{"orpha":391799,"name":"Rare genetic dystonia","type":"Category","group":"Group of disorders","status":"active","flags":[],"synonyms":["Rare genetic dystonic disorder"],"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-391799/","orphanet_url":"https://www.orpha.net/en/disease/detail/391799","names":{"fr":{"name":"Dystonie génétique rare"},"de":{"name":"Seltene genetisch bedingte Dystonie","synonyms":["Seltene genetisch dystonische Störung"]},"es":{"name":"Distonía genética rara","synonyms":["Trastorno distónico genético raro"]},"it":{"name":"Distonia genetica rara","synonyms":["Malattia distonica genetica rara"]},"nl":{"name":"Zeldzame genetische dystonie","synonyms":["Zeldzame genetische dystonische stoornis"]},"pt":{"name":"Distonia genética rara"},"pl":{"name":"Rzadka dystonia genetyczna","synonyms":["Rzadkie genetyczne zaburzenie dystoniczne"]},"cs":{"name":"Vzácná geneticky podmíněná dystonie","synonyms":["Vzácná geneticky podmíněná dystonická porucha"]},"uk":{"name":"Рідкісна генетично обумовлена дистонія","synonyms":["Рідкісне генетичне дистонічне захворювання"]},"zh":{"name":"罕见遗传性肌张力障碍","synonyms":["罕见遗传性肌张力低下"]},"tr":{"name":"Nadir genetik distoni","synonyms":["Nadir genetik distonik bozukluk"]}},"xrefs":[{"source":"UMLS","code":"C5680022","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":98006,"name":"Rare neurologic disease"},"parents":[{"orpha":496916,"name":"Rare genetic hyperkinetic movement disorder","classifications":[156]}],"children":[{"orpha":98203,"name":"Combined dystonia","type":"Category"},{"orpha":156159,"name":"Isolated dystonia","type":"Category"},{"orpha":370106,"name":"Rare disorder with dystonia and other neurologic or systemic manifestation","type":"Category"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}