{"orpha":316235,"name":"Autosomal dominant spastic ataxia","type":"Category","group":"Group of disorders","status":"active","flags":[],"synonyms":["AD-SPAX"],"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-316235/","orphanet_url":"https://www.orpha.net/en/disease/detail/316235","names":{"fr":{"name":"Ataxie spastique autosomique dominante","synonyms":["AD-SPAX"]},"de":{"name":"Spastische Ataxie, autosomal-dominante","synonyms":["AD-SPAX"]},"es":{"name":"Ataxia espástica autosómica dominante","synonyms":["AD-SPAX"]},"it":{"name":"Atassia spastica autosomica dominante","synonyms":["AD-SPAX"]},"nl":{"name":"Autosomaal dominante spastische ataxie","synonyms":["AD-SPAX"]},"pt":{"name":"Ataxia espástica autossómica dominante","synonyms":["AD-SPAX"]},"pl":{"name":"Autosomalna dominująca ataksja spastyczna","synonyms":["AD-SPAX"]},"cs":{"name":"Autozomálně dominantní spastická ataxie","synonyms":["AD-SPAX"]},"uk":{"name":"Аутосомно-домінантна спастична атаксія","synonyms":["AD-SPAX"]},"zh":{"name":"常染色体显性遗传痉挛性共济失调","synonyms":["常染色体显性SPAX"]},"tr":{"name":"Otozomal dominant spastik ataksi","synonyms":["AD-SPAX"]}},"xrefs":[{"source":"MONDO","code":"0017846","qualifier":"E","icd_relation":null,"validated":true},{"source":"MONDO","code":"17846","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5679899","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":98006,"name":"Rare neurologic disease"},"parents":[{"orpha":316226,"name":"Spastic ataxia","classifications":[156,181]}],"children":[{"orpha":251282,"name":"Autosomal dominant spastic ataxia type 1","type":"Disease"},{"orpha":1182,"name":"Spastic ataxia with congenital miosis","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":["Autosomal dominant"],"onset":[],"prevalence":[],"phenotypes":null}