{"orpha":247765,"name":"X-linked cerebellar ataxia","type":"Category","group":"Group of disorders","status":"active","flags":[],"synonyms":[],"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-247765/","orphanet_url":"https://www.orpha.net/en/disease/detail/247765","names":{"fr":{"name":"Ataxie cérébelleuse liée à l'X"},"de":{"name":"Zerebelläre Ataxie, X-chromosomale"},"es":{"name":"Ataxia cerebelosa ligada al cromosoma X"},"it":{"name":"Atassia cerebellare legata all'X"},"nl":{"name":"X-gebonden cerebellaire ataxie"},"pt":{"name":"Ataxia cerebelosa ligada ao X"},"pl":{"name":"Ataksja móżdżkowa sprzężona z X"},"cs":{"name":"X-vázaná spinocerebelární ataxie"},"uk":{"name":"Х-зчеплена мозочкова атаксія"},"zh":{"name":"x连锁遗传小脑性共济失调"},"tr":{"name":"X'e bağlı serebellar ataksi"}},"xrefs":[{"source":"MONDO","code":"0016612","qualifier":"E","icd_relation":null,"validated":true},{"source":"MONDO","code":"16612","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":98006,"name":"Rare neurologic disease"},"parents":[{"orpha":183518,"name":"Hereditary ataxia","classifications":[156,181]}],"children":[{"orpha":1188,"name":"Ataxia-deafness-intellectual disability syndrome","type":"Malformation syndrome"},{"orpha":85278,"name":"Christianson syndrome","type":"Malformation syndrome"},{"orpha":93256,"name":"Fragile X-associated tremor/ataxia syndrome","type":"Malformation syndrome"},{"orpha":1187,"name":"Lethal ataxia with deafness and optic atrophy","type":"Disease"},{"orpha":85338,"name":"X-linked intellectual disability-ataxia-apraxia syndrome","type":"Disease"},{"orpha":314978,"name":"X-linked non progressive cerebellar ataxia","type":"Disease"},{"orpha":1175,"name":"X-linked progressive cerebellar ataxia","type":"Disease"},{"orpha":2802,"name":"X-linked sideroblastic anemia and spinocerebellar ataxia","type":"Disease"},{"orpha":85297,"name":"X-linked spinocerebellar ataxia type 3","type":"Malformation syndrome"},{"orpha":85292,"name":"X-linked spinocerebellar ataxia type 4","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":["X-linked dominant","X-linked recessive"],"onset":[],"prevalence":[],"phenotypes":null}