'en:pigmented paravenous chorioretinal atrophy'
(id=8725897 ; fe=en:pigmented paravenous chorioretinal atrophy ; type=1 ; niveau=200 ; luminosité=25 ; somme entrante=11968 creation date=2017-08-20 touchdate=2025-12-24 01:14:30.000)

≈ 557 relations sortantes en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 50 / 1 -> en:congenital hydrocele n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital hydrocele | rel=r_associated | relid=0 | w=50 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 50 / 1 -> en:retinal degeneration n1=en:pigmented paravenous chorioretinal atrophy | n2=en:retinal degeneration | rel=r_associated | relid=0 | w=50 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 49 / 0.98 -> en:behr syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:behr syndrome | rel=r_associated | relid=0 | w=49 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 49 / 0.98 -> en:congenital contracture of gastrocnemius muscle n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital contracture of gastrocnemius muscle | rel=r_associated | relid=0 | w=49 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 48 / 0.96 -> en:congenital anomaly of mother complicating pregnancy n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital anomaly of mother complicating pregnancy | rel=r_associated | relid=0 | w=48 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 47 / 0.94 -> en:pfeiffer mayer syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:pfeiffer mayer syndrome | rel=r_associated | relid=0 | w=47 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 46 / 0.92 -> en:colobomatous microphthalmia, rhizomelic dysplasia syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:colobomatous microphthalmia, rhizomelic dysplasia syndrome | rel=r_associated | relid=0 | w=46 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 46 / 0.92 -> en:congenital dacryocele n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital dacryocele | rel=r_associated | relid=0 | w=46 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 46 / 0.92 -> en:congenital obstruction of bile duct n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital obstruction of bile duct | rel=r_associated | relid=0 | w=46 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 46 / 0.92 -> en:congenital palato-esophageal incoordination n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital palato-esophageal incoordination | rel=r_associated | relid=0 | w=46 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 46 / 0.92 -> en:congenital rearfoot varus n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital rearfoot varus | rel=r_associated | relid=0 | w=46 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 46 / 0.92 -> en:deafness, encephaloneuropathy, obesity, valvulopathy syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:deafness, encephaloneuropathy, obesity, valvulopathy syndrome | rel=r_associated | relid=0 | w=46 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 46 / 0.92 -> en:duane anomaly, myopathy, scoliosis syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:duane anomaly, myopathy, scoliosis syndrome | rel=r_associated | relid=0 | w=46 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 46 / 0.92 -> en:encephalopathy, intracerebral calcification, retinal degeneration syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:encephalopathy, intracerebral calcification, retinal degeneration syndrome | rel=r_associated | relid=0 | w=46 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 46 / 0.92 -> en:epidermoid cyst of spleen n1=en:pigmented paravenous chorioretinal atrophy | n2=en:epidermoid cyst of spleen | rel=r_associated | relid=0 | w=46 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 45 / 0.9 -> en:alpha-fetoprotein deficiency n1=en:pigmented paravenous chorioretinal atrophy | n2=en:alpha-fetoprotein deficiency | rel=r_associated | relid=0 | w=45 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 45 / 0.9 -> en:angioid streaks n1=en:pigmented paravenous chorioretinal atrophy | n2=en:angioid streaks | rel=r_associated | relid=0 | w=45 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 45 / 0.9 -> en:congenital celiac disease n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital celiac disease | rel=r_associated | relid=0 | w=45 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 45 / 0.9 -> en:congenital nephrotic syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital nephrotic syndrome | rel=r_associated | relid=0 | w=45 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 45 / 0.9 -> en:extensive congenital erosions, vesicles and reticulate scarring n1=en:pigmented paravenous chorioretinal atrophy | n2=en:extensive congenital erosions, vesicles and reticulate scarring | rel=r_associated | relid=0 | w=45 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 45 / 0.9 -> en:fetal congenital tumor causing disproportion n1=en:pigmented paravenous chorioretinal atrophy | n2=en:fetal congenital tumor causing disproportion | rel=r_associated | relid=0 | w=45 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 45 / 0.9 -> en:hereditary retinal dystrophy n1=en:pigmented paravenous chorioretinal atrophy | n2=en:hereditary retinal dystrophy | rel=r_associated | relid=0 | w=45 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 45 / 0.9 -> en:myotonia congenita n1=en:pigmented paravenous chorioretinal atrophy | n2=en:myotonia congenita | rel=r_associated | relid=0 | w=45 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 45 / 0.9 -> en:right atrial appendage absent n1=en:pigmented paravenous chorioretinal atrophy | n2=en:right atrial appendage absent | rel=r_associated | relid=0 | w=45 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 44 / 0.88 -> en:abruzzo erickson syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:abruzzo erickson syndrome | rel=r_associated | relid=0 | w=44 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 44 / 0.88 -> en:autosomal dominant cystoid macular edema n1=en:pigmented paravenous chorioretinal atrophy | n2=en:autosomal dominant cystoid macular edema | rel=r_associated | relid=0 | w=44 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 44 / 0.88 -> en:congenital choroidal fold n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital choroidal fold | rel=r_associated | relid=0 | w=44 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 44 / 0.88 -> en:congenital pancreatic trypsin deficiency n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital pancreatic trypsin deficiency | rel=r_associated | relid=0 | w=44 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 44 / 0.88 -> en:congenital plasminogen activator inhibitor deficiency type 1 n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital plasminogen activator inhibitor deficiency type 1 | rel=r_associated | relid=0 | w=44 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 44 / 0.88 -> en:goniodysgenesis-mental retardation-short stature syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:goniodysgenesis-mental retardation-short stature syndrome | rel=r_associated | relid=0 | w=44 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 44 / 0.88 -> en:hemifacial hyperplasia with strabismus n1=en:pigmented paravenous chorioretinal atrophy | n2=en:hemifacial hyperplasia with strabismus | rel=r_associated | relid=0 | w=44 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 44 / 0.88 -> en:joubert syndrome with ocular defect n1=en:pigmented paravenous chorioretinal atrophy | n2=en:joubert syndrome with ocular defect | rel=r_associated | relid=0 | w=44 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 44 / 0.88 -> en:microphthalmia, syndromic 3 n1=en:pigmented paravenous chorioretinal atrophy | n2=en:microphthalmia, syndromic 3 | rel=r_associated | relid=0 | w=44 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 44 / 0.88 -> en:mydriasis, congenital n1=en:pigmented paravenous chorioretinal atrophy | n2=en:mydriasis, congenital | rel=r_associated | relid=0 | w=44 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 44 / 0.88 -> en:myostatin-related muscle hypertrophy n1=en:pigmented paravenous chorioretinal atrophy | n2=en:myostatin-related muscle hypertrophy | rel=r_associated | relid=0 | w=44 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 44 / 0.88 -> en:peripapillary chorioretinal atrophy n1=en:pigmented paravenous chorioretinal atrophy | n2=en:peripapillary chorioretinal atrophy | rel=r_associated | relid=0 | w=44 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 44 / 0.88 -> en:right inferior caval vein connecting to left atrium and right atrium n1=en:pigmented paravenous chorioretinal atrophy | n2=en:right inferior caval vein connecting to left atrium and right atrium | rel=r_associated | relid=0 | w=44 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 44 / 0.88 -> en:siegler brewer carey syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:siegler brewer carey syndrome | rel=r_associated | relid=0 | w=44 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 44 / 0.88 -> en:spinal muscular atrophy, distal, congenital nonprogressive (disorder) n1=en:pigmented paravenous chorioretinal atrophy | n2=en:spinal muscular atrophy, distal, congenital nonprogressive (disorder) | rel=r_associated | relid=0 | w=44 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 44 / 0.88 -> en:sveinsson chorioretinal atrophy n1=en:pigmented paravenous chorioretinal atrophy | n2=en:sveinsson chorioretinal atrophy | rel=r_associated | relid=0 | w=44 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 44 / 0.88 -> en:temtamy syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:temtamy syndrome | rel=r_associated | relid=0 | w=44 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 44 / 0.88 -> ERG n1=en:pigmented paravenous chorioretinal atrophy | n2=ERG | rel=r_associated | relid=0 | w=44 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 44 / 0.88 -> vision scotopique n1=en:pigmented paravenous chorioretinal atrophy | n2=vision scotopique | rel=r_associated | relid=0 | w=44 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 43 / 0.86 -> électrorétinogramme n1=en:pigmented paravenous chorioretinal atrophy | n2=électrorétinogramme | rel=r_associated | relid=0 | w=43 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 43 / 0.86 -> en:action myoclonus renal failure syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:action myoclonus renal failure syndrome | rel=r_associated | relid=0 | w=43 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 43 / 0.86 -> en:congenital dysarthria n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital dysarthria | rel=r_associated | relid=0 | w=43 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 43 / 0.86 -> en:congenital dysphasia n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital dysphasia | rel=r_associated | relid=0 | w=43 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 43 / 0.86 -> en:congenital hypogonadotropic hypogonadism n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital hypogonadotropic hypogonadism | rel=r_associated | relid=0 | w=43 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 43 / 0.86 -> en:congenital kyphosis n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital kyphosis | rel=r_associated | relid=0 | w=43 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 43 / 0.86 -> en:congenital rectal fissure n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital rectal fissure | rel=r_associated | relid=0 | w=43 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 43 / 0.86 -> en:hydrophthalmos n1=en:pigmented paravenous chorioretinal atrophy | n2=en:hydrophthalmos | rel=r_associated | relid=0 | w=43 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 43 / 0.86 -> en:kallmann syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:kallmann syndrome | rel=r_associated | relid=0 | w=43 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 43 / 0.86 -> en:ohdo syndrome, maat-kievit-brunner type n1=en:pigmented paravenous chorioretinal atrophy | n2=en:ohdo syndrome, maat-kievit-brunner type | rel=r_associated | relid=0 | w=43 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 43 / 0.86 -> en:revesz syndrome (disorder) n1=en:pigmented paravenous chorioretinal atrophy | n2=en:revesz syndrome (disorder) | rel=r_associated | relid=0 | w=43 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 43 / 0.86 -> en:spinocerebellar ataxia, autosomal recessive 1 n1=en:pigmented paravenous chorioretinal atrophy | n2=en:spinocerebellar ataxia, autosomal recessive 1 | rel=r_associated | relid=0 | w=43 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 42 / 0.84 -> en:angioid streaks of choroid n1=en:pigmented paravenous chorioretinal atrophy | n2=en:angioid streaks of choroid | rel=r_associated | relid=0 | w=42 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 42 / 0.84 -> en:cerebellar ataxia, areflexia, pes cavus, optic atrophy, sensorineural hearing loss syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:cerebellar ataxia, areflexia, pes cavus, optic atrophy, sensorineural hearing loss syndrome | rel=r_associated | relid=0 | w=42 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 42 / 0.84 -> en:chorioretinal degeneration n1=en:pigmented paravenous chorioretinal atrophy | n2=en:chorioretinal degeneration | rel=r_associated | relid=0 | w=42 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 42 / 0.84 -> en:congenital achalasia of esophagus n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital achalasia of esophagus | rel=r_associated | relid=0 | w=42 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 42 / 0.84 -> en:congenital anomaly of right sternocleidomastoid muscle n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital anomaly of right sternocleidomastoid muscle | rel=r_associated | relid=0 | w=42 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 42 / 0.84 -> en:congenital blood disorder n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital blood disorder | rel=r_associated | relid=0 | w=42 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 42 / 0.84 -> en:congenital chromosomal disease n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital chromosomal disease | rel=r_associated | relid=0 | w=42 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 42 / 0.84 -> en:congenital leptomeningeal angiomatosis n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital leptomeningeal angiomatosis | rel=r_associated | relid=0 | w=42 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 42 / 0.84 -> en:congenital pneumonia n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital pneumonia | rel=r_associated | relid=0 | w=42 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 42 / 0.84 -> en:congenital pterygium of nail n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital pterygium of nail | rel=r_associated | relid=0 | w=42 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 42 / 0.84 -> en:congenital viral hepatitis n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital viral hepatitis | rel=r_associated | relid=0 | w=42 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 42 / 0.84 -> en:digeorge syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:digeorge syndrome | rel=r_associated | relid=0 | w=42 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 42 / 0.84 -> en:glaucoma and sleep apnea syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:glaucoma and sleep apnea syndrome | rel=r_associated | relid=0 | w=42 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 42 / 0.84 -> en:growth retardation, alopecia, pseudoanodontia and optic atrophy n1=en:pigmented paravenous chorioretinal atrophy | n2=en:growth retardation, alopecia, pseudoanodontia and optic atrophy | rel=r_associated | relid=0 | w=42 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 42 / 0.84 -> en:ichthyosiform erythroderma, congenital n1=en:pigmented paravenous chorioretinal atrophy | n2=en:ichthyosiform erythroderma, congenital | rel=r_associated | relid=0 | w=42 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 42 / 0.84 -> en:inclusion body myopathy 3, autosomal dominant n1=en:pigmented paravenous chorioretinal atrophy | n2=en:inclusion body myopathy 3, autosomal dominant | rel=r_associated | relid=0 | w=42 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 42 / 0.84 -> en:isolated congenital alacrima n1=en:pigmented paravenous chorioretinal atrophy | n2=en:isolated congenital alacrima | rel=r_associated | relid=0 | w=42 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 42 / 0.84 -> en:lactase deficiency, congenital n1=en:pigmented paravenous chorioretinal atrophy | n2=en:lactase deficiency, congenital | rel=r_associated | relid=0 | w=42 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 42 / 0.84 -> en:lethal congenital erythroderma n1=en:pigmented paravenous chorioretinal atrophy | n2=en:lethal congenital erythroderma | rel=r_associated | relid=0 | w=42 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 42 / 0.84 -> en:microcornea with corectopia and macular hypoplasia syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:microcornea with corectopia and macular hypoplasia syndrome | rel=r_associated | relid=0 | w=42 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 42 / 0.84 -> en:microphthalmia, syndromic 7 n1=en:pigmented paravenous chorioretinal atrophy | n2=en:microphthalmia, syndromic 7 | rel=r_associated | relid=0 | w=42 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 42 / 0.84 -> en:neonatal intestinal perforation with in utero intraluminal obstruction n1=en:pigmented paravenous chorioretinal atrophy | n2=en:neonatal intestinal perforation with in utero intraluminal obstruction | rel=r_associated | relid=0 | w=42 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 42 / 0.84 -> en:peripapillary crescent n1=en:pigmented paravenous chorioretinal atrophy | n2=en:peripapillary crescent | rel=r_associated | relid=0 | w=42 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 42 / 0.84 -> en:peters-plus syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:peters-plus syndrome | rel=r_associated | relid=0 | w=42 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 42 / 0.84 -> en:primrose syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:primrose syndrome | rel=r_associated | relid=0 | w=42 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 42 / 0.84 -> en:ptosis, strabismus, and ectopic pupils n1=en:pigmented paravenous chorioretinal atrophy | n2=en:ptosis, strabismus, and ectopic pupils | rel=r_associated | relid=0 | w=42 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 42 / 0.84 -> en:regional congenital anomaly n1=en:pigmented paravenous chorioretinal atrophy | n2=en:regional congenital anomaly | rel=r_associated | relid=0 | w=42 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 42 / 0.84 -> en:robinow-like syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:robinow-like syndrome | rel=r_associated | relid=0 | w=42 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 42 / 0.84 -> en:rolandic epilepsy, speech dyspraxia syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:rolandic epilepsy, speech dyspraxia syndrome | rel=r_associated | relid=0 | w=42 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 42 / 0.84 -> en:spinocerebellar ataxia, autosomal recessive 5 n1=en:pigmented paravenous chorioretinal atrophy | n2=en:spinocerebellar ataxia, autosomal recessive 5 | rel=r_associated | relid=0 | w=42 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 42 / 0.84 -> en:stomach in right sided position n1=en:pigmented paravenous chorioretinal atrophy | n2=en:stomach in right sided position | rel=r_associated | relid=0 | w=42 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 42 / 0.84 -> en:visceral myopathy familial external ophthalmoplegia n1=en:pigmented paravenous chorioretinal atrophy | n2=en:visceral myopathy familial external ophthalmoplegia | rel=r_associated | relid=0 | w=42 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 42 / 0.84 -> en:wagr syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:wagr syndrome | rel=r_associated | relid=0 | w=42 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 41 / 0.82 -> en:acrootoocular syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:acrootoocular syndrome | rel=r_associated | relid=0 | w=41 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 41 / 0.82 -> en:anophthalmia plus syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:anophthalmia plus syndrome | rel=r_associated | relid=0 | w=41 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 41 / 0.82 -> en:basal ganglia disease, biotin-responsive n1=en:pigmented paravenous chorioretinal atrophy | n2=en:basal ganglia disease, biotin-responsive | rel=r_associated | relid=0 | w=41 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 41 / 0.82 -> en:blepharophimosis with ptosis, syndactyly, and short stature n1=en:pigmented paravenous chorioretinal atrophy | n2=en:blepharophimosis with ptosis, syndactyly, and short stature | rel=r_associated | relid=0 | w=41 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 41 / 0.82 -> en:cataract microcornea syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:cataract microcornea syndrome | rel=r_associated | relid=0 | w=41 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 41 / 0.82 -> en:cerebellar ataxia, intellectual disability, oculomotor apraxia, cerebellar cysts syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:cerebellar ataxia, intellectual disability, oculomotor apraxia, cerebellar cysts syndrome | rel=r_associated | relid=0 | w=41 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 41 / 0.82 -> en:charcot-marie-tooth neuropathy x type 1 n1=en:pigmented paravenous chorioretinal atrophy | n2=en:charcot-marie-tooth neuropathy x type 1 | rel=r_associated | relid=0 | w=41 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 41 / 0.82 -> en:chronic diarrhea due to glucoamylase deficiency n1=en:pigmented paravenous chorioretinal atrophy | n2=en:chronic diarrhea due to glucoamylase deficiency | rel=r_associated | relid=0 | w=41 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 41 / 0.82 -> en:congenital anomaly of vagina n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital anomaly of vagina | rel=r_associated | relid=0 | w=41 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 41 / 0.82 -> en:congenital anomaly of vulva n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital anomaly of vulva | rel=r_associated | relid=0 | w=41 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 41 / 0.82 -> en:congenital arcus juvenilis n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital arcus juvenilis | rel=r_associated | relid=0 | w=41 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 41 / 0.82 -> en:congenital atrophy of optic nerve n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital atrophy of optic nerve | rel=r_associated | relid=0 | w=41 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 41 / 0.82 -> en:congenital cataract ichthyosis syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital cataract ichthyosis syndrome | rel=r_associated | relid=0 | w=41 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 41 / 0.82 -> en:congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration | rel=r_associated | relid=0 | w=41 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 41 / 0.82 -> en:congenital ear disorder n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital ear disorder | rel=r_associated | relid=0 | w=41 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 41 / 0.82 -> en:congenital facial asymmetry n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital facial asymmetry | rel=r_associated | relid=0 | w=41 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 41 / 0.82 -> en:congenital forefoot varus n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital forefoot varus | rel=r_associated | relid=0 | w=41 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 41 / 0.82 -> en:congenital keratoderma n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital keratoderma | rel=r_associated | relid=0 | w=41 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 41 / 0.82 -> en:congenital leptin deficiency n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital leptin deficiency | rel=r_associated | relid=0 | w=41 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 41 / 0.82 -> en:congenital neurologic anomalies n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital neurologic anomalies | rel=r_associated | relid=0 | w=41 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 41 / 0.82 -> en:congenital paraplegia n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital paraplegia | rel=r_associated | relid=0 | w=41 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 41 / 0.82 -> en:congenital sequelae of disorders n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital sequelae of disorders | rel=r_associated | relid=0 | w=41 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 41 / 0.82 -> en:congenital talipes calcaneovalgus n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital talipes calcaneovalgus | rel=r_associated | relid=0 | w=41 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 41 / 0.82 -> en:congenital uremia n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital uremia | rel=r_associated | relid=0 | w=41 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 41 / 0.82 -> en:corneal dystrophy, endothelial, x-linked n1=en:pigmented paravenous chorioretinal atrophy | n2=en:corneal dystrophy, endothelial, x-linked | rel=r_associated | relid=0 | w=41 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 41 / 0.82 -> en:fleck retina of kandori n1=en:pigmented paravenous chorioretinal atrophy | n2=en:fleck retina of kandori | rel=r_associated | relid=0 | w=41 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 41 / 0.82 -> en:focal palmoplantar and gingival keratoderma n1=en:pigmented paravenous chorioretinal atrophy | n2=en:focal palmoplantar and gingival keratoderma | rel=r_associated | relid=0 | w=41 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 41 / 0.82 -> en:generalized congenital intestinal dysmotility n1=en:pigmented paravenous chorioretinal atrophy | n2=en:generalized congenital intestinal dysmotility | rel=r_associated | relid=0 | w=41 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 41 / 0.82 -> en:gnmt deficiency n1=en:pigmented paravenous chorioretinal atrophy | n2=en:gnmt deficiency | rel=r_associated | relid=0 | w=41 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 41 / 0.82 -> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=41 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 41 / 0.82 -> en:isolated congenital megalocornea n1=en:pigmented paravenous chorioretinal atrophy | n2=en:isolated congenital megalocornea | rel=r_associated | relid=0 | w=41 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 41 / 0.82 -> en:methylmalonic acidemia due to methylmalonyl-coenzyme a epimerase deficiency n1=en:pigmented paravenous chorioretinal atrophy | n2=en:methylmalonic acidemia due to methylmalonyl-coenzyme a epimerase deficiency | rel=r_associated | relid=0 | w=41 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 41 / 0.82 -> en:microphthalmia, syndromic 10 n1=en:pigmented paravenous chorioretinal atrophy | n2=en:microphthalmia, syndromic 10 | rel=r_associated | relid=0 | w=41 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 41 / 0.82 -> en:nathalie syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:nathalie syndrome | rel=r_associated | relid=0 | w=41 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 41 / 0.82 -> en:norrie disease n1=en:pigmented paravenous chorioretinal atrophy | n2=en:norrie disease | rel=r_associated | relid=0 | w=41 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 41 / 0.82 -> en:primary refluxing megaureter n1=en:pigmented paravenous chorioretinal atrophy | n2=en:primary refluxing megaureter | rel=r_associated | relid=0 | w=41 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 41 / 0.82 -> en:pure mitochondrial myopathy n1=en:pigmented paravenous chorioretinal atrophy | n2=en:pure mitochondrial myopathy | rel=r_associated | relid=0 | w=41 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 41 / 0.82 -> en:right ventricular myocardial sinusoids n1=en:pigmented paravenous