{"orpha":101107,"name":"Spinocerebellar ataxia type 22","type":"Disease","group":"Disorder","status":"inactive","flags":["Deprecated entity"],"synonyms":["SCA22"],"definition":null,"note":"This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Spinocerebellar ataxia type 19/22","url":"https://raremap.alftech.space/d/ORPHA-101107/","orphanet_url":"https://www.orpha.net/en/disease/detail/101107","names":{"fr":{"name":"Ataxie spinocérébelleuse type 22","synonyms":["SCA22"]},"de":{"name":"Ataxie, spinozerebelläre, Typ 22","synonyms":["SCA22"]},"es":{"name":"Ataxia espinocerebolosa tipo 22","synonyms":["SCA22"]},"it":{"name":"Atassia spinocerebellare, tipo 22","synonyms":["SCA22"]},"nl":{"name":"Spinocerebellaire ataxie type 22","synonyms":["SCA22"]},"pt":{"name":"Ataxia espinocerebelosa tipo 22","synonyms":["SCA22"]},"pl":{"name":"Ataksja rdzeniowo-móżdżkowa typu 22","synonyms":["SCA22"]},"cs":{"name":"Spinocerebelární ataxie, typ 22","synonyms":["SCA22"]},"uk":{"name":"Спіноцеребеллярна атаксія, тип 22","synonyms":["SCA22"]},"zh":{"name":"脊髓小脑共济失调22型","synonyms":["SCA22"]},"tr":{"name":"Spinoserebellar ataksi tip 22","synonyms":["SCA22"]}},"xrefs":[{"source":"MeSH","code":"C542540","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C2746067","qualifier":"E","icd_relation":null,"validated":true}],"associations":[{"type":"Moved to","orpha":98772,"name":"Spinocerebellar ataxia type 19/22"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}