{"orpha":307064,"name":"Rare genetic 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-307064/","orphanet_url":"https://www.orpha.net/en/disease/detail/307064","names":{"fr":{"name":"Myoclonie génétique rare"},"de":{"name":"Myoklonus, seltener, genetisch bedingter"},"es":{"name":"Mioclono genético raro"},"it":{"name":"Mioclonia genetica rara"},"nl":{"name":"Zeldzame genetische myoclonus"},"pt":{"name":"Mioclonia genética rara"},"pl":{"name":"Rzadki mioklonus uwarunkowany genetycznie"},"cs":{"name":"Vzácné geneticky podmíněné myoklony"},"uk":{"name":"Рідкісний генетично обумовлений міоклонус"},"zh":{"name":"罕见遗传性肌阵挛"},"tr":{"name":"Nadir genetik miyoklonus"}},"xrefs":[{"source":"MONDO","code":"17663","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5681059","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":306750,"name":"Primary myoclonus","type":"Category"},{"orpha":307067,"name":"Rare genetic disease with myoclonus as a major feature","type":"Category"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}