'en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome'
(id=9103032 ; fe=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome ; type=1 ; niveau=200 ; luminosité=25 ; somme entrante=13537 creation date=2017-10-29 touchdate=2025-12-02 07:02:02.000)

≈ 628 relations sortantes en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 43 / 1 -> en:arthrogryposis-like hand anomaly and sensorineural deafness n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:arthrogryposis-like hand anomaly and sensorineural deafness | rel=r_associated | relid=0 | w=43 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 43 / 1 -> en:cleft palate with stapes fixation and oligodontia syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:cleft palate with stapes fixation and oligodontia syndrome | rel=r_associated | relid=0 | w=43 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 43 / 1 -> en:epilepsy, myoclonic, benign adult familial, type 2 n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:epilepsy, myoclonic, benign adult familial, type 2 | rel=r_associated | relid=0 | w=43 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 43 / 1 -> en:high tone sensori-neuronal hearing loss n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:high tone sensori-neuronal hearing loss | rel=r_associated | relid=0 | w=43 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 43 / 1 -> en:peutz-jeghers syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=43 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 43 / 1 -> en:shprintzen omphalocele syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:shprintzen omphalocele syndrome | rel=r_associated | relid=0 | w=43 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 43 / 1 -> en:spinocerebellar ataxia 17 n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:spinocerebellar ataxia 17 | rel=r_associated | relid=0 | w=43 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 42 / 0.977 -> en:acute intermittent porphyria n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:acute intermittent porphyria | rel=r_associated | relid=0 | w=42 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 42 / 0.977 -> en:albinism-deafness syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:albinism-deafness syndrome | rel=r_associated | relid=0 | w=42 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 42 / 0.977 -> en:amelogenesis imperfecta - hypoplastic autosomal dominant - smooth n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:amelogenesis imperfecta - hypoplastic autosomal dominant - smooth | rel=r_associated | relid=0 | w=42 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 42 / 0.977 -> en:congenital sensorineural hearing loss n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:congenital sensorineural hearing loss | rel=r_associated | relid=0 | w=42 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 42 / 0.977 -> en:cooper jabs syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:cooper jabs syndrome | rel=r_associated | relid=0 | w=42 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 42 / 0.977 -> en:lissencephaly due to tuba1a (tubulin alpha 1a) mutation n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:lissencephaly due to tuba1a (tubulin alpha 1a) mutation | rel=r_associated | relid=0 | w=42 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 42 / 0.977 -> en:vasculopathy, retinal, with cerebral leukodystrophy n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:vasculopathy, retinal, with cerebral leukodystrophy | rel=r_associated | relid=0 | w=42 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 41 / 0.953 -> en:autosomal dominant cerebellar ataxia, deafness, and narcolepsy n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness, and narcolepsy | rel=r_associated | relid=0 | w=41 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 41 / 0.953 -> en:cochleosaccular degeneration of the inner ear and progressive cataracts n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:cochleosaccular degeneration of the inner ear and progressive cataracts | rel=r_associated | relid=0 | w=41 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 41 / 0.953 -> en:dermoodontodysplasia n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:dermoodontodysplasia | rel=r_associated | relid=0 | w=41 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 41 / 0.953 -> en:finger-nose ataxia n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:finger-nose ataxia | rel=r_associated | relid=0 | w=41 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 41 / 0.953 -> en:hereditary cystatin c amyloid angiopathy n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:hereditary cystatin c amyloid angiopathy | rel=r_associated | relid=0 | w=41 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 41 / 0.953 -> en:heritable pulmonary arterial hypertension due to bmpr2 mutation n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:heritable pulmonary arterial hypertension due to bmpr2 mutation | rel=r_associated | relid=0 | w=41 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 41 / 0.953 -> en:mowat-wilson syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:mowat-wilson syndrome | rel=r_associated | relid=0 | w=41 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 41 / 0.953 -> en:paraganglioma and gastric stromal sarcoma n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:paraganglioma and gastric stromal sarcoma | rel=r_associated | relid=0 | w=41 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 41 / 0.953 -> en:synpolydactyly n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:synpolydactyly | rel=r_associated | relid=0 | w=41 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 41 / 0.953 -> en:thiel-behnke corneal dystrophy n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:thiel-behnke corneal dystrophy | rel=r_associated | relid=0 | w=41 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 40 / 0.93 -> en:blindness, scoliosis, arachnodactyly syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:blindness, scoliosis, arachnodactyly syndrome | rel=r_associated | relid=0 | w=40 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 40 / 0.93 -> en:bork stender schmidt syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:bork stender schmidt syndrome | rel=r_associated | relid=0 | w=40 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 40 / 0.93 -> en:czech dysplasia, metatarsal type n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:czech dysplasia, metatarsal type | rel=r_associated | relid=0 | w=40 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 40 / 0.93 -> en:fibrodysplasia ossificans progressiva n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:fibrodysplasia ossificans progressiva | rel=r_associated | relid=0 | w=40 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 40 / 0.93 -> en:frontotemporal dementia n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:frontotemporal dementia | rel=r_associated | relid=0 | w=40 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 40 / 0.93 -> en:mild spondyloepiphyseal dysplasia due to col2a1 mutation with early onset osteoarthritis n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:mild spondyloepiphyseal dysplasia due to col2a1 mutation with early onset osteoarthritis | rel=r_associated | relid=0 | w=40 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 40 / 0.93 -> en:myoclonic cerebellar dyssynergia n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:myoclonic cerebellar dyssynergia | rel=r_associated | relid=0 | w=40 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 39 / 0.907 -> en:spondyloepiphyseal dysplasia-brachydactyly and distinctive speech n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:spondyloepiphyseal dysplasia-brachydactyly and distinctive speech | rel=r_associated | relid=0 | w=39 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 38 / 0.884 -> en:autosomal dominant palmoplantar keratoderma and congenital alopecia n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:autosomal dominant palmoplantar keratoderma and congenital alopecia | rel=r_associated | relid=0 | w=38 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 38 / 0.884 -> en:charcot-marie-tooth disease, autosomal dominant, type 2k n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:charcot-marie-tooth disease, autosomal dominant, type 2k | rel=r_associated | relid=0 | w=38 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 38 / 0.884 -> en:cleft palate with short stature and vertebral anomaly syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:cleft palate with short stature and vertebral anomaly syndrome | rel=r_associated | relid=0 | w=38 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 38 / 0.884 -> en:familial digital arthropathy and brachydactyly syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:familial digital arthropathy and brachydactyly syndrome | rel=r_associated | relid=0 | w=38 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 38 / 0.884 -> en:hyperparathyroidism-jaw tumor syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:hyperparathyroidism-jaw tumor syndrome | rel=r_associated | relid=0 | w=38 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 38 / 0.884 -> en:jones syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:jones syndrome | rel=r_associated | relid=0 | w=38 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 38 / 0.884 -> en:mastocytosis, cutaneous, with short stature, conductive hearing loss and microtia n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:mastocytosis, cutaneous, with short stature, conductive hearing loss and microtia | rel=r_associated | relid=0 | w=38 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 38 / 0.884 -> en:pituitary adenoma, familial isolated (disorder) n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:pituitary adenoma, familial isolated (disorder) | rel=r_associated | relid=0 | w=38 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 37 / 0.86 -> en:autosomal dominant intermediate charcot-marie-tooth disease type e n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:autosomal dominant intermediate charcot-marie-tooth disease type e | rel=r_associated | relid=0 | w=37 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 37 / 0.86 -> en:dysplasia, saddan n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:dysplasia, saddan | rel=r_associated | relid=0 | w=37 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 37 / 0.86 -> en:hereditary gastrogenic lactose intolerance n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:hereditary gastrogenic lactose intolerance | rel=r_associated | relid=0 | w=37 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 37 / 0.86 -> en:mesomelic dysplasia, kantaputra type n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:mesomelic dysplasia, kantaputra type | rel=r_associated | relid=0 | w=37 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 37 / 0.86 -> en:osteosclerosis, developmental delay, craniosynostosis syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:osteosclerosis, developmental delay, craniosynostosis syndrome | rel=r_associated | relid=0 | w=37 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 36 / 0.837 -> en:bilateral microtia with deafness and cleft palate syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:bilateral microtia with deafness and cleft palate syndrome | rel=r_associated | relid=0 | w=36 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 36 / 0.837 -> en:hypoparathyroidism - autosomal dominant n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:hypoparathyroidism - autosomal dominant | rel=r_associated | relid=0 | w=36 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 36 / 0.837 -> en:popliteal pterygium syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:popliteal pterygium syndrome | rel=r_associated | relid=0 | w=36 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 36 / 0.837 -> en:syndactyly, type iv n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:syndactyly, type iv | rel=r_associated | relid=0 | w=36 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 35 / 0.814 -> en:ablepharon-macrostomia syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:ablepharon-macrostomia syndrome | rel=r_associated | relid=0 | w=35 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 35 / 0.814 -> en:alopecia, epilepsy, pyorrhea, mental subnormality n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:alopecia, epilepsy, pyorrhea, mental subnormality | rel=r_associated | relid=0 | w=35 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 35 / 0.814 -> en:aniridia and absent patella n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:aniridia and absent patella | rel=r_associated | relid=0 | w=35 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 35 / 0.814 -> en:atelosteogenesis, type 1 n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:atelosteogenesis, type 1 | rel=r_associated | relid=0 | w=35 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 35 / 0.814 -> en:atrophic degeneration n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:atrophic degeneration | rel=r_associated | relid=0 | w=35 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 35 / 0.814 -> en:autoimmune lymphoproliferative syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:autoimmune lymphoproliferative syndrome | rel=r_associated | relid=0 | w=35 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 35 / 0.814 -> en:autosomal dominant charcot-marie-tooth disease type 2c n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:autosomal dominant charcot-marie-tooth disease type 2c | rel=r_associated | relid=0 | w=35 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 35 / 0.814 -> en:autosomal dominant inheritance n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:autosomal dominant inheritance | rel=r_associated | relid=0 | w=35 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 35 / 0.814 -> en:autosomal dominant macrothrombocytopenia n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:autosomal dominant macrothrombocytopenia | rel=r_associated | relid=0 | w=35 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 35 / 0.814 -> en:brachydactyly with syndactyly zhao type n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:brachydactyly with syndactyly zhao type | rel=r_associated | relid=0 | w=35 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 35 / 0.814 -> en:branchiogenic-deafness syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:branchiogenic-deafness syndrome | rel=r_associated | relid=0 | w=35 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 35 / 0.814 -> en:brooke-spiegler syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:brooke-spiegler syndrome | rel=r_associated | relid=0 | w=35 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 35 / 0.814 -> en:capillary malformation-arteriovenous malformation (disorder) n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:capillary malformation-arteriovenous malformation (disorder) | rel=r_associated | relid=0 | w=35 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 35 / 0.814 -> en:charcot-marie-tooth disease, type 2j n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:charcot-marie-tooth disease, type 2j | rel=r_associated | relid=0 | w=35 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 35 / 0.814 -> en:chorioretinal atrophy, progressive bifocal n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:chorioretinal atrophy, progressive bifocal | rel=r_associated | relid=0 | w=35 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 35 / 0.814 -> en:cleidocranial dysplasia n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:cleidocranial dysplasia | rel=r_associated | relid=0 | w=35 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 35 / 0.814 -> en:cleidorhizomelic syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:cleidorhizomelic syndrome | rel=r_associated | relid=0 | w=35 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 35 / 0.814 -> en:craniofacial deafness hand syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:craniofacial deafness hand syndrome | rel=r_associated | relid=0 | w=35 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 35 / 0.814 -> en:craniosynostosis with dandy-walker malformation and hydrocephalus syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:craniosynostosis with dandy-walker malformation and hydrocephalus syndrome | rel=r_associated | relid=0 | w=35 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 35 / 0.814 -> en:currarino triad n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:currarino triad | rel=r_associated | relid=0 | w=35 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 35 / 0.814 -> en:dicer1 syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:dicer1 syndrome | rel=r_associated | relid=0 | w=35 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 35 / 0.814 -> en:doughnut lesions of skull, familial n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:doughnut lesions of skull, familial | rel=r_associated | relid=0 | w=35 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 35 / 0.814 -> en:dyschondrosteosis and nephritis syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:dyschondrosteosis and nephritis syndrome | rel=r_associated | relid=0 | w=35 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 35 / 0.814 -> en:dystonia 12 n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:dystonia 12 | rel=r_associated | relid=0 | w=35 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 35 / 0.814 -> en:dystrophia myotonica 2 n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:dystrophia myotonica 2 | rel=r_associated | relid=0 | w=35 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 35 / 0.814 -> en:ectodermal dysplasia with natal teeth, turnpenny type n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:ectodermal dysplasia with natal teeth, turnpenny type | rel=r_associated | relid=0 | w=35 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 35 / 0.814 -> en:epiphyseal dysplasia, multiple, 1 n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:epiphyseal dysplasia, multiple, 1 | rel=r_associated | relid=0 | w=35 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 35 / 0.814 -> en:erythrokeratodermia with ataxia n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:erythrokeratodermia with ataxia | rel=r_associated | relid=0 | w=35 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 35 / 0.814 -> en:familial benign neonatal epilepsy n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:familial benign neonatal epilepsy | rel=r_associated | relid=0 | w=35 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 35 / 0.814 -> en:glomuvenous malformations n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:glomuvenous malformations | rel=r_associated | relid=0 | w=35 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 35 / 0.814 -> en:hereditary breast and ovarian cancer syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:hereditary breast and ovarian cancer syndrome | rel=r_associated | relid=0 | w=35 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 35 / 0.814 -> en:hereditary myopathy with early respiratory failure n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:hereditary myopathy with early respiratory failure | rel=r_associated | relid=0 | w=35 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 35 / 0.814 -> en:hereditary nonpolyposis colorectal cancer n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:hereditary nonpolyposis colorectal cancer | rel=r_associated | relid=0 | w=35 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 35 / 0.814 -> en:huntington disease-like 2 n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:huntington disease-like 2 | rel=r_associated | relid=0 | w=35 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 35 / 0.814 -> en:hyperinsulinism due to uncoupling protein 2 deficiency n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=35 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 35 / 0.814 -> en:hyperpigmentation, familial progressive n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:hyperpigmentation, familial progressive | rel=r_associated | relid=0 | w=35 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 35 / 0.814 -> en:hypogonadotropic hypogonadism with frontoparietal alopecia syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:hypogonadotropic hypogonadism with frontoparietal alopecia syndrome | rel=r_associated | relid=0 | w=35 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 35 / 0.814 -> en:hypotrichosis simplex of scalp n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:hypotrichosis simplex of scalp | rel=r_associated | relid=0 | w=35 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 35 / 0.814 -> en:inclusion body myopathy with early-onset paget disease and frontotemporal dementia n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:inclusion body myopathy with early-onset paget disease and frontotemporal dementia | rel=r_associated | relid=0 | w=35 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 35 / 0.814 -> en:intellectual disability, hypoplastic corpus callosum, preauricular tag syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:intellectual disability, hypoplastic corpus callosum, preauricular tag syndrome | rel=r_associated | relid=0 | w=35 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 35 / 0.814 -> en:juvenile cataract, microcornea, renal glucosuria syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:juvenile cataract, microcornea, renal glucosuria syndrome | rel=r_associated | relid=0 | w=35 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 35 / 0.814 -> en:may-hegglin anomaly n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:may-hegglin anomaly | rel=r_associated | relid=0 | w=35 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 35 / 0.814 -> en:melanoma astrocytoma syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:melanoma astrocytoma syndrome | rel=r_associated | relid=0 | w=35 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 35 / 0.814 -> en:mid frequency deafness n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:mid frequency deafness | rel=r_associated | relid=0 | w=35 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 35 / 0.814 -> en:morava mehes syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:morava mehes syndrome | rel=r_associated | relid=0 | w=35 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 35 / 0.814 -> en:muckle-wells syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:muckle-wells syndrome | rel=r_associated | relid=0 | w=35 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 35 / 0.814 -> en:myopathy, distal, tateyama type n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:myopathy, distal, tateyama type | rel=r_associated | relid=0 | w=35 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 35 / 0.814 -> en:neuropathy, hereditary thermosensitive n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:neuropathy, hereditary thermosensitive | rel=r_associated | relid=0 | w=35 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 35 / 0.814 -> en:nicolaides baraitser syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:nicolaides baraitser syndrome | rel=r_associated | relid=0 | w=35 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 35 / 0.814 -> en:nonprogressive cerebellar ataxia n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:nonprogressive cerebellar ataxia | rel=r_associated | relid=0 | w=35 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 35 / 0.814 -> en:olivopontocerebellar atrophy and deafness n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:olivopontocerebellar atrophy and deafness | rel=r_associated | relid=0 | w=35 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 35 / 0.814 -> en:other cerebellar ataxia n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:other cerebellar ataxia | rel=r_associated | relid=0 | w=35 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 35 / 0.814 -> en:pelvis-shoulder dysplasia n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:pelvis-shoulder dysplasia | rel=r_associated | relid=0 | w=35 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 35 / 0.814 -> en:pfeiffer syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:pfeiffer syndrome | rel=r_associated | relid=0 | w=35 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 35 / 0.814 -> en:platelet-type von willebrand disease n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:platelet-type von willebrand disease | rel=r_associated | relid=0 | w=35 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 35 / 0.814 -> en:profound sensorineural hearing impairment n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:profound sensorineural hearing impairment | rel=r_associated | relid=0 | w=35 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 35 / 0.814 -> en:radioulnar synostosis with amegakaryocytic thrombocytopenia syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:radioulnar synostosis with amegakaryocytic thrombocytopenia syndrome | rel=r_associated | relid=0 | w=35 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 35 / 0.814 -> en:sensorineural hearing loss of combined sites n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:sensorineural hearing loss of combined sites | rel=r_associated | relid=0 | w=35 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 35 / 0.814 -> en:spinocerebellar ataxia 23 n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:spinocerebellar ataxia 23 | rel=r_associated | relid=0 | w=35 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 35 / 0.814 -> en:spinocerebellar ataxia 29 n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:spinocerebellar ataxia 29 | rel=r_associated | relid=0 | w=35 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 35 / 0.814 -> en:spinocerebellar ataxia type 37 n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:spinocerebellar ataxia type 37 | rel=r_associated | relid=0 | w=35 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 35 / 0.814 -> en:spinocerebellar ataxia type 4 n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:spinocerebellar ataxia type 4 | rel=r_associated | relid=0 | w=35 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 35 / 0.814 -> en:spondyloepimetaphyseal dysplasia, missouri type n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:spondyloepimetaphyseal dysplasia, missouri type | rel=r_associated | relid=0 | w=35 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 35 / 0.814 -> en:thong douglas ferrante syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:thong douglas ferrante syndrome | rel=r_associated | relid=0 | w=35 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 35 / 0.814 -> en:unilateral sensory hearing loss n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:unilateral sensory hearing loss | rel=r_associated | relid=0 | w=35 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 35 / 0.814 -> en:upper limb defect with eye and ear abnormalities syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:upper limb defect with eye and ear abnormalities syndrome | rel=r_associated | relid=0 | w=35 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 35 / 0.814 -> en:vitreoretinochoroidopathy (disorder) n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:vitreoretinochoroidopathy (disorder) | rel=r_associated | relid=0 | w=35 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 35 / 0.814 -> en:wells jankovic syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:wells jankovic syndrome | rel=r_associated | relid=0 | w=35 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 35 / 0.814 -> en:x-linked sensorineural hearing loss n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:x-linked sensorineural hearing loss | rel=r_associated | relid=0 | w=35 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 35 / 0.814 -> en:x-linked sideroblastic anemia with spinocerebellar ataxia n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:x-linked sideroblastic anemia with spinocerebellar ataxia | rel=r_associated | relid=0 | w=35 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 35 / 0.814 -> en:zimmerman laband syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:zimmerman laband syndrome | rel=r_associated | relid=0 | w=35 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 34 / 0.791 -> en:albinism, ocular, with late-onset sensorineural deafness (disorder) n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:albinism, ocular, with late-onset sensorineural deafness (disorder) | rel=r_associated | relid=0 | w=34 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 34 / 0.791 -> en:alpha-fetoprotein, hereditary persistence of n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:alpha-fetoprotein, hereditary persistence of | rel=r_associated | relid=0 | w=34 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 34 / 0.791 -> en:ameloonychohypohidrotic syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:ameloonychohypohidrotic syndrome | rel=r_associated | relid=0 | w=34 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 34 / 0.791 -> en:amyloid neuropathies, familial n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:amyloid neuropathies, familial | rel=r_associated | relid=0 | w=34 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 34 / 0.791 -> en:angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps | rel=r_associated | relid=0 | w=34 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 34 / 0.791 -> en:arthrogryposis, distal, type 1 n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:arthrogryposis, distal, type 1 | rel=r_associated | relid=0 | w=34 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 34 / 0.791 -> en:autosomal dominant cystoid macular edema n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:autosomal dominant cystoid macular edema | rel=r_associated | relid=0 | w=34 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 34 / 0.791 -> en:autosomal dominant deficiency of plasminogen n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:autosomal dominant deficiency of plasminogen | rel=r_associated | relid=0 | w=34 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 34 / 0.791 -> en:autosomal dominant hypohidrotic ectodermal dysplasia syndrome (disorder) n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:autosomal dominant hypohidrotic ectodermal dysplasia syndrome (disorder) | rel=r_associated | relid=0 | w=34 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 34 / 0.791 -> en:autosomal dominant idiopathic familial dystonia n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:autosomal dominant idiopathic familial dystonia | rel=r_associated | relid=0 | w=34 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 34 / 0.791 -> en:autosomal dominant oculocutaneous albinism n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:autosomal dominant oculocutaneous albinism | rel=r_associated | relid=0 | w=34 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 34 / 0.791 -> en:brachydactyly types b and e combined n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:brachydactyly types b and e combined | rel=r_associated | relid=0 | w=34 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 34 / 0.791 -> en:brachymesophalangy 2 and 5 n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:brachymesophalangy 2 and 5 | rel=r_associated | relid=0 | w=34 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 34 / 0.791 -> en:cataract glaucoma syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:cataract glaucoma syndrome | rel=r_associated | relid=0 | w=34 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 34 / 0.791 -> en:cataract, congenital, cerulean type 1 n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:cataract, congenital, cerulean type 1 | rel=r_associated | relid=0 | w=34 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 34 / 0.791 -> en:cerebellar ataxia, cayman type n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:cerebellar ataxia, cayman type | rel=r_associated | relid=0 | w=34 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 34 / 0.791 -> en:childhood onset sensorineural hearing impairment n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:childhood onset sensorineural hearing impairment | rel=r_associated | relid=0 | w=34 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 34 / 0.791 -> en:chitty hall baraitser syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:chitty hall baraitser syndrome | rel=r_associated | relid=0 | w=34 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 34 / 0.791 -> en:choreoathetosis, hypothyroidism, and neonatal respiratory distress n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:choreoathetosis, hypothyroidism, and neonatal respiratory distress | rel=r_associated | relid=0 | w=34 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 34 / 0.791 -> en:choreoathetosis/spasticity, episodic n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:choreoathetosis/spasticity, episodic | rel=r_associated | relid=0 | w=34 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 34 / 0.791 -> en:chromosome 11p11.2 deletion syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:chromosome 11p11.2 deletion syndrome | rel=r_associated | relid=0 | w=34 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 34 / 0.791 -> en:congenital deafness n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:congenital deafness | rel=r_associated | relid=0 | w=34 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 34 / 0.791 -> en:craniofacial conodysplasia syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:craniofacial conodysplasia syndrome | rel=r_associated | relid=0 | w=34 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 34 / 0.791 -> en:craniosynostosis, philadelphia type n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:craniosynostosis, philadelphia type | rel=r_associated | relid=0 | w=34 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 34 / 0.791 -> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=34 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 34 / 0.791 -> en:dentatorubral-pallidoluysian atrophy n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:dentatorubral-pallidoluysian atrophy | rel=r_associated | relid=0 | w=34 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 34 / 0.791 -> en:dominant sensorineural hearing loss n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:dominant sensorineural hearing loss | rel=r_associated | relid=0 | w=34 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 34 / 0.791 -> en:ehlers-danlos syndrome kyphoscoliotic and deafness type n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:ehlers-danlos syndrome kyphoscoliotic and deafness type | rel=r_associated | relid=0 | w=34 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 34 / 0.791 -> en:ehlers-danlos syndrome, type i n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:ehlers-danlos syndrome, type i | rel=r_associated | relid=0 | w=34 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 34 / 0.791 -> en:familial non-autoimmune autosomal dominant hyperthyroidism n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:familial non-autoimmune autosomal dominant hyperthyroidism | rel=r_associated | relid=0 | w=34 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 34 / 0.791 -> en:fine-lubinsky syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:fine-lubinsky syndrome | rel=r_associated | relid=0 | w=34 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 34 / 0.791 -> en:frontotemporal dementia, chromosome 3-linked n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:frontotemporal dementia, chromosome 3-linked | rel=r_associated | relid=0 | w=34 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 34 / 0.791 -> en:gracile bone dysplasia n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:gracile bone dysplasia | rel=r_associated | relid=0 | w=34 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 34 / 0.791 -> en:hereditary diffuse gastric adenocarcinoma n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:hereditary diffuse gastric adenocarcinoma | rel=r_associated | relid=0 | w=34 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 34 / 0.791 -> en:hereditary sensory autonomic neuropathy, type 1 n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:hereditary sensory autonomic neuropathy, type 1 | rel=r_associated | relid=0 | w=34 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 34 / 0.791 -> en:hereditary systemic amyloidosis n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:hereditary systemic amyloidosis | rel=r_associated | relid=0 | w=34 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 34 / 0.791 -> en:hyaline dystrophy of bruch's membrane n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:hyaline dystrophy of bruch's membrane | rel=r_associated | relid=0 | w=34 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 34 / 0.791 -> en:isotretinoin embryopathy like syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:isotretinoin embryopathy like syndrome | rel=r_associated | relid=0 | w=34 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 34 / 0.791 -> en:li-fraumeni syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:li-fraumeni syndrome | rel=r_associated | relid=0 | w=34 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 34 / 0.791 -> en:lowry maclean syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:lowry maclean syndrome | rel=r_associated | relid=0 | w=34 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 34 / 0.791 -> en:lymphedema and cerebral arteriovenous anomaly syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:lymphedema and cerebral arteriovenous anomaly syndrome | rel=r_associated | relid=0 | w=34 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 34 / 0.791 -> en:mammary-digital-nail syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:mammary-digital-nail syndrome | rel=r_associated | relid=0 | w=34 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 34 / 0.791 -> en:marfan syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:marfan syndrome | rel=r_associated | relid=0 | w=34 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 34 / 0.791 -> en:microcornea with glaucoma and absent frontal sinus syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:microcornea with glaucoma and absent frontal sinus syndrome | rel=r_associated | relid=0 | w=34 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 34 / 0.791 -> en:narcolepsy without cataplexy n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:narcolepsy without cataplexy | rel=r_associated | relid=0 | w=34 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 34 / 0.791 -> en:optic atrophy, autosomal dominant n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:optic atrophy, autosomal dominant | rel=r_associated | relid=0 | w=34 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 34 / 0.791 -> en:orofaciodigital syndrome 11 n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:orofaciodigital syndrome 11 | rel=r_associated | relid=0 | w=34 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 34 / 0.791 -> en:pfeiffer kapferer syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:pfeiffer kapferer syndrome | rel=r_associated | relid=0 | w=34 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 34 / 0.791 -> en:phosphoserine aminotransferase deficiency n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:phosphoserine aminotransferase deficiency | rel=r_associated | relid=0 | w=34 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 34 / 0.791 -> en:piebaldism n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:piebaldism | rel=r_associated | relid=0 | w=34 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 34 / 0.791 -> en:profound sensorineural hearing loss n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:profound sensorineural hearing loss | rel=r_associated | relid=0 | w=34 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 34 / 0.791 -> en:reticulate acropigmentation of kitamura n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:reticulate acropigmentation of kitamura | rel=r_associated | relid=0 | w=34 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 34 / 0.791 -> en:sellars beighton syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:sellars beighton syndrome | rel=r_associated | relid=0 | w=34 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 34 / 0.791 -> en:spastic ataxia n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:spastic ataxia | rel=r_associated | relid=0 | w=34 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 34 / 0.791 -> en:spinocerebellar ataxia 10 n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:spinocerebellar ataxia 10 | rel=r_associated | relid=0 | w=34 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 34 / 0.791 -> en:spinocerebellar ataxia 12 n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:spinocerebellar ataxia 12 | rel=r_associated | relid=0 | w=34 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 34 / 0.791 -> en:spinocerebellar ataxia 13 n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:spinocerebellar ataxia 13 | rel=r_associated | relid=0 | w=34 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 34 / 0.791 -> en:spinocerebellar ataxia 26 n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:spinocerebellar ataxia 26 | rel=r_associated | relid=0 | w=34 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 34 / 0.791 -> en:spinocerebellar ataxia 27 n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:spinocerebellar ataxia 27 | rel=r_associated | relid=0 | w=34 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 34 / 0.791 -> en:spinocerebellar ataxia 28 n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:spinocerebellar ataxia 28 | rel=r_associated | relid=0 | w=34 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 34 / 0.791 -> en:spinocerebellar ataxia 31 (disorder) n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:spinocerebellar ataxia 31 (disorder) | rel=r_associated | relid=0 | w=34 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 34 / 0.791 -> en:spondyloepiphyseal dysplasia reardon type n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:spondyloepiphyseal dysplasia reardon type | rel=r_associated | relid=0 | w=34 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 34 / 0.791 -> en:steatocystoma multiplex n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:steatocystoma multiplex | rel=r_associated | relid=0 | w=34 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 34 / 0.791 -> en:sudden sensorineural hearing loss n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:sudden sensorineural hearing loss | rel=r_associated | relid=0 | w=34 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 34 / 0.791 -> en:syndromes, narcolepsy-cataplexy n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:syndromes, narcolepsy-cataplexy | rel=r_associated | relid=0 | w=34 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 34 / 0.791 -> en:unilateral neural hearing loss n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:unilateral neural hearing loss | rel=r_associated | relid=0 | w=34 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 34 / 0.791 -> en:wellesley carman french syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:wellesley carman french syndrome | rel=r_associated | relid=0 | w=34 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 34 / 0.791 -> en:white platelet syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:white platelet syndrome | rel=r_associated | relid=0 | w=34 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 32 / 0.744 -> en:acute cerebellar ataxia due to varicella n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:acute cerebellar ataxia due to varicella | rel=r_associated | relid=0 | w=32 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 32 / 0.744 -> en:adult-onset leukoencephalopathy with axonal spheroids and pigmented glia n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:adult-onset leukoencephalopathy with axonal spheroids and pigmented glia | rel=r_associated | relid=0 | w=32 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 32 / 0.744 -> en:advanced sleep-phase syndrome, familial n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:advanced sleep-phase syndrome, familial | rel=r_associated | relid=0 | w=32 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 32 / 0.744 -> en:amelogenesis imperfecta - hypoplastic autosomal dominant - rough n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:amelogenesis imperfecta - hypoplastic autosomal dominant - rough | rel=r_associated | relid=0 | w=32 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 32 / 0.744 -> en:amelogenesis imperfecta, type ib n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:amelogenesis imperfecta, type ib | rel=r_associated | relid=0 | w=32 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 32 / 0.744 -> en:andersen syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:andersen syndrome | rel=r_associated | relid=0 | w=32 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 32 / 0.744 -> en:anonychia-onychodystrophy with hypoplasia or absence of distal phalanges n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:anonychia-onychodystrophy with hypoplasia or absence of distal phalanges | rel=r_associated | relid=0 | w=32 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 32 / 0.744 -> en:autosomal dominant epidermolysis bullosa simplex n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:autosomal dominant epidermolysis bullosa simplex | rel=r_associated | relid=0 | w=32 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 32 / 0.744 -> en:autosomal dominant hypophosphatemic bone disease n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:autosomal dominant hypophosphatemic bone disease | rel=r_associated | relid=0 | w=32 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 32 / 0.744 -> en:autosomal dominant progressive nephropathy with hypertension n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:autosomal dominant progressive nephropathy with hypertension | rel=r_associated | relid=0 | w=32 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 32 / 0.744 -> en:autosomal dominant retinitis pigmentosa n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:autosomal dominant retinitis pigmentosa | rel=r_associated | relid=0 | w=32 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 32 / 0.744 -> en:ayazi syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:ayazi syndrome | rel=r_associated | relid=0 | w=32 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 32 / 0.744 -> en:basal cell nevus syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:basal cell nevus syndrome | rel=r_associated | relid=0 | w=32 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 32 / 0.744 -> en:blepharoptosis, myopia, ectopia lentis syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:blepharoptosis, myopia, ectopia lentis syndrome | rel=r_associated | relid=0 | w=32 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 32 / 0.744 -> en:bosley-salih-alorainy syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:bosley-salih-alorainy syndrome | rel=r_associated | relid=0 | w=32 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 32 / 0.744 -> en:brachydactyly, type a2 n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:brachydactyly, type a2 | rel=r_associated | relid=0 | w=32 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 32 / 0.744 -> en:charcot-marie-tooth disease, axonal, type 2b (disorder) n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:charcot-marie-tooth disease, axonal, type 2b (disorder) | rel=r_associated | relid=0 | w=32 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 32 / 0.744 -> en:charcot-marie-tooth disease, axonal, type 2e (disorder) n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:charcot-marie-tooth disease, axonal, type 2e (disorder) | rel=r_associated | relid=0 | w=32 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 32 / 0.744 -> en:congenital anomaly of ear with impairment of hearing n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:congenital anomaly of ear with impairment of hearing | rel=r_associated | relid=0 | w=32 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 32 / 0.744 -> en:congenital cataract with ataxia and deafness syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:congenital cataract with ataxia and deafness syndrome | rel=r_associated | relid=0 | w=32 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 32 / 0.744 -> en:congenital qualifier n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:congenital qualifier | rel=r_associated | relid=0 | w=32 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 32 / 0.744 -> en:corneal dystrophy, posterior amorphous n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:corneal dystrophy, posterior amorphous | rel=r_associated | relid=0 | w=32 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 32 / 0.744 -> en:developmental malformation, deafness, dystonia syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:developmental malformation, deafness, dystonia syndrome | rel=r_associated | relid=0 | w=32 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 32 / 0.744 -> en:diffuse palmoplantar keratoderma and acrocyanosis syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:diffuse palmoplantar keratoderma and acrocyanosis syndrome | rel=r_associated | relid=0 | w=32 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 32 / 0.744 -> en:dnmt1, ala570val n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:dnmt1, ala570val | rel=r_associated | relid=0 | w=32 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 32 / 0.744 -> en:dnmt1, val606phe n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:dnmt1, val606phe | rel=r_associated | relid=0 | w=32 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 32 / 0.744 -> en:dominant autosomal hereditary disorder, incomplete penetrance n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:dominant autosomal hereditary disorder, incomplete penetrance | rel=r_associated | relid=0 | w=32 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 32 / 0.744 -> en:ehlers-danlos syndrome vascular-like type n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:ehlers-danlos syndrome vascular-like type | rel=r_associated | relid=0 | w=32 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 32 / 0.744 -> en:episodic ataxia n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:episodic ataxia | rel=r_associated | relid=0 | w=32 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 32 / 0.744 -> en:familial encephalopathy with neuroserpin inclusion bodies n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:familial encephalopathy with neuroserpin inclusion bodies | rel=r_associated | relid=0 | w=32 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 32 / 0.744 -> en:familial osteochondritis dissecans n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:familial osteochondritis dissecans | rel=r_associated | relid=0 | w=32 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 32 / 0.744 -> en:fibular aplasia and ectrodactyly syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:fibular aplasia and ectrodactyly syndrome | rel=r_associated | relid=0 | w=32 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 32 / 0.744 -> en:freeman-sheldon syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:freeman-sheldon syndrome | rel=r_associated | relid=0 | w=32 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 32 / 0.744 -> en:geniospasm 1 n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:geniospasm 1 | rel=r_associated | relid=0 | w=32 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 32 / 0.744 -> en:glucose transporter protein type 1 deficiency syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:glucose transporter protein type 1 deficiency syndrome | rel=r_associated | relid=0 | w=32 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 32 / 0.744 -> en:hereditary papillary renal carcinoma n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:hereditary papillary renal carcinoma | rel=r_associated | relid=0 | w=32 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 32 / 0.744 -> en:hip dysplasia, beukes type n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:hip dysplasia, beukes type | rel=r_associated | relid=0 | w=32 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 32 / 0.744 -> en:hyperinsulinism due to hnf1a deficiency n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:hyperinsulinism due to hnf1a deficiency | rel=r_associated | relid=0 | w=32 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 32 / 0.744 -> en:isolated cryptophthalmos n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:isolated cryptophthalmos | rel=r_associated | relid=0 | w=32 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 32 / 0.744 -> en:johnson neuroectodermal syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:johnson neuroectodermal syndrome | rel=r_associated | relid=0 | w=32 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 32 / 0.744 -> en:keratitis, hereditary n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:keratitis, hereditary | rel=r_associated | relid=0 | w=32 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 32 / 0.744 -> en:leopard syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:leopard syndrome | rel=r_associated | relid=0 | w=32 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 32 / 0.744 -> en:leukokeratosis, hereditary mucosal n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:leukokeratosis, hereditary mucosal | rel=r_associated | relid=0 | w=32 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 32 / 0.744 -> en:low tone sensorineural hearing loss n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:low tone sensorineural hearing loss | rel=r_associated | relid=0 | w=32 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 32 / 0.744 -> en:lowry yong syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:lowry yong syndrome | rel=r_associated | relid=0 | w=32 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 32 / 0.744 -> en:mandibulofacial dysostosis n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:mandibulofacial dysostosis | rel=r_associated | relid=0 | w=32 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 32 / 0.744 -> en:mesomelic dwarfism reinhardt pfeiffer type n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:mesomelic dwarfism reinhardt pfeiffer type | rel=r_associated | relid=0 | w=32 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 32 / 0.744 -> en:multiple epiphyseal dysplasia beighton type n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:multiple epiphyseal dysplasia beighton type | rel=r_associated | relid=0 | w=32 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 32 / 0.744 -> en:neurofibromatosis 1 n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:neurofibromatosis 1 | rel=r_associated | relid=0 | w=32 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 32 / 0.744 -> en:nothnagel's syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:nothnagel's syndrome | rel=r_associated | relid=0 | w=32 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 32 / 0.744 -> en:oculodigitoesophagoduodenal syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:oculodigitoesophagoduodenal syndrome | rel=r_associated | relid=0 | w=32 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 32 / 0.744 -> en:perinatal sensorineural hearing loss n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:perinatal sensorineural hearing loss | rel=r_associated | relid=0 | w=32 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 32 / 0.744 -> en:progressive heterotopic heteroplasia n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:progressive heterotopic heteroplasia | rel=r_associated | relid=0 | w=32 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 32 / 0.744 -> en:progressive sensorineural hearing impairment n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:progressive sensorineural hearing impairment | rel=r_associated | relid=0 | w=32 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 32 / 0.744 -> en:pseudohypoaldosteronism, type 1, dominant form n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:pseudohypoaldosteronism, type 1, dominant form | rel=r_associated | relid=0 | w=32 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 32 / 0.744 -> en:pten hamartoma tumor syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:pten hamartoma tumor syndrome | rel=r_associated | relid=0 | w=32 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 32 / 0.744 -> en:radial hypoplasia, triphalangeal thumbs and hypospadias n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:radial hypoplasia, triphalangeal thumbs and hypospadias | rel=r_associated | relid=0 | w=32 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 32 / 0.744 -> en:recessive sensorineural hearing loss n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:recessive sensorineural hearing loss | rel=r_associated | relid=0 | w=32 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 32 / 0.744 -> en:secondary narcolepsy n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:secondary narcolepsy | rel=r_associated | relid=0 | w=32 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 32 / 0.744 -> en:sensorineural hearing loss in left ear n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:sensorineural hearing loss in left ear | rel=r_associated | relid=0 | w=32 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 32 / 0.744 -> en:sesame syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:sesame syndrome | rel=r_associated | relid=0 | w=32 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 32 / 0.744 -> en:small patella syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:small patella syndrome | rel=r_associated | relid=0 | w=32 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 32 / 0.744 -> en:spastic paraplegia, hereditary n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:spastic paraplegia, hereditary | rel=r_associated | relid=0 | w=32 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 32 / 0.744 -> en:spinocerebellar ataxia 36 n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:spinocerebellar ataxia 36 | rel=r_associated | relid=0 | w=32 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 32 / 0.744 -> en:spinocerebellar ataxia type 7 n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:spinocerebellar ataxia type 7 | rel=r_associated | relid=0 | w=32 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 32 / 0.744 -> en:spinocerebellar ataxia with epilepsy n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:spinocerebellar ataxia with epilepsy | rel=r_associated | relid=0 | w=32 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 32 / 0.744 -> en:split-hand-foot malformation with long bone deficiency 1 n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:split-hand-foot malformation with long bone deficiency 1 | rel=r_associated | relid=0 | w=32 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 32 / 0.744 -> en:spondyloepiphyseal dysplasia, maroteaux type n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:spondyloepiphyseal dysplasia, maroteaux type | rel=r_associated | relid=0 | w=32 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 32 / 0.744 -> en:syndactyly, type v n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:syndactyly, type v | rel=r_associated | relid=0 | w=32 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 32 / 0.744 -> en:timothy syndrome type 2 n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:timothy syndrome type 2 | rel=r_associated | relid=0 | w=32 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 32 / 0.744 -> en:turcot syndrome (disorder) n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:turcot syndrome (disorder) | rel=r_associated | relid=0 | w=32 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 31 / 0.721 -> en:abruzzo erickson syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:abruzzo erickson syndrome | rel=r_associated | relid=0 | w=31 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 31 / 0.721 -> en:absence of fingerprints with congenital milia syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:absence of fingerprints with congenital milia syndrome | rel=r_associated | relid=0 | w=31 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 31 / 0.721 -> en:acrodysostosis n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:acrodysostosis | rel=r_associated | relid=0 | w=31 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 31 / 0.721 -> en:adult onset autosomal dominant leukodystrophy n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:adult onset autosomal dominant leukodystrophy | rel=r_associated | relid=0 | w=31 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 31 / 0.721 -> en:alcoholic cerebellar degeneration n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:alcoholic cerebellar degeneration | rel=r_associated | relid=0 | w=31 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 31 / 0.721 -> en:aniridia and intellectual disability syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:aniridia and intellectual disability syndrome | rel=r_associated | relid=0 | w=31 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 31 / 0.721 -> en:asymmetrical sensorineural hearing loss n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:asymmetrical sensorineural hearing loss | rel=r_associated | relid=0 | w=31 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 31 / 0.721 -> en:ataxia with deafness and intellectual disability syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:ataxia with deafness and intellectual disability syndrome | rel=r_associated | relid=0 | w=31 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 31 / 0.721 -> en:ataxia, spinocerebellar n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:ataxia, spinocerebellar | rel=r_associated | relid=0 | w=31 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 31 / 0.721 -> en:ataxias, appendicular n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:ataxias, appendicular | rel=r_associated | relid=0 | w=31 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 31 / 0.721 -> en:ataxic gait n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:ataxic gait | rel=r_associated | relid=0 | w=31 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 31 / 0.721 -> en:auriculo-condylar syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:auriculo-condylar syndrome | rel=r_associated | relid=0 | w=31 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 31 / 0.721 -> en:autosomal dominant familial woolly hair n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:autosomal dominant familial woolly hair | rel=r_associated | relid=0 | w=31 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 31 / 0.721 -> en:autosomal dominant ichthyosis n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:autosomal dominant ichthyosis | rel=r_associated | relid=0 | w=31 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 31 / 0.721 -> en:bads syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:bads syndrome | rel=r_associated | relid=0 | w=31 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 31 / 0.721 -> en:behavioral variant of frontotemporal dementia n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:behavioral variant of frontotemporal dementia | rel=r_associated | relid=0 | w=31 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 31 / 0.721 -> en:bilateral neural hearing loss n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:bilateral neural hearing loss | rel=r_associated | relid=0 | w=31 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 31 / 0.721 -> en:blau syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:blau syndrome | rel=r_associated | relid=0 | w=31 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 31 / 0.721 -> en:blepharo-cheilo-dontic syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:blepharo-cheilo-dontic syndrome | rel=r_associated | relid=0 | w=31 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 31 / 0.721 -> en:brachydactyly type a6 n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:brachydactyly type a6 | rel=r_associated | relid=0 | w=31 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 31 / 0.721 -> en:camptodactyly and tall stature with scoliosis and hearing loss syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:camptodactyly and tall stature with scoliosis and hearing loss syndrome | rel=r_associated | relid=0 | w=31 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 31 / 0.721 -> en:cardiac anomaly and heterotaxy syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:cardiac anomaly and heterotaxy syndrome | rel=r_associated | relid=0 | w=31 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 31 / 0.721 -> en:cerebellar ataxia associated with quadrupedal gait n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:cerebellar ataxia associated with quadrupedal gait | rel=r_associated | relid=0 | w=31 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 31 / 0.721 -> en:chorioretinal dystrophy, spinocerebellar ataxia, and hypogonadotropic hypogonadism n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:chorioretinal dystrophy, spinocerebellar ataxia, and hypogonadotropic hypogonadism | rel=r_associated | relid=0 | w=31 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 31 / 0.721 -> en:chromosome 17q21.31 deletion syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:chromosome 17q21.31 deletion