{"orpha":307058,"name":"Miscellaneous movement disorder due to genetic neurodegenerative disease","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-307058/","orphanet_url":"https://www.orpha.net/en/disease/detail/307058","names":{"fr":{"name":"Troubles divers du mouvement dus à une maladie génétique neurodégénérative"},"de":{"name":"Gemischte Bewegungsstörung bei genetischer neurodegenerativer Störung"},"es":{"name":"Trastornos del movimiento diversos por una enfermedad neurodegenerativa genética"},"it":{"name":"Disturbi vari del movimento da malattia neurodegenerativa genetica"},"nl":{"name":"Gevarieerde bewegingsstoornis door genetische neurodegeneratieve ziekte"},"pt":{"name":"Alterações diversas do movimento por doença neurodegenerativa genética"},"pl":{"name":"Różne zaburzenia ruchu spowdowane genetycznie uwarunowaną chorobą neurodegeneracyjną"},"cs":{"name":"Různé poruchy hybnosti na podkladě geneticky podmíněných neurodegenerativních onemocnění"},"uk":{"name":"Різні рухові розлади внаслідок генетично обумовленого нейродегенеративного захворювання"},"zh":{"name":"遗传性神经退行性病变所致多种运动障碍"},"tr":{"name":"Genetik nörodejeneratif hastalığa bağlı çeşitli hareket bozuklukları"}},"xrefs":[{"source":"MONDO","code":"17662","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5681056","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":98006,"name":"Rare neurologic disease"},"parents":[{"orpha":183521,"name":"Rare genetic movement disorder","classifications":[156]}],"children":[{"orpha":500180,"name":"Childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder","type":"Disease"},{"orpha":306708,"name":"Frontotemporal neurodegeneration with movement disorder","type":"Category"},{"orpha":157946,"name":"Huntington disease-like 3","type":"Disease"},{"orpha":1576,"name":"Infantile bilateral striatal necrosis","type":"Clinical group"},{"orpha":282166,"name":"Inherited Creutzfeldt-Jakob disease","type":"Disease"},{"orpha":263440,"name":"Neuroacanthocytosis","type":"Clinical group"},{"orpha":385,"name":"Neurodegeneration with brain iron accumulation","type":"Clinical group"},{"orpha":401768,"name":"Proximal myopathy with extrapyramidal signs","type":"Disease"},{"orpha":98759,"name":"Spinocerebellar ataxia type 17","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}