'en:autosomal dominant cerebellar ataxia, deafness, and narcolepsy'
(id=8568167 ; fe=en:autosomal dominant cerebellar ataxia, deafness, and narcolepsy ; type=1 ; niveau=200 ; luminosité=25 ; somme entrante=964 creation date=2017-08-03 touchdate=2025-11-20 20:51:23.000)

≈ 17 relations sortantes en:autosomal dominant cerebellar ataxia, deafness, and narcolepsy -- r_associated #0: 30 / 1 -> démence n1=en:autosomal dominant cerebellar ataxia, deafness, and narcolepsy | n2=démence | rel=r_associated | relid=0 | w=30 en:autosomal dominant cerebellar ataxia, deafness, and narcolepsy -- r_associated #0: 28 / 0.933 -> 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 cerebellar ataxia, deafness, and narcolepsy -- r_associated #0: 26 / 0.867 -> en:sensorineural hearing loss n1=en:autosomal dominant cerebellar ataxia, deafness, and narcolepsy | n2=en:sensorineural hearing loss | rel=r_associated | relid=0 | w=26 en:autosomal dominant cerebellar ataxia, deafness, and narcolepsy -- r_associated #0: 25 / 0.833 -> en:autosomal n1=en:autosomal dominant cerebellar ataxia, deafness, and narcolepsy | n2=en:autosomal | rel=r_associated | relid=0 | w=25 en:autosomal dominant cerebellar ataxia, deafness, and narcolepsy -- r_associated #0: 25 / 0.833 -> en:autosomal dominant n1=en:autosomal dominant cerebellar ataxia, deafness, and narcolepsy | n2=en:autosomal dominant | rel=r_associated | relid=0 | w=25 en:autosomal dominant cerebellar ataxia, deafness, and narcolepsy -- r_associated #0: 24 / 0.8 -> en:dementia n1=en:autosomal dominant cerebellar ataxia, deafness, and narcolepsy | n2=en:dementia | rel=r_associated | relid=0 | w=24 en:autosomal dominant cerebellar ataxia, deafness, and narcolepsy -- r_associated #0: 22 / 0.733 -> perte d'audition sensorineurale n1=en:autosomal dominant cerebellar ataxia, deafness, and narcolepsy | n2=perte d'audition sensorineurale | rel=r_associated | relid=0 | w=22 en:autosomal dominant cerebellar ataxia, deafness, and narcolepsy -- r_associated #0: 20 / 0.667 -> demence n1=en:autosomal dominant cerebellar ataxia, deafness, and narcolepsy | n2=demence | rel=r_associated | relid=0 | w=20 en:autosomal dominant cerebellar ataxia, deafness, and narcolepsy -- r_associated #0: 20 / 0.667 -> démence héréditaire et infarctus multiples cérébraux n1=en:autosomal dominant cerebellar ataxia, deafness, and narcolepsy | n2=démence héréditaire et infarctus multiples cérébraux | rel=r_associated | relid=0 | w=20 en:autosomal dominant cerebellar ataxia, deafness, and narcolepsy -- r_associated #0: 20 / 0.667 -> en:autosomal dominant inheritance n1=en:autosomal dominant cerebellar ataxia, deafness, and narcolepsy | n2=en:autosomal dominant inheritance | rel=r_associated | relid=0 | w=20 en:autosomal dominant cerebellar ataxia, deafness, and narcolepsy -- r_associated #0: 20 / 0.667 -> en:decreased csf hypocretin n1=en:autosomal dominant cerebellar ataxia, deafness, and narcolepsy | n2=en:decreased csf hypocretin | rel=r_associated | relid=0 | w=20 en:autosomal dominant cerebellar ataxia, deafness, and narcolepsy -- r_associated #0: 20 / 0.667 -> en:excessive daytime somnolence n1=en:autosomal dominant cerebellar ataxia, deafness, and narcolepsy | n2=en:excessive daytime somnolence | rel=r_associated | relid=0 | w=20 en:autosomal dominant cerebellar ataxia, deafness, and narcolepsy -- r_associated #0: 20 / 0.667 -> en:limb lymphedema (in some patients) n1=en:autosomal dominant cerebellar ataxia, deafness, and narcolepsy | n2=en:limb lymphedema (in some patients) | rel=r_associated | relid=0 | w=20 en:autosomal dominant cerebellar ataxia, deafness, and narcolepsy -- r_associated #0: 20 / 0.667 -> en:narcolepsy n1=en:autosomal dominant cerebellar ataxia, deafness, and narcolepsy | n2=en:narcolepsy | rel=r_associated | relid=0 | w=20 en:autosomal dominant cerebellar ataxia, deafness, and narcolepsy -- r_associated #0: 20 / 0.667 -> en:optic atrophy (in some patients) n1=en:autosomal dominant cerebellar ataxia, deafness, and narcolepsy | n2=en:optic atrophy (in some patients) | rel=r_associated | relid=0 | w=20 en:autosomal dominant cerebellar ataxia, deafness, and narcolepsy -- r_associated #0: 20 / 0.667 -> narcolepsie n1=en:autosomal dominant cerebellar ataxia, deafness, and narcolepsy | n2=narcolepsie | rel=r_associated | relid=0 | w=20 en:autosomal dominant cerebellar ataxia, deafness, and narcolepsy -- r_associated #0: 20 / 0.667 -> narcolepsy n1=en:autosomal dominant cerebellar ataxia, deafness, and narcolepsy | n2=narcolepsy | rel=r_associated | relid=0 | w=20