syndrome | rel=r_associated | relid=0 | w=31 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 31 / 0.721 -> en:congenital reticular ichthyosiform erythroderma n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:congenital reticular ichthyosiform erythroderma | rel=r_associated | relid=0 | w=31 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 31 / 0.721 -> en:corneal cerebellar syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:corneal cerebellar syndrome | rel=r_associated | relid=0 | w=31 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 31 / 0.721 -> en:deafness oligodontia syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:deafness oligodontia syndrome | rel=r_associated | relid=0 | w=31 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 31 / 0.721 -> en:digitorenocerebral syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:digitorenocerebral syndrome | rel=r_associated | relid=0 | w=31 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 31 / 0.721 -> en:dysphasia, familial developmental n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:dysphasia, familial developmental | rel=r_associated | relid=0 | w=31 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 31 / 0.721 -> en:epithelial recurrent erosion dystrophy n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:epithelial recurrent erosion dystrophy | rel=r_associated | relid=0 | w=31 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 31 / 0.721 -> en:epithelio-exfoliative colitis and deafness syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:epithelio-exfoliative colitis and deafness syndrome | rel=r_associated | relid=0 | w=31 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 31 / 0.721 -> en:familial hypodontia n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:familial hypodontia | rel=r_associated | relid=0 | w=31 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 31 / 0.721 -> en:fechtner syndrome (disorder) n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:fechtner syndrome (disorder) | rel=r_associated | relid=0 | w=31 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 31 / 0.721 -> en:feigenbaum bergeron richardson syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:feigenbaum bergeron richardson syndrome | rel=r_associated | relid=0 | w=31 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 31 / 0.721 -> en:foxg1 syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:foxg1 syndrome | rel=r_associated | relid=0 | w=31 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 31 / 0.721 -> en:glomerulopathy with fibronectin deposits 2 (disorder) n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:glomerulopathy with fibronectin deposits 2 (disorder) | rel=r_associated | relid=0 | w=31 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 31 / 0.721 -> en:grayson wilbrandt corneal dystrophy n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:grayson wilbrandt corneal dystrophy | rel=r_associated | relid=0 | w=31 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 31 / 0.721 -> en:hereditary benign intraepithelial dyskeratosis n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:hereditary benign intraepithelial dyskeratosis | rel=r_associated | relid=0 | w=31 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 31 / 0.721 -> en:hereditary vascular retinopathy n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:hereditary vascular retinopathy | rel=r_associated | relid=0 | w=31 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 31 / 0.721 -> en:hyperinsulinism due to deficiency of glucokinase n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:hyperinsulinism due to deficiency of glucokinase | rel=r_associated | relid=0 | w=31 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 31 / 0.721 -> en:hypoplastic tibia and postaxial polydactyly syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:hypoplastic tibia and postaxial polydactyly syndrome | rel=r_associated | relid=0 | w=31 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 31 / 0.721 -> en:ichthyosis, cyclic, with epidermolytic hyperkeratosis n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:ichthyosis, cyclic, with epidermolytic hyperkeratosis | rel=r_associated | relid=0 | w=31 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 31 / 0.721 -> en:isolated autosomal dominant hypomagnesemia glaudemans type n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:isolated autosomal dominant hypomagnesemia glaudemans type | rel=r_associated | relid=0 | w=31 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 31 / 0.721 -> en:keratosis palmoplantaris papulosa n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:keratosis palmoplantaris papulosa | rel=r_associated | relid=0 | w=31 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 31 / 0.721 -> en:late onset cerebellar ataxia n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:late onset cerebellar ataxia | rel=r_associated | relid=0 | w=31 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 31 / 0.721 -> en:microphthalmia, syndromic 3 n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:microphthalmia, syndromic 3 | rel=r_associated | relid=0 | w=31 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 31 / 0.721 -> en:mitral regurgitation, conductive deafness, and fusion of cervical vertebrae and of carpal and tarsal bones n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:mitral regurgitation, conductive deafness, and fusion of cervical vertebrae and of carpal and tarsal bones | rel=r_associated | relid=0 | w=31 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 31 / 0.721 -> en:mullerian duct and limb anomalies syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:mullerian duct and limb anomalies syndrome | rel=r_associated | relid=0 | w=31 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 31 / 0.721 -> en:multiple epiphyseal dysplasia type 5 n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:multiple epiphyseal dysplasia type 5 | rel=r_associated | relid=0 | w=31 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 31 / 0.721 -> en:myopathy, distal 2 n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:myopathy, distal 2 | rel=r_associated | relid=0 | w=31 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 31 / 0.721 -> en:neurofibromatosis 2 n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:neurofibromatosis 2 | rel=r_associated | relid=0 | w=31 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 31 / 0.721 -> en:neurofibromatosis, type 1-like syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:neurofibromatosis, type 1-like syndrome | rel=r_associated | relid=0 | w=31 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 31 / 0.721 -> en:neuropathy, hereditary motor and sensory, okinawa type n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:neuropathy, hereditary motor and sensory, okinawa type | rel=r_associated | relid=0 | w=31 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 31 / 0.721 -> en:oculootoradial syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:oculootoradial syndrome | rel=r_associated | relid=0 | w=31 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 31 / 0.721 -> en:peripheral resistance to thyroid hormone n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:peripheral resistance to thyroid hormone | rel=r_associated | relid=0 | w=31 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 31 / 0.721 -> en:pili torti-deafness syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:pili torti-deafness syndrome | rel=r_associated | relid=0 | w=31 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 31 / 0.721 -> en:polydactyly, preaxial ii (disorder) n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:polydactyly, preaxial ii (disorder) | rel=r_associated | relid=0 | w=31 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 31 / 0.721 -> en:potassium aggravated myotonia n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:potassium aggravated myotonia | rel=r_associated | relid=0 | w=31 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 31 / 0.721 -> en:roch leri mesosomatous lipomatosis n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:roch leri mesosomatous lipomatosis | rel=r_associated | relid=0 | w=31 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 31 / 0.721 -> en:rudd klimek syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:rudd klimek syndrome | rel=r_associated | relid=0 | w=31 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 31 / 0.721 -> en:sensorineural hearing loss in right ear n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:sensorineural hearing loss in right ear | rel=r_associated | relid=0 | w=31 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 31 / 0.721 -> en:severe x-linked intellectual disability gustavson type n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:severe x-linked intellectual disability gustavson type | rel=r_associated | relid=0 | w=31 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 31 / 0.721 -> en:short fifth metacarpal insulin resistance syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:short fifth metacarpal insulin resistance syndrome | rel=r_associated | relid=0 | w=31 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 31 / 0.721 -> en:spinocerebellar ataxia 14 n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:spinocerebellar ataxia 14 | rel=r_associated | relid=0 | w=31 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 31 / 0.721 -> en:spinocerebellar ataxia type 5 n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:spinocerebellar ataxia type 5 | rel=r_associated | relid=0 | w=31 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 31 / 0.721 -> en:spinocerebellar ataxia, x-linked 3 n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:spinocerebellar ataxia, x-linked 3 | rel=r_associated | relid=0 | w=31 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 31 / 0.721 -> en:spondyloepiphyseal dysplasia macdermot type n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:spondyloepiphyseal dysplasia macdermot type | rel=r_associated | relid=0 | w=31 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 31 / 0.721 -> en:sting-associated vasculopathy with onset in infancy n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:sting-associated vasculopathy with onset in infancy | rel=r_associated | relid=0 | w=31 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 31 / 0.721 -> en:tubular renal disease with cardiomyopathy syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:tubular renal disease with cardiomyopathy syndrome | rel=r_associated | relid=0 | w=31 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 31 / 0.721 -> en:whyte hemingway carpal tarsal phalangeal osteolyses n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:whyte hemingway carpal tarsal phalangeal osteolyses | rel=r_associated | relid=0 | w=31 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 31 / 0.721 -> en:x-linked hereditary sensory and autonomic neuropathy with deafness n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:x-linked hereditary sensory and autonomic neuropathy with deafness | rel=r_associated | relid=0 | w=31 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 31 / 0.721 -> en:x-linked intellectual disability with ataxia and apraxia syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:x-linked intellectual disability with ataxia and apraxia syndrome | rel=r_associated | relid=0 | w=31 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 31 / 0.721 -> en:yemenite deaf-blind hypopigmentation syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:yemenite deaf-blind hypopigmentation syndrome | rel=r_associated | relid=0 | w=31 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 30 / 0.698 -> en:17q11.2 microduplication syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:17q11.2 microduplication syndrome | rel=r_associated | relid=0 | w=30 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 30 / 0.698 -> en:acquired sensorineural hearing loss n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:acquired sensorineural hearing loss | rel=r_associated | relid=0 | w=30 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 30 / 0.698 -> en:acropectorovertebral dysplasia, f-form n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:acropectorovertebral dysplasia, f-form | rel=r_associated | relid=0 | w=30 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 30 / 0.698 -> en:acute cerebellar ataxia n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:acute cerebellar ataxia | rel=r_associated | relid=0 | w=30 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 30 / 0.698 -> en:alport syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:alport syndrome | rel=r_associated | relid=0 | w=30 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 30 / 0.698 -> en:angioedemas, hereditary n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:angioedemas, hereditary | rel=r_associated | relid=0 | w=30 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 30 / 0.698 -> en:autosomal dominant muscular dystrophy with limb girdle distribution n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:autosomal dominant muscular dystrophy with limb girdle distribution | rel=r_associated | relid=0 | w=30 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 30 / 0.698 -> en:autosomal dominant variant form of albumin n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:autosomal dominant variant form of albumin | rel=r_associated | relid=0 | w=30 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 30 / 0.698 -> en:avascular necrosis of femur head n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:avascular necrosis of femur head | rel=r_associated | relid=0 | w=30 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 30 / 0.698 -> en:bilateral multiple fibroadenoma of breast n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:bilateral multiple fibroadenoma of breast | rel=r_associated | relid=0 | w=30 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 30 / 0.698 -> en:brachymorphism-onychodysplasia-dysphalangism syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:brachymorphism-onychodysplasia-dysphalangism syndrome | rel=r_associated | relid=0 | w=30 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 30 / 0.698 -> en:cataplexy n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:cataplexy | rel=r_associated | relid=0 | w=30 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 30 / 0.698 -> en:char syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:char syndrome | rel=r_associated | relid=0 | w=30 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 30 / 0.698 -> en:cole disease n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:cole disease | rel=r_associated | relid=0 | w=30 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 30 / 0.698 -> en:congenital hereditary facial paralysis with variable hearing loss syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:congenital hereditary facial paralysis with variable hearing loss syndrome | rel=r_associated | relid=0 | w=30 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 30 / 0.698 -> en:deafness enamel hypoplasia nail defects n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:deafness enamel hypoplasia nail defects | rel=r_associated | relid=0 | w=30 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 30 / 0.698 -> en:dentin dyspalsia, shields type 2 n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:dentin dyspalsia, shields type 2 | rel=r_associated | relid=0 | w=30 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 30 / 0.698 -> en:dopa-responsive dystonia n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:dopa-responsive dystonia | rel=r_associated | relid=0 | w=30 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 30 / 0.698 -> en:familial partial lipodystrophy, type 2 n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:familial partial lipodystrophy, type 2 | rel=r_associated | relid=0 | w=30 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 30 / 0.698 -> en:familial spontaneous pneumothorax n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:familial spontaneous pneumothorax | rel=r_associated | relid=0 | w=30 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 30 / 0.698 -> en:hereditary cerebral amyloid angiopathy, icelandic type n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:hereditary cerebral amyloid angiopathy, icelandic type | rel=r_associated | relid=0 | w=30 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 30 / 0.698 -> en:hereditary elliptocytosis due to alpha spectrin defect n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:hereditary elliptocytosis due to alpha spectrin defect | rel=r_associated | relid=0 | w=30 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 30 / 0.698 -> en:hereditary elliptocytosis due to deficiency of protein 4.1 n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:hereditary elliptocytosis due to deficiency of protein 4.1 | rel=r_associated | relid=0 | w=30 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 30 / 0.698 -> en:hereditary oculoleptomeningeal amyloid angiopathy n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=30 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 30 / 0.698 -> en:hyperinsulinism due to hnf4a deficiency n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:hyperinsulinism due to hnf4a deficiency | rel=r_associated | relid=0 | w=30 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 30 / 0.698 -> en:hypertrichosis terminalis, generalized, with or without gingival hyperplasia n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:hypertrichosis terminalis, generalized, with or without gingival hyperplasia | rel=r_associated | relid=0 | w=30 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 30 / 0.698 -> en:jackson-weiss syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:jackson-weiss syndrome | rel=r_associated | relid=0 | w=30 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 30 / 0.698 -> en:lamellar ichthyosis, autosomal dominant form n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:lamellar ichthyosis, autosomal dominant form | rel=r_associated | relid=0 | w=30 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 30 / 0.698 -> en:mild neurosensory hearing impairment n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:mild neurosensory hearing impairment | rel=r_associated | relid=0 | w=30 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 30 / 0.698 -> en:nemaline myopathy 3 n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:nemaline myopathy 3 | rel=r_associated | relid=0 | w=30 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 30 / 0.698 -> en:neural hearing loss n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:neural hearing loss | rel=r_associated | relid=0 | w=30 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 30 / 0.698 -> en:noise-induced hearing loss n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:noise-induced hearing loss | rel=r_associated | relid=0 | w=30 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 30 / 0.698 -> en:oculodental syndrome rutherfurd syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=30 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 30 / 0.698 -> en:odontotrichoungual-digital-palmar syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:odontotrichoungual-digital-palmar syndrome | rel=r_associated | relid=0 | w=30 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 30 / 0.698 -> en:palmoplantar keratoderma with deafness n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:palmoplantar keratoderma with deafness | rel=r_associated | relid=0 | w=30 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 30 / 0.698 -> en:preaxial deficiency, postaxial polydactyly and hypospadias n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:preaxial deficiency, postaxial polydactyly and hypospadias | rel=r_associated | relid=0 | w=30 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 30 / 0.698 -> en:richards-rundle syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:richards-rundle syndrome | rel=r_associated | relid=0 | w=30 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 30 / 0.698 -> en:rombo syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:rombo syndrome | rel=r_associated | relid=0 | w=30 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 30 / 0.698 -> en:sanger-brown cerebellar ataxia n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:sanger-brown cerebellar ataxia | rel=r_associated | relid=0 | w=30 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 30 / 0.698 -> en:schnyder crystalline corneal dystrophy n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:schnyder crystalline corneal dystrophy | rel=r_associated | relid=0 | w=30 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 30 / 0.698 -> en:sensorineural hearing loss, bilateral n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:sensorineural hearing loss, bilateral | rel=r_associated | relid=0 | w=30 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 30 / 0.698 -> en:sensorineural hearing loss, unilateral n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:sensorineural hearing loss, unilateral | rel=r_associated | relid=0 | w=30 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 30 / 0.698 -> en:shprintzen-goldberg syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:shprintzen-goldberg syndrome | rel=r_associated | relid=0 | w=30 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 30 / 0.698 -> en:spinocerebellar ataxia 21 n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:spinocerebellar ataxia 21 | rel=r_associated | relid=0 | w=30 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 30 / 0.698 -> en:spinocerebellar ataxia 8 n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:spinocerebellar ataxia 8 | rel=r_associated | relid=0 | w=30 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 30 / 0.698 -> en:split-hand with congenital nystagmus, fundal changes, and cataracts n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:split-hand with congenital nystagmus, fundal changes, and cataracts | rel=r_associated | relid=0 | w=30 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 30 / 0.698 -> en:spondylometaphyseal dysplasia, algerian type n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:spondylometaphyseal dysplasia, algerian type | rel=r_associated | relid=0 | w=30 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 30 / 0.698 -> en:syndrome, branchio-oculo-facial n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:syndrome, branchio-oculo-facial | rel=r_associated | relid=0 | w=30 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 30 / 0.698 -> en:thickened earlobe with conductive deafness syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:thickened earlobe with conductive deafness syndrome | rel=r_associated | relid=0 | w=30 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 30 / 0.698 -> en:timothy syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:timothy syndrome | rel=r_associated | relid=0 | w=30 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 30 / 0.698 -> en:wnt4 mullerian aplasia and ovarian dysfunction n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:wnt4 mullerian aplasia and ovarian dysfunction | rel=r_associated | relid=0 | w=30 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 30 / 0.698 -> en:yorifuji okuno syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:yorifuji okuno syndrome | rel=r_associated | relid=0 | w=30 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 30 / 0.698 -> en:zunich neuroectodermal syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:zunich neuroectodermal syndrome | rel=r_associated | relid=0 | w=30 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 29 / 0.674 -> en:acro-dermato-ungual-lacrimal-tooth syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:acro-dermato-ungual-lacrimal-tooth syndrome | rel=r_associated | relid=0 | w=29 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 29 / 0.674 -> en:aniridia, ptosis, intellectual disability, familial obesity syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:aniridia, ptosis, intellectual disability, familial obesity syndrome | rel=r_associated | relid=0 | w=29 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 29 / 0.674 -> en:autosomal dominant focal dystonia dyt25 type n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:autosomal dominant focal dystonia dyt25 type | rel=r_associated | relid=0 | w=29 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 29 / 0.674 -> en:autosomal dominant hyperinsulinism due to kir6.2 deficiency n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:autosomal dominant hyperinsulinism due to kir6.2 deficiency | rel=r_associated | relid=0 | w=29 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 29 / 0.674 -> en:autosomal dominant ichthyosis vulgaris n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:autosomal dominant ichthyosis vulgaris | rel=r_associated | relid=0 | w=29 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 29 / 0.674 -> en:autosomal dominant polycystic kidney disease n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:autosomal dominant polycystic kidney disease | rel=r_associated | relid=0 | w=29 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 29 / 0.674 -> en:beare-stevenson cutis gyrata syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:beare-stevenson cutis gyrata syndrome | rel=r_associated | relid=0 | w=29 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 29 / 0.674 -> en:brachydactyly type a5 nail dysplasia n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:brachydactyly type a5 nail dysplasia | rel=r_associated | relid=0 | w=29 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 29 / 0.674 -> en:brachydactyly with hypertension n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:brachydactyly with hypertension | rel=r_associated | relid=0 | w=29 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 29 / 0.674 -> en:brachyolmia type 3 n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:brachyolmia type 3 | rel=r_associated | relid=0 | w=29 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 29 / 0.674 -> en:burn-mckeown syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:burn-mckeown syndrome | rel=r_associated | relid=0 | w=29 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 29 / 0.674 -> en:centronuclear myopathy 1 n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:centronuclear myopathy 1 | rel=r_associated | relid=0 | w=29 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 29 / 0.674 -> en:cerebellar ataxia associated with another disorder n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:cerebellar ataxia associated with another disorder | rel=r_associated | relid=0 | w=29 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 29 / 0.674 -> en:cerebellar ataxia ectodermal dysplasia n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:cerebellar ataxia ectodermal dysplasia | rel=r_associated | relid=0 | w=29 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 29 / 0.674 -> en:cerebellar ataxia, areflexia, pes cavus, optic atrophy, sensorineural hearing loss syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:cerebellar ataxia, areflexia, pes cavus, optic atrophy, sensorineural hearing loss syndrome | rel=r_associated | relid=0 | w=29 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 29 / 0.674 -> en:charcot-marie-tooth disease, axonal, type 2f n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:charcot-marie-tooth disease, axonal, type 2f | rel=r_associated | relid=0 | w=29 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 29 / 0.674 -> en:charcot-marie-tooth disease, demyelinating, type 1e n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:charcot-marie-tooth disease, demyelinating, type 1e | rel=r_associated | relid=0 | w=29 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 29 / 0.674 -> en:chromosome 3q29 deletion syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:chromosome 3q29 deletion syndrome | rel=r_associated | relid=0 | w=29 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 29 / 0.674 -> en:coloboma of macula with type b brachydactyly n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:coloboma of macula with type b brachydactyly | rel=r_associated | relid=0 | w=29 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 29 / 0.674 -> en:congenital dyserythropoietic anemia type iv n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:congenital dyserythropoietic anemia type iv | rel=r_associated | relid=0 | w=29 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 29 / 0.674 -> en:craniosynostosis with facial dysmorphism and brachydactyly syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:craniosynostosis with facial dysmorphism and brachydactyly syndrome | rel=r_associated | relid=0 | w=29 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 29 / 0.674 -> en:cutis laxa, autosomal dominant n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:cutis laxa, autosomal dominant | rel=r_associated | relid=0 | w=29 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 29 / 0.674 -> en:deafness labyrinthine n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:deafness labyrinthine | rel=r_associated | relid=0 | w=29 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 29 / 0.674 -> en:dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome | rel=r_associated | relid=0 | w=29 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 29 / 0.674 -> en:edict syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:edict syndrome | rel=r_associated | relid=0 | w=29 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 29 / 0.674 -> en:familial hemiplegic migraine n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:familial hemiplegic migraine | rel=r_associated | relid=0 | w=29 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 29 / 0.674 -> en:goniodysgenesis-mental retardation-short stature syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:goniodysgenesis-mental retardation-short stature syndrome | rel=r_associated | relid=0 | w=29 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 29 / 0.674 -> en:haspeslagh fryns muelenaere syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:haspeslagh fryns muelenaere syndrome | rel=r_associated | relid=0 | w=29 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 29 / 0.674 -> en:hereditary sensory and autonomic neuropathy type 1b n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:hereditary sensory and autonomic neuropathy type 1b | rel=r_associated | relid=0 | w=29 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 29 / 0.674 -> en:hyperferritinemia, hereditary, with congenital cataracts n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:hyperferritinemia, hereditary, with congenital cataracts | rel=r_associated | relid=0 | w=29 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 29 / 0.674 -> en:hyperinsulinism due to insulin receptor deficiency n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:hyperinsulinism due to insulin receptor deficiency | rel=r_associated | relid=0 | w=29 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 29 / 0.674 -> en:image syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:image syndrome | rel=r_associated | relid=0 | w=29 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 29 / 0.674 -> en:loeys-dietz syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:loeys-dietz syndrome | rel=r_associated | relid=0 | w=29 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 29 / 0.674 -> en:low-frequency sensorineural hearing impairment n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:low-frequency sensorineural hearing impairment | rel=r_associated | relid=0 | w=29 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 29 / 0.674 -> en:mixed hearing loss n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:mixed hearing loss | rel=r_associated | relid=0 | w=29 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 29 / 0.674 -> en:okihiro syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:okihiro syndrome | rel=r_associated | relid=0 | w=29 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 29 / 0.674 -> en:overgrowth, macrocephaly, facial dysmorphism syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:overgrowth, macrocephaly, facial dysmorphism syndrome | rel=r_associated | relid=0 | w=29 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 29 / 0.674 -> en:pitt-hopkins syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:pitt-hopkins syndrome | rel=r_associated | relid=0 | w=29 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 29 / 0.674 -> en:primary pigmented nodular adrenocortical disease n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:primary pigmented nodular adrenocortical