{"orpha":94149,"name":"Autosomal dominant cerebellar ataxia type IV","type":"Clinical group","group":"Group of disorders","status":"active","flags":[],"synonyms":["ADCA4","ADCAIV","Autosomal dominant cerebellar ataxia type 4"],"definition":null,"note":"This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.","url":"https://raremap.alftech.space/d/ORPHA-94149/","orphanet_url":"https://www.orpha.net/en/disease/detail/94149","names":{"fr":{"name":"Ataxie cérébelleuse autosomique dominante type IV","synonyms":["ADCA4","ADCAIV","Ataxie cérébelleuse autosomique dominante type 4"]},"de":{"name":"Ataxie, zerebelläre, autosomal-dominante, Typ IV","synonyms":["ADCA4","ADCAIV","Ataxie, zerebelläre, autosomal-dominante, Typ 4"]},"es":{"name":"Ataxia cerebelosa autosómica dominante tipo IV","synonyms":["ADCA4","ADCAIV","Ataxia cerebelosa autosómica dominante tipo 4"]},"it":{"name":"Atassia cerebellare autosomica dominante, tipo 4","synonyms":["ADCA4","ADCAIV","Atassia cerebellare autosomica dominante, tipo IV"]},"nl":{"name":"Autosomaal dominante cerebellaire ataxie type IV","synonyms":["ADCA4","ADCAIV","Autosomaal dominante cerebellaire ataxie type 4"]},"pt":{"name":"Ataxia cerebelosa autossómica dominante tipo IV","synonyms":["ADCA4"]},"pl":{"name":"Autosomalna dominująca ataksja móżdżkowa typu IV","synonyms":["ADCA4","ADCAIV","Autosomalna dominująca ataksja móżdżkowa typu 4"]},"cs":{"name":"Autozomálně dominantní cerebelární ataxie, typ 4","synonyms":["ADCA4","ADCAIV","Autozomálně dominantní cerebelární ataxie, typ IV"]},"uk":{"name":"Аутосомно-домінантна мозочкова атаксія, тип IV","synonyms":["ADCA4","ADCAIV","Аутосомно-домінантна мозочкова атаксія типу 4"]},"zh":{"name":"常染色体显性遗传性小脑共济失调共济失调IV型","synonyms":["常染色体显性遗传性小脑共济失调4型"]},"tr":{"name":"Otozomal dominant serebellar ataksi tip IV","synonyms":["ADCA4","ADCAIV","Otozomal baskın serebellar ataksi tip 4"]}},"xrefs":[{"source":"MONDO","code":"0019794","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5680261","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":98006,"name":"Rare neurologic disease"},"parents":[{"orpha":99,"name":"Autosomal dominant cerebellar ataxia","classifications":[156,181]}],"children":[{"orpha":101,"name":"Dentatorubral pallidoluysian atrophy","type":"Disease"},{"orpha":98761,"name":"Spinocerebellar ataxia type 10","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":["Autosomal dominant"],"onset":[],"prevalence":[],"phenotypes":null}