{"orpha":306750,"name":"Primary 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-306750/","orphanet_url":"https://www.orpha.net/en/disease/detail/306750","names":{"fr":{"name":"Myoclonie primaire"},"de":{"name":"Myoklonie, primäre"},"es":{"name":"Mioclono primario"},"it":{"name":"Mioclonia primitiva"},"nl":{"name":"Primaire myoclonus"},"pt":{"name":"Mioclonia primária"},"pl":{"name":"Mioklonus pierwotny"},"cs":{"name":"Primární myoklonus"},"uk":{"name":"Первинний міоклонус"},"zh":{"name":"原发性肌阵挛"},"tr":{"name":"Primer miyoklonus"}},"xrefs":[{"source":"MONDO","code":"17651","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5681052","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":98006,"name":"Rare neurologic disease"},"parents":[{"orpha":307064,"name":"Rare genetic myoclonus","classifications":[156]},{"orpha":306747,"name":"Rare myoclonus","classifications":[181]}],"children":[{"orpha":86814,"name":"Familial adult myoclonic epilepsy","type":"Disease"},{"orpha":319189,"name":"Familial cortical myoclonus","type":"Disease"},{"orpha":221083,"name":"Hemifacial spasm","type":"Disease"},{"orpha":36899,"name":"Myoclonus-dystonia syndrome","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}