{"orpha":98070,"name":"OBSOLETE: Autosomal dominant spinocerebellar ataxia due to repeat expansions that do not encode polyglutamine","type":"Category","group":"Group of disorders","status":"inactive","flags":["Obsolete entity"],"synonyms":[],"definition":null,"note":"This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>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.<br/><br/>Instead, consider using Autosomal dominant cerebellar ataxia","url":"https://raremap.alftech.space/d/ORPHA-98070/","orphanet_url":"https://www.orpha.net/en/disease/detail/98070","names":{"fr":{"name":"OBSOLETE : Ataxie spinocérébelleuse autosomique dominante due à des expansions non codantes pour la polyglutamine"},"de":{"name":"OBSOLET: Ataxie, spinozerebelläre, bei Repeat-Expansionen, die nicht Polyglutamin betreffen"},"es":{"name":"OBSOLETO: Ataxia espinocerebelosa autosómica dominante por expansiones repetidas que no codifican para poliglutamina"},"it":{"name":"OBSOLETO: Atassia spinocerebellare da ripetute espansioni che non codificano per poliglutamine"},"nl":{"name":"OBSOLEET: Autosomaal dominante spinocerebellaire ataxie als gevolg van herhaalde expansies die geen polyglutamine coderen"},"pt":{"name":"OBSOLETO: Ataxia espinocerebelosa autossómica dominante por expansões repetitivas que não codificam poliglutamina"},"pl":{"name":"NIEAKTUALNE: Autosomalna dominujaca ataksja rdzeniowo-mózdzkowa z powodu ekspansji powtórzen, które nie koduja poliglutaminy"},"cs":{"name":"NEAKTUÁLNÍ: Autozomálně dominantní spinocerebelární ataxie způsobená expanzí repetitivních sekvencí nekódujících polyglutamin"},"uk":{"name":"ЗАСТАРІЛО: Аутосомно-домінантна спіноцеребеллярна атаксія внаслідок повторних експансій, які не кодують поліглутамін."},"zh":{"name":"弃用：不编码多聚谷氨酰胺重复扩张致常染色体显性遗传脊髓小脑性共济失调"},"tr":{"name":"Eski adı: Poliglutamini kodlamayan tekrarlayan genişlemelere bağlı otozomal dominant spinoserebellar ataksi"}},"xrefs":[],"associations":[{"type":"Referred to","orpha":99,"name":"Autosomal dominant cerebellar ataxia"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}