{"orpha":306747,"name":"Rare myoclonus","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-306747/","orphanet_url":"https://www.orpha.net/en/disease/detail/306747","names":{"fr":{"name":"Myoclonie rare"},"de":{"name":"Myoklonie, seltene"},"es":{"name":"Mioclono raro"},"it":{"name":"Mioclonia rara"},"nl":{"name":"Zeldzame myoclonus"},"pt":{"name":"Mioclonia rara"},"pl":{"name":"Rzadki mioklonus"},"cs":{"name":"Vzácné myoklony"},"uk":{"name":"Рідкісний міоклонус"},"zh":{"name":"罕见肌阵挛"},"tr":{"name":"Nadir miyoklonus"}},"xrefs":[{"source":"MONDO","code":"17650","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5681067","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":98006,"name":"Rare neurologic disease"},"parents":[{"orpha":494457,"name":"Rare hyperkinetic movement disorder","classifications":[181]}],"children":[{"orpha":306750,"name":"Primary myoclonus","type":"Category"},{"orpha":306753,"name":"Rare disease with myoclonus as a major feature","type":"Category"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}