≈ 20 relations entrantes en:sensorineural hearing loss --- r_associated #0: 185 --> en:autosomal dominant cerebellar ataxia, deafness, and narcolepsy n1=en:sensorineural hearing loss | n2=en:autosomal dominant cerebellar ataxia, deafness, and narcolepsy | rel=r_associated | relid=0 | w=185 perte d'audition sensorineurale --- r_associated #0: 184 --> en:autosomal dominant cerebellar ataxia, deafness, and narcolepsy n1=perte d'audition sensorineurale | n2=en:autosomal dominant cerebellar ataxia, deafness, and narcolepsy | rel=r_associated | relid=0 | w=184 narcolepsie --- r_associated #0: 63 --> en:autosomal dominant cerebellar ataxia, deafness, and narcolepsy n1=narcolepsie | n2=en:autosomal dominant cerebellar ataxia, deafness, and narcolepsy | rel=r_associated | relid=0 | w=63 en:narcolepsy --- r_associated #0: 61 --> en:autosomal dominant cerebellar ataxia, deafness, and narcolepsy n1=en:narcolepsy | n2=en:autosomal dominant cerebellar ataxia, deafness, and narcolepsy | rel=r_associated | relid=0 | w=61 narcolepsy --- r_associated #0: 61 --> en:autosomal dominant cerebellar ataxia, deafness, and narcolepsy n1=narcolepsy | n2=en:autosomal dominant cerebellar ataxia, deafness, and narcolepsy | rel=r_associated | relid=0 | w=61 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome --- r_associated #0: 41 --> 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 demence --- r_associated #0: 34 --> en:autosomal dominant cerebellar ataxia, deafness, and narcolepsy n1=demence | n2=en:autosomal dominant cerebellar ataxia, deafness, and narcolepsy | rel=r_associated | relid=0 | w=34 en:dementia --- r_associated #0: 34 --> en:autosomal dominant cerebellar ataxia, deafness, and narcolepsy n1=en:dementia | n2=en:autosomal dominant cerebellar ataxia, deafness, and narcolepsy | rel=r_associated | relid=0 | w=34 démence héréditaire et infarctus multiples cérébraux --- r_associated #0: 31 --> en:autosomal dominant cerebellar ataxia, deafness, and narcolepsy n1=démence héréditaire et infarctus multiples cérébraux | n2=en:autosomal dominant cerebellar ataxia, deafness, and narcolepsy | rel=r_associated | relid=0 | w=31 en:decreased csf hypocretin --- r_associated #0: 31 --> en:autosomal dominant cerebellar ataxia, deafness, and narcolepsy n1=en:decreased csf hypocretin | n2=en:autosomal dominant cerebellar ataxia, deafness, and narcolepsy | rel=r_associated | relid=0 | w=31 en:autosomal dominant inheritance --- r_associated #0: 28 --> en:autosomal dominant cerebellar ataxia, deafness, and narcolepsy n1=en:autosomal dominant inheritance | n2=en:autosomal dominant cerebellar ataxia, deafness, and narcolepsy | rel=r_associated | relid=0 | w=28 en:limb lymphedema (in some patients) --- r_associated #0: 28 --> en:autosomal dominant cerebellar ataxia, deafness, and narcolepsy n1=en:limb lymphedema (in some patients) | n2=en:autosomal dominant cerebellar ataxia, deafness, and narcolepsy | rel=r_associated | relid=0 | w=28 en:excessive daytime somnolence --- r_associated #0: 27 --> en:autosomal dominant cerebellar ataxia, deafness, and narcolepsy n1=en:excessive daytime somnolence | n2=en:autosomal dominant cerebellar ataxia, deafness, and narcolepsy | rel=r_associated | relid=0 | w=27 en:optic atrophy (in some patients) --- r_associated #0: 26 --> en:autosomal dominant cerebellar ataxia, deafness, and narcolepsy n1=en:optic atrophy (in some patients) | n2=en:autosomal dominant cerebellar ataxia, deafness, and narcolepsy | rel=r_associated | relid=0 | w=26 démence --- r_associated #0: 20 --> en:autosomal dominant cerebellar ataxia, deafness, and narcolepsy n1=démence | n2=en:autosomal dominant cerebellar ataxia, deafness, and narcolepsy | rel=r_associated | relid=0 | w=20 Narcolepsie --- r_associated #0: 10 --> en:autosomal dominant cerebellar ataxia, deafness, and narcolepsy n1=Narcolepsie | n2=en:autosomal dominant cerebellar ataxia, deafness, and narcolepsy | rel=r_associated | relid=0 | w=10 démence (sémiologie) --- r_associated #0: 10 --> en:autosomal dominant cerebellar ataxia, deafness, and narcolepsy n1=démence (sémiologie) | n2=en:autosomal dominant cerebellar ataxia, deafness, and narcolepsy | rel=r_associated | relid=0 | w=10 en:hereditary multi-infarct type --- r_associated #0: 10 --> en:autosomal dominant cerebellar ataxia, deafness, and narcolepsy n1=en:hereditary multi-infarct type | n2=en:autosomal dominant cerebellar ataxia, deafness, and narcolepsy | rel=r_associated | relid=0 | w=10 en:sleep epilepsy --- r_associated #0: 10 --> en:autosomal dominant cerebellar ataxia, deafness, and narcolepsy n1=en:sleep epilepsy | n2=en:autosomal dominant cerebellar ataxia, deafness, and narcolepsy | rel=r_associated | relid=0 | w=10 en:sleeping disease --- r_associated #0: 10 --> en:autosomal dominant cerebellar ataxia, deafness, and narcolepsy n1=en:sleeping disease | n2=en:autosomal dominant cerebellar ataxia, deafness, and narcolepsy | rel=r_associated | relid=0 | w=10