 en:congenital nephritis --- r_associated #0: 37 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital nephritis | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=37 en:congenital pterygium of nail --- r_associated #0: 37 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital pterygium of nail | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=37 en:kallmann syndrome --- r_associated #0: 36 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:kallmann syndrome | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=36 porphyrie érythropoïétique --- r_associated #0: 36 --> en:adrenocortical hypofunction, chronic primary congenital n1=porphyrie érythropoïétique | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=36 dysplasie olfactogénitale --- r_associated #0: 35 --> en:adrenocortical hypofunction, chronic primary congenital n1=dysplasie olfactogénitale | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=35 en:Prader-Willi syndrome --- r_associated #0: 35 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:Prader-Willi syndrome | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=35 en:adrenocortical insufficiency --- r_associated #0: 35 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:adrenocortical insufficiency | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=35 en:cap myopathy --- r_associated #0: 35 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:cap myopathy | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=35 en:congenital atrophy of left lobe of liver --- r_associated #0: 35 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital atrophy of left lobe of liver | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=35 en:congenital auditory imperception --- r_associated #0: 35 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital auditory imperception | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=35 en:congenital blepharophimosis --- r_associated #0: 35 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital blepharophimosis | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=35 en:congenital celiac disease --- r_associated #0: 35 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital celiac disease | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=35 en:congenital cyst of fallopian tube --- r_associated #0: 35 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital cyst of fallopian tube | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=35 en:congenital dysarthria --- r_associated #0: 35 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital dysarthria | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=35 en:congenital end-plate acetylcholinesterase deficiency --- r_associated #0: 35 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital end-plate acetylcholinesterase deficiency | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=35 en:congenital fecaliths causing obstruction --- r_associated #0: 35 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital fecaliths causing obstruction | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=35 en:congenital hepatic porphyria --- r_associated #0: 35 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital hepatic porphyria | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=35 en:congenital ischemic atrophy of central nervous system structure --- r_associated #0: 35 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital ischemic atrophy of central nervous system structure | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=35 en:congenital kyphosis --- r_associated #0: 35 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital kyphosis | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=35 en:congenital male infertility --- r_associated #0: 35 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital male infertility | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=35 en:congenital reproductive system disorder --- r_associated #0: 35 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital reproductive system disorder | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=35 en:congenital stenosis --- r_associated #0: 35 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital stenosis | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=35 en:congenital uremia --- r_associated #0: 35 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital uremia | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=35 en:congenital von willebrand's disease --- r_associated #0: 35 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital von willebrand's disease | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=35 en:obstructed interchordal space of tricuspid chordae tendinae --- r_associated #0: 35 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:obstructed interchordal space of tricuspid chordae tendinae | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=35 en:prader-willi syndrome --- r_associated #0: 35 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:prader-willi syndrome | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=35 en:rudimentary left ventricle --- r_associated #0: 35 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:rudimentary left ventricle | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=35 en:tricuspid valve primary chords absent --- r_associated #0: 35 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:tricuspid valve primary chords absent | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=35 en:urachal cyst --- r_associated #0: 35 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:urachal cyst | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=35 Maladie congénitale --- r_associated #0: 34 --> en:adrenocortical hypofunction, chronic primary congenital n1=Maladie congénitale | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=34 en:basal ganglia disease, biotin-responsive --- r_associated #0: 34 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:basal ganglia disease, biotin-responsive | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=34 en:congenital complete atrioventricular block --- r_associated #0: 34 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital complete atrioventricular block | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=34 en:congenital factor ix deficiency variant --- r_associated #0: 34 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital factor ix deficiency variant | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=34 en:congenital fibrinogen abnormality --- r_associated #0: 34 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital fibrinogen abnormality | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=34 en:congenital hearing disorder --- r_associated #0: 34 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital hearing disorder | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=34 en:congenital hydrosalpinx --- r_associated #0: 34 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital hydrosalpinx | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=34 en:congenital immunodeficiency disease --- r_associated #0: 34 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital immunodeficiency disease | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=34 en:congenital neutrophil actin dysfunction --- r_associated #0: 34 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital neutrophil actin dysfunction | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=34 en:congenital occlusion of anus --- r_associated #0: 34 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital occlusion of anus | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=34 en:congenital quadriplegia --- r_associated #0: 34 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital quadriplegia | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=34 en:congenital skeletal disorder --- r_associated #0: 34 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital skeletal disorder | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=34 en:congenital velopharyngeal dysfunction --- r_associated #0: 34 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital velopharyngeal dysfunction | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=34 en:double orifice of right atrioventricular valve in double inlet ventricle --- r_associated #0: 34 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:double orifice of right atrioventricular valve in double inlet ventricle | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=34 en:glucocorticoid deficiency --- r_associated #0: 34 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:glucocorticoid deficiency | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=34 en:myostatin-related muscle hypertrophy --- r_associated #0: 34 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:myostatin-related muscle hypertrophy | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=34 en:regional congenital anomaly --- r_associated #0: 34 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:regional