disease | rel=r_associated | relid=0 | w=29 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 29 / 0.674 -> en:progressive sensorineural hearing loss and hypertrophic cardiomyopathy syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:progressive sensorineural hearing loss and hypertrophic cardiomyopathy syndrome | rel=r_associated | relid=0 | w=29 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 29 / 0.674 -> en:proteus-like syndrome (disorder) n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:proteus-like syndrome (disorder) | rel=r_associated | relid=0 | w=29 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 29 / 0.674 -> en:pseudohypoparathyroidism type 1c n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:pseudohypoparathyroidism type 1c | rel=r_associated | relid=0 | w=29 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 29 / 0.674 -> en:reis-bucklers' corneal dystrophy n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:reis-bucklers' corneal dystrophy | rel=r_associated | relid=0 | w=29 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 29 / 0.674 -> en:sensorineural hearing loss of combined types n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:sensorineural hearing loss of combined types | rel=r_associated | relid=0 | w=29 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 29 / 0.674 -> en:spinocerebellar ataxia 30 n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:spinocerebellar ataxia 30 | rel=r_associated | relid=0 | w=29 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 29 / 0.674 -> en:spinocerebellar ataxia type 6 (disorder) n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:spinocerebellar ataxia type 6 (disorder) | rel=r_associated | relid=0 | w=29 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 29 / 0.674 -> en:spondylocostal dysostosis 4, autosomal dominant n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:spondylocostal dysostosis 4, autosomal dominant | rel=r_associated | relid=0 | w=29 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 29 / 0.674 -> en:spondyloperipheral dysplasia short ulna n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:spondyloperipheral dysplasia short ulna | rel=r_associated | relid=0 | w=29 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 29 / 0.674 -> en:stapes ankylosis with broad thumb and toes (disorder) n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:stapes ankylosis with broad thumb and toes (disorder) | rel=r_associated | relid=0 | w=29 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 29 / 0.674 -> en:strudwick syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:strudwick syndrome | rel=r_associated | relid=0 | w=29 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 29 / 0.674 -> en:syndactyly, type iii n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:syndactyly, type iii | rel=r_associated | relid=0 | w=29 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 29 / 0.674 -> en:trigonocephaly with broad thumb syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:trigonocephaly with broad thumb syndrome | rel=r_associated | relid=0 | w=29 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 29 / 0.674 -> en:wt limb blood syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:wt limb blood syndrome | rel=r_associated | relid=0 | w=29 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 28 / 0.651 -> en:acromicric dysplasia n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:acromicric dysplasia | rel=r_associated | relid=0 | w=28 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 28 / 0.651 -> en:alagille syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:alagille syndrome | rel=r_associated | relid=0 | w=28 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 28 / 0.651 -> en:angel shaped phalangoepiphyseal dysplasia n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:angel shaped phalangoepiphyseal dysplasia | rel=r_associated | relid=0 | w=28 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 28 / 0.651 -> en:aplasia of lacrimal and salivary glands n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:aplasia of lacrimal and salivary glands | rel=r_associated | relid=0 | w=28 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 28 / 0.651 -> en:ataxias, truncal n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:ataxias, truncal | rel=r_associated | relid=0 | w=28 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 28 / 0.651 -> en:auditory neuropathy n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:auditory neuropathy | rel=r_associated | relid=0 | w=28 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 28 / 0.651 -> en:autosomal dominant beta2-microglobulinic amyloidosis n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:autosomal dominant beta2-microglobulinic amyloidosis | rel=r_associated | relid=0 | w=28 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 28 / 0.651 -> en:autosomal dominant excess of transthyretin n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:autosomal dominant excess of transthyretin | rel=r_associated | relid=0 | w=28 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 28 / 0.651 -> en:autosomal dominant hyperinsulinism due to sur1 deficiency n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:autosomal dominant hyperinsulinism due to sur1 deficiency | rel=r_associated | relid=0 | w=28 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 28 / 0.651 -> en:autosomal dominant late onset basal ganglia degeneration n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:autosomal dominant late onset basal ganglia degeneration | rel=r_associated | relid=0 | w=28 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 28 / 0.651 -> en:autosomal dominant pterygium of conjunctiva n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:autosomal dominant pterygium of conjunctiva | rel=r_associated | relid=0 | w=28 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 28 / 0.651 -> en:benign autosomal dominant osteopetrosis n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:benign autosomal dominant osteopetrosis | rel=r_associated | relid=0 | w=28 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 28 / 0.651 -> en:branchio-oto-renal syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:branchio-oto-renal syndrome | rel=r_associated | relid=0 | w=28 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 28 / 0.651 -> en:carnevale hernandez castillo syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:carnevale hernandez castillo syndrome | rel=r_associated | relid=0 | w=28 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 28 / 0.651 -> en:cerebellar ataxia in diseases classified elsewhere n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:cerebellar ataxia in diseases classified elsewhere | rel=r_associated | relid=0 | w=28 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 28 / 0.651 -> en:cochlear function disorder n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:cochlear function disorder | rel=r_associated | relid=0 | w=28 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 28 / 0.651 -> en:combined perceptive hearing loss n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:combined perceptive hearing loss | rel=r_associated | relid=0 | w=28 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 28 / 0.651 -> en:congenital dyserythropoietic anemia, type iii n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:congenital dyserythropoietic anemia, type iii | rel=r_associated | relid=0 | w=28 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 28 / 0.651 -> en:corneal dystrophy, congenital stromal n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:corneal dystrophy, congenital stromal | rel=r_associated | relid=0 | w=28 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 28 / 0.651 -> en:deafness and intellectual disability martin probst type syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:deafness and intellectual disability martin probst type syndrome | rel=r_associated | relid=0 | w=28 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 28 / 0.651 -> en:deafness-hypogonadism syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:deafness-hypogonadism syndrome | rel=r_associated | relid=0 | w=28 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 28 / 0.651 -> en:early onset cerebellar ataxia n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:early onset cerebellar ataxia | rel=r_associated | relid=0 | w=28 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 28 / 0.651 -> en:functional observable n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:functional observable | rel=r_associated | relid=0 | w=28 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 28 / 0.651 -> en:gemss syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:gemss syndrome | rel=r_associated | relid=0 | w=28 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 28 / 0.651 -> en:generalized myotonia of thomsen n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:generalized myotonia of thomsen | rel=r_associated | relid=0 | w=28 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 28 / 0.651 -> en:genitopatellar syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:genitopatellar syndrome | rel=r_associated | relid=0 | w=28 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 28 / 0.651 -> en:hemochromatosis, type 4 n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:hemochromatosis, type 4 | rel=r_associated | relid=0 | w=28 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 28 / 0.651 -> en:hereditary elliptocytosis due to beta spectrin defect in self-association n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:hereditary elliptocytosis due to beta spectrin defect in self-association | rel=r_associated | relid=0 | w=28 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 28 / 0.651 -> en:high frequency hearing loss n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:high frequency hearing loss | rel=r_associated | relid=0 | w=28 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 28 / 0.651 -> en:late-onset retinal degeneration (disorder) n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:late-onset retinal degeneration (disorder) | rel=r_associated | relid=0 | w=28 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 28 / 0.651 -> en:laurin-sandrow syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:laurin-sandrow syndrome | rel=r_associated | relid=0 | w=28 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 28 / 0.651 -> en:liddle syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:liddle syndrome | rel=r_associated | relid=0 | w=28 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 28 / 0.651 -> en:limb-mammary syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:limb-mammary syndrome | rel=r_associated | relid=0 | w=28 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 28 / 0.651 -> en:lipodystrophy, intellectual disability, deafness syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:lipodystrophy, intellectual disability, deafness syndrome | rel=r_associated | relid=0 | w=28 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 28 / 0.651 -> en:lopes gorlin syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:lopes gorlin syndrome | rel=r_associated | relid=0 | w=28 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 28 / 0.651 -> en:median nodule of upper lip n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:median nodule of upper lip | rel=r_associated | relid=0 | w=28 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 28 / 0.651 -> en:moderate sensorineural hearing impairment n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:moderate sensorineural hearing impairment | rel=r_associated | relid=0 | w=28 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 28 / 0.651 -> en:mohr-tranebjaerg syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:mohr-tranebjaerg syndrome | rel=r_associated | relid=0 | w=28 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 28 / 0.651 -> en:multiple endocrine neoplasia type 2b n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:multiple endocrine neoplasia type 2b | rel=r_associated | relid=0 | w=28 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 28 / 0.651 -> en:nathalie syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:nathalie syndrome | rel=r_associated | relid=0 | w=28 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 28 / 0.651 -> en:noonan syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:noonan syndrome | rel=r_associated | relid=0 | w=28 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 28 / 0.651 -> en:other anomalies of ear causing impairment of hearing n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:other anomalies of ear causing impairment of hearing | rel=r_associated | relid=0 | w=28 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 28 / 0.651 -> en:other anomalies of external ear with impairment of hearing n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:other anomalies of external ear with impairment of hearing | rel=r_associated | relid=0 | w=28 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 28 / 0.651 -> en:progressive cerebellar ataxia n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:progressive cerebellar ataxia | rel=r_associated | relid=0 | w=28 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 28 / 0.651 -> en:spinocerebellar ataxia 15 n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:spinocerebellar ataxia 15 | rel=r_associated | relid=0 | w=28 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 28 / 0.651 -> en:spinocerebellar ataxia type 35 n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:spinocerebellar ataxia type 35 | rel=r_associated | relid=0 | w=28 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 28 / 0.651 -> en:spondyloepiphyseal dysplasia, kimberley type n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:spondyloepiphyseal dysplasia, kimberley type | rel=r_associated | relid=0 | w=28 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 28 / 0.651 -> en:syndromic orbital border hypoplasia n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:syndromic orbital border hypoplasia | rel=r_associated | relid=0 | w=28 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 27 / 0.628 -> en:acromegaloid facial appearance syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:acromegaloid facial appearance syndrome | rel=r_associated | relid=0 | w=27 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 27 / 0.628 -> en:alport syndrome, autosomal dominant n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:alport syndrome, autosomal dominant | rel=r_associated | relid=0 | w=27 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 27 / 0.628 -> en:aphalangy and syndactyly with microcephaly syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:aphalangy and syndactyly with microcephaly syndrome | rel=r_associated | relid=0 | w=27 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 27 / 0.628 -> en:ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia | rel=r_associated | relid=0 | w=27 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 27 / 0.628 -> en:autosomal dominant charcot-marie-tooth disease type 2a1 n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:autosomal dominant charcot-marie-tooth disease type 2a1 | rel=r_associated | relid=0 | w=27 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 27 / 0.628 -> en:autosomal dominant charcot-marie-tooth disease type 2m n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:autosomal dominant charcot-marie-tooth disease type 2m | rel=r_associated | relid=0 | w=27 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 27 / 0.628 -> en:bethlem myopathy 1 n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:bethlem myopathy 1 | rel=r_associated | relid=0 | w=27 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 27 / 0.628 -> en:bilateral pheochromocytoma and islet cell adenoma of the pancreas n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:bilateral pheochromocytoma and islet cell adenoma of the pancreas | rel=r_associated | relid=0 | w=27 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 27 / 0.628 -> en:bixler christian gorlin syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:bixler christian gorlin syndrome | rel=r_associated | relid=0 | w=27 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 27 / 0.628 -> en:book syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:book syndrome | rel=r_associated | relid=0 | w=27 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 27 / 0.628 -> en:brachydactyly, type a1 (disorder) n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:brachydactyly, type a1 (disorder) | rel=r_associated | relid=0 | w=27 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 27 / 0.628 -> en:brachytelephalangy, facial dysmorphism, kallmann syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:brachytelephalangy, facial dysmorphism, kallmann syndrome | rel=r_associated | relid=0 | w=27 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 27 / 0.628 -> en:cap myopathy n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:cap myopathy | rel=r_associated | relid=0 | w=27 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 27 / 0.628 -> en:central hearing loss n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:central hearing loss | rel=r_associated | relid=0 | w=27 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 27 / 0.628 -> en:cerebellar ataxia due to toxin n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:cerebellar ataxia due to toxin | rel=r_associated | relid=0 | w=27 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 27 / 0.628 -> en:cerebral hemorrhage with amyloidosis, hereditary, dutch type n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:cerebral hemorrhage with amyloidosis, hereditary, dutch type | rel=r_associated | relid=0 | w=27 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 27 / 0.628 -> en:cerebrooculonasal syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:cerebrooculonasal syndrome | rel=r_associated | relid=0 | w=27 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 27 / 0.628 -> en:charcot-marie-tooth disease, axonal, type 2l (disorder) n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:charcot-marie-tooth disease, axonal, type 2l (disorder) | rel=r_associated | relid=0 | w=27 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 27 / 0.628 -> en:charcot-marie-tooth disease, axonal, type 2n n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:charcot-marie-tooth disease, axonal, type 2n | rel=r_associated | relid=0 | w=27 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 27 / 0.628 -> en:chromosome 22q11.2 microduplication syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:chromosome 22q11.2 microduplication syndrome | rel=r_associated | relid=0 | w=27 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 27 / 0.628 -> en:congenital deaf mutism n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:congenital deaf mutism | rel=r_associated | relid=0 | w=27 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 27 / 0.628 -> en:craniosynostosis, type 2 n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:craniosynostosis, type 2 | rel=r_associated | relid=0 | w=27 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 27 / 0.628 -> en:deafness, sensorineural, and male infertility n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:deafness, sensorineural, and male infertility | rel=r_associated | relid=0 | w=27 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 27 / 0.628 -> en:dnmt1, gly605ala n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:dnmt1, gly605ala | rel=r_associated | relid=0 | w=27 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 27 / 0.628 -> en:dominant autosomal hereditary disorder, complete penetrance n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:dominant autosomal hereditary disorder, complete penetrance | rel=r_associated | relid=0 | w=27 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 27 / 0.628 -> en:dyskeratosis congenita, autosomal dominant n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:dyskeratosis congenita, autosomal dominant | rel=r_associated | relid=0 | w=27 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 27 / 0.628 -> en:familial cerebral cavernous malformation n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:familial cerebral cavernous malformation | rel=r_associated | relid=0 | w=27 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 27 / 0.628 -> en:familial isolated arrhythmogenic right ventricular dysplasia n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:familial isolated arrhythmogenic right ventricular dysplasia | rel=r_associated | relid=0 | w=27 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 27 / 0.628 -> en:fountain syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:fountain syndrome | rel=r_associated | relid=0 | w=27 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 27 / 0.628 -> en:glutamate dehydrogenase 1 hyperinsulinism n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:glutamate dehydrogenase 1 hyperinsulinism | rel=r_associated | relid=0 | w=27 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 27 / 0.628 -> en:hawkinsinuria n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:hawkinsinuria | rel=r_associated | relid=0 | w=27 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 27 / 0.628 -> en:heart-hand syndrome, slovenian type n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:heart-hand syndrome, slovenian type | rel=r_associated | relid=0 | w=27 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 27 / 0.628 -> en:hereditary elliptocytosis due to abnormal protein 4.1 n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:hereditary elliptocytosis due to abnormal protein 4.1 | rel=r_associated | relid=0 | w=27 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 27 / 0.628 -> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=27 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 27 / 0.628 -> en:hereditary multiple exostoses n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:hereditary multiple exostoses | rel=r_associated | relid=0 | w=27 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 27 / 0.628 -> en:hereditary stomatocytosis n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:hereditary stomatocytosis | rel=r_associated | relid=0 | w=27 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 27 / 0.628 -> en:high-frequency sensorineural hearing impairment n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:high-frequency sensorineural hearing impairment | rel=r_associated | relid=0 | w=27 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 27 / 0.628 -> en:hnsha due to triosephosphate isomerase deficiency n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:hnsha due to triosephosphate isomerase deficiency | rel=r_associated | relid=0 | w=27 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 27 / 0.628 -> en:holt-oram syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:holt-oram syndrome | rel=r_associated | relid=0 | w=27 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 27 / 0.628 -> en:hunter-mcalpine craniosynostosis syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:hunter-mcalpine craniosynostosis syndrome | rel=r_associated | relid=0 | w=27 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 27 / 0.628 -> en:hyperuricemia, anemia, renal failure syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:hyperuricemia, anemia, renal failure syndrome | rel=r_associated | relid=0 | w=27 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 27 / 0.628 -> en:idiopathic narcolepsy n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:idiopathic narcolepsy | rel=r_associated | relid=0 | w=27 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 27 / 0.628 -> en:insulin autoimmune syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:insulin autoimmune syndrome | rel=r_associated | relid=0 | w=27 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 27 / 0.628 -> en:keratoderma, palmoplantar, diffuse n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:keratoderma, palmoplantar, diffuse | rel=r_associated | relid=0 | w=27 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 27 / 0.628 -> en:macular dystrophy, concentric annular n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:macular dystrophy, concentric annular | rel=r_associated | relid=0 | w=27 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 27 / 0.628 -> en:osteogenesis imperfecta, levin type n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:osteogenesis imperfecta, levin type | rel=r_associated | relid=0 | w=27 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 27 / 0.628 -> en:osteopoikilosis and dacryocystitis n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:osteopoikilosis and dacryocystitis | rel=r_associated | relid=0 | w=27 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 27 / 0.628 -> en:otoonychoperoneal syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:otoonychoperoneal syndrome | rel=r_associated | relid=0 | w=27 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 27 / 0.628 -> en:paroxysmal extreme pain disorder n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:paroxysmal extreme pain disorder | rel=r_associated | relid=0 | w=27 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 27 / 0.628 -> en:presbycusis n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:presbycusis | rel=r_associated | relid=0 | w=27 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 27 / 0.628 -> en:rubella deafness n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:rubella deafness | rel=r_associated | relid=0 | w=27 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 27 / 0.628 -> en:sensory hearing loss, bilateral n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:sensory hearing loss, bilateral | rel=r_associated | relid=0 | w=27 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 27 / 0.628 -> en:spinocerebellar ataxia type 19 n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:spinocerebellar ataxia type 19 | rel=r_associated | relid=0 | w=27 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 27 / 0.628 -> en:spinocerebellar ataxia, autosomal recessive 2 n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:spinocerebellar ataxia, autosomal recessive 2 | rel=r_associated | relid=0 | w=27 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 27 / 0.628 -> en:spinocerebellar ataxia, x-linked 4 n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:spinocerebellar ataxia, x-linked 4 | rel=r_associated | relid=0 | w=27 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 27 / 0.628 -> en:steinfeld syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:steinfeld syndrome | rel=r_associated | relid=0 | w=27 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 27 / 0.628 -> en:tungland bellman syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:tungland bellman syndrome | rel=r_associated | relid=0 | w=27 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 27 / 0.628 -> en:ulnar-mammary syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:ulnar-mammary syndrome | rel=r_associated | relid=0 | w=27 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 27 / 0.628 -> en:upington disease n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:upington disease | rel=r_associated | relid=0 | w=27 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 27 / 0.628 -> en:usher syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:usher syndrome | rel=r_associated | relid=0 | w=27 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 27 / 0.628 -> en:uveal coloboma with cleft lip and palate and intellectual disability syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:uveal coloboma with cleft lip and palate and intellectual disability syndrome | rel=r_associated | relid=0 | w=27 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 27 / 0.628 -> en:vestibulocochlear nerve injuries n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:vestibulocochlear nerve injuries | rel=r_associated | relid=0 | w=27 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 27 / 0.628 -> en:vitelliform macular dystrophy n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:vitelliform macular dystrophy | rel=r_associated | relid=0 | w=27 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 27 / 0.628 -> syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=syndrome | rel=r_associated | relid=0 | w=27 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 26 / 0.605 -> en:aase smith syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:aase smith syndrome | rel=r_associated | relid=0 | w=26 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 26 / 0.605 -> en:acropectoral syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:acropectoral syndrome | rel=r_associated | relid=0 | w=26 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 26 / 0.605 -> en:adult onset sensorineural hearing impairment n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:adult onset sensorineural hearing impairment | rel=r_associated | relid=0 | w=26 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 26 / 0.605 -> en:ankylosing vertebral hyperostosis with tylosis syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:ankylosing vertebral hyperostosis with tylosis syndrome | rel=r_associated | relid=0 | w=26 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 26 / 0.605 -> en:apert syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:apert syndrome | rel=r_associated | relid=0 | w=26 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 26 / 0.605 -> en:ataxia n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:ataxia | rel=r_associated | relid=0 | w=26 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 26 / 0.605 -> en:autosomal dominant muscular dystrophy not predominantly limb girdle n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:autosomal dominant muscular dystrophy not predominantly limb girdle | rel=r_associated | relid=0 | w=26 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 26 / 0.605 -> en:autosomal dominant mutilating keratoderma n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:autosomal dominant mutilating keratoderma | rel=r_associated | relid=0 | w=26 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 26 / 0.605 -> en:bannayan-riley-ruvalcaba syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:bannayan-riley-ruvalcaba syndrome | rel=r_associated | relid=0 | w=26 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 26 / 0.605 -> en:charcot-marie-tooth disease type 2d n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:charcot-marie-tooth disease type 2d | rel=r_associated | relid=0 | w=26 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 26 / 0.605 -> en:charcot-marie-tooth disease, axonal, type 2g n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:charcot-marie-tooth disease, axonal, type 2g | rel=r_associated | relid=0 | w=26 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 26 / 0.605 -> en:congenital nephrogenic diabetes insipidus n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:congenital nephrogenic diabetes insipidus | rel=r_associated | relid=0 | w=26 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 26 / 0.605 -> en:corneal dystrophy and perceptive deafness n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:corneal dystrophy and perceptive deafness | rel=r_associated | relid=0 | w=26 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 26 / 0.605 -> en:deafness and myopia syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:deafness and myopia syndrome | rel=r_associated | relid=0 | w=26 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 26 / 0.605 -> en:deafness-craniofacial syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:deafness-craniofacial syndrome | rel=r_associated | relid=0 | w=26 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 26 / 0.605 -> en:deafness, prelingual n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:deafness, prelingual | rel=r_associated | relid=0 | w=26 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 26 / 0.605 -> en:deafness, progressive, with stapes fixation n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:deafness, progressive, with stapes fixation | rel=r_associated | relid=0 | w=26 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 26 / 0.605 -> en:distal renal tubular acidosis co-occurrent with sensorineural deafness n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:distal renal tubular acidosis co-occurrent with sensorineural deafness | rel=r_associated | relid=0 | w=26 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 26 / 0.605 -> en:dominant beta-thalassemia n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:dominant beta-thalassemia | rel=r_associated | relid=0 | w=26 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 26 / 0.605 -> en:dysdiadochokinesis n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:dysdiadochokinesis | rel=r_associated | relid=0 | w=26 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 26 / 0.605 -> en:dysmetrias, cerebellar n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:dysmetrias, cerebellar | rel=r_associated | relid=0 | w=26 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 26 / 0.605 -> en:erythrokeratodermia variabilis 3 (disorder) n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:erythrokeratodermia variabilis 3 (disorder) | rel=r_associated | relid=0 | w=26 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 26 / 0.605 -> en:familial alzheimer-like prion disease n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:familial alzheimer-like prion disease | rel=r_associated | relid=0 | w=26 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 26 / 0.605 -> en:familial amyloid polyneuropathy, type v n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:familial amyloid polyneuropathy, type v | rel=r_associated | relid=0 | w=26 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 26 / 0.605 -> en:familial creutzfeldt-jakob n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:familial creutzfeldt-jakob | rel=r_associated | relid=0 | w=26 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 26 / 0.605 -> en:frontotemporal lobar degeneration with tdp43 inclusions, grn-related n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:frontotemporal lobar degeneration with tdp43 inclusions, grn-related | rel=r_associated | relid=0 | w=26 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 26 / 0.605 -> en:generalized epilepsy and paroxysmal dyskinesia syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:generalized epilepsy and paroxysmal dyskinesia syndrome | rel=r_associated | relid=0 | w=26 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 26 / 0.605 -> en:hand foot uterus syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:hand foot uterus syndrome | rel=r_associated | relid=0 | w=26 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 26 / 0.605 -> en:hearing n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:hearing | rel=r_associated | relid=0 | w=26 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 26 / 0.605 -> en:hereditary motor and sensory neuropathy type i n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:hereditary motor and sensory neuropathy type i | rel=r_associated | relid=0 | w=26 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 26 / 0.605 -> en:hyperinsulinemic hypoglycemia, familial, 7 n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:hyperinsulinemic hypoglycemia, familial, 7 | rel=r_associated | relid=0 | w=26 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 26 / 0.605 -> en:insulin-dependent diabetes mellitus secretory diarrhea syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:insulin-dependent diabetes mellitus secretory diarrhea syndrome | rel=r_associated | relid=0 | w=26 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 26 / 0.605 -> en:iris coloboma with ptosis, hypertelorism, and mental retardation n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:iris coloboma with ptosis, hypertelorism, and mental retardation | rel=r_associated | relid=0 | w=26 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 26 / 0.605 -> en:jervell-lange nielsen syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:jervell-lange nielsen syndrome | rel=r_associated | relid=0 | w=26 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 26 / 0.605 -> en:kbg syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:kbg syndrome | rel=r_associated | relid=0 | w=26 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 26 / 0.605 -> en:keratoacanthoma familial n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:keratoacanthoma familial | rel=r_associated | relid=0 | w=26 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 26 / 0.605 -> en:low frequency hearing loss n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:low frequency hearing loss | rel=r_associated | relid=0 | w=26 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 26 / 0.605 -> en:metaphyseal dysplasia, braun-tinschert type n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:metaphyseal dysplasia, braun-tinschert type | rel=r_associated | relid=0 | w=26 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 26 / 0.605 -> en:microcephaly deafness syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:microcephaly deafness syndrome | rel=r_associated | relid=0 | w=26 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 26 / 0.605 -> en:microphthalmia, syndromic 5 n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:microphthalmia, syndromic 5 | rel=r_associated | relid=0 | w=26 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 26 / 0.605 -> en:microphthalmia, syndromic 6 (disorder) n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:microphthalmia, syndromic 6 (disorder) | rel=r_associated | relid=0 | w=26 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 26 / 0.605 -> en:narcolepsy aggravated n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:narcolepsy aggravated | rel=r_associated | relid=0 | w=26 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 26 / 0.605 -> en:osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome | rel=r_associated | relid=0 | w=26 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 26 / 0.605 -> en:osteopenia, myopia, hearing loss, intellectual disability, facial dysmorphism syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:osteopenia, myopia, hearing loss, intellectual disability, facial dysmorphism syndrome | rel=r_associated | relid=0 | w=26 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 26 / 0.605 -> en:parastremmatic dwarfism n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:parastremmatic dwarfism | rel=r_associated | relid=0 | w=26 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 26 / 0.605 -> en:parietal foramina n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:parietal foramina | rel=r_associated | relid=0 | w=26 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 26 / 0.605 -> en:santos mateus leal syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:santos mateus leal syndrome | rel=r_associated | relid=0 | w=26 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 26 / 0.605 -> en:scalp-ear-nipple syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:scalp-ear-nipple syndrome | rel=r_associated | relid=0 | w=26 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 26 / 0.605 -> en:schaap taylor baraitser syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:schaap taylor baraitser syndrome | rel=r_associated | relid=0 | w=26 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 26 / 0.605 -> en:schilbach-rott syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:schilbach-rott syndrome | rel=r_associated | relid=0 | w=26 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 26 / 0.605 -> en:sensory hearing loss n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:sensory hearing loss | rel=r_associated | relid=0 | w=26 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 26 / 0.605 -> en:severe sensorineural hearing impairment n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:severe sensorineural hearing impairment | rel=r_associated | relid=0 | w=26 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 26 / 0.605 -> en:short stature with valvular heart disease and characteristic facies syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:short stature with valvular heart disease and characteristic facies syndrome | rel=r_associated | relid=0 | w=26 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 26 / 0.605 -> en:short stature, pituitary and cerebellar defect and small sella turcica syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:short stature, pituitary and cerebellar defect and small sella turcica syndrome | rel=r_associated | relid=0 | w=26 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 26 / 0.605 -> en:spinocerebellar ataxia 11 n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:spinocerebellar ataxia 11 | rel=r_associated | relid=0 | w=26 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 26 / 0.605 -> en:spinocerebellar ataxia 18 n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:spinocerebellar ataxia 18 | rel=r_associated | relid=0 | w=26 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 26 / 0.605 -> en:spinocerebellar ataxia 20 n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:spinocerebellar ataxia 20 | rel=r_associated | relid=0 | w=26 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 26 / 0.605 -> en:spinocerebellar ataxia 25 n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:spinocerebellar ataxia 25 | rel=r_associated | relid=0 | w=26 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 26 / 0.605 -> en:spinocerebellar ataxia type 1 n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:spinocerebellar ataxia type 1 | rel=r_associated | relid=0 | w=26 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 26 / 0.605 -> en:spinocerebellar ataxia type 2 n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:spinocerebellar ataxia type 2 | rel=r_associated | relid=0 | w=26 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 26 / 0.605 -> en:spinocerebellar ataxia type 32 n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:spinocerebellar ataxia type 32 | rel=r_associated | relid=0 | w=26 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 26 / 0.605 -> en:syndactyly, type i n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:syndactyly, type i | rel=r_associated | relid=0 | w=26 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 26 / 0.605 -> en:tarsal-carpal coalition syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:tarsal-carpal coalition syndrome | rel=r_associated | relid=0 | w=26 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 26 / 0.605 -> en:transthyretin related familial amyloid cardiomyopathy n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:transthyretin related familial amyloid cardiomyopathy | rel=r_associated | relid=0 | w=26 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 26 / 0.605 -> en:ulna metaphyseal dysplasia syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:ulna metaphyseal dysplasia syndrome | rel=r_associated | relid=0 | w=26 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 25 / 0.581 -> en:autosomal n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:autosomal | rel=r_associated | relid=0 | w=25 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 25 / 0.581 -> en:autosomal dominant n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:autosomal dominant | rel=r_associated | relid=0 | w=25 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 20 / 0.465 -> en:ataxia co-occurrent and due to abetalipoproteinemia n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:ataxia co-occurrent and due to abetalipoproteinemia | rel=r_associated | relid=0 | w=20 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 20 / 0.465 -> en:ataxia co-occurrent and due to cerebrotendinous xanthomatosis n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:ataxia co-occurrent and due to cerebrotendinous xanthomatosis | rel=r_associated | relid=0 | w=20 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 20 / 0.465 -> en:corneal dystrophy, subepithelial mucinous n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:corneal dystrophy, subepithelial mucinous | rel=r_associated | relid=0 | w=20 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 20 / 0.465 -> en:deafness, genital anomaly, metacarpal and metatarsal synostosis syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:deafness, genital anomaly, metacarpal and metatarsal synostosis syndrome | rel=r_associated | relid=0 | w=20 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 20 / 0.465 -> en:epiphyseal dysplasia, multiple, 2 n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:epiphyseal dysplasia, multiple, 2 | rel=r_associated | relid=0 | w=20 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 20 / 0.465 -> en:metaphyseal dysplasia, maxillary hypoplasia, brachydactyly syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:metaphyseal dysplasia, maxillary hypoplasia, brachydactyly syndrome | rel=r_associated | relid=0 | w=20 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 20 / 0.465 -> en:piussan lenaerts mathieu syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:piussan lenaerts mathieu syndrome | rel=r_associated | relid=0 | w=20 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 20 / 0.465 -> en:polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, cataract syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, cataract syndrome | rel=r_associated | relid=0 | w=20 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 20 / 0.465 -> en:sporadic adult-onset ataxia of unknown etiology n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:sporadic adult-onset ataxia of unknown etiology | rel=r_associated | relid=0 | w=20 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome -- r_associated #0: 1 / 0.023 -> en:disease or syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:disease or syndrome | rel=r_associated | relid=0 | w=1

≈ 654 relations entrantes en:autosomal dominant beta2-microglobulinic amyloidosis --- r_associated #0: 43 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:autosomal dominant beta2-microglobulinic amyloidosis | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=43 en:polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, cataract syndrome --- r_associated #0: 42 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, cataract syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=42 en:17q11.2 microduplication syndrome --- r_associated #0: 35 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:17q11.2 microduplication syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=35 en:bethlem myopathy 1 --- r_associated #0: 35 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:bethlem myopathy 1 | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=35 en:dnmt1, ala570val --- r_associated #0: 35 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:dnmt1, ala570val | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=35 en:fountain syndrome --- r_associated #0: 35 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:fountain syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=35 en:hyperinsulinism due to insulin receptor deficiency --- r_associated #0: 35 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:hyperinsulinism due to insulin receptor deficiency | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=35 en:primary pigmented nodular adrenocortical disease --- r_associated #0: 35 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:primary pigmented nodular adrenocortical disease | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=35 en:autosomal dominant charcot-marie-tooth disease type 2m --- r_associated #0: 34 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:autosomal dominant charcot-marie-tooth disease type 2m | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=34 en:cooper jabs syndrome --- r_associated #0: 34 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:cooper jabs syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=34 en:corneal dystrophy, subepithelial mucinous --- r_associated #0: 34 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:corneal dystrophy, subepithelial mucinous | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=34 en:czech dysplasia, metatarsal type --- r_associated #0: 34 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:czech dysplasia, metatarsal type | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=34 en:diffuse palmoplantar keratoderma and acrocyanosis syndrome --- r_associated #0: 34 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:diffuse palmoplantar keratoderma and acrocyanosis syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=34 en:distal renal tubular acidosis co-occurrent with sensorineural deafness --- r_associated #0: 34 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:distal renal tubular acidosis co-occurrent with sensorineural deafness | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=34 en:epithelio-exfoliative colitis and deafness syndrome --- r_associated #0: 34 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:epithelio-exfoliative colitis and deafness syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=34 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome --- r_associated #0: 34 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=34 en:sporadic adult-onset ataxia of unknown etiology --- r_associated #0: 34 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:sporadic adult-onset ataxia of unknown etiology | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=34 en:gracile bone dysplasia --- r_associated #0: 32 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:gracile bone dysplasia | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=32 en:hereditary sensory and autonomic neuropathy type 1b --- r_associated #0: 32 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:hereditary sensory and autonomic neuropathy type 1b | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=32 en:timothy syndrome type 2 --- r_associated #0: 32 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:timothy syndrome type 2 | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=32 en:acro-dermato-ungual-lacrimal-tooth syndrome --- r_associated #0: 31 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:acro-dermato-ungual-lacrimal-tooth syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=31 en:aniridia, ptosis, intellectual disability, familial obesity syndrome --- r_associated #0: 31 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:aniridia, ptosis, intellectual disability, familial obesity syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=31 en:deafness and myopia syndrome --- r_associated #0: 31 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:deafness and myopia syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=31 en:hyperinsulinism due to hnf1a deficiency --- r_associated #0: 31 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:hyperinsulinism due to hnf1a deficiency | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=31 en:hyperinsulinism due to uncoupling protein 2 deficiency --- r_associated #0: 31 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=31 en:hyperuricemia, anemia, renal failure syndrome --- r_associated #0: 31 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:hyperuricemia, anemia, renal failure syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=31 en:preaxial deficiency, postaxial polydactyly and hypospadias --- r_associated #0: 31 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:preaxial deficiency, postaxial polydactyly and hypospadias | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=31 en:tubular renal disease with cardiomyopathy syndrome --- r_associated #0: 31 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:tubular renal disease with cardiomyopathy syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=31 en:aniridia and intellectual disability syndrome --- r_associated #0: 30 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:aniridia and intellectual disability syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=30 en:anonychia-onychodystrophy with hypoplasia or absence of distal phalanges --- r_associated #0: 30 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:anonychia-onychodystrophy with hypoplasia or absence of distal phalanges | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=30 en:autosomal dominant palmoplantar keratoderma and congenital alopecia --- r_associated #0: 30 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:autosomal dominant palmoplantar keratoderma and congenital alopecia | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=30 en:craniosynostosis with facial dysmorphism and brachydactyly syndrome --- r_associated #0: 30 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:craniosynostosis with facial dysmorphism and brachydactyly syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=30 en:dyschondrosteosis and nephritis syndrome --- r_associated #0: 30 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:dyschondrosteosis and nephritis syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=30 en:morava mehes syndrome --- r_associated #0: 30 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:morava mehes syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=30 en:short fifth metacarpal insulin resistance syndrome --- r_associated #0: 30 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:short fifth metacarpal insulin resistance syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=30 en:spinocerebellar ataxia type 32 --- r_associated #0: 30 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:spinocerebellar ataxia type 32 | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=30 en:yemenite deaf-blind hypopigmentation syndrome --- r_associated #0: 30 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:yemenite deaf-blind hypopigmentation syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=30 en:ataxia co-occurrent and due to cerebrotendinous xanthomatosis --- r_associated #0: 29 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:ataxia co-occurrent and due to cerebrotendinous xanthomatosis | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=29 en:cardiac anomaly and heterotaxy syndrome --- r_associated #0: 29 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:cardiac anomaly and heterotaxy syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=29 en:cataract glaucoma syndrome --- r_associated #0: 29 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:cataract glaucoma syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=29 en:cleidorhizomelic syndrome --- r_associated #0: 29 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:cleidorhizomelic syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=29 en:dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome --- r_associated #0: 29 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=29 en:ehlers-danlos syndrome vascular-like type --- r_associated #0: 29 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:ehlers-danlos syndrome vascular-like type | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=29 en:osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome --- r_associated #0: 29 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=29 en:autosomal dominant cerebellar ataxia, deafness, and narcolepsy --- r_associated #0: 28 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:autosomal dominant cerebellar ataxia, deafness, and narcolepsy | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=28 en:autosomal dominant focal dystonia dyt25 type --- r_associated #0: 28 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:autosomal dominant focal dystonia dyt25 type | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=28 en:congenital cataract with ataxia and deafness syndrome --- r_associated #0: 28 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:congenital cataract with ataxia and deafness syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=28 en:deafness, genital anomaly, metacarpal and metatarsal synostosis syndrome --- r_associated #0: 28 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:deafness, genital anomaly, metacarpal and metatarsal synostosis syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=28 en:dnmt1, gly605ala --- r_associated #0: 28 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:dnmt1, gly605ala | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=28 en:dnmt1, val606phe --- r_associated #0: 28 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:dnmt1, val606phe | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=28 en:polydactyly, preaxial ii (disorder) --- r_associated #0: 28 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:polydactyly, preaxial ii (disorder) | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=28 en:absence of fingerprints with congenital milia syndrome --- r_associated #0: 27 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:absence of fingerprints with congenital milia syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=27 en:aphalangy and syndactyly with microcephaly syndrome --- r_associated #0: 27 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:aphalangy and syndactyly with microcephaly syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=27 en:ehlers-danlos syndrome kyphoscoliotic and deafness type --- r_associated #0: 27 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:ehlers-danlos syndrome kyphoscoliotic and deafness type | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=27 en:epiphyseal dysplasia, multiple, 2 --- r_associated #0: 27 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:epiphyseal dysplasia, multiple, 2 | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=27 en:piussan lenaerts mathieu syndrome --- r_associated #0: 27 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:piussan lenaerts mathieu syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=27 en:spinocerebellar ataxia type 37 --- r_associated #0: 27 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:spinocerebellar ataxia type 37 | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=27 en:x-linked intellectual disability with ataxia and apraxia syndrome --- r_associated #0: 27 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:x-linked intellectual disability with ataxia and apraxia syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=27 en:ataxia co-occurrent and due to abetalipoproteinemia --- r_associated #0: 26 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:ataxia co-occurrent and due to abetalipoproteinemia | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=26 en:brachytelephalangy, facial dysmorphism, kallmann syndrome --- r_associated #0: 26 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:brachytelephalangy, facial dysmorphism, kallmann syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=26 en:metaphyseal dysplasia, maxillary hypoplasia, brachydactyly syndrome --- r_associated #0: 26 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:metaphyseal dysplasia, maxillary hypoplasia, brachydactyly syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=26 démence fronto-temporale --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=démence fronto-temporale | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:aase smith syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:aase smith syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:ablepharon-macrostomia syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:ablepharon-macrostomia syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:abruzzo erickson syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:abruzzo erickson syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:acquired sensorineural hearing loss --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:acquired sensorineural hearing loss | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:acrodysostosis --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:acrodysostosis | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:acromegaloid facial appearance syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:acromegaloid facial appearance syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:acromicric dysplasia --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:acromicric dysplasia | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:acropectoral syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:acropectoral syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:acropectorovertebral dysplasia, f-form --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:acropectorovertebral dysplasia, f-form | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:acute cerebellar ataxia --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:acute cerebellar ataxia | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:acute cerebellar ataxia due to varicella --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:acute cerebellar ataxia due to varicella | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:acute intermittent porphyria --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:acute intermittent porphyria | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:adult onset autosomal dominant leukodystrophy --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:adult onset autosomal dominant leukodystrophy | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:adult onset sensorineural hearing impairment --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:adult onset sensorineural hearing impairment | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:adult-onset leukoencephalopathy with axonal spheroids and pigmented glia --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:adult-onset leukoencephalopathy with axonal spheroids and pigmented glia | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:advanced sleep-phase syndrome, familial --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:advanced sleep-phase syndrome, familial | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:alagille syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:alagille syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:albinism, ocular, with late-onset sensorineural deafness (disorder) --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:albinism, ocular, with late-onset sensorineural deafness (disorder) | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:albinism-deafness syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:albinism-deafness syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:alcoholic cerebellar degeneration --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:alcoholic cerebellar degeneration | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:alopecia, epilepsy, pyorrhea, mental subnormality --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:alopecia, epilepsy, pyorrhea, mental subnormality | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:alpha-fetoprotein, hereditary persistence of --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:alpha-fetoprotein, hereditary persistence of | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:alport syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:alport syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:alport syndrome, autosomal dominant --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:alport syndrome, autosomal dominant | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:amelogenesis imperfecta - hypoplastic autosomal dominant - rough --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:amelogenesis imperfecta - hypoplastic autosomal dominant - rough | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:amelogenesis imperfecta - hypoplastic autosomal dominant - smooth --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:amelogenesis imperfecta - hypoplastic autosomal dominant - smooth | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:amelogenesis imperfecta, type ib --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:amelogenesis imperfecta, type ib | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:ameloonychohypohidrotic syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:ameloonychohypohidrotic syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:amyloid neuropathies, familial --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:amyloid neuropathies, familial | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:andersen syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:andersen syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:angel shaped phalangoepiphyseal dysplasia --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:angel shaped phalangoepiphyseal dysplasia | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:angioedemas, hereditary --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:angioedemas, hereditary | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:aniridia and absent patella --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:aniridia and absent patella | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:ankylosing vertebral hyperostosis with tylosis syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:ankylosing vertebral hyperostosis with tylosis syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:apert syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:apert syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:aplasia of lacrimal and