chorioretinal atrophy | n2=en:right ventricular myocardial sinusoids | rel=r_associated | relid=0 | w=41 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 41 / 0.82 -> en:spondyloepiphyseal dysplasia macdermot type n1=en:pigmented paravenous chorioretinal atrophy | n2=en:spondyloepiphyseal dysplasia macdermot type | rel=r_associated | relid=0 | w=41 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 41 / 0.82 -> en:stomach in central position n1=en:pigmented paravenous chorioretinal atrophy | n2=en:stomach in central position | rel=r_associated | relid=0 | w=41 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 41 / 0.82 -> en:tooth abnormalities n1=en:pigmented paravenous chorioretinal atrophy | n2=en:tooth abnormalities | rel=r_associated | relid=0 | w=41 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 41 / 0.82 -> en:upper limb defect with eye and ear abnormalities syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:upper limb defect with eye and ear abnormalities syndrome | rel=r_associated | relid=0 | w=41 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 41 / 0.82 -> en:x-linked non progressive cerebellar ataxia n1=en:pigmented paravenous chorioretinal atrophy | n2=en:x-linked non progressive cerebellar ataxia | rel=r_associated | relid=0 | w=41 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 41 / 0.82 -> scotopique n1=en:pigmented paravenous chorioretinal atrophy | n2=scotopique | rel=r_associated | relid=0 | w=41 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> en:abnormal root proximity between adjacent teeth n1=en:pigmented paravenous chorioretinal atrophy | n2=en:abnormal root proximity between adjacent teeth | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> en:aniridia, ptosis, intellectual disability, familial obesity syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:aniridia, ptosis, intellectual disability, familial obesity syndrome | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> en:aplasia cutis congenita with epibulbar dermoids n1=en:pigmented paravenous chorioretinal atrophy | n2=en:aplasia cutis congenita with epibulbar dermoids | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> en:autosomal dominant pterygium of conjunctiva n1=en:pigmented paravenous chorioretinal atrophy | n2=en:autosomal dominant pterygium of conjunctiva | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> en:autosomal recessive cerebellar ataxia with saccadic intrusion syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:autosomal recessive cerebellar ataxia with saccadic intrusion syndrome | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> en:cahmr syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:cahmr syndrome | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> en:cataract glaucoma syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:cataract glaucoma syndrome | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> en:charcot-marie-tooth disease, dominant intermediate d n1=en:pigmented paravenous chorioretinal atrophy | n2=en:charcot-marie-tooth disease, dominant intermediate d | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> en:choriocapillaris atrophy n1=en:pigmented paravenous chorioretinal atrophy | n2=en:choriocapillaris atrophy | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> en:choroidal sclerosis n1=en:pigmented paravenous chorioretinal atrophy | n2=en:choroidal sclerosis | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> en:congenital absence of right upper limb n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital absence of right upper limb | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> en:congenital alpha-2-antiplasmin deficiency n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital alpha-2-antiplasmin deficiency | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> en:congenital and developmental myasthenia n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital and developmental myasthenia | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> en:congenital blepharophimosis of upper eyelid n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital blepharophimosis of upper eyelid | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> en:congenital blocked tear duct n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital blocked tear duct | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> en:congenital cataract with ataxia and deafness syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital cataract with ataxia and deafness syndrome | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> en:congenital chylothorax n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital chylothorax | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> en:congenital constriction of pylorus n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital constriction of pylorus | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> en:congenital cutaneous angiomatosis n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital cutaneous angiomatosis | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> en:congenital cyst of orbit n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital cyst of orbit | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> en:congenital debility of fetus n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital debility of fetus | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> en:congenital disorder of gallbladder and biliary tract n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital disorder of gallbladder and biliary tract | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> en:congenital diverticulitis of small intestine n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital diverticulitis of small intestine | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> en:congenital esotropia n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital esotropia | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> en:congenital hypothyroidism n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital hypothyroidism | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> en:congenital infectious disease n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital infectious disease | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> en:congenital inguinal hernia n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital inguinal hernia | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> en:congenital laryngeal abductor palsy n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital laryngeal abductor palsy | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> en:congenital laryngeal cyst n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital laryngeal cyst | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> en:congenital malignant melanoma n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital malignant melanoma | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> en:congenital monosaccharide malabsorption n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital monosaccharide malabsorption | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> en:congenital muscle disorder n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital muscle disorder | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> en:congenital neutrophil actin dysfunction n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital neutrophil actin dysfunction | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> en:congenital obstruction of bladder neck n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital obstruction of bladder neck | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> en:congenital pelviureteric junction obstruction n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital pelviureteric junction obstruction | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> en:congenital pseudobulbar palsy n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital pseudobulbar palsy | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> en:congenital qualifier n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital qualifier | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> en:congenital secondary hydronephrosis n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital secondary hydronephrosis | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> en:congenital skeletal disorder n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital skeletal disorder | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> en:congenital syringomyelia n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital syringomyelia | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> en:congenital velopharyngeal dysfunction n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital velopharyngeal dysfunction | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> en:corpus callosum, agenesis of, with mental retardation, ocular coloboma, and micrognathia n1=en:pigmented paravenous chorioretinal atrophy | n2=en:corpus callosum, agenesis of, with mental retardation, ocular coloboma, and micrognathia | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> en:cryptophthalmos syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:cryptophthalmos syndrome | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> en:dermoids of cornea n1=en:pigmented paravenous chorioretinal atrophy | n2=en:dermoids of cornea | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> en:ectopic bone tissue congenital n1=en:pigmented paravenous chorioretinal atrophy | n2=en:ectopic bone tissue congenital | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> en:encephalopathy due to sulfite oxidase deficiency n1=en:pigmented paravenous chorioretinal atrophy | n2=en:encephalopathy due to sulfite oxidase deficiency | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> en:epilepsy telangiectasia syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:epilepsy telangiectasia syndrome | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> en:erythema palmare hereditarium n1=en:pigmented paravenous chorioretinal atrophy | n2=en:erythema palmare hereditarium | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> en:eye diseases, hereditary n1=en:pigmented paravenous chorioretinal atrophy | n2=en:eye diseases, hereditary | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> en:familial hypophosphatemic rickets n1=en:pigmented paravenous chorioretinal atrophy | n2=en:familial hypophosphatemic rickets | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> en:fetal disorder n1=en:pigmented paravenous chorioretinal atrophy | n2=en:fetal disorder | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> en:flatfoot, rigid n1=en:pigmented paravenous chorioretinal atrophy | n2=en:flatfoot, rigid | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> en:fordyce's disease n1=en:pigmented paravenous chorioretinal atrophy | n2=en:fordyce's disease | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> en:hereditary vascular retinopathy n1=en:pigmented paravenous chorioretinal atrophy | n2=en:hereditary vascular retinopathy | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> en:hereditary x linked recessive spastic paraplegia n1=en:pigmented paravenous chorioretinal atrophy | n2=en:hereditary x linked recessive spastic paraplegia | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> en:hyperferritinemia, hereditary, with congenital cataracts n1=en:pigmented paravenous chorioretinal atrophy | n2=en:hyperferritinemia, hereditary, with congenital cataracts | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> en:hypermethioninemia encephalopathy due to deficiency of adenosine kinase n1=en:pigmented paravenous chorioretinal atrophy | n2=en:hypermethioninemia encephalopathy due to deficiency of adenosine kinase | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> en:hypoplasia and coloboma of alar cartilage with telecanthus syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:hypoplasia and coloboma of alar cartilage with telecanthus syndrome | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> en:isolated optic nerve hypoplasia n1=en:pigmented paravenous chorioretinal atrophy | n2=en:isolated optic nerve hypoplasia | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> en:leukoencephalopathy with brain stem and spinal cord involvement and high lactate syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:leukoencephalopathy with brain stem and spinal cord involvement and high lactate syndrome | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> en:leukoencephalopathy, ataxia, hypodontia, hypomyelination syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:leukoencephalopathy, ataxia, hypodontia, hypomyelination syndrome | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> en:leukoencephalopathy, thalamus and brainstem anomalies, high lactate syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:leukoencephalopathy, thalamus and brainstem anomalies, high lactate syndrome | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> en:microcornea with glaucoma and absent frontal sinus syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:microcornea with glaucoma and absent frontal sinus syndrome | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> en:microtia with nasolacrimal duct imperforation and eye coloboma n1=en:pigmented paravenous chorioretinal atrophy | n2=en:microtia with nasolacrimal duct imperforation and eye coloboma | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> en:muscle filaminopathy n1=en:pigmented paravenous chorioretinal atrophy | n2=en:muscle filaminopathy | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> en:muscular dystrophy, oculopharyngeal n1=en:pigmented paravenous chorioretinal atrophy | n2=en:muscular dystrophy, oculopharyngeal | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> en:myelocele n1=en:pigmented paravenous chorioretinal atrophy | n2=en:myelocele | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> en:myosclerosis n1=en:pigmented paravenous chorioretinal atrophy | n2=en:myosclerosis | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> en:nance-horan syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:nance-horan syndrome | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> en:nasopalpebral lipoma coloboma syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:nasopalpebral lipoma coloboma syndrome | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> en:nonfenestrated interatrial communication within oval fossa n1=en:pigmented paravenous chorioretinal atrophy | n2=en:nonfenestrated interatrial communication within oval fossa | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> en:obstructed pulmonary venous connection at coronary sinus orifice n1=en:pigmented paravenous chorioretinal atrophy | n2=en:obstructed pulmonary venous connection at coronary sinus orifice | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> en:orofaciodigital syndrome 9 n1=en:pigmented paravenous chorioretinal atrophy | n2=en:orofaciodigital syndrome 9 | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> en:palmoplantar porokeratosis n1=en:pigmented paravenous chorioretinal atrophy | n2=en:palmoplantar porokeratosis | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> en:parachute malformation of right atrioventricular valve n1=en:pigmented paravenous chorioretinal atrophy | n2=en:parachute malformation of right atrioventricular valve | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> en:pericellular fibrosis of congenital syphilis n1=en:pigmented paravenous chorioretinal atrophy | n2=en:pericellular fibrosis of congenital syphilis | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> en:platelet storage pool deficiency n1=en:pigmented paravenous chorioretinal atrophy | n2=en:platelet storage pool deficiency | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> en:progressive external ophthalmoplegia, myopathy, emaciation syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:progressive external ophthalmoplegia, myopathy, emaciation syndrome | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> en:pulmonic stenosis and congenital nephrosis n1=en:pigmented paravenous chorioretinal atrophy | n2=en:pulmonic stenosis and congenital nephrosis | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> en:renal coloboma syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:renal coloboma syndrome | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> en:right atrial appendage - left - juxtaposition n1=en:pigmented paravenous chorioretinal atrophy | n2=en:right atrial appendage - left - juxtaposition | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> en:right atrial endocardial fibroelastosis n1=en:pigmented paravenous chorioretinal atrophy | n2=en:right atrial endocardial fibroelastosis | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> en:right-sided pulmonary arterial trunk n1=en:pigmented paravenous chorioretinal atrophy | n2=en:right-sided pulmonary arterial trunk | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> en:rotation of tooth n1=en:pigmented paravenous chorioretinal atrophy | n2=en:rotation of tooth | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> en:severe x-linked intellectual disability gustavson type n1=en:pigmented paravenous chorioretinal atrophy | n2=en:severe x-linked intellectual disability gustavson type | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> en:slowed nerve conduction velocity, autosomal dominant n1=en:pigmented paravenous chorioretinal atrophy | n2=en:slowed nerve conduction velocity, autosomal dominant | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> en:spastic paraplegia, glaucoma, intellectual disability syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:spastic paraplegia, glaucoma, intellectual disability syndrome | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> en:spectrin-associated autosomal recessive cerebellar ataxia n1=en:pigmented paravenous chorioretinal atrophy | n2=en:spectrin-associated autosomal recessive cerebellar ataxia | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> en:spondyloepiphyseal dysplasia, craniosynostosis, cleft palate, cataract and intellectual disability syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:spondyloepiphyseal dysplasia, craniosynostosis, cleft palate, cataract and intellectual disability syndrome | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> en:striate palmoplantar keratoderma n1=en:pigmented paravenous chorioretinal atrophy | n2=en:striate palmoplantar keratoderma | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> en:tricuspid valve primary chords absent n1=en:pigmented paravenous chorioretinal atrophy | n2=en:tricuspid valve primary chords absent | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> en:urachal cyst n1=en:pigmented paravenous chorioretinal atrophy | n2=en:urachal cyst | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> en:uveal coloboma with cleft lip and palate and intellectual disability syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:uveal coloboma with cleft lip and palate and intellectual disability syndrome | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> en:verloes van maldergem marneffe syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:verloes van maldergem marneffe syndrome | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> en:white forelock with malformations n1=en:pigmented paravenous chorioretinal atrophy | n2=en:white forelock with malformations | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> en:x-linked distal spinal muscular atrophy type 3 n1=en:pigmented paravenous chorioretinal atrophy | n2=en:x-linked distal spinal muscular atrophy type 3 | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 40 / 0.8 -> rétinite pigmentaire liée à la périphérine (pro219leu) n1=en:pigmented paravenous chorioretinal atrophy | n2=rétinite pigmentaire liée à la périphérine (pro219leu) | rel=r_associated | relid=0 | w=40 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 39 / 0.78 -> 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 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 39 / 0.78 -> en:aicardi's syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:aicardi's syndrome | rel=r_associated | relid=0 | w=39 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 39 / 0.78 -> en:anophthalmia and pulmonary hypoplasia n1=en:pigmented paravenous chorioretinal atrophy | n2=en:anophthalmia and pulmonary hypoplasia | rel=r_associated | relid=0 | w=39 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 39 / 0.78 -> en:asexual dwarfism n1=en:pigmented paravenous chorioretinal atrophy | n2=en:asexual dwarfism | rel=r_associated | relid=0 | w=39 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 39 / 0.78 -> en:autosomal recessive cerebellar ataxia, pyramidal signs, nystagmus, oculomotor apraxia syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:autosomal recessive cerebellar ataxia, pyramidal signs, nystagmus, oculomotor apraxia syndrome | rel=r_associated | relid=0 | w=39 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 39 / 0.78 -> en:benign congenital myopathy n1=en:pigmented paravenous chorioretinal atrophy | n2=en:benign congenital myopathy | rel=r_associated | relid=0 | w=39 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 39 / 0.78 -> en:cap myopathy n1=en:pigmented paravenous chorioretinal atrophy | n2=en:cap myopathy | rel=r_associated | relid=0 | w=39 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 39 / 0.78 -> en:charcot-marie-tooth disease, dominant intermediate c n1=en:pigmented paravenous chorioretinal atrophy | n2=en:charcot-marie-tooth disease, dominant intermediate c | rel=r_associated | relid=0 | w=39 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 39 / 0.78 -> en:coloboma of macula with type b brachydactyly n1=en:pigmented paravenous chorioretinal atrophy | n2=en:coloboma of macula with type b brachydactyly | rel=r_associated | relid=0 | w=39 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 39 / 0.78 -> en:combined pancreatic lipase and colipase deficiency n1=en:pigmented paravenous chorioretinal atrophy | n2=en:combined pancreatic lipase and colipase deficiency | rel=r_associated | relid=0 | w=39 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 39 / 0.78 -> en:congenital atrophy of thyroid n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital atrophy of thyroid | rel=r_associated | relid=0 | w=39 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 39 / 0.78 -> en:congenital auditory imperception n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital auditory imperception | rel=r_associated | relid=0 | w=39 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 39 / 0.78 -> en:congenital blepharophimosis n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital blepharophimosis | rel=r_associated | relid=0 | w=39 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 39 / 0.78 -> en:congenital brain damage n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital brain damage | rel=r_associated | relid=0 | w=39 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 39 / 0.78 -> en:congenital cataracts, facial dysmorphism, and neuropathy n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital cataracts, facial dysmorphism, and neuropathy | rel=r_associated | relid=0 | w=39 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 39 / 0.78 -> en:congenital disease of brain n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital disease of brain | rel=r_associated | relid=0 | w=39 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 39 / 0.78 -> en:congenital elephantiasis n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital elephantiasis | rel=r_associated | relid=0 | w=39 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 39 / 0.78 -> en:congenital hepatic fibrosis n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital hepatic fibrosis | rel=r_associated | relid=0 | w=39 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 39 / 0.78 -> en:congenital hereditary facial paralysis with variable hearing loss syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital hereditary facial paralysis with variable hearing loss syndrome | rel=r_associated | relid=0 | w=39 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 39 / 0.78 -> en:congenital hernia of bladder n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital hernia of bladder | rel=r_associated | relid=0 | w=39 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 39 / 0.78 -> en:congenital ischemic atrophy of central nervous system structure n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital ischemic atrophy of central nervous system structure | rel=r_associated | relid=0 | w=39 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 39 / 0.78 -> en:congenital kidney disorder n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital kidney disorder | rel=r_associated | relid=0 | w=39 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 39 / 0.78 -> en:congenital male infertility n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital male infertility | rel=r_associated | relid=0 | w=39 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 39 / 0.78 -> en:congenital malposition of eyelid n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital malposition of eyelid | rel=r_associated | relid=0 | w=39 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 39 / 0.78 -> en:congenital meningocele n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital meningocele | rel=r_associated | relid=0 | w=39 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 39 / 0.78 -> en:congenital myasthenic syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital myasthenic syndrome | rel=r_associated | relid=0 | w=39 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 39 / 0.78 -> en:congenital myotonic dystrophy n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital myotonic dystrophy | rel=r_associated | relid=0 | w=39 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 39 / 0.78 -> en:congenital nasolacrimal duct obstruction n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital nasolacrimal duct obstruction | rel=r_associated | relid=0 | w=39 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 39 / 0.78 -> en:congenital nephritis n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital nephritis | rel=r_associated | relid=0 | w=39 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 39 / 0.78 -> en:congenital obstruction of small intestine n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital obstruction of small intestine | rel=r_associated | relid=0 | w=39 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 39 / 0.78 -> en:congenital obstruction of urethra n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital obstruction of urethra | rel=r_associated | relid=0 | w=39 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 39 / 0.78 -> en:congenital occlusion of ureter n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital occlusion of ureter | rel=r_associated | relid=0 | w=39 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 39 / 0.78 -> en:congenital onychoatrophy n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital onychoatrophy | rel=r_associated | relid=0 | w=39 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 39 / 0.78 -> en:congenital porencephalic cyst n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital porencephalic cyst | rel=r_associated | relid=0 | w=39 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 39 / 0.78 -> en:congenital positional talipes n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital positional talipes | rel=r_associated | relid=0 | w=39 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 39 / 0.78 -> en:congenital pseudostrabismus n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital pseudostrabismus | rel=r_associated | relid=0 | w=39 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 39 / 0.78 -> en:congenital skin contracture n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital skin contracture | rel=r_associated | relid=0 | w=39 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 39 / 0.78 -> en:congenital talipes equinus n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital talipes equinus | rel=r_associated | relid=0 | w=39 