congenital anomaly | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=34 en:erythropoietic porphyria --- r_associated #0: 33 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:erythropoietic porphyria | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=33 en:congenital blocked tear duct --- r_associated #0: 32 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital blocked tear duct | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=32 en:congenital brain damage --- r_associated #0: 32 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital brain damage | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=32 en:congenital constriction of pylorus --- r_associated #0: 32 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital constriction of pylorus | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=32 en:congenital exophthalmos --- r_associated #0: 32 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital exophthalmos | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=32 en:congenital factor ix deficiency without inhibitor --- r_associated #0: 32 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital factor ix deficiency without inhibitor | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=32 en:congenital pancreatic trypsin deficiency --- r_associated #0: 32 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital pancreatic trypsin deficiency | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=32 en:congenital pseudobulbar palsy --- r_associated #0: 32 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital pseudobulbar palsy | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=32 en:congenital thrombocytopenic purpura --- r_associated #0: 32 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital thrombocytopenic purpura | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=32 en:drug-induced adrenocortical insufficiency --- r_associated #0: 32 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:drug-induced adrenocortical insufficiency | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=32 en:familial adrenocortical hypoplasia --- r_associated #0: 32 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:familial adrenocortical hypoplasia | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=32 en:fascial dystrophy, congenital --- r_associated #0: 32 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:fascial dystrophy, congenital | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=32 en:fenestrated interatrial communication within oval fossa --- r_associated #0: 32 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:fenestrated interatrial communication within oval fossa | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=32 en:parachute malformation of common atrioventricular valve --- r_associated #0: 32 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:parachute malformation of common atrioventricular valve | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=32 en:right atrial endocardial fibroelastosis --- r_associated #0: 32 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:right atrial endocardial fibroelastosis | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=32 en:right-sided pulmonary arterial trunk --- r_associated #0: 32 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:right-sided pulmonary arterial trunk | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=32 en:secondary megacolon - congenital --- r_associated #0: 32 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:secondary megacolon - congenital | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=32 en:true cleft of common atrioventricular valve leaflet --- r_associated #0: 32 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:true cleft of common atrioventricular valve leaflet | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=32 en:vitamin d-dependent rickets, type 1 --- r_associated #0: 32 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:vitamin d-dependent rickets, type 1 | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=32 en:adrenogenital syndrome --- r_associated #0: 31 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:adrenogenital syndrome | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=31 en:chronic diarrhea due to glucoamylase deficiency --- r_associated #0: 31 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:chronic diarrhea due to glucoamylase deficiency | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=31 en:congenital adrenal gland hypoplasia --- r_associated #0: 31 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital adrenal gland hypoplasia | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=31 en:congenital analbuminemia --- r_associated #0: 31 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital analbuminemia | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=31 en:congenital dysphasia --- r_associated #0: 31 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital dysphasia | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=31 en:congenital malignant melanoma --- r_associated #0: 31 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital malignant melanoma | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=31 en:congenital peripheral aneurysm --- r_associated #0: 31 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital peripheral aneurysm | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=31 en:congenital retinoschisis --- r_associated #0: 31 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital retinoschisis | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=31 en:congenital viral hepatitis --- r_associated #0: 31 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital viral hepatitis | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=31 en:cortisol deficiency --- r_associated #0: 31 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:cortisol deficiency | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=31 en:genetic diseases, inborn --- r_associated #0: 31 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:genetic diseases, inborn | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=31 en:lactase deficiency, congenital --- r_associated #0: 31 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:lactase deficiency, congenital | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=31 en:megophthalmos --- r_associated #0: 31 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:megophthalmos | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=31 en:obstructed pulmonary venous connection at coronary sinus orifice --- r_associated #0: 31 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:obstructed pulmonary venous connection at coronary sinus orifice | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=31 en:palmoplantar porokeratosis --- r_associated #0: 31 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:palmoplantar porokeratosis | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=31 en:precocious exfoliation of teeth related to root resorption associated with trauma --- r_associated #0: 31 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:precocious exfoliation of teeth related to root resorption associated with trauma | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=31 en:right atrial appendage - left - juxtaposition --- r_associated #0: 31 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:right atrial appendage - left - juxtaposition | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=31 en:right ventricular myocardial sinusoids --- r_associated #0: 31 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:right ventricular myocardial sinusoids | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=31 en:rotation of tooth --- r_associated #0: 31 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:rotation of tooth | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=31 en:secondary adrenal insufficiency --- r_associated #0: 31 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:secondary adrenal insufficiency | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=31 en:shortened trunk --- r_associated #0: 31 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:shortened trunk | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=31 en:stomach in right sided position --- r_associated #0: 31 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:stomach in right sided position | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=31 myofibromatose infantile --- r_associated #0: 31 --> en:adrenocortical hypofunction, chronic primary congenital n1=myofibromatose infantile | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=31 nystagmus congénital isolé --- r_associated #0: 31 --> en:adrenocortical hypofunction, chronic primary congenital n1=nystagmus congénital isolé | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=31 ARTHROGRYPOSE --- r_associated #0: 30 --> en:adrenocortical hypofunction, chronic primary congenital n1=ARTHROGRYPOSE | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=30 adrénoleucodystrophie liée à l'X --- r_associated #0: 30 --> en:adrenocortical hypofunction, chronic primary congenital n1=adrénoleucodystrophie liée à l'X | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=30 adrénoleucodystrophie néonatale récessive --- r_associated #0: 30 --> en:adrenocortical hypofunction, chronic primary congenital n1=adrénoleucodystrophie néonatale récessive | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=30 anomalie chromosomique --- r_associated #0: 30 --> en:adrenocortical hypofunction, chronic primary congenital n1=anomalie chromosomique | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=30 anomalie cytogénétique --- r_associated #0: 30 --> en:adrenocortical hypofunction, chronic primary congenital n1=anomalie cytogénétique | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=30 anormalité des chromosomes --- r_associated #0: 30 --> en:adrenocortical hypofunction, chronic primary congenital n1=anormalité des chromosomes | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=30 en:Addison disease --- r_associated #0: 30 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:Addison disease | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=30 en:adrenal insufficiency due to adrenal metastasis --- r_associated #0: 30 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:adrenal insufficiency due to adrenal metastasis | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=30 en:becker generalized myotonia --- r_associated #0: 30 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:becker generalized myotonia | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=30 en:chromosomal abnormality --- r_associated #0: 30 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:chromosomal abnormality | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=30 en:chromosome disorder --- r_associated #0: 30 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:chromosome disorder | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=30 en:congenital achalasia of esophagus --- r_associated #0: 30 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital achalasia of esophagus | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=30 en:congenital and developmental myasthenia --- r_associated #0: 30 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital and developmental myasthenia | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=30 en:congenital arcus juvenilis --- r_associated #0: 30 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital arcus juvenilis | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=30 en:congenital biliary tract disorder --- r_associated #0: 30 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital biliary tract disorder | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=30 en:congenital calcium pyrophosphate dihydrate crystal deposition disease --- r_associated #0: 30 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital calcium pyrophosphate dihydrate crystal deposition disease | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=30 en:congenital cyst of aryepiglottic fold --- r_associated #0: 30 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital cyst of aryepiglottic fold | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=30 en:congenital esotropia --- r_associated #0: 30 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital esotropia | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=30 en:congenital hepatomegaly --- r_associated #0: 30 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital hepatomegaly | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=30 en:congenital neurogenic ileus syndrome --- r_associated #0: 30 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital neurogenic ileus syndrome | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=30 en:congenital obstruction of bladder neck --- r_associated #0: 30 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital obstruction of bladder neck | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=30 en:congenital oral/facial/cranial defect --- r_associated #0: 30 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital oral/facial/cranial defect | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=30 en:congenital plasminogen activator inhibitor deficiency type 1 --- r_associated #0: 30 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital plasminogen activator inhibitor deficiency type 1 | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=30 en:congenital skin contracture --- r_associated #0: 30 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital skin contracture | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=30 en:developmental fault --- r_associated #0: 30 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:developmental fault | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=30 en:generalized intestinal dysmotility --- r_associated #0: 30 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:generalized intestinal dysmotility | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=30 en:leber congenital amaurosis --- r_associated #0: 30 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:leber congenital amaurosis | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=30 en:microvillus inclusion disease --- r_associated #0: 30 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:microvillus inclusion disease | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=30 en:mineralocorticoid deficiency --- r_associated #0: 30 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:mineralocorticoid deficiency | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=30 en:myelocele --- r_associated #0: 30 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:myelocele | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=30 en:night blindness, congenital stationary --- r_associated #0: 30 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:night blindness, congenital stationary | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=30 en:nystagmus --- r_associated #0: 30 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:nystagmus | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=30 en:posterior deviation of infundibular septum of obstructive aortic arch type --- r_associated #0: 30 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:posterior deviation of infundibular septum of obstructive aortic arch type | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=30 en:pseudomonas pyocyaneus congenital infection --- r_associated #0: 30 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:pseudomonas pyocyaneus congenital infection | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=30 en:truncal valve overriding ventricular septum --- r_associated #0: 30 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:truncal valve overriding ventricular septum | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=30 en:vocal cord dysfunction familial --- r_associated #0: 30 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:vocal cord dysfunction familial | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=30 trouble chromosomique --- r_associated #0: 30 --> en:adrenocortical hypofunction, chronic primary congenital n1=trouble chromosomique | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=30 adrénoleucodystrophie de l?enfant --- r_associated #0: 29 --> en:adrenocortical hypofunction, chronic primary congenital n1=adrénoleucodystrophie de l?enfant | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=29 contractures congénitales et arachnodactylie --- r_associated #0: 29 --> en:adrenocortical hypofunction, chronic primary congenital n1=contractures congénitales et arachnodactylie | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=29 en:adrenal insufficiency neonatal --- r_associated #0: 29 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:adrenal insufficiency neonatal | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=29 en:congenital axial myopia --- r_associated #0: 29 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital axial myopia | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=29 en:congenital blepharophimosis of lower eyelid --- r_associated #0: 29 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital blepharophimosis of lower eyelid | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=29 en:congenital cardiovascular disorder --- r_associated #0: 29 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital cardiovascular disorder | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=29 en:congenital cardiovascular disorders during pregnancy, childbirth and the puerperium --- r_associated #0: 29 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital cardiovascular disorders during pregnancy, childbirth and the puerperium | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=29 en:congenital color blindness --- r_associated #0: 29 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital