{"orpha":98069,"name":"OBSOLETE: Autosomal dominant spinocerebellar ataxia due to a channelopathy","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-98069/","orphanet_url":"https://www.orpha.net/en/disease/detail/98069","names":{"fr":{"name":"OBSOLETE : Ataxie spinocérébelleuse autosomique dominante due à une canalopathie"},"de":{"name":"OBSOLET: Ataxie, spinozerebelläre, bei Ionenkanalkrankheit"},"es":{"name":"OBSOLETO: Ataxia espinocerebelosa autosómica dominante por canalopatía"},"it":{"name":"OBSOLETO: Atassia spinocerebellare da canalopatia"},"nl":{"name":"OBSOLEET: Autosomaal dominante spinocerebellaire ataxie als gevolg van een kanalopathie"},"pt":{"name":"OBSOLETO: Ataxia espinhocerebelosa autossómica dominante por canalopatia"},"pl":{"name":"NIEAKTUALNE: Autosomalna dominujaca ataksja rdzeniowo-mózdzkowa z powodu kanalopatii"},"cs":{"name":"NEAKTUÁLNÍ: Autozomálně dominantní spinocerebelární ataxie způsobená kanálopatií"},"uk":{"name":"ЗАСТАРІЛО: Аутосомно-домінантна спіноцеребеллярна атаксія внаслідок каналопатії"},"zh":{"name":"弃用：离子通道病致常染色体显性脊髓小脑共济失调遗传病"},"tr":{"name":"Eski adı: Kanalopatiye 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}