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 39 / 0.78 -> en:congenital talipes varus n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital talipes varus | rel=r_associated | relid=0 | w=39 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 39 / 0.78 -> en:congenital volvulus of stomach n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital volvulus of stomach | rel=r_associated | relid=0 | w=39 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 39 / 0.78 -> en:diffuse palmoplantar keratoderma and acrocyanosis syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:diffuse palmoplantar keratoderma and acrocyanosis syndrome | rel=r_associated | relid=0 | w=39 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 39 / 0.78 -> en:disorder of eye co-occurrent and due to marfan syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:disorder of eye co-occurrent and due to marfan syndrome | rel=r_associated | relid=0 | w=39 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 39 / 0.78 -> en:epilepsy, partial, with variable foci n1=en:pigmented paravenous chorioretinal atrophy | n2=en:epilepsy, partial, with variable foci | rel=r_associated | relid=0 | w=39 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 39 / 0.78 -> en:factor xi deficiency n1=en:pigmented paravenous chorioretinal atrophy | n2=en:factor xi deficiency | rel=r_associated | relid=0 | w=39 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 39 / 0.78 -> en:foxg1 syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:foxg1 syndrome | rel=r_associated | relid=0 | w=39 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 39 / 0.78 -> en:hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 n1=en:pigmented paravenous chorioretinal atrophy | n2=en:hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 | rel=r_associated | relid=0 | w=39 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 39 / 0.78 -> en:hypotrichosis with juvenile macular degeneration syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:hypotrichosis with juvenile macular degeneration syndrome | rel=r_associated | relid=0 | w=39 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 39 / 0.78 -> en:inborn errors of metabolism n1=en:pigmented paravenous chorioretinal atrophy | n2=en:inborn errors of metabolism | rel=r_associated | relid=0 | w=39 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 39 / 0.78 -> en:keratitis, hereditary n1=en:pigmented paravenous chorioretinal atrophy | n2=en:keratitis, hereditary | rel=r_associated | relid=0 | w=39 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 39 / 0.78 -> en:left atrioventricular valve bifoliate with fused left sided superior and inferior bridging leaflet n1=en:pigmented paravenous chorioretinal atrophy | n2=en:left atrioventricular valve bifoliate with fused left sided superior and inferior bridging leaflet | rel=r_associated | relid=0 | w=39 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 39 / 0.78 -> en:longitudinal deficiency of limb n1=en:pigmented paravenous chorioretinal atrophy | n2=en:longitudinal deficiency of limb | rel=r_associated | relid=0 | w=39 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 39 / 0.78 -> en:lowry maclean syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:lowry maclean syndrome | rel=r_associated | relid=0 | w=39 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 39 / 0.78 -> en:macular coloboma, cleft palate, hallux valgus syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:macular coloboma, cleft palate, hallux valgus syndrome | rel=r_associated | relid=0 | w=39 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 39 / 0.78 -> en:microphthalmia, syndromic 6 (disorder) n1=en:pigmented paravenous chorioretinal atrophy | n2=en:microphthalmia, syndromic 6 (disorder) | rel=r_associated | relid=0 | w=39 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 39 / 0.78 -> en:mobius ii syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:mobius ii syndrome | rel=r_associated | relid=0 | w=39 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 39 / 0.78 -> en:nephrogenic syndrome of inappropriate antidiuresis n1=en:pigmented paravenous chorioretinal atrophy | n2=en:nephrogenic syndrome of inappropriate antidiuresis | rel=r_associated | relid=0 | w=39 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 39 / 0.78 -> en:neuhauser syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:neuhauser syndrome | rel=r_associated | relid=0 | w=39 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 39 / 0.78 -> en:night blindness, congenital stationary n1=en:pigmented paravenous chorioretinal atrophy | n2=en:night blindness, congenital stationary | rel=r_associated | relid=0 | w=39 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 39 / 0.78 -> en:oculoauricular syndrome schorderet type n1=en:pigmented paravenous chorioretinal atrophy | n2=en:oculoauricular syndrome schorderet type | rel=r_associated | relid=0 | w=39 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 39 / 0.78 -> en:oliver-mcfarlane syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:oliver-mcfarlane syndrome | rel=r_associated | relid=0 | w=39 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 39 / 0.78 -> en:osteopoikilosis and dacryocystitis n1=en:pigmented paravenous chorioretinal atrophy | n2=en:osteopoikilosis and dacryocystitis | rel=r_associated | relid=0 | w=39 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 39 / 0.78 -> en:paravenous chorioretinal atrophy n1=en:pigmented paravenous chorioretinal atrophy | n2=en:paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=39 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 39 / 0.78 -> en:polydactyly, postaxial, with progressive myopia n1=en:pigmented paravenous chorioretinal atrophy | n2=en:polydactyly, postaxial, with progressive myopia | rel=r_associated | relid=0 | w=39 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 39 / 0.78 -> en:precocious exfoliation of teeth related to idiopathic root resorption n1=en:pigmented paravenous chorioretinal atrophy | n2=en:precocious exfoliation of teeth related to idiopathic root resorption | rel=r_associated | relid=0 | w=39 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 39 / 0.78 -> en:pulmonary valve overriding ventricular septum n1=en:pigmented paravenous chorioretinal atrophy | n2=en:pulmonary valve overriding ventricular septum | rel=r_associated | relid=0 | w=39 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 39 / 0.78 -> en:redundant prepuce n1=en:pigmented paravenous chorioretinal atrophy | n2=en:redundant prepuce | rel=r_associated | relid=0 | w=39 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 39 / 0.78 -> en:short stature and locking fingers n1=en:pigmented paravenous chorioretinal atrophy | n2=en:short stature and locking fingers | rel=r_associated | relid=0 | w=39 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 39 / 0.78 -> en:shortened trunk n1=en:pigmented paravenous chorioretinal atrophy | n2=en:shortened trunk | rel=r_associated | relid=0 | w=39 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 39 / 0.78 -> en:smith-lemli-opitz syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:smith-lemli-opitz syndrome | rel=r_associated | relid=0 | w=39 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 39 / 0.78 -> en:spondylo-ocular syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:spondylo-ocular syndrome | rel=r_associated | relid=0 | w=39 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 39 / 0.78 -> en:telecanthus n1=en:pigmented paravenous chorioretinal atrophy | n2=en:telecanthus | rel=r_associated | relid=0 | w=39 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 39 / 0.78 -> en:tripartite right ventricle n1=en:pigmented paravenous chorioretinal atrophy | n2=en:tripartite right ventricle | rel=r_associated | relid=0 | w=39 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 39 / 0.78 -> en:vitamin d-dependent rickets, type 1 n1=en:pigmented paravenous chorioretinal atrophy | n2=en:vitamin d-dependent rickets, type 1 | rel=r_associated | relid=0 | w=39 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 39 / 0.78 -> en:williams syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:williams syndrome | rel=r_associated | relid=0 | w=39 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 39 / 0.78 -> en:yemenite deaf-blind hypopigmentation syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:yemenite deaf-blind hypopigmentation syndrome | rel=r_associated | relid=0 | w=39 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 38 / 0.76 -> en:congenital atrophy of left lobe of liver n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital atrophy of left lobe of liver | rel=r_associated | relid=0 | w=38 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 38 / 0.76 -> en:spheroid body myopathy n1=en:pigmented paravenous chorioretinal atrophy | n2=en:spheroid body myopathy | rel=r_associated | relid=0 | w=38 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 38 / 0.76 -> en:toe syndactyly, telecanthus, and anogenital and renal malformations n1=en:pigmented paravenous chorioretinal atrophy | n2=en:toe syndactyly, telecanthus, and anogenital and renal malformations | rel=r_associated | relid=0 | w=38 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 37 / 0.74 -> en:ablepharon-macrostomia syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:ablepharon-macrostomia syndrome | rel=r_associated | relid=0 | w=37 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 37 / 0.74 -> en:albinism, ocular n1=en:pigmented paravenous chorioretinal atrophy | n2=en:albinism, ocular | rel=r_associated | relid=0 | w=37 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 37 / 0.74 -> en:aplasia cutis with myopia syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:aplasia cutis with myopia syndrome | rel=r_associated | relid=0 | w=37 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 37 / 0.74 -> en:arthrogryposis n1=en:pigmented paravenous chorioretinal atrophy | n2=en:arthrogryposis | rel=r_associated | relid=0 | w=37 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 37 / 0.74 -> en:ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia n1=en:pigmented paravenous chorioretinal atrophy | n2=en:ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia | rel=r_associated | relid=0 | w=37 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 37 / 0.74 -> en:blepharoptosis, myopia, ectopia lentis syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:blepharoptosis, myopia, ectopia lentis syndrome | rel=r_associated | relid=0 | w=37 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 37 / 0.74 -> en:brittle cornea syndrome 1 n1=en:pigmented paravenous chorioretinal atrophy | n2=en:brittle cornea syndrome 1 | rel=r_associated | relid=0 | w=37 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 37 / 0.74 -> en:cataract, congenital heart disease, neural tube defect syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:cataract, congenital heart disease, neural tube defect syndrome | rel=r_associated | relid=0 | w=37 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 37 / 0.74 -> en:cerebroretinal microangiopathy with calcifications and cysts (disorder) n1=en:pigmented paravenous chorioretinal atrophy | n2=en:cerebroretinal microangiopathy with calcifications and cysts (disorder) | rel=r_associated | relid=0 | w=37 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 37 / 0.74 -> en:congenital anemia n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital anemia | rel=r_associated | relid=0 | w=37 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 37 / 0.74 -> en:congenital hepatic porphyria n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital hepatic porphyria | rel=r_associated | relid=0 | w=37 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 37 / 0.74 -> en:congenital hypertonia n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital hypertonia | rel=r_associated | relid=0 | w=37 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 37 / 0.74 -> en:congenital megaprepuce n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital megaprepuce | rel=r_associated | relid=0 | w=37 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 37 / 0.74 -> en:congenital membranous nephropathy due to maternal anti-neutral endopeptidase alloimmunization n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital membranous nephropathy due to maternal anti-neutral endopeptidase alloimmunization | rel=r_associated | relid=0 | w=37 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 37 / 0.74 -> en:congenital pes cavus n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital pes cavus | rel=r_associated | relid=0 | w=37 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 37 / 0.74 -> en:congenital respiratory disorder n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital respiratory disorder | rel=r_associated | relid=0 | w=37 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 37 / 0.74 -> en:congenital scoliosis due to bony malformation n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital scoliosis due to bony malformation | rel=r_associated | relid=0 | w=37 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 37 / 0.74 -> en:congenital sutural cataract n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital sutural cataract | rel=r_associated | relid=0 | w=37 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 37 / 0.74 -> en:cyanotic congenital heart disease n1=en:pigmented paravenous chorioretinal atrophy | n2=en:cyanotic congenital heart disease | rel=r_associated | relid=0 | w=37 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 37 / 0.74 -> en:dental arch length loss secondary to congenitally missing teeth n1=en:pigmented paravenous chorioretinal atrophy | n2=en:dental arch length loss secondary to congenitally missing teeth | rel=r_associated | relid=0 | w=37 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 37 / 0.74 -> en:dental midlines coincident and incorrect n1=en:pigmented paravenous chorioretinal atrophy | n2=en:dental midlines coincident and incorrect | rel=r_associated | relid=0 | w=37 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 37 / 0.74 -> en:familial isolated trichomegaly n1=en:pigmented paravenous chorioretinal atrophy | n2=en:familial isolated trichomegaly | rel=r_associated | relid=0 | w=37 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 37 / 0.74 -> en:foramen ovale, patent n1=en:pigmented paravenous chorioretinal atrophy | n2=en:foramen ovale, patent | rel=r_associated | relid=0 | w=37 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 37 / 0.74 -> en:gaze palsy, familial horizontal, with progressive scoliosis, 1 n1=en:pigmented paravenous chorioretinal atrophy | n2=en:gaze palsy, familial horizontal, with progressive scoliosis, 1 | rel=r_associated | relid=0 | w=37 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 37 / 0.74 -> en:gemss syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:gemss syndrome | rel=r_associated | relid=0 | w=37 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 37 / 0.74 -> en:gyrate atrophy n1=en:pigmented paravenous chorioretinal atrophy | n2=en:gyrate atrophy | rel=r_associated | relid=0 | w=37 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 37 / 0.74 -> en:hereditary choroidal dystrophy n1=en:pigmented paravenous chorioretinal atrophy | n2=en:hereditary choroidal dystrophy | rel=r_associated | relid=0 | w=37 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 37 / 0.74 -> en:hereditary disorder of endocrine system n1=en:pigmented paravenous chorioretinal atrophy | n2=en:hereditary disorder of endocrine system | rel=r_associated | relid=0 | w=37 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 37 / 0.74 -> en:hereditary vitreoretinopathy n1=en:pigmented paravenous chorioretinal atrophy | n2=en:hereditary vitreoretinopathy | rel=r_associated | relid=0 | w=37 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 37 / 0.74 -> en:hypogonadism-cataract syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:hypogonadism-cataract syndrome | rel=r_associated | relid=0 | w=37 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 37 / 0.74 -> en:infantile myofibromatosis n1=en:pigmented paravenous chorioretinal atrophy | n2=en:infantile myofibromatosis | rel=r_associated | relid=0 | w=37 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 37 / 0.74 -> en:juvenile cataract, microcornea, renal glucosuria syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:juvenile cataract, microcornea, renal glucosuria syndrome | rel=r_associated | relid=0 | w=37 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 37 / 0.74 -> en:krasnow qazi syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:krasnow qazi syndrome | rel=r_associated | relid=0 | w=37 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 37 / 0.74 -> en:longitudinal deficiency of part of limb n1=en:pigmented paravenous chorioretinal atrophy | n2=en:longitudinal deficiency of part of limb | rel=r_associated | relid=0 | w=37 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 37 / 0.74 -> en:mackay shek carr syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:mackay shek carr syndrome | rel=r_associated | relid=0 | w=37 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 37 / 0.74 -> en:multifocal pattern dystrophy of retinal pigment epithelium simulating fundus flavimaculatus n1=en:pigmented paravenous chorioretinal atrophy | n2=en:multifocal pattern dystrophy of retinal pigment epithelium simulating fundus flavimaculatus | rel=r_associated | relid=0 | w=37 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 37 / 0.74 -> en:multiple supernumerary teeth unrelated to systemic condition n1=en:pigmented paravenous chorioretinal atrophy | n2=en:multiple supernumerary teeth unrelated to systemic condition | rel=r_associated | relid=0 | w=37 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 37 / 0.74 -> en:myopic crescent n1=en:pigmented paravenous chorioretinal atrophy | n2=en:myopic crescent | rel=r_associated | relid=0 | w=37 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 37 / 0.74 -> en:okihiro syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:okihiro syndrome | rel=r_associated | relid=0 | w=37 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 37 / 0.74 -> en:paraganglioma and gastric stromal sarcoma n1=en:pigmented paravenous chorioretinal atrophy | n2=en:paraganglioma and gastric stromal sarcoma | rel=r_associated | relid=0 | w=37 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 37 / 0.74 -> en:precocious exfoliation of teeth related to root resorption associated with trauma n1=en:pigmented paravenous chorioretinal atrophy | n2=en:precocious exfoliation of teeth related to root resorption associated with trauma | rel=r_associated | relid=0 | w=37 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 37 / 0.74 -> en:primary left ventricular endocardial fibroelastosis n1=en:pigmented paravenous chorioretinal atrophy | n2=en:primary left ventricular endocardial fibroelastosis | rel=r_associated | relid=0 | w=37 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 37 / 0.74 -> en:pulmonary alveolar proteinosis, congenital n1=en:pigmented paravenous chorioretinal atrophy | n2=en:pulmonary alveolar proteinosis, congenital | rel=r_associated | relid=0 | w=37 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 37 / 0.74 -> en:retinal arterial macroaneurysm with supravalvular pulmonic stenosis n1=en:pigmented paravenous chorioretinal atrophy | n2=en:retinal arterial macroaneurysm with supravalvular pulmonic stenosis | rel=r_associated | relid=0 | w=37 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 37 / 0.74 -> en:ring dermoid of cornea n1=en:pigmented paravenous chorioretinal atrophy | n2=en:ring dermoid of cornea | rel=r_associated | relid=0 | w=37 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 37 / 0.74 -> en:rudimentary left ventricle n1=en:pigmented paravenous chorioretinal atrophy | n2=en:rudimentary left ventricle | rel=r_associated | relid=0 | w=37 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 37 / 0.74 -> en:seemanova lesny syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:seemanova lesny syndrome | rel=r_associated | relid=0 | w=37 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 37 / 0.74 -> en:senile atrophy of choroid n1=en:pigmented paravenous chorioretinal atrophy | n2=en:senile atrophy of choroid | rel=r_associated | relid=0 | w=37 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 37 / 0.74 -> en:ter haar syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:ter haar syndrome | rel=r_associated | relid=0 | w=37 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 37 / 0.74 -> en:trifoliate left atrioventricular valve n1=en:pigmented paravenous chorioretinal atrophy | n2=en:trifoliate left atrioventricular valve | rel=r_associated | relid=0 | w=37 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 37 / 0.74 -> en:x-linked retinal dysplasia n1=en:pigmented paravenous chorioretinal atrophy | n2=en:x-linked retinal dysplasia | rel=r_associated | relid=0 | w=37 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 37 / 0.74 -> en:xte syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:xte syndrome | rel=r_associated | relid=0 | w=37 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 36 / 0.72 -> en:absent eyebrows and eyelashes with mental retardation n1=en:pigmented paravenous chorioretinal atrophy | n2=en:absent eyebrows and eyelashes with mental retardation | rel=r_associated | relid=0 | w=36 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 36 / 0.72 -> en:albinism, oculocutaneous n1=en:pigmented paravenous chorioretinal atrophy | n2=en:albinism, oculocutaneous | rel=r_associated | relid=0 | w=36 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 36 / 0.72 -> en:albinotic fundus n1=en:pigmented paravenous chorioretinal atrophy | n2=en:albinotic fundus | rel=r_associated | relid=0 | w=36 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 36 / 0.72 -> en:alstrom syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:alstrom syndrome | rel=r_associated | relid=0 | w=36 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 36 / 0.72 -> en:aniridia and absent patella n1=en:pigmented paravenous chorioretinal atrophy | n2=en:aniridia and absent patella | rel=r_associated | relid=0 | w=36 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 36 / 0.72 -> en:aniridia renal agenesis psychomotor retardation n1=en:pigmented paravenous chorioretinal atrophy | n2=en:aniridia renal agenesis psychomotor retardation | rel=r_associated | relid=0 | w=36 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 36 / 0.72 -> en:aplasia of lacrimal and salivary glands n1=en:pigmented paravenous chorioretinal atrophy | n2=en:aplasia of lacrimal and salivary glands | rel=r_associated | relid=0 | w=36 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 36 / 0.72 -> en:bleeding disorder due to p2ry12 defect n1=en:pigmented paravenous chorioretinal atrophy | n2=en:bleeding disorder due to p2ry12 defect | rel=r_associated | relid=0 | w=36 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 36 / 0.72 -> en:bornholm eye disease n1=en:pigmented paravenous chorioretinal atrophy | n2=en:bornholm eye disease | rel=r_associated | relid=0 | w=36 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 36 / 0.72 -> en:charcot-marie-tooth disease type 4 n1=en:pigmented paravenous chorioretinal atrophy | n2=en:charcot-marie-tooth disease type 4 | rel=r_associated | relid=0 | w=36 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 36 / 0.72 -> en:congenital abnormality n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital abnormality | rel=r_associated | relid=0 | w=36 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 36 / 0.72 -> en:congenital anal fissure n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital anal fissure | rel=r_associated | relid=0 | w=36 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 36 / 0.72 -> en:congenital axial myopia n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital axial myopia | rel=r_associated | relid=0 | w=36 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 36 / 0.72 -> en:congenital biliary tract disorder n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital biliary tract disorder | rel=r_associated | relid=0 | w=36 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 36 / 0.72 -> en:congenital connective tissue disorder n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital connective tissue disorder | rel=r_associated | relid=0 | w=36 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 36 / 0.72 -> en:congenital digestive system disorder n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital digestive system disorder | rel=r_associated | relid=0 | w=36 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 36 / 0.72 -> en:congenital end-plate acetylcholinesterase deficiency n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital end-plate acetylcholinesterase deficiency | rel=r_associated | relid=0 | w=36 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 36 / 0.72 -> en:congenital eye disorder n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital eye disorder | rel=r_associated | relid=0 | w=36 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 36 / 0.72 -> en:congenital fecaliths causing obstruction n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital fecaliths causing obstruction | rel=r_associated | relid=0 | w=36 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 36 / 0.72 -> en:congenital hydrosalpinx n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital hydrosalpinx | rel=r_associated | relid=0 | w=36 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 36 / 0.72 -> en:congenital long qt syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital long qt syndrome | rel=r_associated | relid=0 | w=36 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 36 / 0.72 -> en:congenital posterior subcapsular polar cataract n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital posterior subcapsular polar cataract | rel=r_associated | relid=0 | w=36 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 36 / 0.72 -> en:congenital quadriplegia n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital quadriplegia | rel=r_associated | relid=0 | w=36 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 36 / 0.72 -> en:corneal hypesthesia, familial n1=en:pigmented paravenous chorioretinal atrophy | n2=en:corneal hypesthesia, familial | rel=r_associated | relid=0 | w=36 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 36 / 0.72 -> en:crome syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:crome syndrome | rel=r_associated | relid=0 | w=36 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 36 / 0.72 -> en:diffuse secondary choroid atrophy n1=en:pigmented paravenous chorioretinal atrophy | n2=en:diffuse secondary choroid atrophy | rel=r_associated | relid=0 | w=36 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 36 / 0.72 -> en:ectodermal dysplasia with blindness syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:ectodermal dysplasia with blindness syndrome | rel=r_associated | relid=0 | w=36 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 36 / 0.72 -> en:edict syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:edict syndrome | rel=r_associated | relid=0 | w=36 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 36 / 0.72 -> en:erythrocyte lactate transporter defect n1=en:pigmented paravenous chorioretinal atrophy | n2=en:erythrocyte lactate transporter defect | rel=r_associated | relid=0 | w=36 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 36 / 0.72 -> en:facial dysmorphism, macrocephaly, myopia, dandy-walker malformation syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:facial dysmorphism, macrocephaly, myopia, dandy-walker malformation syndrome | rel=r_associated | relid=0 | w=36 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 36 / 0.72 -> en:hyperammonemic encephalopathy due to carbonic anhydrase va deficiency n1=en:pigmented paravenous chorioretinal atrophy | n2=en:hyperammonemic encephalopathy due to carbonic anhydrase va deficiency | rel=r_associated | relid=0 | w=36 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 36 / 0.72 -> en:intellectual disability, alacrima, achalasia syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:intellectual