salivary glands --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:aplasia of lacrimal and salivary glands | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:arthrogryposis, distal, type 1 --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:arthrogryposis, distal, type 1 | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:arthrogryposis-like hand anomaly and sensorineural deafness --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:arthrogryposis-like hand anomaly and sensorineural deafness | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:asymmetrical sensorineural hearing loss --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:asymmetrical sensorineural hearing loss | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:ataxia --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:ataxia | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:ataxia with deafness and intellectual disability syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:ataxia with deafness and intellectual disability syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:ataxia, spinocerebellar --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:ataxia, spinocerebellar | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:ataxias, appendicular --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:ataxias, appendicular | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:ataxias, truncal --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:ataxias, truncal | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:ataxic gait --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:ataxic gait | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:atelosteogenesis, type 1 --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:atelosteogenesis, type 1 | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:atrophic degeneration --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:atrophic degeneration | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:auditory neuropathy --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:auditory neuropathy | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:auriculo-condylar syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:auriculo-condylar syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:autoimmune lymphoproliferative syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:autoimmune lymphoproliferative syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:autosomal dominant charcot-marie-tooth disease type 2a1 --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:autosomal dominant charcot-marie-tooth disease type 2a1 | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:autosomal dominant charcot-marie-tooth disease type 2c --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:autosomal dominant charcot-marie-tooth disease type 2c | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:autosomal dominant cystoid macular edema --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:autosomal dominant cystoid macular edema | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:autosomal dominant deficiency of plasminogen --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:autosomal dominant deficiency of plasminogen | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:autosomal dominant epidermolysis bullosa simplex --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:autosomal dominant epidermolysis bullosa simplex | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:autosomal dominant excess of transthyretin --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:autosomal dominant excess of transthyretin | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:autosomal dominant familial woolly hair --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:autosomal dominant familial woolly hair | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:autosomal dominant hyperinsulinism due to kir6.2 deficiency --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:autosomal dominant hyperinsulinism due to kir6.2 deficiency | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:autosomal dominant hyperinsulinism due to sur1 deficiency --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:autosomal dominant hyperinsulinism due to sur1 deficiency | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:autosomal dominant hypohidrotic ectodermal dysplasia syndrome (disorder) --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:autosomal dominant hypohidrotic ectodermal dysplasia syndrome (disorder) | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:autosomal dominant hypophosphatemic bone disease --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:autosomal dominant hypophosphatemic bone disease | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:autosomal dominant ichthyosis --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:autosomal dominant ichthyosis | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:autosomal dominant ichthyosis vulgaris --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:autosomal dominant ichthyosis vulgaris | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:autosomal dominant idiopathic familial dystonia --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:autosomal dominant idiopathic familial dystonia | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:autosomal dominant inheritance --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:autosomal dominant inheritance | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:autosomal dominant intermediate charcot-marie-tooth disease type e --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:autosomal dominant intermediate charcot-marie-tooth disease type e | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:autosomal dominant late onset basal ganglia degeneration --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:autosomal dominant late onset basal ganglia degeneration | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:autosomal dominant macrothrombocytopenia --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:autosomal dominant macrothrombocytopenia | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:autosomal dominant muscular dystrophy not predominantly limb girdle --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:autosomal dominant muscular dystrophy not predominantly limb girdle | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:autosomal dominant muscular dystrophy with limb girdle distribution --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:autosomal dominant muscular dystrophy with limb girdle distribution | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:autosomal dominant mutilating keratoderma --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:autosomal dominant mutilating keratoderma | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:autosomal dominant oculocutaneous albinism --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:autosomal dominant oculocutaneous albinism | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:autosomal dominant polycystic kidney disease --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:autosomal dominant polycystic kidney disease | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:autosomal dominant progressive nephropathy with hypertension --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:autosomal dominant progressive nephropathy with hypertension | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:autosomal dominant pterygium of conjunctiva --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:autosomal dominant pterygium of conjunctiva | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:autosomal dominant retinitis pigmentosa --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:autosomal dominant retinitis pigmentosa | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:autosomal dominant variant form of albumin --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:autosomal dominant variant form of albumin | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:avascular necrosis of femur head --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:avascular necrosis of femur head | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:ayazi syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:ayazi syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:bads syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:bads syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:bannayan-riley-ruvalcaba syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:bannayan-riley-ruvalcaba syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:basal cell nevus syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:basal cell nevus syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:beare-stevenson cutis gyrata syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:beare-stevenson cutis gyrata syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:behavioral variant of frontotemporal dementia --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:behavioral variant of frontotemporal dementia | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:benign autosomal dominant osteopetrosis --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:benign autosomal dominant osteopetrosis | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:bilateral microtia with deafness and cleft palate syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:bilateral microtia with deafness and cleft palate syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:bilateral multiple fibroadenoma of breast --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:bilateral multiple fibroadenoma of breast | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:bilateral neural hearing loss --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:bilateral neural hearing loss | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:bilateral pheochromocytoma and islet cell adenoma of the pancreas --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:bilateral pheochromocytoma and islet cell adenoma of the pancreas | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:bixler christian gorlin syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:bixler christian gorlin syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:blau syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:blau syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:blepharo-cheilo-dontic syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:blepharo-cheilo-dontic syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:blepharoptosis, myopia, ectopia lentis syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:blepharoptosis, myopia, ectopia lentis syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:blindness, scoliosis, arachnodactyly syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:blindness, scoliosis, arachnodactyly syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:book syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:book syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:bork stender schmidt syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:bork stender schmidt syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:bosley-salih-alorainy syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:bosley-salih-alorainy syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:brachydactyly type a5 nail dysplasia --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:brachydactyly type a5 nail dysplasia | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:brachydactyly type a6 --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:brachydactyly type a6 | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:brachydactyly types b and e combined --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:brachydactyly types b and e combined | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:brachydactyly with hypertension --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:brachydactyly with hypertension | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:brachydactyly with syndactyly zhao type --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:brachydactyly with syndactyly zhao type | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:brachydactyly, type a1 (disorder) --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:brachydactyly, type a1 (disorder) | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:brachydactyly, type a2 --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:brachydactyly, type a2 | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:brachymesophalangy 2 and 5 --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:brachymesophalangy 2 and 5 | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:brachymorphism-onychodysplasia-dysphalangism syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:brachymorphism-onychodysplasia-dysphalangism syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:brachyolmia type 3 --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:brachyolmia type 3 | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:branchio-oto-renal syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:branchio-oto-renal syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:branchiogenic-deafness syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:branchiogenic-deafness syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:brooke-spiegler syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:brooke-spiegler syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:burn-mckeown syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:burn-mckeown syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:camptodactyly and tall stature with scoliosis and hearing loss syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:camptodactyly and tall stature with scoliosis and hearing loss syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:cap myopathy --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:cap myopathy | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:capillary malformation-arteriovenous malformation (disorder) --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:capillary malformation-arteriovenous malformation (disorder) | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:carnevale hernandez castillo syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:carnevale hernandez castillo syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:cataplexy --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:cataplexy | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:cataract, congenital, cerulean type 1 --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:cataract, congenital, cerulean type 1 | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:central hearing loss --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:central hearing loss | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:centronuclear myopathy 1 --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:centronuclear myopathy 1 | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:cerebellar ataxia associated with another disorder --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:cerebellar ataxia associated with another disorder | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:cerebellar ataxia associated with quadrupedal gait --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:cerebellar ataxia associated with quadrupedal gait | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:cerebellar ataxia due to toxin --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:cerebellar ataxia due to toxin | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:cerebellar ataxia ectodermal dysplasia --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:cerebellar ataxia ectodermal dysplasia | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:cerebellar ataxia in diseases classified elsewhere --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:cerebellar ataxia in diseases classified elsewhere | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:cerebellar ataxia, areflexia, pes cavus, optic atrophy, sensorineural hearing loss syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:cerebellar ataxia, areflexia, pes cavus, optic atrophy, sensorineural hearing loss syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:cerebellar ataxia, cayman type --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:cerebellar ataxia, cayman type | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:cerebral hemorrhage with amyloidosis, hereditary, dutch type --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:cerebral hemorrhage with amyloidosis, hereditary, dutch type | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:cerebrooculonasal syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:cerebrooculonasal syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:char syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:char syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:charcot-marie-tooth disease type 2d --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:charcot-marie-tooth disease type 2d | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:charcot-marie-tooth disease, autosomal dominant, type 2k --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:charcot-marie-tooth disease, autosomal dominant, type 2k | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:charcot-marie-tooth disease, axonal, type 2b (disorder) --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:charcot-marie-tooth disease, axonal, type 2b (disorder) | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:charcot-marie-tooth disease, axonal, type 2e (disorder) --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:charcot-marie-tooth disease, axonal, type 2e (disorder) | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:charcot-marie-tooth disease, axonal, type 2f --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:charcot-marie-tooth disease, axonal, type 2f | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:charcot-marie-tooth disease, axonal, type 2g --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:charcot-marie-tooth disease, axonal, type 2g | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:charcot-marie-tooth disease, axonal, type 2l (disorder) --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:charcot-marie-tooth disease, axonal, type 2l (disorder) | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:charcot-marie-tooth disease, axonal, type 2n --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:charcot-marie-tooth disease, axonal, type 2n | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:charcot-marie-tooth disease, demyelinating, type 1e --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:charcot-marie-tooth disease, demyelinating, type 1e | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:charcot-marie-tooth disease, type 2j --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:charcot-marie-tooth disease, type 2j | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:childhood onset sensorineural hearing impairment --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:childhood onset sensorineural hearing impairment | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:chitty hall baraitser syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:chitty hall baraitser syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:choreoathetosis, hypothyroidism, and neonatal respiratory distress --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:choreoathetosis, hypothyroidism, and neonatal respiratory distress | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:choreoathetosis/spasticity, episodic --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:choreoathetosis/spasticity, episodic | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:chorioretinal atrophy, progressive bifocal --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:chorioretinal atrophy, progressive bifocal | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:chorioretinal dystrophy, spinocerebellar ataxia, and hypogonadotropic hypogonadism --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:chorioretinal dystrophy, spinocerebellar ataxia, and hypogonadotropic hypogonadism | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:chromosome 11p11.2 deletion syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:chromosome 11p11.2 deletion syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:chromosome 17q21.31 deletion syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:chromosome 17q21.31 deletion syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:chromosome 22q11.2 microduplication syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:chromosome 22q11.2 microduplication syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:chromosome 3q29 deletion syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:chromosome 3q29 deletion syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:cleft palate with short stature and vertebral anomaly syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:cleft palate with short stature and vertebral anomaly syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:cleft palate with stapes fixation and oligodontia syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:cleft palate with stapes fixation and oligodontia syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:cleidocranial dysplasia --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:cleidocranial dysplasia | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:cochlear function disorder --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:cochlear function disorder | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:cochleosaccular degeneration of the inner ear and progressive cataracts --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:cochleosaccular degeneration of the inner ear and progressive cataracts | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:cole disease --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:cole disease | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:coloboma of macula with type b brachydactyly --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:coloboma of macula with type b brachydactyly | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:combined perceptive hearing loss --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:combined perceptive hearing loss | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:congenital anomaly of ear with impairment of hearing --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:congenital anomaly of ear with impairment of hearing | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:congenital deaf mutism --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:congenital deaf mutism | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:congenital deafness --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:congenital deafness | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:congenital dyserythropoietic anemia type iv --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:congenital dyserythropoietic anemia type iv | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:congenital dyserythropoietic anemia, type iii --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:congenital dyserythropoietic anemia, type iii | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:congenital hereditary facial paralysis with variable hearing loss syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:congenital hereditary facial paralysis with variable hearing loss syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:congenital nephrogenic diabetes insipidus --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:congenital nephrogenic diabetes insipidus | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:congenital qualifier --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:congenital qualifier | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:congenital reticular ichthyosiform erythroderma --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:congenital reticular ichthyosiform erythroderma | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:congenital sensorineural hearing loss --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:congenital sensorineural hearing loss | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:corneal cerebellar syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:corneal cerebellar syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:corneal dystrophy and perceptive deafness --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:corneal dystrophy and perceptive deafness | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:corneal dystrophy, congenital stromal --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:corneal dystrophy, congenital stromal | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:corneal dystrophy, posterior amorphous --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:corneal dystrophy, posterior amorphous | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:craniofacial conodysplasia syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:craniofacial conodysplasia syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:craniofacial deafness hand syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:craniofacial deafness hand syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:craniosynostosis with dandy-walker malformation and hydrocephalus syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:craniosynostosis with dandy-walker malformation and hydrocephalus syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:craniosynostosis, philadelphia type --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:craniosynostosis, philadelphia type | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:craniosynostosis, type 2 --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:craniosynostosis, type 2 | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:currarino triad --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:currarino triad | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:cutis laxa, autosomal dominant --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:cutis laxa, autosomal dominant | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:deafness and intellectual disability martin probst type syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:deafness and intellectual disability martin probst type syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:deafness enamel hypoplasia nail defects --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:deafness enamel hypoplasia nail defects | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:deafness labyrinthine --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:deafness labyrinthine | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:deafness oligodontia syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:deafness oligodontia syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:deafness, prelingual --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:deafness, prelingual | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:deafness, progressive, with stapes fixation --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:deafness, progressive, with stapes fixation | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:deafness, sensorineural, and male infertility --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:deafness, sensorineural, and male infertility | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:deafness-craniofacial syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:deafness-craniofacial syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:deafness-hypogonadism syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:deafness-hypogonadism syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:dentatorubral-pallidoluysian atrophy --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:dentatorubral-pallidoluysian atrophy | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:dentin dyspalsia, shields type 2 --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:dentin dyspalsia, shields type 2 | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:dermoodontodysplasia --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:dermoodontodysplasia | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:developmental malformation, deafness, dystonia syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:developmental malformation, deafness, dystonia syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:dicer1 syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:dicer1 syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:digitorenocerebral syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:digitorenocerebral syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:dominant autosomal hereditary disorder, complete penetrance --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:dominant autosomal hereditary disorder, complete penetrance | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:dominant autosomal hereditary disorder, incomplete penetrance --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:dominant autosomal hereditary disorder, incomplete penetrance | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:dominant beta-thalassemia --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:dominant beta-thalassemia | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:dominant sensorineural hearing loss --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:dominant sensorineural hearing loss | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:dopa-responsive dystonia --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:dopa-responsive dystonia | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:doughnut lesions of skull, familial --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:doughnut lesions of skull, familial | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:dysdiadochokinesis --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:dysdiadochokinesis | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:dyskeratosis congenita, autosomal dominant --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:dyskeratosis congenita, autosomal dominant | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:dysmetrias, cerebellar --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:dysmetrias, cerebellar | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:dysphasia, familial developmental --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:dysphasia, familial developmental | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:dysplasia, saddan --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:dysplasia, saddan | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:dystonia 12 --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:dystonia 12 | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:dystrophia myotonica 2 --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:dystrophia myotonica 2 | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:early onset cerebellar ataxia --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:early onset cerebellar ataxia | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:ectodermal dysplasia with natal teeth, turnpenny type --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:ectodermal dysplasia with natal teeth, turnpenny type | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:edict syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:edict syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:ehlers-danlos syndrome, type i --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:ehlers-danlos syndrome, type i | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:epilepsy, myoclonic, benign adult familial, type 2 --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:epilepsy, myoclonic, benign adult familial, type 2 | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:epiphyseal dysplasia, multiple, 1 --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:epiphyseal dysplasia, multiple, 1 | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:episodic ataxia --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:episodic ataxia | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:epithelial recurrent erosion dystrophy --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:epithelial recurrent erosion dystrophy | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:erythrokeratodermia variabilis 3 (disorder) --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:erythrokeratodermia variabilis 3 (disorder) | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:erythrokeratodermia with ataxia --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:erythrokeratodermia with ataxia | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:familial alzheimer-like prion