color blindness | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=29 en:congenital digestive system disorder --- r_associated #0: 29 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital digestive system disorder | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=29 en:congenital disorder of facial nerve --- r_associated #0: 29 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital disorder of facial nerve | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=29 en:congenital disorder of gallbladder and biliary tract --- r_associated #0: 29 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital disorder of gallbladder and biliary tract | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=29 en:congenital factor ix deficiency with inhibitor --- r_associated #0: 29 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital factor ix deficiency with inhibitor | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=29 en:congenital functional disorders of the colon --- r_associated #0: 29 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital functional disorders of the colon | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=29 en:congenital leptomeningeal angiomatosis --- r_associated #0: 29 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital leptomeningeal angiomatosis | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=29 en:congenital melanocytic nevus of trunk --- r_associated #0: 29 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital melanocytic nevus of trunk | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=29 en:congenital metabolic disorder --- r_associated #0: 29 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital metabolic disorder | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=29 en:congenital monosaccharide malabsorption --- r_associated #0: 29 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital monosaccharide malabsorption | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=29 en:congenital nasolacrimal duct obstruction --- r_associated #0: 29 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital nasolacrimal duct obstruction | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=29 en:congenital nervous system disorder --- r_associated #0: 29 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital nervous system disorder | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=29 en:congenital obstruction of small intestine --- r_associated #0: 29 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital obstruction of small intestine | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=29 en:congenital spastic foot --- r_associated #0: 29 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital spastic foot | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=29 en:congenital vocal cord palsy --- r_associated #0: 29 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital vocal cord palsy | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=29 en:fetal congenital tumor causing disproportion --- r_associated #0: 29 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:fetal congenital tumor causing disproportion | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=29 en:fetal disorder --- r_associated #0: 29 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:fetal disorder | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=29 en:fordyce's disease --- r_associated #0: 29 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:fordyce's disease | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=29 en:hutch diverticulum --- r_associated #0: 29 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:hutch diverticulum | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=29 en:iatrogenic adrenal insufficiency --- r_associated #0: 29 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:iatrogenic adrenal insufficiency | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=29 en:longitudinal deficiency of limb --- r_associated #0: 29 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:longitudinal deficiency of limb | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=29 en:nonfenestrated interatrial communication within oval fossa --- r_associated #0: 29 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:nonfenestrated interatrial communication within oval fossa | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=29 en:post-adrenalectomy adrenal insufficiency --- r_associated #0: 29 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:post-adrenalectomy adrenal insufficiency | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=29 en:primary left ventricular endocardial fibroelastosis --- r_associated #0: 29 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:primary left ventricular endocardial fibroelastosis | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=29 en:pulmonary valve overriding ventricular septum --- r_associated #0: 29 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:pulmonary valve overriding ventricular septum | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=29 en:redundant prepuce --- r_associated #0: 29 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:redundant prepuce | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=29 en:systemic venovenous collateral vein --- r_associated #0: 29 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:systemic venovenous collateral vein | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=29 en:upper esophageal web --- r_associated #0: 29 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:upper esophageal web | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=29 en:vitamin d-dependent rickets, type 2 --- r_associated #0: 29 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:vitamin d-dependent rickets, type 2 | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=29 en:adrenal androgen deficiency --- r_associated #0: 28 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:adrenal androgen deficiency | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=28 en:amyoplasia congenita --- r_associated #0: 28 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:amyoplasia congenita | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=28 en:benign congenital myopathy --- r_associated #0: 28 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:benign congenital myopathy | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=28 en:congenital accessory skin tag --- r_associated #0: 28 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital accessory skin tag | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=28 en:congenital blepharophimosis of upper eyelid --- r_associated #0: 28 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital blepharophimosis of upper eyelid | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=28 en:congenital cerebellar cortical atrophy --- r_associated #0: 28 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital cerebellar cortical atrophy | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=28 en:congenital fecaliths --- r_associated #0: 28 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital fecaliths | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=28 en:congenital myasthenic syndrome --- r_associated #0: 28 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital myasthenic syndrome | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=28 en:congenital obstruction of aqueduct of sylvius --- r_associated #0: 28 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital obstruction of aqueduct of sylvius | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=28 en:congenital onychatrophy --- r_associated #0: 28 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital onychatrophy | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=28 en:congenital pain insensitivity --- r_associated #0: 28 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital pain insensitivity | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=28 en:congenital palato-esophageal incoordination --- r_associated #0: 28 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital palato-esophageal incoordination | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=28 en:dental arch length loss secondary to congenitally missing teeth --- r_associated #0: 28 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:dental arch length loss secondary to congenitally missing teeth | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=28 en:digeorge syndrome --- r_associated #0: 28 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:digeorge syndrome | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=28 en:parachute malformation of left atrioventricular valve --- r_associated #0: 28 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:parachute malformation of left atrioventricular valve | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=28 en:precocious exfoliation of teeth related to idiopathic root resorption --- r_associated #0: 28 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:precocious exfoliation of teeth related to idiopathic root resorption | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=28 en:right atrial appendage absent --- r_associated #0: 28 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:right atrial appendage absent | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=28 en:trifoliate left atrioventricular valve --- r_associated #0: 28 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:trifoliate left atrioventricular valve | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=28 hypofonctionnement corticosurrénalien primaire congénital --- r_associated #0: 28 --> en:adrenocortical hypofunction, chronic primary congenital n1=hypofonctionnement corticosurrénalien primaire congénital | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=28 en:Günther's disease --- r_associated #0: 27 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:Günther's disease | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=27 en:adrenal crisis --- r_associated #0: 27 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:adrenal crisis | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=27 en:congenital amegakaryocytic thrombocytopenia --- r_associated #0: 27 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital amegakaryocytic thrombocytopenia | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=27 en:congenital bundle of his tachycardia --- r_associated #0: 27 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital bundle of his tachycardia | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=27 en:congenital cardiac failure --- r_associated #0: 27 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital cardiac failure | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=27 en:congenital choroidal fold --- r_associated #0: 27 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital choroidal fold | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=27 en:congenital chylothorax --- r_associated #0: 27 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital chylothorax | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=27 en:congenital facial asymmetry --- r_associated #0: 27 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital facial asymmetry | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=27 en:congenital hypertonia --- r_associated #0: 27 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital hypertonia | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=27 en:congenital nephrotic syndrome --- r_associated #0: 27 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital nephrotic syndrome | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=27 en:congenital pancreatic cyst --- r_associated #0: 27 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital pancreatic cyst | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=27 en:congenital secretory diarrhea --- r_associated #0: 27 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital secretory diarrhea | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=27 en:ectopic bone tissue congenital --- r_associated #0: 27 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:ectopic bone tissue congenital | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=27 en:hereditary adrenal unresponsiveness to corticotropin --- r_associated #0: 27 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:hereditary adrenal unresponsiveness to corticotropin | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=27 en:infantile myofibromatosis --- r_associated #0: 27 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:infantile myofibromatosis | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=27 en:intestinal epithelial dysplasia --- r_associated #0: 27 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:intestinal epithelial dysplasia | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=27 en:longitudinal deficiency of part of limb --- r_associated #0: 27 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:longitudinal deficiency of part of limb | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=27 en:parachute malformation of right atrioventricular valve --- r_associated #0: 27 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:parachute malformation of right atrioventricular valve | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=27 en:tooth malformation --- r_associated #0: 27 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:tooth malformation | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=27 une anomalie congénitale --- r_associated #0: 27 --> en:adrenocortical hypofunction, chronic primary congenital n1=une anomalie congénitale | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=27 en:adrenal atrophy --- r_associated #0: 26 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:adrenal atrophy | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=26 en:allgrove syndrome --- r_associated #0: 26 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:allgrove syndrome | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=26 en:combined pituitary hormone deficiency genetic form --- r_associated #0: 26 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:combined pituitary hormone deficiency genetic form | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=26 en:congenital disease of brain --- r_associated #0: 26 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital disease of brain | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=26 en:congenital elephantiasis --- r_associated #0: 26 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital elephantiasis | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=26 en:congenital flat foot --- r_associated #0: 26 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital flat foot | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=26 en:congenital hydrocele --- r_associated #0: 26 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital hydrocele | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=26 en:congenital laryngeal cyst --- r_associated #0: 26 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital laryngeal cyst | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=26 en:congenital long qt syndrome --- r_associated #0: 26 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital long qt syndrome | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=26 en:congenital megaprepuce --- r_associated #0: 26 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital megaprepuce | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=26 en:congenital obstruction of bile duct --- r_associated #0: 26 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital obstruction of bile duct | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=26 en:congenital paraplegia --- r_associated #0: 26 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital paraplegia | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=26 en:congenital pericardial effusion --- r_associated #0: 26 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital pericardial effusion | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=26 en:congenital posterior subcapsular polar cataract --- r_associated #0: 26 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital posterior subcapsular polar cataract | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=26 en:congenital pseudoporencephaly --- r_associated #0: 26 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital pseudoporencephaly | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=26 en:congenital scoliosis due to bony malformation --- r_associated #0: 26 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital scoliosis due to bony malformation | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=26 en:congenital sequelae of disorders --- r_associated #0: 26 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital sequelae of disorders | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=26 en:cushing syndrome --- r_associated #0: 26 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:cushing syndrome | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=26 en:dental midlines coincident and incorrect --- r_associated #0: 26 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:dental midlines coincident and incorrect | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=26 en:extensive congenital erosions, vesicles and reticulate scarring --- r_associated #0: 26 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:extensive congenital erosions, vesicles and reticulate scarring | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=26 en:infant metachromatic leukodystrophies --- r_associated #0: 26 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:infant metachromatic leukodystrophies | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=26 en:keratitis, hereditary --- r_associated #0: 26 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:keratitis, hereditary | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=26 en:left atrioventricular valve bifoliate with fused left sided superior and inferior bridging leaflet --- r_associated #0: 26 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:left atrioventricular valve bifoliate with fused left sided superior and inferior bridging leaflet | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=26 en:pseudohypoaldosteronism type 1 --- r_associated #0: 26 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:pseudohypoaldosteronism type 1 | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=26 en:right inferior caval vein connecting to left atrium and right atrium --- r_associated #0: 26 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:right inferior caval vein connecting to left atrium and right atrium | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=26 en:testicular hypofunction due to defect in adrenocortical hormone synthesis --- r_associated #0: 26 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:testicular hypofunction due to defect in adrenocortical hormone synthesis | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=26 insuffisance surrénale --- r_associated #0: 26 --> en:adrenocortical hypofunction, chronic primary congenital n1=insuffisance surrénale | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=26 en:buphthalmia --- r_associated #0: 25 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:buphthalmia | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=25 en:chromosomal aberration --- r_associated #0: 25 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:chromosomal aberration | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=25 en:congenital blood disorder --- r_associated #0: 25 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital blood disorder | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=25 en:congenital cyst of vulva --- r_associated #0: 25 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital cyst of vulva | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=25 en:congenital hepatic fibrosis --- r_associated #0: 25 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital hepatic fibrosis | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=25 en:congenital muscle disorder --- r_associated #0: 25 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital muscle disorder | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=25 en:congenital nystagmus --- r_associated #0: 25 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital nystagmus | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=25 en:congenital pseudostrabismus --- r_associated #0: 25 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital pseudostrabismus | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=25 en:congenital sixth nerve palsy --- r_associated #0: 25 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital sixth nerve palsy | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=25 en:congenital volvulus of stomach --- r_associated #0: 25 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital volvulus of stomach | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=25 en:multiple supernumerary teeth unrelated to systemic condition --- r_associated #0: 25 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:multiple supernumerary teeth unrelated to systemic condition | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=25 en:tripartite right ventricle --- r_associated #0: 25 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:tripartite right ventricle | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=25 hypogonadisme avec anosmie --- r_associated #0: 25 --> en:adrenocortical hypofunction, chronic primary congenital n1=hypogonadisme avec anosmie | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=25 en:adrenocortical insufficiency neonatal --- r_associated #0: 24 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:adrenocortical insufficiency neonatal | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=24 en:alpha-fetoprotein deficiency --- r_associated #0: 24 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:alpha-fetoprotein deficiency | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=24 en:congenital alpha-2-antiplasmin deficiency --- r_associated #0: 24 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital alpha-2-antiplasmin deficiency | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=24 en:congenital hernia of bladder --- r_associated #0: 24 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital hernia of bladder | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=24 en:congenital malalignment of the toenails --- r_associated #0: 24 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital malalignment of the toenails | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=24 en:congenital mass of mitral leaflet --- r_associated #0: 24 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital mass of mitral leaflet | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=24 en:congenital myotonic dystrophy --- r_associated #0: 24 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital myotonic dystrophy | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=24 en:congenital pneumonia --- r_associated #0: 24 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital pneumonia | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=24 en:congenital porphyria --- r_associated #0: 24 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital porphyria | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=24 en:congenital single renal cyst --- r_associated #0: 24 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital single renal cyst | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=24 en:congenital skin disorder --- r_associated #0: 24 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital skin disorder | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=24 en:congenital vascular disorder --- r_associated #0: 24 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital vascular disorder | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=24 en:developmental anomaly --- r_associated #0: 24 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:developmental anomaly | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=24 en:ear dimple --- r_associated #0: 24 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:ear dimple | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=24 en:generalized myotonia of thomsen --- r_associated #0: 24 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:generalized myotonia of thomsen | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=24 en:smith-lemli-opitz syndrome --- r_associated #0: 24 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:smith-lemli-opitz syndrome | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=24 en:steroid withdrawal syndrome --- r_associated #0: 24 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:steroid withdrawal syndrome | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=24 adrénoleucodystrophie liée à l?X --- r_associated #0: 23 --> en:adrenocortical hypofunction, chronic primary congenital n1=adrénoleucodystrophie liée à l?X | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=23 en:congenital anemia --- r_associated #0: 23 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital anemia | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=23 en:congenital cutaneous angiomatosis --- r_associated #0: 23 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital cutaneous angiomatosis | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=23 en:congenital fissure of tongue --- r_associated #0: 23 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital fissure of tongue | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=23 en:congenital infectious disease --- r_associated #0: 23 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital infectious disease | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=23 en:congenital laryngeal adductor palsy --- r_associated #0: 23 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital laryngeal adductor palsy | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=23 en:erythropoietic uroporphyria --- r_associated #0: 23 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:erythropoietic uroporphyria | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=23 en:mydriasis, congenital --- r_associated #0: 23 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:mydriasis, congenital | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=23 en:prominent valve of inferior vena cava --- r_associated #0: 23 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:prominent valve of inferior vena cava | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=23 syndrome de Williams --- r_associated #0: 23 --> en:adrenocortical hypofunction, chronic primary congenital n1=syndrome de Williams | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=23 