{"orpha":306719,"name":"Neurodegenerative disease with chorea","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-306719/","orphanet_url":"https://www.orpha.net/en/disease/detail/306719","names":{"fr":{"name":"Maladie neurodégénérative avec mouvements choréiques"},"de":{"name":"Neurodegenerative Krankheit mit Chorea"},"es":{"name":"Enfermedad neurodegenerativa con corea"},"it":{"name":"Malattia neurodegenerativa con corea"},"nl":{"name":"Neurodegeneratieve ziekte met chorea"},"pt":{"name":"Doença neurodegenerativa com coreia"},"pl":{"name":"Choroba neurodegeneracyjna z pląsawicą"},"cs":{"name":"Neurodegenerativní onemocnění s choreou"},"uk":{"name":"Нейродегенеративне захворювання з хореєю"},"zh":{"name":"神经退行性疾病伴舞蹈病"},"tr":{"name":"Kore ile seyreden nörodejeneratif hastalık"}},"xrefs":[{"source":"MONDO","code":"17646","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5681064","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":98006,"name":"Rare neurologic disease"},"parents":[{"orpha":306715,"name":"Rare choreic movement disorder","classifications":[181]},{"orpha":496916,"name":"Rare genetic hyperkinetic movement disorder","classifications":[156]}],"children":[{"orpha":1429,"name":"Benign hereditary chorea","type":"Disease"},{"orpha":209905,"name":"Brain-lung-thyroid syndrome","type":"Disease"},{"orpha":494541,"name":"Childhood-onset benign chorea with striatal involvement","type":"Disease"},{"orpha":399,"name":"Huntington disease","type":"Disease"},{"orpha":157941,"name":"Huntington disease-like 1","type":"Disease"},{"orpha":401901,"name":"Huntington disease-like syndrome due to C9ORF72 expansions","type":"Disease"},{"orpha":248111,"name":"Juvenile Huntington disease","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}