disease --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:familial alzheimer-like prion disease | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:familial amyloid polyneuropathy, type v --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:familial amyloid polyneuropathy, type v | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:familial benign neonatal epilepsy --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:familial benign neonatal epilepsy | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:familial cerebral cavernous malformation --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:familial cerebral cavernous malformation | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:familial creutzfeldt-jakob --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:familial creutzfeldt-jakob | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:familial digital arthropathy and brachydactyly syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:familial digital arthropathy and brachydactyly syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:familial encephalopathy with neuroserpin inclusion bodies --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:familial encephalopathy with neuroserpin inclusion bodies | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:familial hemiplegic migraine --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:familial hemiplegic migraine | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:familial hypodontia --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:familial hypodontia | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:familial isolated arrhythmogenic right ventricular dysplasia --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:familial isolated arrhythmogenic right ventricular dysplasia | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:familial non-autoimmune autosomal dominant hyperthyroidism --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:familial non-autoimmune autosomal dominant hyperthyroidism | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:familial osteochondritis dissecans --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:familial osteochondritis dissecans | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:familial partial lipodystrophy, type 2 --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:familial partial lipodystrophy, type 2 | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:familial spontaneous pneumothorax --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:familial spontaneous pneumothorax | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:fechtner syndrome (disorder) --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:fechtner syndrome (disorder) | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:feigenbaum bergeron richardson syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:feigenbaum bergeron richardson syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:fibrodysplasia ossificans progressiva --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:fibrodysplasia ossificans progressiva | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:fibular aplasia and ectrodactyly syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:fibular aplasia and ectrodactyly syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:fine-lubinsky syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:fine-lubinsky syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:finger-nose ataxia --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:finger-nose ataxia | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:foxg1 syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:foxg1 syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:freeman-sheldon syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:freeman-sheldon syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:frontotemporal dementia --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:frontotemporal dementia | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:frontotemporal dementia, chromosome 3-linked --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:frontotemporal dementia, chromosome 3-linked | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:frontotemporal lobar degeneration with tdp43 inclusions, grn-related --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:frontotemporal lobar degeneration with tdp43 inclusions, grn-related | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:functional observable --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:functional observable | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:gemss syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:gemss syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:generalized epilepsy and paroxysmal dyskinesia syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:generalized epilepsy and paroxysmal dyskinesia syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:generalized myotonia of thomsen --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:generalized myotonia of thomsen | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:geniospasm 1 --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:geniospasm 1 | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:genitopatellar syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:genitopatellar syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:glomerulopathy with fibronectin deposits 2 (disorder) --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:glomerulopathy with fibronectin deposits 2 (disorder) | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:glomuvenous malformations --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:glomuvenous malformations | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:glucose transporter protein type 1 deficiency syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:glucose transporter protein type 1 deficiency syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:glutamate dehydrogenase 1 hyperinsulinism --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:glutamate dehydrogenase 1 hyperinsulinism | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:goniodysgenesis-mental retardation-short stature syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:goniodysgenesis-mental retardation-short stature syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:grayson wilbrandt corneal dystrophy --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:grayson wilbrandt corneal dystrophy | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:hand foot uterus syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:hand foot uterus syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:haspeslagh fryns muelenaere syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:haspeslagh fryns muelenaere syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:hawkinsinuria --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:hawkinsinuria | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:hearing --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:hearing | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:heart-hand syndrome, slovenian type --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:heart-hand syndrome, slovenian type | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:hemochromatosis, type 4 --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:hemochromatosis, type 4 | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:hereditary benign intraepithelial dyskeratosis --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:hereditary benign intraepithelial dyskeratosis | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:hereditary breast and ovarian cancer syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:hereditary breast and ovarian cancer syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:hereditary cerebral amyloid angiopathy, icelandic type --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:hereditary cerebral amyloid angiopathy, icelandic type | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:hereditary cystatin c amyloid angiopathy --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:hereditary cystatin c amyloid angiopathy | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:hereditary diffuse gastric adenocarcinoma --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:hereditary diffuse gastric adenocarcinoma | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:hereditary elliptocytosis due to abnormal protein 4.1 --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:hereditary elliptocytosis due to abnormal protein 4.1 | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:hereditary elliptocytosis due to alpha spectrin defect --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:hereditary elliptocytosis due to alpha spectrin defect | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:hereditary elliptocytosis due to beta spectrin defect in self-association --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:hereditary elliptocytosis due to beta spectrin defect in self-association | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:hereditary elliptocytosis due to deficiency of protein 4.1 --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:hereditary elliptocytosis due to deficiency of protein 4.1 | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:hereditary gastrogenic lactose intolerance --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:hereditary gastrogenic lactose intolerance | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:hereditary motor and sensory neuropathy type i --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:hereditary motor and sensory neuropathy type i | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:hereditary multiple exostoses --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:hereditary multiple exostoses | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:hereditary myopathy with early respiratory failure --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:hereditary myopathy with early respiratory failure | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:hereditary nonpolyposis colorectal cancer --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:hereditary nonpolyposis colorectal cancer | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:hereditary oculoleptomeningeal amyloid angiopathy --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:hereditary papillary renal carcinoma --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:hereditary papillary renal carcinoma | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:hereditary sensory autonomic neuropathy, type 1 --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:hereditary sensory autonomic neuropathy, type 1 | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:hereditary stomatocytosis --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:hereditary stomatocytosis | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:hereditary systemic amyloidosis --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:hereditary systemic amyloidosis | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:hereditary vascular retinopathy --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:hereditary vascular retinopathy | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:heritable pulmonary arterial hypertension due to bmpr2 mutation --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:heritable pulmonary arterial hypertension due to bmpr2 mutation | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:high frequency hearing loss --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:high frequency hearing loss | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:high tone sensori-neuronal hearing loss --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:high tone sensori-neuronal hearing loss | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:high-frequency sensorineural hearing impairment --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:high-frequency sensorineural hearing impairment | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:hip dysplasia, beukes type --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:hip dysplasia, beukes type | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:hnsha due to triosephosphate isomerase deficiency --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:hnsha due to triosephosphate isomerase deficiency | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:holt-oram syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:holt-oram syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:hunter-mcalpine craniosynostosis syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:hunter-mcalpine craniosynostosis syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:huntington disease-like 2 --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:huntington disease-like 2 | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:hyaline dystrophy of bruch's membrane --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:hyaline dystrophy of bruch's membrane | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:hyperferritinemia, hereditary, with congenital cataracts --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:hyperferritinemia, hereditary, with congenital cataracts | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:hyperinsulinemic hypoglycemia, familial, 7 --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:hyperinsulinemic hypoglycemia, familial, 7 | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:hyperinsulinism due to deficiency of glucokinase --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:hyperinsulinism due to deficiency of glucokinase | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:hyperinsulinism due to hnf4a deficiency --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:hyperinsulinism due to hnf4a deficiency | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:hyperparathyroidism-jaw tumor syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:hyperparathyroidism-jaw tumor syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:hyperpigmentation, familial progressive --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:hyperpigmentation, familial progressive | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:hypertrichosis terminalis, generalized, with or without gingival hyperplasia --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:hypertrichosis terminalis, generalized, with or without gingival hyperplasia | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:hypogonadotropic hypogonadism with frontoparietal alopecia syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:hypogonadotropic hypogonadism with frontoparietal alopecia syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:hypoparathyroidism - autosomal dominant --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:hypoparathyroidism - autosomal dominant | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:hypoplastic tibia and postaxial polydactyly syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:hypoplastic tibia and postaxial polydactyly syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:hypotrichosis simplex of scalp --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:hypotrichosis simplex of scalp | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:ichthyosis, cyclic, with epidermolytic hyperkeratosis --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:ichthyosis, cyclic, with epidermolytic hyperkeratosis | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:idiopathic narcolepsy --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:idiopathic narcolepsy | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:image syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:image syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:inclusion body myopathy with early-onset paget disease and frontotemporal dementia --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:inclusion body myopathy with early-onset paget disease and frontotemporal dementia | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:insulin autoimmune syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:insulin autoimmune syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:insulin-dependent diabetes mellitus secretory diarrhea syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:insulin-dependent diabetes mellitus secretory diarrhea syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:intellectual disability, hypoplastic corpus callosum, preauricular tag syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:intellectual disability, hypoplastic corpus callosum, preauricular tag syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:iris coloboma with ptosis, hypertelorism, and mental retardation --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:iris coloboma with ptosis, hypertelorism, and mental retardation | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:isolated autosomal dominant hypomagnesemia glaudemans type --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:isolated autosomal dominant hypomagnesemia glaudemans type | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:isolated cryptophthalmos --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:isolated cryptophthalmos | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:isotretinoin embryopathy like syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:isotretinoin embryopathy like syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:jackson-weiss syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:jackson-weiss syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:jervell-lange nielsen syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:jervell-lange nielsen syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:johnson neuroectodermal syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:johnson neuroectodermal syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:jones syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:jones syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:juvenile cataract, microcornea, renal glucosuria syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:juvenile cataract, microcornea, renal glucosuria syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:kbg syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:kbg syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:keratitis, hereditary --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:keratitis, hereditary | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:keratoacanthoma familial --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:keratoacanthoma familial | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:keratoderma, palmoplantar, diffuse --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:keratoderma, palmoplantar, diffuse | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:keratosis palmoplantaris papulosa --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:keratosis palmoplantaris papulosa | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:lamellar ichthyosis, autosomal dominant form --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:lamellar ichthyosis, autosomal dominant form | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:late onset cerebellar ataxia --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:late onset cerebellar ataxia | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:late-onset retinal degeneration (disorder) --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:late-onset retinal degeneration (disorder) | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:laurin-sandrow syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:laurin-sandrow syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:leopard syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:leopard syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:leukokeratosis, hereditary mucosal --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:leukokeratosis, hereditary mucosal | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:li-fraumeni syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:li-fraumeni syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:liddle syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:liddle syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:limb-mammary syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:limb-mammary syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:lipodystrophy, intellectual disability, deafness syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:lipodystrophy, intellectual disability, deafness syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:lissencephaly due to tuba1a (tubulin alpha 1a) mutation --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:lissencephaly due to tuba1a (tubulin alpha 1a) mutation | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:loeys-dietz syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:loeys-dietz syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:lopes gorlin syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:lopes gorlin syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:low frequency hearing loss --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:low frequency hearing loss | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:low tone sensorineural hearing loss --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:low tone sensorineural hearing loss | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:low-frequency sensorineural hearing impairment --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:low-frequency sensorineural hearing impairment | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:lowry maclean syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:lowry maclean syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:lowry yong syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:lowry yong syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:lymphedema and cerebral arteriovenous anomaly syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:lymphedema and cerebral arteriovenous anomaly syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:macular dystrophy, concentric annular --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:macular dystrophy, concentric annular | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:mammary-digital-nail syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:mammary-digital-nail syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:mandibulofacial dysostosis --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:mandibulofacial dysostosis | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:marfan syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:marfan syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:mastocytosis, cutaneous, with short stature, conductive hearing loss and microtia --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:mastocytosis, cutaneous, with short stature, conductive hearing loss and microtia | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:may-hegglin anomaly --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:may-hegglin anomaly | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:median nodule of upper lip --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:median nodule of upper lip | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:melanoma astrocytoma syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:melanoma astrocytoma syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:mesomelic dwarfism reinhardt pfeiffer type --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:mesomelic dwarfism reinhardt pfeiffer type | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:mesomelic dysplasia, kantaputra type --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:mesomelic dysplasia, kantaputra type | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:metaphyseal dysplasia, braun-tinschert type --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:metaphyseal dysplasia, braun-tinschert type | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:microcephaly deafness syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:microcephaly deafness syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:microcornea with glaucoma and absent frontal sinus syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:microcornea with glaucoma and absent frontal sinus syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:microphthalmia, syndromic 3 --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:microphthalmia, syndromic 3 | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:microphthalmia, syndromic 5 --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:microphthalmia, syndromic 5 | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:microphthalmia, syndromic 6 (disorder) --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:microphthalmia, syndromic 6 (disorder) | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:mid frequency deafness --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:mid frequency deafness | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:mild neurosensory hearing impairment --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:mild neurosensory hearing impairment | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:mild spondyloepiphyseal dysplasia due to col2a1 mutation with early onset osteoarthritis --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:mild spondyloepiphyseal dysplasia due to col2a1 mutation with early onset osteoarthritis | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:mitral regurgitation, conductive deafness, and fusion of cervical vertebrae and of carpal and tarsal bones --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:mitral regurgitation, conductive deafness, and fusion of cervical vertebrae and of carpal and tarsal bones | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:mixed hearing loss --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:mixed hearing loss | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:moderate sensorineural hearing impairment --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:moderate sensorineural hearing impairment | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:mohr-tranebjaerg syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:mohr-tranebjaerg syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:mowat-wilson syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:mowat-wilson syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:muckle-wells syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:muckle-wells syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:mullerian duct and limb anomalies syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:mullerian duct and limb anomalies syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:multiple endocrine neoplasia type 2b --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:multiple endocrine neoplasia type 2b | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:multiple epiphyseal dysplasia beighton type --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:multiple epiphyseal dysplasia beighton type | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:multiple epiphyseal dysplasia type 5 --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:multiple epiphyseal dysplasia type 5 | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:myoclonic cerebellar dyssynergia --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:myoclonic cerebellar dyssynergia | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:myopathy, distal 2 --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:myopathy, distal 2 | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:myopathy, distal, tateyama type --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:myopathy, distal, tateyama type | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:narcolepsy aggravated --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:narcolepsy aggravated | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:narcolepsy without cataplexy --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:narcolepsy without cataplexy | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:nathalie syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:nathalie syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:nemaline myopathy 3 --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:nemaline myopathy 3 | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:neural hearing loss --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:neural hearing loss | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:neurofibromatosis 1 --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:neurofibromatosis 1 | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:neurofibromatosis 2 --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:neurofibromatosis 2 | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:neurofibromatosis, type 1-like syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:neurofibromatosis, type 1-like syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:neuropathy, hereditary motor and sensory, okinawa type --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:neuropathy, hereditary motor and sensory, okinawa type | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:neuropathy, hereditary thermosensitive --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:neuropathy, hereditary thermosensitive | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:nicolaides baraitser syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:nicolaides baraitser syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:noise-induced hearing loss --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:noise-induced hearing loss | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:nonprogressive cerebellar ataxia --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:nonprogressive cerebellar ataxia | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:noonan syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:noonan syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:nothnagel's syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:nothnagel's syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:oculodigitoesophagoduodenal syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:oculodigitoesophagoduodenal syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:oculootoradial syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:oculootoradial syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:odontotrichoungual-digital-palmar syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:odontotrichoungual-digital-palmar syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:okihiro syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:okihiro syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:olivopontocerebellar atrophy and deafness --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:olivopontocerebellar atrophy and deafness | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:optic atrophy, autosomal dominant --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:optic atrophy, autosomal dominant | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:orofaciodigital syndrome 11 --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:orofaciodigital syndrome 11 | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:osteogenesis imperfecta, levin type --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:osteogenesis imperfecta, levin type | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:osteopenia, myopia, hearing loss, intellectual disability, facial dysmorphism syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:osteopenia, myopia, hearing loss, intellectual disability, facial dysmorphism syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:osteopoikilosis and dacryocystitis --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:osteopoikilosis and dacryocystitis | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:osteosclerosis, developmental delay, craniosynostosis syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:osteosclerosis, developmental delay, craniosynostosis syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:other anomalies of ear causing impairment of hearing --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:other anomalies of ear causing impairment of hearing | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:other anomalies of external ear with impairment of hearing --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:other anomalies of external ear with impairment of hearing | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:other cerebellar ataxia --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:other cerebellar ataxia | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:otoonychoperoneal syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:otoonychoperoneal syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:overgrowth, macrocephaly, facial dysmorphism syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:overgrowth, macrocephaly, facial dysmorphism syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:palmoplantar keratoderma with deafness --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:palmoplantar keratoderma with deafness | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:paraganglioma and gastric stromal sarcoma --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:paraganglioma and gastric stromal sarcoma | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:parastremmatic dwarfism --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:parastremmatic dwarfism | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:parietal foramina --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:parietal foramina | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:paroxysmal extreme pain disorder --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:paroxysmal extreme pain disorder | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:pelvis-shoulder dysplasia --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:pelvis-shoulder dysplasia | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:perinatal sensorineural hearing loss --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:perinatal sensorineural hearing loss | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:peripheral resistance to thyroid hormone --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:peripheral resistance to thyroid hormone | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:peutz-jeghers syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:peutz-jeghers syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:pfeiffer kapferer syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:pfeiffer kapferer syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:pfeiffer syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:pfeiffer syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:phosphoserine aminotransferase deficiency --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:phosphoserine aminotransferase deficiency | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:piebaldism --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:piebaldism | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:pili torti-deafness syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:pili torti-deafness syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:pitt-hopkins syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:pitt-hopkins syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:pituitary adenoma, familial isolated (disorder) --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:pituitary adenoma, familial isolated (disorder) | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:platelet-type von willebrand disease --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:platelet-type von willebrand disease | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:popliteal pterygium syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:popliteal pterygium syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:potassium aggravated myotonia --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:potassium aggravated myotonia | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:presbycusis --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:presbycusis | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:profound sensorineural hearing impairment --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:profound sensorineural hearing impairment | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:profound sensorineural hearing loss --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:profound sensorineural hearing loss | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:progressive cerebellar ataxia --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:progressive cerebellar ataxia | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:progressive heterotopic heteroplasia --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:progressive heterotopic heteroplasia | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:progressive sensorineural hearing impairment --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:progressive sensorineural hearing impairment | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:progressive sensorineural hearing loss and hypertrophic cardiomyopathy syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:progressive sensorineural hearing loss and hypertrophic cardiomyopathy syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:proteus-like syndrome (disorder) --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:proteus-like syndrome (disorder) | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:pseudohypoaldosteronism, type 1, dominant form --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:pseudohypoaldosteronism, type 1, dominant form | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:pseudohypoparathyroidism type 1c --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:pseudohypoparathyroidism type 1c | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:pten hamartoma tumor syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:pten hamartoma tumor syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:radial hypoplasia, triphalangeal thumbs and hypospadias --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:radial hypoplasia, triphalangeal thumbs and hypospadias | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:radioulnar synostosis with amegakaryocytic thrombocytopenia syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:radioulnar synostosis with amegakaryocytic thrombocytopenia syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:recessive sensorineural hearing loss --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:recessive sensorineural hearing loss | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:reis-bucklers' corneal dystrophy --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:reis-bucklers' corneal dystrophy | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:reticulate acropigmentation of kitamura --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:reticulate acropigmentation of kitamura | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:richards-rundle syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:richards-rundle syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:roch leri mesosomatous lipomatosis --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:roch leri mesosomatous lipomatosis | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:rombo syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:rombo syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:rubella deafness --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:rubella deafness | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:rudd klimek syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:rudd klimek syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:sanger-brown cerebellar ataxia --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:sanger-brown cerebellar ataxia | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:santos mateus leal syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:santos mateus leal syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:scalp-ear-nipple syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:scalp-ear-nipple syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:schaap taylor baraitser syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:schaap taylor baraitser syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:schilbach-rott syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:schilbach-rott syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:schnyder crystalline corneal dystrophy --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:schnyder crystalline corneal dystrophy | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:secondary narcolepsy --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:secondary narcolepsy | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:sellars beighton syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:sellars beighton syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:sensorineural hearing loss in left ear --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:sensorineural hearing loss in left ear | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:sensorineural hearing loss in right ear --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:sensorineural hearing loss in right ear | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:sensorineural hearing loss of combined sites --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:sensorineural hearing loss of combined sites | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:sensorineural hearing loss of combined types --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:sensorineural hearing loss of combined types | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:sensorineural hearing loss, bilateral --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:sensorineural hearing loss, bilateral | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:sensorineural hearing loss, unilateral --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:sensorineural hearing loss, unilateral | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:sensory hearing loss --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:sensory hearing loss | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:sensory hearing loss, bilateral --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:sensory hearing loss, bilateral | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:sesame syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:sesame syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:severe sensorineural hearing impairment --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:severe sensorineural hearing impairment | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:severe x-linked intellectual disability gustavson type --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:severe x-linked intellectual disability gustavson type | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:short stature with valvular heart disease and characteristic facies syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:short stature with valvular heart disease and characteristic facies syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:short stature, pituitary and cerebellar defect and small sella turcica syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:short stature, pituitary and cerebellar defect and small sella turcica syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:shprintzen omphalocele syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:shprintzen omphalocele syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:shprintzen-goldberg syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:shprintzen-goldberg syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:small patella syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:small patella syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:spastic ataxia --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:spastic ataxia | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:spastic paraplegia, hereditary --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:spastic paraplegia, hereditary | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:spinocerebellar ataxia 10 --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:spinocerebellar ataxia 10 | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:spinocerebellar ataxia 11 --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:spinocerebellar ataxia 11 | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:spinocerebellar ataxia 12 --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:spinocerebellar ataxia 12 | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:spinocerebellar ataxia 13 --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:spinocerebellar ataxia 13 | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:spinocerebellar ataxia 14 --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:spinocerebellar ataxia 14 | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:spinocerebellar ataxia 15 --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:spinocerebellar ataxia 15 | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:spinocerebellar ataxia 17 --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:spinocerebellar ataxia 17 | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:spinocerebellar ataxia 18 --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:spinocerebellar ataxia 18 | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:spinocerebellar ataxia 20 --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:spinocerebellar ataxia 20 | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:spinocerebellar ataxia 21 --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:spinocerebellar ataxia 21 | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:spinocerebellar ataxia 23 --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:spinocerebellar ataxia 23 | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:spinocerebellar ataxia 25 --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:spinocerebellar ataxia 25 | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:spinocerebellar ataxia 26 --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:spinocerebellar ataxia 26 | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:spinocerebellar ataxia 27 --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:spinocerebellar ataxia 27 | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:spinocerebellar ataxia 28 --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:spinocerebellar ataxia 28 | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:spinocerebellar ataxia 29 --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:spinocerebellar ataxia 29 | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:spinocerebellar ataxia 30 --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:spinocerebellar ataxia 30 | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:spinocerebellar ataxia 31 (disorder) --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:spinocerebellar ataxia 31 (disorder) | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:spinocerebellar ataxia 36 --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:spinocerebellar ataxia 36 | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:spinocerebellar ataxia 8 --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:spinocerebellar ataxia 8 | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:spinocerebellar ataxia type 1 --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:spinocerebellar ataxia type 1 | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:spinocerebellar ataxia type 19 --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:spinocerebellar ataxia type 19 | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:spinocerebellar ataxia type 2 --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:spinocerebellar ataxia type 2 | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:spinocerebellar ataxia type 35 --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:spinocerebellar ataxia type 35 | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:spinocerebellar ataxia type 4 --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:spinocerebellar ataxia type 4 | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:spinocerebellar ataxia type 5 --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:spinocerebellar ataxia type 5 | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:spinocerebellar ataxia type 6 (disorder) --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:spinocerebellar ataxia type 6 (disorder) | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:spinocerebellar ataxia type 7 --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:spinocerebellar ataxia type 7 | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:spinocerebellar ataxia with epilepsy --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:spinocerebellar ataxia with epilepsy | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:spinocerebellar ataxia, autosomal recessive 2 --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:spinocerebellar ataxia, autosomal recessive 2 | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:spinocerebellar ataxia, x-linked 3 --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:spinocerebellar ataxia, x-linked 3 | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:spinocerebellar ataxia, x-linked 4 --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:spinocerebellar ataxia, x-linked 4 | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:split-hand with congenital nystagmus, fundal changes, and cataracts --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:split-hand with congenital nystagmus, fundal changes, and cataracts | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:split-hand-foot malformation with long bone deficiency 1 --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:split-hand-foot malformation with long bone deficiency 1 | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:spondylocostal dysostosis 4, autosomal dominant --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:spondylocostal dysostosis 4, autosomal dominant | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:spondyloepimetaphyseal dysplasia, missouri type --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:spondyloepimetaphyseal dysplasia, missouri type | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:spondyloepiphyseal dysplasia macdermot type --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:spondyloepiphyseal dysplasia macdermot type | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:spondyloepiphyseal dysplasia reardon type --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:spondyloepiphyseal dysplasia reardon type | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:spondyloepiphyseal dysplasia, kimberley type --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:spondyloepiphyseal dysplasia, kimberley type | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:spondyloepiphyseal dysplasia, maroteaux type --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:spondyloepiphyseal dysplasia, maroteaux type | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:spondyloepiphyseal dysplasia-brachydactyly and distinctive speech --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:spondyloepiphyseal dysplasia-brachydactyly and distinctive speech | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:spondylometaphyseal dysplasia, algerian type --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:spondylometaphyseal dysplasia, algerian type | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:spondyloperipheral dysplasia short ulna --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:spondyloperipheral dysplasia short ulna | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:stapes ankylosis with broad thumb and toes (disorder) --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:stapes ankylosis with broad thumb and toes (disorder) | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:steatocystoma multiplex --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:steatocystoma multiplex | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:steinfeld syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:steinfeld syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:sting-associated vasculopathy with onset in infancy --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:sting-associated vasculopathy with onset in infancy | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:strudwick syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:strudwick syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:sudden sensorineural hearing loss --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:sudden sensorineural hearing loss | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:syndactyly, type i --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:syndactyly, type i | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:syndactyly, type iii --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:syndactyly, type iii | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:syndactyly, type iv --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:syndactyly, type iv | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:syndactyly, type v --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:syndactyly, type v | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:syndrome, branchio-oculo-facial --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:syndrome, branchio-oculo-facial | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:syndromes, narcolepsy-cataplexy --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:syndromes, narcolepsy-cataplexy | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:syndromic orbital border hypoplasia --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:syndromic orbital border hypoplasia | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:synpolydactyly --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:synpolydactyly | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:tarsal-carpal coalition syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:tarsal-carpal coalition syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:thickened earlobe with conductive deafness syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:thickened earlobe with conductive deafness syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:thiel-behnke corneal dystrophy --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:thiel-behnke corneal dystrophy | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:thong douglas ferrante syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:thong douglas ferrante syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:timothy syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:timothy syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:transthyretin related familial amyloid cardiomyopathy --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:transthyretin related familial amyloid cardiomyopathy | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:trigonocephaly with broad thumb syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:trigonocephaly with broad thumb syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:tungland bellman syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:tungland bellman syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:turcot syndrome (disorder) --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:turcot syndrome (disorder) | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:ulna metaphyseal dysplasia syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:ulna metaphyseal dysplasia syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:ulnar-mammary syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:ulnar-mammary syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:unilateral neural hearing loss --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:unilateral neural hearing loss | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:unilateral sensory hearing loss --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:unilateral sensory hearing loss | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:upington disease --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:upington disease | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:upper limb defect with eye and ear abnormalities syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:upper limb defect with eye and ear abnormalities syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:usher syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:usher syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:uveal coloboma with cleft lip and palate and intellectual disability syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:uveal coloboma with cleft lip and palate and intellectual disability syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:vasculopathy, retinal, with cerebral leukodystrophy --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:vasculopathy, retinal, with cerebral leukodystrophy | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:vestibulocochlear nerve injuries --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:vestibulocochlear nerve injuries | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:vitelliform macular dystrophy --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:vitelliform macular dystrophy | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:vitreoretinochoroidopathy (disorder) --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:vitreoretinochoroidopathy (disorder) | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:wellesley carman french syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:wellesley carman french syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:wells jankovic syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:wells jankovic syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:white platelet syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:white platelet syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:whyte hemingway carpal tarsal phalangeal osteolyses --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:whyte hemingway carpal tarsal phalangeal osteolyses | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:wnt4 mullerian aplasia and ovarian dysfunction --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:wnt4 mullerian aplasia and ovarian dysfunction | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:wt limb blood syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:wt limb blood syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:x-linked hereditary sensory and autonomic neuropathy with deafness --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:x-linked hereditary sensory and autonomic neuropathy with deafness | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:x-linked sensorineural hearing loss --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:x-linked sensorineural hearing loss | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:x-linked sideroblastic anemia with spinocerebellar ataxia --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:x-linked sideroblastic anemia with spinocerebellar ataxia | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:yorifuji okuno syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:yorifuji okuno syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:zimmerman laband syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:zimmerman laband syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:zunich neuroectodermal syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:zunich neuroectodermal syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 syndrome --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 aclasie diaphysaire --- r_associated #0: 15 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=aclasie diaphysaire | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=15 chondrodysplasie héréditaire déformante --- r_associated #0: 15 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=chondrodysplasie héréditaire déformante | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=15 exostose héréditaire multiple --- r_associated #0: 15 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=exostose héréditaire multiple | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=15 absence d'empreintes digitales avec syndrome de milia congénital --- r_associated #0: 10 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=absence d'empreintes digitales avec syndrome de milia congénital | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=10 acuité auditive --- r_associated #0: 10 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=acuité auditive | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=10 arachnodactylie --- r_associated #0: 10 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=arachnodactylie | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=10 ataxie appendiculaire --- r_associated #0: 10 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=ataxie appendiculaire | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=10 cataplexie --- r_associated #0: 10 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=cataplexie | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=10 chondrodysplasie déformante héréditaire --- r_associated #0: 10 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=chondrodysplasie déformante héréditaire | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=10 maladie de Bessel-Hagen --- r_associated #0: 10 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=maladie de Bessel-Hagen | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=10 maladie exostosante multiple --- r_associated #0: 10 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=maladie exostosante multiple | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=10 maladie ostéogénique --- r_associated #0: 10 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=maladie ostéogénique | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=10 piebaldisme --- r_associated #0: 10 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=piebaldisme | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=10 piébaldisme --- r_associated #0: 10 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=piébaldisme | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=10 steatocystoma multiplex --- r_associated #0: 10 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=steatocystoma multiplex | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=10 stéatocystomes multiples --- r_associated #0: 10 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=stéatocystomes multiples | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=10 surdité congénitale --- r_associated #0: 10 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=surdité congénitale | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=10 surdité du labyrinthe --- r_associated #0: 10 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=surdité du labyrinthe | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=10 surdité héréditaire --- r_associated #0: 10 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=surdité héréditaire | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=10 syndrome de bor --- r_associated #0: 10 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=syndrome de bor | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=10 syndrome de prédisposition héréditaire au cancer du sein et de l'ovaire --- r_associated #0: 10 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=syndrome de prédisposition héréditaire au cancer du sein et de l'ovaire | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=10 syndrome des hamartomes multiples lié à PTEN --- r_associated #0: 10 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=syndrome des hamartomes multiples lié à PTEN | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=10 syndrome héréditaire de cancer du sein et de l'ovaire --- r_associated #0: 10 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=syndrome héréditaire de cancer du sein et de l'ovaire | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=10 syndrome héréditaire de prédisposition au cancer du sein et de l'ovaire --- r_associated #0: 10 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=syndrome héréditaire de prédisposition au cancer du sein et de l'ovaire | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=10 maladie des exostoses multiples --- r_associated #0: 5 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=maladie des exostoses multiples | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=5 neuropathie sensitive héréditaire dominante de type i --- r_associated #0: 5 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=neuropathie sensitive héréditaire dominante de type i | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=5 surdité neurosensorielle bilatérale --- r_associated #0: 5 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=surdité neurosensorielle bilatérale | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=5 syndrome lymphoprolifératif avec autoimmunité --- r_associated #0: 5 --> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=syndrome lymphoprolifératif avec autoimmunité | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=5