déficit congénital en mégacaryocytes --- r_associated #0: 22 --> en:adrenocortical hypofunction, chronic primary congenital n1=déficit congénital en mégacaryocytes | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=22 en:abnormal root proximity between adjacent teeth --- r_associated #0: 22 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:abnormal root proximity between adjacent teeth | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=22 en:congenital inguinal hernia --- r_associated #0: 22 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital inguinal hernia | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=22 en:congenital kidney disorder --- r_associated #0: 22 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital kidney disorder | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=22 en:congenital rectal fissure --- r_associated #0: 22 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital rectal fissure | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=22 en:congenital respiratory disorder --- r_associated #0: 22 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital respiratory disorder | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=22 en:foxg1 syndrome --- r_associated #0: 22 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:foxg1 syndrome | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=22 en:impervious urethra --- r_associated #0: 22 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:impervious urethra | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=22 buphtalmie --- r_associated #0: 21 --> en:adrenocortical hypofunction, chronic primary congenital n1=buphtalmie | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=21 en:Fordyce's disease --- r_associated #0: 21 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:Fordyce's disease | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=21 en:adrenocortical (adrenal) insufficiency --- r_associated #0: 21 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:adrenocortical (adrenal) insufficiency | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=21 en:congenital contracture of gastrocnemius muscle --- r_associated #0: 21 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital contracture of gastrocnemius muscle | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=21 en:congenital occlusion of ureter --- r_associated #0: 21 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital occlusion of ureter | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=21 en:congenital renal atrophy --- r_associated #0: 21 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:congenital renal atrophy | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=21 en:gelatinous atrioventricular valve leaflet in atrioventricular septal defect --- r_associated #0: 21 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:gelatinous atrioventricular valve leaflet in atrioventricular septal defect | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=21 en:pericellular fibrosis of congenital syphilis --- r_associated #0: 21 --> 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:stomach in central position --- r_associated #0: 21 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:stomach in central position | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=21 malformation --- r_associated #0: 21 --> en:adrenocortical hypofunction, chronic primary congenital n1=malformation | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=21 méthémoglobinémie héréditaire --- r_associated #0: 21 --> en:adrenocortical hypofunction, chronic primary congenital n1=méthémoglobinémie héréditaire | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=21 syndrome de Prader-Willi --- r_associated #0: 21 --> en:adrenocortical hypofunction, chronic primary congenital n1=syndrome de Prader-Willi | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=21 Malformation congénitale --- r_associated #0: 20 --> en:adrenocortical hypofunction, chronic primary congenital n1=Malformation congénitale | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=20 dysplasie olfactogénitale de De Morsier --- r_associated #0: 20 --> en:adrenocortical hypofunction, chronic primary congenital n1=dysplasie olfactogénitale de De Morsier | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=20 Arthrogrypose --- r_associated #0: 15 --> en:adrenocortical hypofunction, chronic primary congenital n1=Arthrogrypose | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=15 BNV --- r_associated #0: 15 --> en:adrenocortical hypofunction, chronic primary congenital n1=BNV | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=15 Goerttler (théorie de) --- r_associated #0: 15 --> en:adrenocortical hypofunction, chronic primary congenital n1=Goerttler (théorie de) | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=15 Insuffisance surrénale --- r_associated #0: 15 --> en:adrenocortical hypofunction, chronic primary congenital n1=Insuffisance surrénale | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=15 Kallman --- r_associated #0: 15 --> en:adrenocortical hypofunction, chronic primary congenital n1=Kallman | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=15 crétinisme --- r_associated #0: 15 --> en:adrenocortical hypofunction, chronic primary congenital n1=crétinisme | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=15 hypothyroïdie (manifestations neuromusculaires dans l') --- r_associated #0: 15 --> en:adrenocortical hypofunction, chronic primary congenital n1=hypothyroïdie (manifestations neuromusculaires dans l') | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=15 malentendant (enfant) --- r_associated #0: 15 --> en:adrenocortical hypofunction, chronic primary congenital n1=malentendant (enfant) | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=15 syndrome de Kallman-de Morsier --- r_associated #0: 15 --> en:adrenocortical hypofunction, chronic primary congenital n1=syndrome de Kallman-de Morsier | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=15 syndrome de de Morsier-Kallmann --- r_associated #0: 15 --> en:adrenocortical hypofunction, chronic primary congenital n1=syndrome de de Morsier-Kallmann | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=15 blépharophimosis congénital --- r_associated #0: 11 --> en:adrenocortical hypofunction, chronic primary congenital n1=blépharophimosis congénital | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=11 hypothyroïdie néonatale --- r_associated #0: 11 --> en:adrenocortical hypofunction, chronic primary congenital n1=hypothyroïdie néonatale | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=11 Amn --- r_associated #0: 10 --> en:adrenocortical hypofunction, chronic primary congenital n1=Amn | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=10 Anomalie chromosomique --- r_associated #0: 10 --> en:adrenocortical hypofunction, chronic primary congenital n1=Anomalie chromosomique | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=10 CONGENITAL --- r_associated #0: 10 --> en:adrenocortical hypofunction, chronic primary congenital n1=CONGENITAL | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=10 CONGÉNITALE --- r_associated #0: 10 --> en:adrenocortical hypofunction, chronic primary congenital n1=CONGÉNITALE | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=10 Malformation --- r_associated #0: 10 --> en:adrenocortical hypofunction, chronic primary congenital n1=Malformation | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=10 Syndrome de Prader-Willi --- r_associated #0: 10 --> en:adrenocortical hypofunction, chronic primary congenital n1=Syndrome de Prader-Willi | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=10 aberration chromosomique --- r_associated #0: 10 --> en:adrenocortical hypofunction, chronic primary congenital n1=aberration chromosomique | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=10 adrénoleucodystrophie de l'enfant --- r_associated #0: 10 --> en:adrenocortical hypofunction, chronic primary congenital n1=adrénoleucodystrophie de l'enfant | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=10 en:Goerttler's theory --- r_associated #0: 10 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:Goerttler's theory | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=10 en:PWS --- r_associated #0: 10 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:PWS | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=10 en:WBS --- r_associated #0: 10 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:WBS | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=10 en:Williams' syndrome --- r_associated #0: 10 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:Williams' syndrome | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=10 en:Williams-Beuren syndrome --- r_associated #0: 10 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:Williams-Beuren syndrome | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=10 en:buphtalmia --- r_associated #0: 10 