{"orpha":306768,"name":"Rare paroxysmal movement disorder","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-306768/","orphanet_url":"https://www.orpha.net/en/disease/detail/306768","names":{"fr":{"name":"Trouble du mouvement paroxystique rare"},"de":{"name":"Bewegungsstörung, seltene paroxysmale"},"es":{"name":"Trastorno raro del movimiento paroxístico"},"it":{"name":"Disturbo raro del movimento parossistico"},"nl":{"name":"Zeldzame paroxysmale bewegingsstoornis"},"pt":{"name":"Alterações paroxístico raras do movimento"},"pl":{"name":"Rzadkie napadowe zaburzenia ruchu"},"cs":{"name":"Vzácné paroxysmální poruchy hybnosti"},"uk":{"name":"Рідкісний пароксизмальний руховий розлад"},"zh":{"name":"罕见阵发性运动障碍"},"tr":{"name":"Nadir paroksismal hareket bozukluğu"}},"xrefs":[{"source":"MONDO","code":"17657","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5681054","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]},{"orpha":102003,"name":"Rare movement disorder","classifications":[181]}],"children":[{"orpha":1179,"name":"Benign paroxysmal tonic upgaze of childhood with ataxia","type":"Disease"},{"orpha":324588,"name":"Familial dyskinesia and facial myokymia","type":"Disease"},{"orpha":200037,"name":"Paroxysmal dystonia","type":"Clinical group"},{"orpha":71272,"name":"Sandifer syndrome","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}