{"orpha":98068,"name":"OBSOLETE: Autosomal dominant spinocerebellar ataxia due to a polyglutamine anomaly","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-98068/","orphanet_url":"https://www.orpha.net/en/disease/detail/98068","names":{"fr":{"name":"OBSOLETE : Ataxie spinocérébelleuse autosomique dominante due à une anomalie de la polyglutamine"},"de":{"name":"OBSOLET: Ataxie, spinozerebelläre, bei Polyglutamin-Anomalie"},"es":{"name":"OBSOLETO: Ataxia espinocerebelosa autosómica dominante por una anomalía de la poliglutamina"},"it":{"name":"OBSOLETO: Atassia spinocerebellare da anomalia delle poliglutamine"},"nl":{"name":"OBSOLEET: Autosomaal dominante spinocerebellaire ataxie als gevolg van een polyglutamineanomalie"},"pt":{"name":"OBSOLETO: Ataxia espinocerebelosa autossómica dominante por anomalia de poliglutamina"},"pl":{"name":"NIEAKTUALNE: Autosomalna dominujaca ataksja rdzeniowo-mózdzkowa z powodu anomalii poliglutaminy"},"cs":{"name":"NEAKTUÁLNÍ: Autozomálně dominantní spinocerebelární ataxie způsobená anomálií polyglutaminu"},"uk":{"name":"ЗАСТАРІЛО: Аутосомно-домінантна спіноцеребелярна атаксія внаслідок поліглутамінової аномалії"},"zh":{"name":"弃用：多谷氨酰胺异常致常染色体显性失调遗传脊髓小脑性共济失调"},"tr":{"name":"Eski adı: Poliglutamin anomalisine 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}