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:buphtalmia | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=10 en:buphthalmos --- r_associated #0: 10 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:buphthalmos | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=10 en:buphthalmus --- r_associated #0: 10 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:buphthalmus | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=10 en:cacomorphosis --- r_associated #0: 10 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:cacomorphosis | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=10 en:chromosomal disorder --- r_associated #0: 10 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:chromosomal disorder | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=10 en:contractural arachnodactyly --- r_associated #0: 10 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:contractural arachnodactyly | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=10 en:hypoacousic child --- r_associated #0: 10 --> en:adrenocortical hypofunction, chronic primary congenital n1=en:hypoacousic child | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=10 insuffisance surrénalienne --- r_associated #0: 10 --> en:adrenocortical hypofunction, chronic primary congenital n1=insuffisance surrénalienne | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=10 myélocèle --- r_associated #0: 10 --> en:adrenocortical hypofunction, chronic primary congenital n1=myélocèle | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=10 nystagmus --- r_associated #0: 10 --> en:adrenocortical hypofunction, chronic primary congenital n1=nystagmus | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=10 nystagmus héréditaire vertical --- r_associated #0: 10 --> en:adrenocortical hypofunction, chronic primary congenital n1=nystagmus héréditaire vertical | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=10 nystagmus lié au sexe --- r_associated #0: 10 --> en:adrenocortical hypofunction, chronic primary congenital n1=nystagmus lié au sexe | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=10 nystagmus myoclonies --- r_associated #0: 10 --> en:adrenocortical hypofunction, chronic primary congenital n1=nystagmus myoclonies | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=10 porphyrie (anesthésie chez un patient atteint de) --- r_associated #0: 10 --> en:adrenocortical hypofunction, chronic primary congenital n1=porphyrie (anesthésie chez un patient atteint de) | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=10 rétinite pigmentaire liée à la périphérine (pro219leu) --- r_associated #0: 10 --> en:adrenocortical hypofunction, chronic primary congenital n1=rétinite pigmentaire liée à la périphérine (pro219leu) | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=10 syndrome de de Morsier --- r_associated #0: 10 --> en:adrenocortical hypofunction, chronic primary congenital n1=syndrome de de Morsier | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=10 Addison (maladie d') --- r_associated #0: 5 --> en:adrenocortical hypofunction, chronic primary congenital n1=Addison (maladie d') | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=5 Maladie d'Addison --- r_associated #0: 5 --> en:adrenocortical hypofunction, chronic primary congenital n1=Maladie d'Addison | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=5 Williams (syndrome de) --- r_associated #0: 5 --> en:adrenocortical hypofunction, chronic primary congenital n1=Williams (syndrome de) | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=5 forme génétique de déficience combinée en hormones hypophysaires --- r_associated #0: 5 --> en:adrenocortical hypofunction, chronic primary congenital n1=forme génétique de déficience combinée en hormones hypophysaires | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=5 hypotonie plasmatique --- r_associated #0: 5 --> en:adrenocortical hypofunction, chronic primary congenital n1=hypotonie plasmatique | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=5 hypotonie sphinctérienne anale --- r_associated #0: 5 --> en:adrenocortical hypofunction, chronic primary congenital n1=hypotonie sphinctérienne anale | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=5 hypotonie sphinctérienne uréthrale --- r_associated #0: 5 --> en:adrenocortical hypofunction, chronic primary congenital n1=hypotonie sphinctérienne uréthrale | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=5 hypotonie utérine --- r_associated #0: 5 --> en:adrenocortical hypofunction, chronic primary congenital n1=hypotonie utérine | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=5 hypotonie vésicale --- r_associated #0: 5 --> en:adrenocortical hypofunction, chronic primary congenital n1=hypotonie vésicale | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=5 hypotonie, obésité et incisives proéminentes --- r_associated #0: 5 --> en:adrenocortical hypofunction, chronic primary congenital n1=hypotonie, obésité et incisives proéminentes | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=5 hypotonique --- r_associated #0: 5 --> en:adrenocortical hypofunction, chronic primary congenital n1=hypotonique | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=5 hypotrichose --- r_associated #0: 5 --> en:adrenocortical hypofunction, chronic primary congenital n1=hypotrichose | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=5 hypotrichose avec anodontie et anhidrose de Touraine --- r_associated #0: 5 --> en:adrenocortical hypofunction, chronic primary congenital n1=hypotrichose avec anodontie et anhidrose de Touraine | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=5 hypotrichose congénitale des cils --- r_associated #0: 5 --> en:adrenocortical hypofunction, chronic primary congenital n1=hypotrichose congénitale des cils | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=5 hypotrichose congénitale simple --- r_associated #0: 5 --> en:adrenocortical hypofunction, chronic primary congenital n1=hypotrichose congénitale simple | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=5 hypotrichose héréditaire de Marie Unna --- r_associated #0: 5 --> en:adrenocortical hypofunction, chronic primary congenital n1=hypotrichose héréditaire de Marie Unna | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=5 hypotrichose, atrophodermie folliculaire et épithéliomatose --- r_associated #0: 5 --> en:adrenocortical hypofunction, chronic primary congenital n1=hypotrichose, atrophodermie folliculaire et épithéliomatose | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=5 malf ormation dysraphique --- r_associated #0: 5 --> en:adrenocortical hypofunction, chronic primary congenital n1=malf ormation dysraphique | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=5 malformation kystique adénomatoïde du poumon --- r_associated #0: 5 --> en:adrenocortical hypofunction, chronic primary congenital n1=malformation kystique adénomatoïde du poumon | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=5 malformation luxante de la hanche --- r_associated #0: 5 --> en:adrenocortical hypofunction, chronic primary congenital n1=malformation luxante de la hanche | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=5 malformation mamelonnaire --- r_associated #0: 5 --> en:adrenocortical hypofunction, chronic primary congenital n1=malformation mamelonnaire | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=5 malformation mammaire --- r_associated #0: 5 --> en:adrenocortical hypofunction, chronic primary congenital n1=malformation mammaire | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=5 malformation ombilicale --- r_associated #0: 5 --> en:adrenocortical hypofunction, chronic primary congenital n1=malformation ombilicale | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=5 malformation utérine --- r_associated #0: 5 --> en:adrenocortical hypofunction, chronic primary congenital n1=malformation utérine | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=5 malformation vaginale --- r_associated #0: 5 --> en:adrenocortical hypofunction, chronic primary congenital n1=malformation vaginale | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=5 malformation vasculaire cérébrale du nourrisson --- r_associated #0: 5 --> en:adrenocortical hypofunction, chronic primary congenital n1=malformation vasculaire cérébrale du nourrisson | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=5 malformations de la charnière occipitocervicale --- r_associated #0: 5 --> en:adrenocortical hypofunction, chronic primary congenital n1=malformations de la charnière occipitocervicale | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=5 nystagmus (zone de moindre) --- r_associated #0: 5 --> en:adrenocortical hypofunction, chronic primary congenital n1=nystagmus (zone de moindre) | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=5 syndrome olfacto-génital --- r_associated #0: 5 --> en:adrenocortical hypofunction, chronic primary congenital n1=syndrome olfacto-génital | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=5