disability, alacrima, achalasia syndrome | rel=r_associated | relid=0 | w=36 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 36 / 0.72 -> en:keratosis pilaris with ichthyosis and deafness n1=en:pigmented paravenous chorioretinal atrophy | n2=en:keratosis pilaris with ichthyosis and deafness | rel=r_associated | relid=0 | w=36 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 36 / 0.72 -> en:knobloch syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:knobloch syndrome | rel=r_associated | relid=0 | w=36 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 36 / 0.72 -> en:myopathy with hexagonally cross-linked tubular arrays n1=en:pigmented paravenous chorioretinal atrophy | n2=en:myopathy with hexagonally cross-linked tubular arrays | rel=r_associated | relid=0 | w=36 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 36 / 0.72 -> en:peripapillary atrophy n1=en:pigmented paravenous chorioretinal atrophy | n2=en:peripapillary atrophy | rel=r_associated | relid=0 | w=36 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 36 / 0.72 -> en:pierson syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:pierson syndrome | rel=r_associated | relid=0 | w=36 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 36 / 0.72 -> en:posterior deviation of infundibular septum of obstructive aortic arch type n1=en:pigmented paravenous chorioretinal atrophy | n2=en:posterior deviation of infundibular septum of obstructive aortic arch type | rel=r_associated | relid=0 | w=36 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 36 / 0.72 -> en:progressive supranuclear palsy n1=en:pigmented paravenous chorioretinal atrophy | n2=en:progressive supranuclear palsy | rel=r_associated | relid=0 | w=36 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 36 / 0.72 -> en:prominent valve of inferior vena cava n1=en:pigmented paravenous chorioretinal atrophy | n2=en:prominent valve of inferior vena cava | rel=r_associated | relid=0 | w=36 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 36 / 0.72 -> en:ptosis, upper ocular movement limitation, absence of lacrimal punctum syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:ptosis, upper ocular movement limitation, absence of lacrimal punctum syndrome | rel=r_associated | relid=0 | w=36 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 36 / 0.72 -> en:reticulate acropigmentation of kitamura n1=en:pigmented paravenous chorioretinal atrophy | n2=en:reticulate acropigmentation of kitamura | rel=r_associated | relid=0 | w=36 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 36 / 0.72 -> en:von willebrand disease, platelet type n1=en:pigmented paravenous chorioretinal atrophy | n2=en:von willebrand disease, platelet type | rel=r_associated | relid=0 | w=36 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 36 / 0.72 -> vision photopique n1=en:pigmented paravenous chorioretinal atrophy | n2=vision photopique | rel=r_associated | relid=0 | w=36 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 35 / 0.7 -> en:aniridia and intellectual disability syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:aniridia and intellectual disability syndrome | rel=r_associated | relid=0 | w=35 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 35 / 0.7 -> en:atrophic n1=en:pigmented paravenous chorioretinal atrophy | n2=en:atrophic | rel=r_associated | relid=0 | w=35 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 35 / 0.7 -> en:autosomal dominant intermediate charcot-marie-tooth disease type e n1=en:pigmented paravenous chorioretinal atrophy | n2=en:autosomal dominant intermediate charcot-marie-tooth disease type e | rel=r_associated | relid=0 | w=35 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 35 / 0.7 -> en:calcaneus, talipes n1=en:pigmented paravenous chorioretinal atrophy | n2=en:calcaneus, talipes | rel=r_associated | relid=0 | w=35 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 35 / 0.7 -> en:congenital anterior subcapsular polar cataract n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital anterior subcapsular polar cataract | rel=r_associated | relid=0 | w=35 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 35 / 0.7 -> en:congenital cardiovascular disorder n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital cardiovascular disorder | rel=r_associated | relid=0 | w=35 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 35 / 0.7 -> en:congenital cerebellar cortical atrophy n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital cerebellar cortical atrophy | rel=r_associated | relid=0 | w=35 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 35 / 0.7 -> en:congenital chalasia of esophagus n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital chalasia of esophagus | rel=r_associated | relid=0 | w=35 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 35 / 0.7 -> en:congenital hearing disorder n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital hearing disorder | rel=r_associated | relid=0 | w=35 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 35 / 0.7 -> en:congenital hepatomegaly n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital hepatomegaly | rel=r_associated | relid=0 | w=35 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 35 / 0.7 -> en:congenital nystagmus n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital nystagmus | rel=r_associated | relid=0 | w=35 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 35 / 0.7 -> en:congenital obstruction of large intestine n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital obstruction of large intestine | rel=r_associated | relid=0 | w=35 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 35 / 0.7 -> en:congenital pseudoporencephaly n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital pseudoporencephaly | rel=r_associated | relid=0 | w=35 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 35 / 0.7 -> en:congenital reproductive system disorder n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital reproductive system disorder | rel=r_associated | relid=0 | w=35 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 35 / 0.7 -> en:congenital secretory diarrhea n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital secretory diarrhea | rel=r_associated | relid=0 | w=35 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 35 / 0.7 -> en:congenital stenosis n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital stenosis | rel=r_associated | relid=0 | w=35 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 35 / 0.7 -> en:congenital/genetic syndrome with poikiloderma n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital/genetic syndrome with poikiloderma | rel=r_associated | relid=0 | w=35 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 35 / 0.7 -> en:deafness and myopia syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:deafness and myopia syndrome | rel=r_associated | relid=0 | w=35 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 35 / 0.7 -> en:familial aplasia of the vermis n1=en:pigmented paravenous chorioretinal atrophy | n2=en:familial aplasia of the vermis | rel=r_associated | relid=0 | w=35 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 35 / 0.7 -> en:hernandez fragoso syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:hernandez fragoso syndrome | rel=r_associated | relid=0 | w=35 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 35 / 0.7 -> en:microvillus inclusion disease n1=en:pigmented paravenous chorioretinal atrophy | n2=en:microvillus inclusion disease | rel=r_associated | relid=0 | w=35 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 35 / 0.7 -> en:pigmentary retinal dystrophy n1=en:pigmented paravenous chorioretinal atrophy | n2=en:pigmentary retinal dystrophy | rel=r_associated | relid=0 | w=35 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 35 / 0.7 -> en:posterior fusion of lumbosacral vertebrae and blepharoptosis syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:posterior fusion of lumbosacral vertebrae and blepharoptosis syndrome | rel=r_associated | relid=0 | w=35 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 35 / 0.7 -> en:prader-willi syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:prader-willi syndrome | rel=r_associated | relid=0 | w=35 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 35 / 0.7 -> en:prolonged electroretinal response suppression n1=en:pigmented paravenous chorioretinal atrophy | n2=en:prolonged electroretinal response suppression | rel=r_associated | relid=0 | w=35 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 35 / 0.7 -> en:rambaud gallian syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:rambaud gallian syndrome | rel=r_associated | relid=0 | w=35 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 35 / 0.7 -> en:spleen in right sided position n1=en:pigmented paravenous chorioretinal atrophy | n2=en:spleen in right sided position | rel=r_associated | relid=0 | w=35 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 35 / 0.7 -> en:unipartite right ventricle n1=en:pigmented paravenous chorioretinal atrophy | n2=en:unipartite right ventricle | rel=r_associated | relid=0 | w=35 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 34 / 0.68 -> en:charcot-marie-tooth disease, dominant intermediate a n1=en:pigmented paravenous chorioretinal atrophy | n2=en:charcot-marie-tooth disease, dominant intermediate a | rel=r_associated | relid=0 | w=34 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 34 / 0.68 -> en:congenital calcium pyrophosphate dihydrate crystal deposition disease n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital calcium pyrophosphate dihydrate crystal deposition disease | rel=r_associated | relid=0 | w=34 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 34 / 0.68 -> en:congenital color blindness n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital color blindness | rel=r_associated | relid=0 | w=34 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 34 / 0.68 -> en:congenital fecaliths n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital fecaliths | rel=r_associated | relid=0 | w=34 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 34 / 0.68 -> en:congenital muscular dystrophy with infantile cataract and hypogonadism syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital muscular dystrophy with infantile cataract and hypogonadism syndrome | rel=r_associated | relid=0 | w=34 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 34 / 0.68 -> en:congenital renal atrophy n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital renal atrophy | rel=r_associated | relid=0 | w=34 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 34 / 0.68 -> en:congenital sixth nerve palsy n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital sixth nerve palsy | rel=r_associated | relid=0 | w=34 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 34 / 0.68 -> en:congenital thrombocytopenia n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital thrombocytopenia | rel=r_associated | relid=0 | w=34 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 34 / 0.68 -> en:duplication of eyebrow and syndactyly syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:duplication of eyebrow and syndactyly syndrome | rel=r_associated | relid=0 | w=34 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 34 / 0.68 -> en:heide syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:heide syndrome | rel=r_associated | relid=0 | w=34 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 34 / 0.68 -> en:hereditary anetoderma n1=en:pigmented paravenous chorioretinal atrophy | n2=en:hereditary anetoderma | rel=r_associated | relid=0 | w=34 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 34 / 0.68 -> en:hutch diverticulum n1=en:pigmented paravenous chorioretinal atrophy | n2=en:hutch diverticulum | rel=r_associated | relid=0 | w=34 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 34 / 0.68 -> en:macrostomia, preauricular tag, external ophthalmoplegia syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:macrostomia, preauricular tag, external ophthalmoplegia syndrome | rel=r_associated | relid=0 | w=34 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 34 / 0.68 -> en:microphthalmia, syndromic 1 n1=en:pigmented paravenous chorioretinal atrophy | n2=en:microphthalmia, syndromic 1 | rel=r_associated | relid=0 | w=34 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 34 / 0.68 -> en:microphthalmia, syndromic 4 (disorder) n1=en:pigmented paravenous chorioretinal atrophy | n2=en:microphthalmia, syndromic 4 (disorder) | rel=r_associated | relid=0 | w=34 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 34 / 0.68 -> en:porphyria, erythropoietic n1=en:pigmented paravenous chorioretinal atrophy | n2=en:porphyria, erythropoietic | rel=r_associated | relid=0 | w=34 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 34 / 0.68 -> en:pseudomonas pyocyaneus congenital infection n1=en:pigmented paravenous chorioretinal atrophy | n2=en:pseudomonas pyocyaneus congenital infection | rel=r_associated | relid=0 | w=34 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 34 / 0.68 -> en:right inferior caval vein connecting to left sided atrium n1=en:pigmented paravenous chorioretinal atrophy | n2=en:right inferior caval vein connecting to left sided atrium | rel=r_associated | relid=0 | w=34 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 34 / 0.68 -> en:spinal hydromeningocele n1=en:pigmented paravenous chorioretinal atrophy | n2=en:spinal hydromeningocele | rel=r_associated | relid=0 | w=34 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 34 / 0.68 -> en:tricuspid but functionally bicuspid aortic valve n1=en:pigmented paravenous chorioretinal atrophy | n2=en:tricuspid but functionally bicuspid aortic valve | rel=r_associated | relid=0 | w=34 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 34 / 0.68 -> en:upper esophageal web n1=en:pigmented paravenous chorioretinal atrophy | n2=en:upper esophageal web | rel=r_associated | relid=0 | w=34 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 34 / 0.68 -> en:vasculopathy, retinal, with cerebral leukodystrophy n1=en:pigmented paravenous chorioretinal atrophy | n2=en:vasculopathy, retinal, with cerebral leukodystrophy | rel=r_associated | relid=0 | w=34 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 34 / 0.68 -> en:waardenburg anophthalmia syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:waardenburg anophthalmia syndrome | rel=r_associated | relid=0 | w=34 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 33 / 0.66 -> en:ataxia, spastic, with congenital miosis n1=en:pigmented paravenous chorioretinal atrophy | n2=en:ataxia, spastic, with congenital miosis | rel=r_associated | relid=0 | w=33 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 33 / 0.66 -> en:behrens baumann dust syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:behrens baumann dust syndrome | rel=r_associated | relid=0 | w=33 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 33 / 0.66 -> en:biallelic rpe65 mutation associated retinal dystrophy n1=en:pigmented paravenous chorioretinal atrophy | n2=en:biallelic rpe65 mutation associated retinal dystrophy | rel=r_associated | relid=0 | w=33 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 33 / 0.66 -> en:congenital obstruction of aqueduct of sylvius n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital obstruction of aqueduct of sylvius | rel=r_associated | relid=0 | w=33 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 33 / 0.66 -> en:familial nasal acilia n1=en:pigmented paravenous chorioretinal atrophy | n2=en:familial nasal acilia | rel=r_associated | relid=0 | w=33 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 33 / 0.66 -> en:sensory ataxic neuropathy, dysarthria, and ophthalmoparesis n1=en:pigmented paravenous chorioretinal atrophy | n2=en:sensory ataxic neuropathy, dysarthria, and ophthalmoparesis | rel=r_associated | relid=0 | w=33 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 33 / 0.66 -> en:truncal valve overriding ventricular septum n1=en:pigmented paravenous chorioretinal atrophy | n2=en:truncal valve overriding ventricular septum | rel=r_associated | relid=0 | w=33 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 32 / 0.64 -> en:cataract, congenital, cerulean type 1 n1=en:pigmented paravenous chorioretinal atrophy | n2=en:cataract, congenital, cerulean type 1 | rel=r_associated | relid=0 | w=32 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 32 / 0.64 -> en:congenital fibrinogen abnormality n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital fibrinogen abnormality | rel=r_associated | relid=0 | w=32 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 32 / 0.64 -> en:congenital functional disorders of the colon n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital functional disorders of the colon | rel=r_associated | relid=0 | w=32 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 32 / 0.64 -> en:congenital kyphoscoliosis n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital kyphoscoliosis | rel=r_associated | relid=0 | w=32 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 32 / 0.64 -> en:congenital laryngeal adductor palsy n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital laryngeal adductor palsy | rel=r_associated | relid=0 | w=32 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 32 / 0.64 -> en:diarrhea 4, malabsorptive, congenital n1=en:pigmented paravenous chorioretinal atrophy | n2=en:diarrhea 4, malabsorptive, congenital | rel=r_associated | relid=0 | w=32 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 32 / 0.64 -> en:hereditary hemoglobinopathy n1=en:pigmented paravenous chorioretinal atrophy | n2=en:hereditary hemoglobinopathy | rel=r_associated | relid=0 | w=32 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 32 / 0.64 -> en:hereditary sensory autonomic neuropathy, type 5 n1=en:pigmented paravenous chorioretinal atrophy | n2=en:hereditary sensory autonomic neuropathy, type 5 | rel=r_associated | relid=0 | w=32 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 32 / 0.64 -> en:intestinal epithelial dysplasia n1=en:pigmented paravenous chorioretinal atrophy | n2=en:intestinal epithelial dysplasia | rel=r_associated | relid=0 | w=32 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 32 / 0.64 -> en:martsolf syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:martsolf syndrome | rel=r_associated | relid=0 | w=32 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 32 / 0.64 -> en:mitochondrial neurogastrointestinal encephalomyopathy syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:mitochondrial neurogastrointestinal encephalomyopathy syndrome | rel=r_associated | relid=0 | w=32 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 32 / 0.64 -> en:syndromic orbital border hypoplasia n1=en:pigmented paravenous chorioretinal atrophy | n2=en:syndromic orbital border hypoplasia | rel=r_associated | relid=0 | w=32 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 32 / 0.64 -> en:zunich neuroectodermal syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:zunich neuroectodermal syndrome | rel=r_associated | relid=0 | w=32 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 31 / 0.62 -> en:2-methyl-3-hydroxybutyric aciduria n1=en:pigmented paravenous chorioretinal atrophy | n2=en:2-methyl-3-hydroxybutyric aciduria | rel=r_associated | relid=0 | w=31 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 31 / 0.62 -> en:congenital genu valgum of left knee n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital genu valgum of left knee | rel=r_associated | relid=0 | w=31 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 31 / 0.62 -> en:congenital ureterovesical junction obstruction n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital ureterovesical junction obstruction | rel=r_associated | relid=0 | w=31 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 31 / 0.62 -> en:congenital vocal cord palsy n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital vocal cord palsy | rel=r_associated | relid=0 | w=31 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 31 / 0.62 -> en:hereditary corneal dystrophy n1=en:pigmented paravenous chorioretinal atrophy | n2=en:hereditary corneal dystrophy | rel=r_associated | relid=0 | w=31 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 31 / 0.62 -> en:intellectual disability with cataract and kyphosis syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:intellectual disability with cataract and kyphosis syndrome | rel=r_associated | relid=0 | w=31 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 31 / 0.62 -> en:leber congenital amaurosis n1=en:pigmented paravenous chorioretinal atrophy | n2=en:leber congenital amaurosis | rel=r_associated | relid=0 | w=31 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 31 / 0.62 -> en:mottled teeth, congenital n1=en:pigmented paravenous chorioretinal atrophy | n2=en:mottled teeth, congenital | rel=r_associated | relid=0 | w=31 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 31 / 0.62 -> en:parachute malformation of left atrioventricular valve n1=en:pigmented paravenous chorioretinal atrophy | n2=en:parachute malformation of left atrioventricular valve | rel=r_associated | relid=0 | w=31 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 31 / 0.62 -> en:split-hand with congenital nystagmus, fundal changes, and cataracts n1=en:pigmented paravenous chorioretinal atrophy | n2=en:split-hand with congenital nystagmus, fundal changes, and cataracts | rel=r_associated | relid=0 | w=31 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 31 / 0.62 -> en:systemic venovenous collateral vein n1=en:pigmented paravenous chorioretinal atrophy | n2=en:systemic venovenous collateral vein | rel=r_associated | relid=0 | w=31 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 31 / 0.62 -> en:wellesley carman french syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:wellesley carman french syndrome | rel=r_associated | relid=0 | w=31 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 30 / 0.6 -> en:congenital spastic foot n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital spastic foot | rel=r_associated | relid=0 | w=30 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 30 / 0.6 -> en:true cleft of common atrioventricular valve leaflet n1=en:pigmented paravenous chorioretinal atrophy | n2=en:true cleft of common atrioventricular valve leaflet | rel=r_associated | relid=0 | w=30 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 29 / 0.58 -> en:adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy n1=en:pigmented paravenous chorioretinal atrophy | n2=en:adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy | rel=r_associated | relid=0 | w=29 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 29 / 0.58 -> en:atrioventricular septal defect, blepharophimosis, radial and anal defect syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:atrioventricular septal defect, blepharophimosis, radial and anal defect syndrome | rel=r_associated | relid=0 | w=29 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 29 / 0.58 -> en:blindness, scoliosis, arachnodactyly syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:blindness, scoliosis, arachnodactyly syndrome | rel=r_associated | relid=0 | w=29 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 29 / 0.58 -> en:charcot-marie-tooth disease, dominant intermediate b (disorder) n1=en:pigmented paravenous chorioretinal atrophy | n2=en:charcot-marie-tooth disease, dominant intermediate b (disorder) | rel=r_associated | relid=0 | w=29 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 29 / 0.58 -> en:congenital accessory skin tag n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital accessory skin tag | rel=r_associated | relid=0 | w=29 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 29 / 0.58 -> en:congenital cardiovascular disorders during pregnancy, childbirth and the puerperium n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital cardiovascular disorders during pregnancy, childbirth and the puerperium | rel=r_associated | relid=0 | w=29 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 29 / 0.58 -> en:congenital flat foot n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital flat foot | rel=r_associated | relid=0 | w=29 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 29 / 0.58 -> en:congenital functional disorders of the small intestine n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital functional disorders of the small intestine | rel=r_associated | relid=0 | w=29 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 29 / 0.58 -> en:ectopia lentis, chorioretinal dystrophy, myopia syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:ectopia lentis, chorioretinal dystrophy, myopia syndrome | rel=r_associated | relid=0 | w=29 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 29 / 0.58 -> en:infant metachromatic leukodystrophies n1=en:pigmented paravenous chorioretinal atrophy | n2=en:infant metachromatic leukodystrophies | rel=r_associated | relid=0 | w=29 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 29 / 0.58 -> en:karandikar maria kamble syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:karandikar maria kamble syndrome | rel=r_associated | relid=0 | w=29 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 29 / 0.58 -> rétinite pigmentaire paraveineuse n1=en:pigmented paravenous chorioretinal atrophy | n2=rétinite pigmentaire paraveineuse | rel=r_associated | relid=0 | w=29 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 28 / 0.56 -> en:congenital analbuminemia n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital analbuminemia | rel=r_associated | relid=0 | w=28 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 28 / 0.56 -> en:congenital disorder of facial nerve n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital disorder of facial nerve | rel=r_associated | relid=0 | w=28 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 28 / 0.56 -> en:congenital fissure of tongue n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital fissure of tongue | rel=r_associated | relid=0 | w=28 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 28 / 0.56 -> en:congenital neurogenic ileus syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital neurogenic ileus syndrome | rel=r_associated | relid=0 | w=28 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 28 / 0.56 -> en:congenital single renal cyst n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital single renal cyst | rel=r_associated | relid=0 | w=28 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 28 / 0.56 -> en:gelatinous atrioventricular valve leaflet in atrioventricular septal defect n1=en:pigmented paravenous chorioretinal atrophy | n2=en:gelatinous atrioventricular valve leaflet in atrioventricular septal defect | rel=r_associated | relid=0 | w=28 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 28 / 0.56 -> en:hemophilia b n1=en:pigmented paravenous chorioretinal atrophy | n2=en:hemophilia b | rel=r_associated | relid=0 | w=28 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 28 / 0.56 -> en:lopes gorlin syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:lopes gorlin syndrome | rel=r_associated | relid=0 | w=28 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 28 / 0.56 -> en:median nodule of upper lip n1=en:pigmented paravenous chorioretinal atrophy | n2=en:median nodule of upper lip | rel=r_associated | relid=0 | w=28 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 28 / 0.56 -> en:microbrachycephaly, ptosis, cleft lip syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:microbrachycephaly, ptosis, cleft lip syndrome | rel=r_associated | relid=0 | w=28 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 28 / 0.56 -> en:myopic conus n1=en:pigmented paravenous chorioretinal atrophy | n2=en:myopic conus | rel=r_associated | relid=0 | w=28 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 28 / 0.56 -> en:placenta previa centralis n1=en:pigmented paravenous chorioretinal atrophy | n2=en:placenta previa centralis | rel=r_associated | relid=0 | w=28 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 28 / 0.56 -> en:vici syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:vici syndrome | rel=r_associated | relid=0 | w=28 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 28 / 0.56 -> paraveineuse n1=en:pigmented paravenous chorioretinal atrophy | n2=paraveineuse | rel=r_associated | relid=0 | w=28 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 27 / 0.54 -> en:cataract and cardiomyopathy n1=en:pigmented paravenous chorioretinal atrophy | n2=en:cataract and cardiomyopathy | rel=r_associated | relid=0 | w=27 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 27 / 0.54 -> en:cochleosaccular degeneration of the inner ear and progressive cataracts n1=en:pigmented paravenous chorioretinal atrophy | n2=en:cochleosaccular degeneration of the inner ear and progressive cataracts | rel=r_associated | relid=0 | w=27 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 27 / 0.54 -> en:congenital immunodeficiency disease n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital immunodeficiency disease | rel=r_associated | relid=0 | w=27 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 27 / 0.54 -> en:congenital malalignment of the toenails n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital malalignment of the toenails | rel=r_associated | relid=0 | w=27 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 27 / 0.54 -> en:congenital methemoglobinemia n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital methemoglobinemia | rel=r_associated | relid=0 | w=27 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 27 / 0.54 -> en:congenital oral/facial/cranial defect n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital oral/facial/cranial defect | rel=r_associated | relid=0 | w=27 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 27 / 0.54 -> en:cortical blindness, intellectual disability, polydactyly syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:cortical blindness, intellectual disability, polydactyly syndrome | rel=r_associated | relid=0 | w=27 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 27 / 0.54 -> en:crb1, val162met n1=en:pigmented paravenous chorioretinal atrophy | n2=en:crb1, val162met | rel=r_associated | relid=0 | w=27 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 27 / 0.54 -> en:hereditary optic atrophy n1=en:pigmented paravenous chorioretinal atrophy | n2=en:hereditary optic atrophy | rel=r_associated | relid=0 | w=27 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 27 / 0.54 -> en:isolated cryptophthalmos n1=en:pigmented paravenous chorioretinal atrophy | n2=en:isolated cryptophthalmos | rel=r_associated | relid=0 | w=27 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 27 / 0.54 -> en:kaufman oculocerebrofacial syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:kaufman oculocerebrofacial syndrome | rel=r_associated | relid=0 | w=27 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 27 / 0.54 -> en:microphthalmia, syndromic 5 n1=en:pigmented paravenous chorioretinal atrophy | n2=en:microphthalmia, syndromic 5 | rel=r_associated | relid=0 | w=27 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 27 / 0.54 -> en:oculopharyngodistal myopathy n1=en:pigmented paravenous chorioretinal atrophy | n2=en:oculopharyngodistal myopathy | rel=r_associated | relid=0 | w=27 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 27 / 0.54 -> en:otulin-related autoinflammatory syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:otulin-related autoinflammatory syndrome | rel=r_associated | relid=0 | w=27 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 27 / 0.54 -> en:palmoplantar keratoderma nagashima type n1=en:pigmented paravenous chorioretinal atrophy | n2=en:palmoplantar keratoderma nagashima type | rel=r_associated | relid=0 | w=27 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 27 / 0.54 -> en:parachute malformation of common atrioventricular valve n1=en:pigmented paravenous chorioretinal atrophy | n2=en:parachute malformation of common atrioventricular valve | rel=r_associated | relid=0 | w=27 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 27 / 0.54 -> en:schaap taylor baraitser syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:schaap taylor baraitser syndrome | rel=r_associated | relid=0 | w=27 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 27 / 0.54 -> en:spinal muscular atrophy, dandy-walker malformation, cataract syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:spinal muscular atrophy, dandy-walker malformation, cataract syndrome | rel=r_associated | relid=0 | w=27 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 26 / 0.52 -> en:congenital blepharophimosis of lower eyelid n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital blepharophimosis of lower eyelid | rel=r_associated | relid=0 | w=26 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 26 / 0.52 -> en:congenital cyst of vulva n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital cyst of vulva | rel=r_associated | relid=0 | w=26 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 26 / 0.52 -> en:congenital exophthalmos n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital exophthalmos | rel=r_associated | relid=0 | w=26 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 26 / 0.52 -> en:congenital melanosis n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital melanosis | rel=r_associated | relid=0 | w=26 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 26 / 0.52 -> en:congenital retinoschisis n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital retinoschisis | rel=r_associated | relid=0 | w=26 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 26 / 0.52 -> en:congenital von willebrand's disease n1=en:pigmented paravenous chorioretinal atrophy | n2=en:congenital von willebrand's disease | rel=r_associated | relid=0 | w=26 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 26 / 0.52 -> en:cor biloculare n1=en:pigmented paravenous chorioretinal atrophy | n2=en:cor biloculare | rel=r_associated | relid=0 | w=26 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 26 / 0.52 -> en:double orifice of right atrioventricular valve in double inlet ventricle n1=en:pigmented paravenous chorioretinal atrophy | n2=en:double orifice of right atrioventricular valve in double inlet ventricle | rel=r_associated | relid=0 | w=26 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 26 / 0.52 -> en:hypospadias, hypertelorism, coloboma, deafness syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:hypospadias, hypertelorism, coloboma, deafness syndrome | rel=r_associated | relid=0 | w=26 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 26 / 0.52 -> en:macrosomia obesity macrocephaly ocular abnormalities n1=en:pigmented paravenous chorioretinal atrophy | n2=en:macrosomia obesity macrocephaly ocular abnormalities | rel=r_associated | relid=0 | w=26 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 26 / 0.52 -> en:obstructed interchordal space of tricuspid chordae tendinae n1=en:pigmented paravenous chorioretinal atrophy | n2=en:obstructed interchordal space of tricuspid chordae tendinae | rel=r_associated | relid=0 | w=26 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 26 / 0.52 -> en:skin abnormalities n1=en:pigmented paravenous chorioretinal atrophy | n2=en:skin abnormalities | rel=r_associated | relid=0 | w=26 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 25 / 0.5 -> atrophie n1=en:pigmented paravenous chorioretinal atrophy | n2=atrophie | rel=r_associated | relid=0 | w=25 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 25 / 0.5 -> en:peripherin-related n1=en:pigmented paravenous chorioretinal atrophy | n2=en:peripherin-related | rel=r_associated | relid=0 | w=25 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 25 / 0.5 -> en:pigmented n1=en:pigmented paravenous chorioretinal atrophy | n2=en:pigmented | rel=r_associated | relid=0 | w=25 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 25 / 0.5 -> rétine n1=en:pigmented paravenous chorioretinal atrophy | n2=rétine | rel=r_associated | relid=0 | w=25 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 23 / 0.46 -> pigmentaire n1=en:pigmented paravenous chorioretinal atrophy | n2=pigmentaire | rel=r_associated | relid=0 | w=23 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 23 / 0.46 -> rétinite n1=en:pigmented paravenous chorioretinal atrophy | n2=rétinite | rel=r_associated | relid=0 | w=23 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 23 / 0.46 -> rétinite pigmentaire n1=en:pigmented paravenous chorioretinal atrophy | n2=rétinite pigmentaire | rel=r_associated | relid=0 | w=23 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 22 / 0.44 -> rétinite pigmentaire liée à la périphérine n1=en:pigmented paravenous chorioretinal atrophy | n2=rétinite pigmentaire liée à la périphérine | rel=r_associated | relid=0 | w=22 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 21 / 0.42 -> en:retinitis pigmentosa n1=en:pigmented paravenous chorioretinal atrophy | n2=en:retinitis pigmentosa | rel=r_associated | relid=0 | w=21 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 20 / 0.4 -> rétinite pigmentaire sénile n1=en:pigmented paravenous chorioretinal atrophy | n2=rétinite pigmentaire sénile | rel=r_associated | relid=0 | w=20 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 20 / 0.4 -> rétinite pigmentaire, surdité, retard mental, et hypogonadisme n1=en:pigmented paravenous chorioretinal atrophy | n2=rétinite pigmentaire, surdité, retard mental, et hypogonadisme | rel=r_associated | relid=0 | w=20 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 15 / 0.3 -> Rétinite pigmentaire n1=en:pigmented paravenous chorioretinal atrophy | n2=Rétinite pigmentaire | rel=r_associated | relid=0 | w=15 en:pigmented paravenous chorioretinal atrophy -- r_associated #0: 1 / 0.02 -> en:disease or syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:disease or syndrome | rel=r_associated | relid=0 | w=1

≈ 593 relations entrantes en:eye diseases, hereditary --- r_associated #0: 35 --> en:pigmented paravenous chorioretinal atrophy n1=en:eye diseases, hereditary | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=35 en:myopic crescent --- r_associated #0: 35 --> en:pigmented paravenous chorioretinal atrophy n1=en:myopic crescent | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=35 en:congenital laryngeal cyst --- r_associated #0: 34 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital laryngeal cyst | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=34 en:peripherin-related --- r_associated #0: 29 --> en:pigmented paravenous chorioretinal atrophy n1=en:peripherin-related | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=29 rétinite pigmentaire paraveineuse --- r_associated #0: 29 --> en:pigmented paravenous chorioretinal atrophy n1=rétinite pigmentaire paraveineuse | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=29 rétinite pigmentaire, surdité, retard mental, et hypogonadisme --- r_associated #0: 29 --> en:pigmented paravenous chorioretinal atrophy n1=rétinite pigmentaire, surdité, retard mental, et hypogonadisme | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=29 en:disorder of eye co-occurrent and due to marfan syndrome --- r_associated #0: 28 --> en:pigmented paravenous chorioretinal atrophy n1=en:disorder of eye co-occurrent and due to marfan syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=28 en:crb1, val162met --- r_associated #0: 27 --> en:pigmented paravenous chorioretinal atrophy n1=en:crb1, val162met | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=27 rétinite pigmentaire liée à la périphérine (pro219leu) --- r_associated #0: 27 --> en:pigmented paravenous chorioretinal atrophy n1=rétinite pigmentaire liée à la périphérine (pro219leu) | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=27 rétinite pigmentaire sénile --- r_associated #0: 27 --> en:pigmented paravenous chorioretinal atrophy n1=rétinite pigmentaire sénile | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=27 en:retinitis pigmentosa --- r_associated #0: 26 --> en:pigmented paravenous chorioretinal atrophy n1=en:retinitis pigmentosa | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=26 rétinite pigmentaire liée à la rhodopsine --- r_associated #0: 25 --> en:pigmented paravenous chorioretinal atrophy n1=rétinite pigmentaire liée à la rhodopsine | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=25 ERG --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=ERG | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 affection oculaire congénitale --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=affection oculaire congénitale | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 dysplasie olfacto-génitale --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=dysplasie olfacto-génitale | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 dysplasie olfactogénitale --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=dysplasie olfactogénitale | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 dysplasie olfactogénitale de De Morsier --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=dysplasie olfactogénitale de De Morsier | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:2-methyl-3-hydroxybutyric aciduria --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:2-methyl-3-hydroxybutyric aciduria | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:ablepharon-macrostomia syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:ablepharon-macrostomia syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:abnormal root proximity between adjacent teeth --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:abnormal root proximity between adjacent teeth | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:abruzzo erickson syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:abruzzo erickson syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:absent eyebrows and eyelashes with mental retardation --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:absent eyebrows and eyelashes with mental retardation | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:acrootoocular syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:acrootoocular syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:action myoclonus renal failure syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:action myoclonus renal failure syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:adrenocortical hypofunction, chronic primary congenital --- r_associated #0: 20 --> 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:adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:aicardi's syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:aicardi's syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:albinism, ocular --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:albinism, ocular | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:albinism, oculocutaneous --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:albinism, oculocutaneous | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:albinotic fundus --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:albinotic fundus | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:alpha-fetoprotein deficiency --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:alpha-fetoprotein deficiency | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:alstrom syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:alstrom syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:angioid streaks --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:angioid streaks | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:angioid streaks of choroid --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:angioid streaks of choroid | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:aniridia and absent patella --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:aniridia and absent patella | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:aniridia and intellectual disability syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:aniridia and intellectual disability syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:aniridia renal agenesis psychomotor retardation --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:aniridia renal agenesis psychomotor retardation | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:aniridia, ptosis, intellectual disability, familial obesity syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:aniridia, ptosis, intellectual disability, familial obesity syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:anophthalmia and pulmonary hypoplasia --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:anophthalmia and pulmonary hypoplasia | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:anophthalmia plus syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:anophthalmia plus syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:aplasia cutis congenita with epibulbar dermoids --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:aplasia cutis congenita with epibulbar dermoids | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:aplasia cutis with myopia syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:aplasia cutis with myopia syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:aplasia of lacrimal and salivary glands --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:aplasia of lacrimal and salivary glands | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:arthrogryposis --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:arthrogryposis | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:asexual dwarfism --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:asexual dwarfism | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:ataxia, spastic, with congenital miosis --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:ataxia, spastic, with congenital miosis | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:atrioventricular septal defect, blepharophimosis, radial and anal defect syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:atrioventricular septal defect, blepharophimosis, radial and anal defect syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:atrophic --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:atrophic | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:autosomal dominant cystoid macular edema --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:autosomal dominant cystoid macular edema | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:autosomal dominant intermediate charcot-marie-tooth disease type e --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:autosomal dominant intermediate charcot-marie-tooth disease type e | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:autosomal dominant pterygium of conjunctiva --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:autosomal dominant pterygium of conjunctiva | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:autosomal recessive cerebellar ataxia with saccadic intrusion syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:autosomal recessive cerebellar ataxia with saccadic intrusion syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:autosomal recessive cerebellar ataxia, pyramidal signs, nystagmus, oculomotor apraxia syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:autosomal recessive cerebellar ataxia, pyramidal signs, nystagmus, oculomotor apraxia syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:basal ganglia disease, biotin-responsive --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:basal ganglia disease, biotin-responsive | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:behr syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:behr syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:behrens baumann dust syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:behrens baumann dust syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:benign congenital myopathy --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:benign congenital myopathy | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:biallelic rpe65 mutation associated retinal dystrophy --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:biallelic rpe65 mutation associated retinal dystrophy | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:bleeding disorder due to p2ry12 defect --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:bleeding disorder due to p2ry12 defect | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:blepharophimosis with ptosis, syndactyly, and short stature --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:blepharophimosis with ptosis, syndactyly, and short stature | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:blepharoptosis, myopia, ectopia lentis syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:blepharoptosis, myopia, ectopia lentis syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:blindness, scoliosis, arachnodactyly syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:blindness, scoliosis, arachnodactyly syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:bornholm eye disease --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:bornholm eye disease | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:brittle cornea syndrome 1 --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:brittle cornea syndrome 1 | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:cahmr syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:cahmr syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:calcaneus, talipes --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:calcaneus, talipes | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:cap myopathy --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:cap myopathy | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:cataract and cardiomyopathy --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:cataract and cardiomyopathy | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:cataract glaucoma syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:cataract glaucoma syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:cataract microcornea syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:cataract microcornea syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:cataract, congenital heart disease, neural tube defect syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:cataract, congenital heart disease, neural tube defect syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:cataract, congenital, cerulean type 1 --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:cataract, congenital, cerulean type 1 | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:cerebellar ataxia, areflexia, pes cavus, optic atrophy, sensorineural hearing loss syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:cerebellar ataxia, areflexia, pes cavus, optic atrophy, sensorineural hearing loss syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:cerebellar ataxia, intellectual disability, oculomotor apraxia, cerebellar cysts syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:cerebellar ataxia, intellectual disability, oculomotor apraxia, cerebellar cysts syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:cerebroretinal microangiopathy with calcifications and cysts (disorder) --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:cerebroretinal microangiopathy with calcifications and cysts (disorder) | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:charcot-marie-tooth disease type 4 --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:charcot-marie-tooth disease type 4 | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:charcot-marie-tooth disease, dominant intermediate a --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:charcot-marie-tooth disease, dominant intermediate a | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:charcot-marie-tooth disease, dominant intermediate b (disorder) --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:charcot-marie-tooth disease, dominant intermediate b (disorder) | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:charcot-marie-tooth disease, dominant intermediate c --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:charcot-marie-tooth disease, dominant intermediate c | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:charcot-marie-tooth disease, dominant intermediate d --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:charcot-marie-tooth disease, dominant intermediate d | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:charcot-marie-tooth neuropathy x type 1 --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:charcot-marie-tooth neuropathy x type 1 | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:choriocapillaris atrophy --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:choriocapillaris atrophy | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:chorioretinal degeneration --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:chorioretinal degeneration | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:choroidal sclerosis --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:choroidal sclerosis | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:chronic diarrhea due to glucoamylase deficiency --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:chronic diarrhea due to glucoamylase deficiency | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:cochleosaccular degeneration of the inner ear and progressive cataracts --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:cochleosaccular degeneration of the inner ear and progressive cataracts | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:coloboma of macula with type b brachydactyly --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:coloboma of macula with type b brachydactyly | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:colobomatous microphthalmia, rhizomelic dysplasia syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:colobomatous microphthalmia, rhizomelic dysplasia syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:combined pancreatic lipase and colipase deficiency --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:combined pancreatic lipase and colipase deficiency | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital abnormality --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital abnormality | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital absence of right upper limb --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital absence of right upper limb | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital accessory skin tag --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital accessory skin tag | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital achalasia of esophagus --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital achalasia of esophagus | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital alpha-2-antiplasmin deficiency --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital alpha-2-antiplasmin deficiency | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital anal fissure --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital anal fissure | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital analbuminemia --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital analbuminemia | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital and developmental myasthenia --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital and developmental myasthenia | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital anemia --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital anemia | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital anomaly of mother complicating pregnancy --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital anomaly of mother complicating pregnancy | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital anomaly of right sternocleidomastoid muscle --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital anomaly of right sternocleidomastoid muscle | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital anomaly of vagina --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital anomaly of vagina | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital anomaly of vulva --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital anomaly of vulva | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital anterior subcapsular polar cataract --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital anterior subcapsular polar cataract | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital arcus juvenilis --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital arcus juvenilis | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital atrophy of left lobe of liver --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital atrophy of left lobe of liver | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital atrophy of optic nerve --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital atrophy of optic nerve | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital atrophy of thyroid --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital atrophy of thyroid | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital auditory imperception --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital auditory imperception | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital axial myopia --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital axial myopia | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital biliary tract disorder --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital biliary tract disorder | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital blepharophimosis --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital blepharophimosis | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital blepharophimosis of lower eyelid --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital blepharophimosis of lower eyelid | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital blepharophimosis of upper eyelid --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital blepharophimosis of upper eyelid | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital blocked tear duct --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital blocked tear duct | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital blood disorder --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital blood disorder | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital brain damage --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital brain damage | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital calcium pyrophosphate dihydrate crystal deposition disease --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital calcium pyrophosphate dihydrate crystal deposition disease | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital cardiovascular disorder --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital cardiovascular disorder | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital cardiovascular disorders during pregnancy, childbirth and the puerperium --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital cardiovascular disorders during pregnancy, childbirth and the puerperium | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital cataract ichthyosis syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital cataract ichthyosis syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital cataract with ataxia and deafness syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital cataract with ataxia and deafness syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital cataracts, facial dysmorphism, and neuropathy --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital cataracts, facial dysmorphism, and neuropathy | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital celiac disease --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital celiac disease | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital cerebellar cortical atrophy --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital cerebellar cortical atrophy | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital chalasia of esophagus --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital chalasia of esophagus | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital choroidal fold --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital choroidal fold | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital chromosomal disease --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital chromosomal disease | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital chylothorax --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital chylothorax | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital color blindness --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital color blindness | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital connective tissue disorder --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital connective tissue disorder | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital constriction of pylorus --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital constriction of pylorus | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital contracture of gastrocnemius muscle --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital contracture of gastrocnemius muscle | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital cutaneous angiomatosis --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital cutaneous angiomatosis | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital cyst of orbit --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital cyst of orbit | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital cyst of vulva --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital cyst of vulva | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital dacryocele --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital dacryocele | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital debility of fetus --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital debility of fetus | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital digestive system disorder --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital digestive system disorder | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital disease of brain --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital disease of brain | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital disorder of facial nerve --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital disorder of facial nerve | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital disorder of gallbladder and biliary tract --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital disorder of gallbladder and biliary tract | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital diverticulitis of small intestine --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital diverticulitis of small intestine | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital dysarthria --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital dysarthria | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital dysphasia --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital dysphasia | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital ear disorder --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital ear disorder | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital elephantiasis --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital elephantiasis | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital end-plate acetylcholinesterase deficiency --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital end-plate acetylcholinesterase deficiency | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital esotropia --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital esotropia | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital exophthalmos --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital exophthalmos | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital eye disorder --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital eye disorder | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital facial asymmetry --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital facial asymmetry | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital fecaliths --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital fecaliths | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital fecaliths causing obstruction --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital fecaliths causing obstruction | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital fibrinogen abnormality --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital fibrinogen abnormality | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital fissure of tongue --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital fissure of tongue | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital flat foot --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital flat foot | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital forefoot varus --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital forefoot varus | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital functional disorders of the colon --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital functional disorders of the colon | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital functional disorders of the small intestine --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital functional disorders of the small intestine | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital genu valgum of left knee --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital genu valgum of left knee | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital hearing disorder --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital hearing disorder | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital hepatic fibrosis --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital hepatic fibrosis | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital hepatic porphyria --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital hepatic porphyria | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital hepatomegaly --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital hepatomegaly | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital hereditary facial paralysis with variable hearing loss syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital hereditary facial paralysis with variable hearing loss syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital hernia of bladder --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital hernia of bladder | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital hydrocele --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital hydrocele | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital hydrosalpinx --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital hydrosalpinx | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital hypertonia --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital hypertonia | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital hypogonadotropic hypogonadism --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital hypogonadotropic hypogonadism | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital hypothyroidism --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital hypothyroidism | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital immunodeficiency disease --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital immunodeficiency disease | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital infectious disease --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital infectious disease | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital inguinal hernia --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital inguinal hernia | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital ischemic atrophy of central nervous system structure --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital ischemic atrophy of central nervous system structure | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital keratoderma --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital keratoderma | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital kidney disorder --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital kidney disorder | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital kyphoscoliosis --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital kyphoscoliosis | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital kyphosis --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital kyphosis | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital laryngeal abductor palsy --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital laryngeal abductor palsy | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital laryngeal adductor palsy --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital laryngeal adductor palsy | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital leptin deficiency --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital leptin deficiency | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital leptomeningeal angiomatosis --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital leptomeningeal angiomatosis | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital long qt syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital long qt syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital malalignment of the toenails --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital malalignment of the toenails | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital male infertility --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital male infertility | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital malignant melanoma --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital malignant melanoma | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital malposition of eyelid --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital malposition of eyelid | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital megaprepuce --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital megaprepuce | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital melanosis --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital melanosis | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital membranous nephropathy due to maternal anti-neutral endopeptidase alloimmunization --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital membranous nephropathy due to maternal anti-neutral endopeptidase alloimmunization | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital meningocele --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital meningocele | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital methemoglobinemia --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital methemoglobinemia | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital monosaccharide malabsorption --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital monosaccharide malabsorption | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital muscle disorder --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital muscle disorder | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital muscular dystrophy with infantile cataract and hypogonadism syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital muscular dystrophy with infantile cataract and hypogonadism syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital myasthenic syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital myasthenic syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital myotonic dystrophy --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital myotonic dystrophy | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital nasolacrimal duct obstruction --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital nasolacrimal duct obstruction | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital nephritis --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital nephritis | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital nephrotic syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital nephrotic syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital neurogenic ileus syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital neurogenic ileus syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital neurologic anomalies --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital neurologic anomalies | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital neutrophil actin dysfunction --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital neutrophil actin dysfunction | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital nystagmus --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital nystagmus | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital obstruction of aqueduct of sylvius --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital obstruction of aqueduct of sylvius | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital obstruction of bile duct --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital obstruction of bile duct | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital obstruction of bladder neck --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital obstruction of bladder neck | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital obstruction of large intestine --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital obstruction of large intestine | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital obstruction of small intestine --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital obstruction of small intestine | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital obstruction of urethra --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital obstruction of urethra | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital occlusion of ureter --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital occlusion of ureter | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital onychoatrophy --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital onychoatrophy | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital oral/facial/cranial defect --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital oral/facial/cranial defect | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital palato-esophageal incoordination --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital palato-esophageal incoordination | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital pancreatic trypsin deficiency --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital pancreatic trypsin deficiency | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital paraplegia --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital paraplegia | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital pelviureteric junction obstruction --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital pelviureteric junction obstruction | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital pes cavus --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital pes cavus | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital plasminogen activator inhibitor deficiency type 1 --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital plasminogen activator inhibitor deficiency type 1 | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital pneumonia --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital pneumonia | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital porencephalic cyst --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital porencephalic cyst | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital positional talipes --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital positional talipes | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital posterior subcapsular polar cataract --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital posterior subcapsular polar cataract | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital pseudobulbar palsy --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital pseudobulbar palsy | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital pseudoporencephaly --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital pseudoporencephaly | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital pseudostrabismus --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital pseudostrabismus | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital pterygium of nail --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital pterygium of nail | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital quadriplegia --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital quadriplegia | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital qualifier --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital qualifier | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital rearfoot varus --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital rearfoot varus | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital rectal fissure --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital rectal fissure | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital renal atrophy --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital renal atrophy | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital reproductive system disorder --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital reproductive system disorder | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital respiratory disorder --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital respiratory disorder | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital retinoschisis --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital retinoschisis | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital scoliosis due to bony malformation --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital scoliosis due to bony malformation | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital secondary hydronephrosis --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital secondary hydronephrosis | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital secretory diarrhea --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital secretory diarrhea | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital sequelae of disorders --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital sequelae of disorders | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital single renal cyst --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital single renal cyst | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital sixth nerve palsy --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital sixth nerve palsy | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital skeletal disorder --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital skeletal disorder | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital skin contracture --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital skin contracture | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital spastic foot --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital spastic foot | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital stenosis --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital stenosis | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital sutural cataract --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital sutural cataract | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital syringomyelia --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital syringomyelia | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital talipes calcaneovalgus --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital talipes calcaneovalgus | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital talipes equinus --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital talipes equinus | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital talipes varus --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital talipes varus | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital thrombocytopenia --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital thrombocytopenia | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital uremia --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital uremia | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital ureterovesical junction obstruction --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital ureterovesical junction obstruction | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital velopharyngeal dysfunction --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital velopharyngeal dysfunction | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital viral hepatitis --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital viral hepatitis | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital vocal cord palsy --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital vocal cord palsy | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital volvulus of stomach --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital volvulus of stomach | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital von willebrand's disease --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital von willebrand's disease | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:congenital/genetic syndrome with poikiloderma --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital/genetic syndrome with poikiloderma | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:cor biloculare --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:cor biloculare | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:corneal dystrophy, endothelial, x-linked --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:corneal dystrophy, endothelial, x-linked | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:corneal hypesthesia, familial --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:corneal hypesthesia, familial | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:corpus callosum, agenesis of, with mental retardation, ocular coloboma, and micrognathia --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:corpus callosum, agenesis of, with mental retardation, ocular coloboma, and micrognathia | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:cortical blindness, intellectual disability, polydactyly syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:cortical blindness, intellectual disability, polydactyly syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:crome syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:crome syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:cryptophthalmos syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:cryptophthalmos syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:cyanotic congenital heart disease --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:cyanotic congenital heart disease | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:deafness and myopia syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:deafness and myopia syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:deafness, encephaloneuropathy, obesity, valvulopathy syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:deafness, encephaloneuropathy, obesity, valvulopathy syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:dental arch length loss secondary to congenitally missing teeth --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:dental arch length loss secondary to congenitally missing teeth | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:dental midlines coincident and incorrect --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:dental midlines coincident and incorrect | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:dermoids of cornea --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:dermoids of cornea | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:diarrhea 4, malabsorptive, congenital --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:diarrhea 4, malabsorptive, congenital | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:diffuse palmoplantar keratoderma and acrocyanosis syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:diffuse palmoplantar keratoderma and acrocyanosis syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:diffuse secondary choroid atrophy --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:diffuse secondary choroid atrophy | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:digeorge syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:digeorge syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:double orifice of right atrioventricular valve in double inlet ventricle --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:double orifice of right atrioventricular valve in double inlet ventricle | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:duane anomaly, myopathy, scoliosis syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:duane anomaly, myopathy, scoliosis syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:duplication of eyebrow and syndactyly syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:duplication of eyebrow and syndactyly syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:ectodermal dysplasia with blindness syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:ectodermal dysplasia with blindness syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:ectopia lentis, chorioretinal dystrophy, myopia syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:ectopia lentis, chorioretinal dystrophy, myopia syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:ectopic bone tissue congenital --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:ectopic bone tissue congenital | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:edict syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:edict syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:encephalopathy due to sulfite oxidase deficiency --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:encephalopathy due to sulfite oxidase deficiency | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:encephalopathy, intracerebral calcification, retinal degeneration syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:encephalopathy, intracerebral calcification, retinal degeneration syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:epidermoid cyst of spleen --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:epidermoid cyst of spleen | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:epilepsy telangiectasia syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:epilepsy telangiectasia syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:epilepsy, partial, with variable foci --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:epilepsy, partial, with variable foci | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:erythema palmare hereditarium --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:erythema palmare hereditarium | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:erythrocyte lactate transporter defect --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:erythrocyte lactate transporter defect | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:extensive congenital erosions, vesicles and reticulate scarring --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:extensive congenital erosions, vesicles and reticulate scarring | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:facial dysmorphism, macrocephaly, myopia, dandy-walker malformation syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:facial dysmorphism, macrocephaly, myopia, dandy-walker malformation syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:factor xi deficiency --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:factor xi deficiency | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:familial aplasia of the vermis --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:familial aplasia of the vermis | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:familial hypophosphatemic rickets --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:familial hypophosphatemic rickets | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:familial isolated trichomegaly --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:familial isolated trichomegaly | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:familial nasal acilia --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:familial nasal acilia | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:fetal congenital tumor causing disproportion --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:fetal congenital tumor causing disproportion | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:fetal disorder --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:fetal disorder | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:flatfoot, rigid --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:flatfoot, rigid | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:fleck retina of kandori --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:fleck retina of kandori | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:focal palmoplantar and gingival keratoderma --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:focal palmoplantar and gingival keratoderma | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:foramen ovale, patent --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:foramen ovale, patent | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:fordyce's disease --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:fordyce's disease | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:foxg1 syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:foxg1 syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:gaze palsy, familial horizontal, with progressive scoliosis, 1 --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:gaze palsy, familial horizontal, with progressive scoliosis, 1 | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:gelatinous atrioventricular valve leaflet in atrioventricular septal defect --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:gelatinous atrioventricular valve leaflet in atrioventricular septal defect | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:gemss syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:gemss syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:generalized congenital intestinal dysmotility --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:generalized congenital intestinal dysmotility | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:glaucoma and sleep apnea syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:glaucoma and sleep apnea syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:gnmt deficiency --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:gnmt deficiency | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:goniodysgenesis-mental retardation-short stature syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:goniodysgenesis-mental retardation-short stature syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:growth retardation, alopecia, pseudoanodontia and optic atrophy --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:growth retardation, alopecia, pseudoanodontia and optic atrophy | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:gyrate atrophy --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:gyrate atrophy | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:heide syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:heide syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:hemifacial hyperplasia with strabismus --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:hemifacial hyperplasia with strabismus | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:hemophilia b --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:hemophilia b | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:hereditary anetoderma --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:hereditary anetoderma | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:hereditary choroidal dystrophy --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:hereditary choroidal dystrophy | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:hereditary corneal dystrophy --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:hereditary corneal dystrophy | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:hereditary disorder of endocrine system --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:hereditary disorder of endocrine system | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:hereditary hemoglobinopathy --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:hereditary hemoglobinopathy | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:hereditary optic atrophy --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:hereditary optic atrophy | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:hereditary retinal dystrophy --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:hereditary retinal dystrophy | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:hereditary sensory autonomic neuropathy, type 5 --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:hereditary sensory autonomic neuropathy, type 5 | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:hereditary vascular retinopathy --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:hereditary vascular retinopathy | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:hereditary vitreoretinopathy --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:hereditary vitreoretinopathy | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:hereditary x linked recessive spastic paraplegia --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:hereditary x linked recessive spastic paraplegia | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:hernandez fragoso syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:hernandez fragoso syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:hutch diverticulum --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:hutch diverticulum | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:hydrophthalmos --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:hydrophthalmos | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:hyperammonemic encephalopathy due to carbonic anhydrase va deficiency --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:hyperammonemic encephalopathy due to carbonic anhydrase va deficiency | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:hyperferritinemia, hereditary, with congenital cataracts --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:hyperferritinemia, hereditary, with congenital cataracts | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:hypermethioninemia encephalopathy due to deficiency of adenosine kinase --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:hypermethioninemia encephalopathy due to deficiency of adenosine kinase | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:hypogonadism-cataract syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:hypogonadism-cataract syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:hypoplasia and coloboma of alar cartilage with telecanthus syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:hypoplasia and coloboma of alar cartilage with telecanthus syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:hypospadias, hypertelorism, coloboma, deafness syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:hypospadias, hypertelorism, coloboma, deafness syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:hypotrichosis with juvenile macular degeneration syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:hypotrichosis with juvenile macular degeneration syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:ichthyosiform erythroderma, congenital --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:ichthyosiform erythroderma, congenital | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:inborn errors of metabolism --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:inborn errors of metabolism | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:inclusion body myopathy 3, autosomal dominant --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:inclusion body myopathy 3, autosomal dominant | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:infant metachromatic leukodystrophies --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:infant metachromatic leukodystrophies | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:infantile myofibromatosis --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:infantile myofibromatosis | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:intellectual disability with cataract and kyphosis syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:intellectual disability with cataract and kyphosis syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:intellectual disability, alacrima, achalasia syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:intellectual disability, alacrima, achalasia syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:intestinal epithelial dysplasia --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:intestinal epithelial dysplasia | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:isolated congenital alacrima --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:isolated congenital alacrima | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:isolated congenital megalocornea --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:isolated congenital megalocornea | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:isolated cryptophthalmos --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:isolated cryptophthalmos | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:isolated optic nerve hypoplasia --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:isolated optic nerve hypoplasia | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:joubert syndrome with ocular defect --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:joubert syndrome with ocular defect | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:juvenile cataract, microcornea, renal glucosuria syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:juvenile cataract, microcornea, renal glucosuria syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:kallmann syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:kallmann syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:karandikar maria kamble syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:karandikar maria kamble syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:kaufman oculocerebrofacial syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:kaufman oculocerebrofacial syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:keratitis, hereditary --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:keratitis, hereditary | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:keratosis pilaris with ichthyosis and deafness --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:keratosis pilaris with ichthyosis and deafness | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:knobloch syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:knobloch syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:krasnow qazi syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:krasnow qazi syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:lactase deficiency, congenital --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:lactase deficiency, congenital | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:leber congenital amaurosis --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:leber congenital amaurosis | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:left atrioventricular valve bifoliate with fused left sided superior and inferior bridging leaflet --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:left atrioventricular valve bifoliate with fused left sided superior and inferior bridging leaflet | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:lethal congenital erythroderma --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:lethal congenital erythroderma | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:leukoencephalopathy with brain stem and spinal cord involvement and high lactate syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:leukoencephalopathy with brain stem and spinal cord involvement and high lactate syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:leukoencephalopathy, ataxia, hypodontia, hypomyelination syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:leukoencephalopathy, ataxia, hypodontia, hypomyelination syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:leukoencephalopathy, thalamus and brainstem anomalies, high lactate syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:leukoencephalopathy, thalamus and brainstem anomalies, high lactate syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:longitudinal deficiency of limb --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:longitudinal deficiency of limb | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:longitudinal deficiency of part of limb --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:longitudinal deficiency of part of limb | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:lopes gorlin syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:lopes gorlin syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:lowry maclean syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:lowry maclean syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:mackay shek carr syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:mackay shek carr syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:macrosomia obesity macrocephaly ocular abnormalities --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:macrosomia obesity macrocephaly ocular abnormalities | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:macrostomia, preauricular tag, external ophthalmoplegia syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:macrostomia, preauricular tag, external ophthalmoplegia syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:macular coloboma, cleft palate, hallux valgus syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:macular coloboma, cleft palate, hallux valgus syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:martsolf syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:martsolf syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:median nodule of upper lip --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:median nodule of upper lip | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:methylmalonic acidemia due to methylmalonyl-coenzyme a epimerase deficiency --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:methylmalonic acidemia due to methylmalonyl-coenzyme a epimerase deficiency | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:microbrachycephaly, ptosis, cleft lip syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:microbrachycephaly, ptosis, cleft lip syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:microcornea with corectopia and macular hypoplasia syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:microcornea with corectopia and macular hypoplasia syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:microcornea with glaucoma and absent frontal sinus syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:microcornea with glaucoma and absent frontal sinus syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:microphthalmia, syndromic 1 --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:microphthalmia, syndromic 1 | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:microphthalmia, syndromic 10 --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:microphthalmia, syndromic 10 | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:microphthalmia, syndromic 3 --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:microphthalmia, syndromic 3 | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:microphthalmia, syndromic 4 (disorder) --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:microphthalmia, syndromic 4 (disorder) | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:microphthalmia, syndromic 5 --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:microphthalmia, syndromic 5 | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:microphthalmia, syndromic 6 (disorder) --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:microphthalmia, syndromic 6 (disorder) | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:microphthalmia, syndromic 7 --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:microphthalmia, syndromic 7 | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:microtia with nasolacrimal duct imperforation and eye coloboma --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:microtia with nasolacrimal duct imperforation and eye coloboma | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:microvillus inclusion disease --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:microvillus inclusion disease | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:mitochondrial neurogastrointestinal encephalomyopathy syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:mitochondrial neurogastrointestinal encephalomyopathy syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:mobius ii syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:mobius ii syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:mottled teeth, congenital --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:mottled teeth, congenital | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:multifocal pattern dystrophy of retinal pigment epithelium simulating fundus flavimaculatus --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:multifocal pattern dystrophy of retinal pigment epithelium simulating fundus flavimaculatus | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:multiple supernumerary teeth unrelated to systemic condition --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:multiple supernumerary teeth unrelated to systemic condition | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:muscle filaminopathy --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:muscle filaminopathy | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:muscular dystrophy, oculopharyngeal --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:muscular dystrophy, oculopharyngeal | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:mydriasis, congenital --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:mydriasis, congenital | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:myelocele --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:myelocele | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:myopathy with hexagonally cross-linked tubular arrays --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:myopathy with hexagonally cross-linked tubular arrays | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:myopic conus --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:myopic conus | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:myosclerosis --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:myosclerosis | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:myostatin-related muscle hypertrophy --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:myostatin-related muscle hypertrophy | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:myotonia congenita --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:myotonia congenita | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:nance-horan syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:nance-horan syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:nasopalpebral lipoma coloboma syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:nasopalpebral lipoma coloboma syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:nathalie syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:nathalie syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:neonatal intestinal perforation with in utero intraluminal obstruction --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:neonatal intestinal perforation with in utero intraluminal obstruction | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:nephrogenic syndrome of inappropriate antidiuresis --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:nephrogenic syndrome of inappropriate antidiuresis | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:neuhauser syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:neuhauser syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:night blindness, congenital stationary --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:night blindness, congenital stationary | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:nonfenestrated interatrial communication within oval fossa --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:nonfenestrated interatrial communication within oval fossa | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:norrie disease --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:norrie disease | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:obstructed interchordal space of tricuspid chordae tendinae --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:obstructed interchordal space of tricuspid chordae tendinae | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:obstructed pulmonary venous connection at coronary sinus orifice --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:obstructed pulmonary venous connection at coronary sinus orifice | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:oculoauricular syndrome schorderet type --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:oculoauricular syndrome schorderet type | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:oculopharyngodistal myopathy --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:oculopharyngodistal myopathy | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:ohdo syndrome, maat-kievit-brunner type --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:ohdo syndrome, maat-kievit-brunner type | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:okihiro syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:okihiro syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:oliver-mcfarlane syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:oliver-mcfarlane syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:orofaciodigital syndrome 9 --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:orofaciodigital syndrome 9 | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:osteopoikilosis and dacryocystitis --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:osteopoikilosis and dacryocystitis | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:otulin-related autoinflammatory syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:otulin-related autoinflammatory syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:palmoplantar keratoderma nagashima type --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:palmoplantar keratoderma nagashima type | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:palmoplantar porokeratosis --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:palmoplantar porokeratosis | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:parachute malformation of common atrioventricular valve --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:parachute malformation of common atrioventricular valve | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:parachute malformation of left atrioventricular valve --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:parachute malformation of left atrioventricular valve | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:parachute malformation of right atrioventricular valve --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:parachute malformation of right atrioventricular valve | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:paraganglioma and gastric stromal sarcoma --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:paraganglioma and gastric stromal sarcoma | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:paravenous chorioretinal atrophy --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:paravenous chorioretinal atrophy | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:pericellular fibrosis of congenital syphilis --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:pericellular fibrosis of congenital syphilis | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:peripapillary atrophy --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:peripapillary atrophy | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:peripapillary chorioretinal atrophy --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:peripapillary chorioretinal atrophy | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:peripapillary crescent --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:peripapillary crescent | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:peters-plus syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:peters-plus syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:pfeiffer mayer syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:pfeiffer mayer syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:pierson syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:pierson syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:pigmentary retinal dystrophy --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:pigmentary retinal dystrophy | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:placenta previa centralis --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:placenta previa centralis | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:platelet storage pool deficiency --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:platelet storage pool deficiency | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:polydactyly, postaxial, with progressive myopia --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:polydactyly, postaxial, with progressive myopia | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:porphyria, erythropoietic --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:porphyria, erythropoietic | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:posterior deviation of infundibular septum of obstructive aortic arch type --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:posterior deviation of infundibular septum of obstructive aortic arch type | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:posterior fusion of lumbosacral vertebrae and blepharoptosis syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:posterior fusion of lumbosacral vertebrae and blepharoptosis syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:prader-willi syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:prader-willi syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:precocious exfoliation of teeth related to idiopathic root resorption --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:precocious exfoliation of teeth related to idiopathic root resorption | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:precocious exfoliation of teeth related to root resorption associated with trauma --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:precocious exfoliation of teeth related to root resorption associated with trauma | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:primary left ventricular endocardial fibroelastosis --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:primary left ventricular endocardial fibroelastosis | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:primary refluxing megaureter --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:primary refluxing megaureter | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:primrose syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:primrose syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:progressive external ophthalmoplegia, myopathy, emaciation syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:progressive external ophthalmoplegia, myopathy, emaciation syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:progressive supranuclear palsy --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:progressive supranuclear palsy | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:prolonged electroretinal response suppression --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:prolonged electroretinal response suppression | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:prominent valve of inferior vena cava --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:prominent valve of inferior vena cava | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:pseudomonas pyocyaneus congenital infection --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:pseudomonas pyocyaneus congenital infection | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:ptosis, strabismus, and ectopic pupils --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:ptosis, strabismus, and ectopic pupils | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:ptosis, upper ocular movement limitation, absence of lacrimal punctum syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:ptosis, upper ocular movement limitation, absence of lacrimal punctum syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:pulmonary alveolar proteinosis, congenital --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:pulmonary alveolar proteinosis, congenital | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:pulmonary valve overriding ventricular septum --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:pulmonary valve overriding ventricular septum | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:pulmonic stenosis and congenital nephrosis --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:pulmonic stenosis and congenital nephrosis | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:pure mitochondrial myopathy --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:pure mitochondrial myopathy | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:rambaud gallian syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:rambaud gallian syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:redundant prepuce --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:redundant prepuce | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:regional congenital anomaly --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:regional congenital anomaly | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:renal coloboma syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:renal coloboma syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:reticulate acropigmentation of kitamura --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:reticulate acropigmentation of kitamura | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:retinal arterial macroaneurysm with supravalvular pulmonic stenosis --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:retinal arterial macroaneurysm with supravalvular pulmonic stenosis | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:retinal degeneration --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:retinal degeneration | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:revesz syndrome (disorder) --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:revesz syndrome (disorder) | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:right atrial appendage - left - juxtaposition --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:right atrial appendage - left - juxtaposition | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:right atrial appendage absent --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:right atrial appendage absent | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:right atrial endocardial fibroelastosis --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:right atrial endocardial fibroelastosis | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:right inferior caval vein connecting to left atrium and right atrium --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:right inferior caval vein connecting to left atrium and right atrium | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:right inferior caval vein connecting to left sided atrium --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:right inferior caval vein connecting to left sided atrium | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:right ventricular myocardial sinusoids --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:right ventricular myocardial sinusoids | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:right-sided pulmonary arterial trunk --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:right-sided pulmonary arterial trunk | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:ring dermoid of cornea --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:ring dermoid of cornea | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:robinow-like syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:robinow-like syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:rolandic epilepsy, speech dyspraxia syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:rolandic epilepsy, speech dyspraxia syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:rotation of tooth --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:rotation of tooth | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:rudimentary left ventricle --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:rudimentary left ventricle | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:schaap taylor baraitser syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:schaap taylor baraitser syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:seemanova lesny syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:seemanova lesny syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:senile atrophy of choroid --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:senile atrophy of choroid | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:sensory ataxic neuropathy, dysarthria, and ophthalmoparesis --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:sensory ataxic neuropathy, dysarthria, and ophthalmoparesis | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:severe x-linked intellectual disability gustavson type --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:severe x-linked intellectual disability gustavson type | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:short stature and locking fingers --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:short stature and locking fingers | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:shortened trunk --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:shortened trunk | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:siegler brewer carey syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:siegler brewer carey syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:skin abnormalities --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:skin abnormalities | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:slowed nerve conduction velocity, autosomal dominant --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:slowed nerve conduction velocity, autosomal dominant | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:smith-lemli-opitz syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:smith-lemli-opitz syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:spastic paraplegia, glaucoma, intellectual disability syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:spastic paraplegia, glaucoma, intellectual disability syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:spectrin-associated autosomal recessive cerebellar ataxia --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:spectrin-associated autosomal recessive cerebellar ataxia | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:spheroid body myopathy --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:spheroid body myopathy | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:spinal hydromeningocele --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:spinal hydromeningocele | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:spinal muscular atrophy, dandy-walker malformation, cataract syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:spinal muscular atrophy, dandy-walker malformation, cataract syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:spinal muscular atrophy, distal, congenital nonprogressive (disorder) --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:spinal muscular atrophy, distal, congenital nonprogressive (disorder) | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:spinocerebellar ataxia, autosomal recessive 1 --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:spinocerebellar ataxia, autosomal recessive 1 | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:spinocerebellar ataxia, autosomal recessive 5 --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:spinocerebellar ataxia, autosomal recessive 5 | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:spleen in right sided position --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:spleen in right sided position | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:split-hand with congenital nystagmus, fundal changes, and cataracts --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:split-hand with congenital nystagmus, fundal changes, and cataracts | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:spondylo-ocular syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:spondylo-ocular syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:spondyloepiphyseal dysplasia macdermot type --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:spondyloepiphyseal dysplasia macdermot type | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:spondyloepiphyseal dysplasia, craniosynostosis, cleft palate, cataract and intellectual disability syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:spondyloepiphyseal dysplasia, craniosynostosis, cleft palate, cataract and intellectual disability syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:stomach in central position --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:stomach in central position | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:stomach in right sided position --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:stomach in right sided position | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:striate palmoplantar keratoderma --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:striate palmoplantar keratoderma | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:sveinsson chorioretinal atrophy --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:sveinsson chorioretinal atrophy | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:syndromic orbital border hypoplasia --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:syndromic orbital border hypoplasia | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:systemic venovenous collateral vein --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:systemic venovenous collateral vein | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:telecanthus --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:telecanthus | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:temtamy syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:temtamy syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:ter haar syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:ter haar syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:toe syndactyly, telecanthus, and anogenital and renal malformations --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:toe syndactyly, telecanthus, and anogenital and renal malformations | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:tooth abnormalities --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:tooth abnormalities | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:tricuspid but functionally bicuspid aortic valve --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:tricuspid but functionally bicuspid aortic valve | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:tricuspid valve primary chords absent --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:tricuspid valve primary chords absent | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:trifoliate left atrioventricular valve --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:trifoliate left atrioventricular valve | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:tripartite right ventricle --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:tripartite right ventricle | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:true cleft of common atrioventricular valve leaflet --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:true cleft of common atrioventricular valve leaflet | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:truncal valve overriding ventricular septum --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:truncal valve overriding ventricular septum | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:unipartite right ventricle --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:unipartite right ventricle | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:upper esophageal web --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:upper esophageal web | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:upper limb defect with eye and ear abnormalities syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:upper limb defect with eye and ear abnormalities syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:urachal cyst --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:urachal cyst | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:uveal coloboma with cleft lip and palate and intellectual disability syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:uveal coloboma with cleft lip and palate and intellectual disability syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:vasculopathy, retinal, with cerebral leukodystrophy --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:vasculopathy, retinal, with cerebral leukodystrophy | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:verloes van maldergem marneffe syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:verloes van maldergem marneffe syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:vici syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:vici syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:visceral myopathy familial external ophthalmoplegia --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:visceral myopathy familial external ophthalmoplegia | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:vitamin d-dependent rickets, type 1 --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:vitamin d-dependent rickets, type 1 | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:von willebrand disease, platelet type --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:von willebrand disease, platelet type | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:waardenburg anophthalmia syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:waardenburg anophthalmia syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:wagr syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:wagr syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:wellesley carman french syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:wellesley carman french syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:white forelock with malformations --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:white forelock with malformations | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:williams syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:williams syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:x-linked distal spinal muscular atrophy type 3 --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:x-linked distal spinal muscular atrophy type 3 | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:x-linked non progressive cerebellar ataxia --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:x-linked non progressive cerebellar ataxia | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:x-linked retinal dysplasia --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:x-linked retinal dysplasia | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:xte syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:xte syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:yemenite deaf-blind hypopigmentation syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:yemenite deaf-blind hypopigmentation syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:zunich neuroectodermal syndrome --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=en:zunich neuroectodermal syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 hypogonadisme avec anosmie --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=hypogonadisme avec anosmie | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 paraveineuse --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=paraveineuse | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 scotopique --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=scotopique | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 vision photopique --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=vision photopique | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 vision scotopique --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=vision scotopique | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 électrorétinogramme --- r_associated #0: 20 --> en:pigmented paravenous chorioretinal atrophy n1=électrorétinogramme | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 Kallman --- r_associated #0: 15 --> en:pigmented paravenous chorioretinal atrophy n1=Kallman | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=15 débilité congénitale foetale --- r_associated #0: 15 --> en:pigmented paravenous chorioretinal atrophy n1=débilité congénitale foetale | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=15 rétinite pigmentaire liée au sexe récessive 3 --- r_associated #0: 15 --> en:pigmented paravenous chorioretinal atrophy n1=rétinite pigmentaire liée au sexe récessive 3 | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=15 syndrome de Kallman-de Morsier --- r_associated #0: 15 --> en:pigmented paravenous chorioretinal atrophy n1=syndrome de Kallman-de Morsier | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=15 syndrome de de Morsier-Kallmann --- r_associated #0: 15 --> en:pigmented paravenous chorioretinal atrophy n1=syndrome de de Morsier-Kallmann | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=15 Vision photopique --- r_associated #0: 10 --> en:pigmented paravenous chorioretinal atrophy n1=Vision photopique | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=10 Vision scotopique --- r_associated #0: 10 --> en:pigmented paravenous chorioretinal atrophy n1=Vision scotopique | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=10 anomalie congénitale de l'oeil --- r_associated #0: 10 --> en:pigmented paravenous chorioretinal atrophy n1=anomalie congénitale de l'oeil | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=10 arthrogrypose --- r_associated #0: 10 --> en:pigmented paravenous chorioretinal atrophy n1=arthrogrypose | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=10 choroïdose --- r_associated #0: 10 --> en:pigmented paravenous chorioretinal atrophy n1=choroïdose | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=10 dystrophie rétinienne héréditaire --- r_associated #0: 10 --> en:pigmented paravenous chorioretinal atrophy n1=dystrophie rétinienne héréditaire | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=10 débilité congénitale du foetus --- r_associated #0: 10 --> en:pigmented paravenous chorioretinal atrophy n1=débilité congénitale du foetus | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=10 déficience congénitale --- r_associated #0: 10 --> en:pigmented paravenous chorioretinal atrophy n1=déficience congénitale | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=10 déformation congénitale --- r_associated #0: 10 --> en:pigmented paravenous chorioretinal atrophy n1=déformation congénitale | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=10 en:Aicardi's syndrome --- r_associated #0: 10 --> en:pigmented paravenous chorioretinal atrophy n1=en:Aicardi's syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=10 en:Primrose syndrome --- r_associated #0: 10 --> en:pigmented paravenous chorioretinal atrophy n1=en:Primrose syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=10 myotonia congenita --- r_associated #0: 10 --> en:pigmented paravenous chorioretinal atrophy n1=myotonia congenita | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=10 myélocèle --- r_associated #0: 10 --> en:pigmented paravenous chorioretinal atrophy n1=myélocèle | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=10 rétinite pigmentaire --- r_associated #0: 10 --> en:pigmented paravenous chorioretinal atrophy n1=rétinite pigmentaire | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=10 rétinite pigmentaire péricentrale dominante --- r_associated #0: 10 --> en:pigmented paravenous chorioretinal atrophy n1=rétinite pigmentaire péricentrale dominante | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=10 rétinite pigmentaire péricentrale récessive --- r_associated #0: 10 --> en:pigmented paravenous chorioretinal atrophy n1=rétinite pigmentaire péricentrale récessive | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=10 rétinite pigmentaire-10 --- r_associated #0: 10 --> en:pigmented paravenous chorioretinal atrophy n1=rétinite pigmentaire-10 | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=10 rétinite pigmentaire-2 --- r_associated #0: 10 --> en:pigmented paravenous chorioretinal atrophy n1=rétinite pigmentaire-2 | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=10 rétinite pigmentaire-3 --- r_associated #0: 10 --> en:pigmented paravenous chorioretinal atrophy n1=rétinite pigmentaire-3 | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=10 rétinite pigmentaire-4 --- r_associated #0: 10 --> en:pigmented paravenous chorioretinal atrophy n1=rétinite pigmentaire-4 | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=10 rétinite pigmentaire-5 --- r_associated #0: 10 --> en:pigmented paravenous chorioretinal atrophy n1=rétinite pigmentaire-5 | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=10 rétinite pigmentaire-6 --- r_associated #0: 10 --> en:pigmented paravenous chorioretinal atrophy n1=rétinite pigmentaire-6 | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=10 rétinite pigmentaire-7 --- r_associated #0: 10 --> en:pigmented paravenous chorioretinal atrophy n1=rétinite pigmentaire-7 | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=10 rétinite pigmentaire-8 --- r_associated #0: 10 --> en:pigmented paravenous chorioretinal atrophy n1=rétinite pigmentaire-8 | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=10 rétinopathie pigmentaire --- r_associated #0: 10 --> en:pigmented paravenous chorioretinal atrophy n1=rétinopathie pigmentaire | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=10 syndrome de de Morsier --- r_associated #0: 10 --> en:pigmented paravenous chorioretinal atrophy n1=syndrome de de Morsier | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=10 anomalie congénitale --- r_associated #0: 5 --> en:pigmented paravenous chorioretinal atrophy n1=anomalie congénitale | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=5 dystrophie musculaire oculo-pharyngée --- r_associated #0: 5 --> en:pigmented paravenous chorioretinal atrophy n1=dystrophie musculaire oculo-pharyngée | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=5 dystrophie musculaire oculopharyngée --- r_associated #0: 5 --> en:pigmented paravenous chorioretinal atrophy n1=dystrophie musculaire oculopharyngée | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=5 en:congenital anomaly --- r_associated #0: 5 --> en:pigmented paravenous chorioretinal atrophy n1=en:congenital anomaly | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=5 malformation congénitale --- r_associated #0: 5 --> en:pigmented paravenous chorioretinal atrophy n1=malformation congénitale | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=5 méthémoglobinémie congénitale --- r_associated #0: 5 --> en:pigmented paravenous chorioretinal atrophy n1=méthémoglobinémie congénitale | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=5 non précisée, dystrophie rétinienne héréditaire --- r_associated #0: 5 --> en:pigmented paravenous chorioretinal atrophy n1=non précisée, dystrophie rétinienne héréditaire | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=5 syndrome olfacto-génital --- r_associated #0: 5 --> en:pigmented paravenous chorioretinal atrophy n1=syndrome olfacto-génital | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=5