{"orpha":307061,"name":"Rare genetic tremor 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-307061/","orphanet_url":"https://www.orpha.net/en/disease/detail/307061","names":{"fr":{"name":"Tremblement génétique rare"},"de":{"name":"Tremorkrankheit, seltene, genetisch bedingte"},"es":{"name":"Temblor genético raro"},"it":{"name":"Tremore genetico raro"},"nl":{"name":"Zeldzame genetische tremorstoornis"},"pt":{"name":"Alterações raras genéticas do tremor"},"pl":{"name":"Rzadkie zaburzenia z drżeniem uwarunkowane genetycznie"},"cs":{"name":"Vzácné geneticky podmíněné třesové poruchy"},"uk":{"name":"Рідкісне генетично обумовлений тремор"},"zh":{"name":"罕见遗传性震颤障碍"},"tr":{"name":"Nadir genetik titreme bozukluğu"}},"xrefs":[{"source":"MONDO","code":"17663","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5681058","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":93256,"name":"Fragile X-associated tremor/ataxia syndrome","type":"Malformation syndrome"},{"orpha":53372,"name":"Hereditary geniospasm","type":"Disease"},{"orpha":457212,"name":"Progressive essential tremor-speech impairment-facial dysmorphism-intellectual disability-abnormal behavior syndrome","type":"Disease"},{"orpha":66633,"name":"Sensorineural hearing loss-early graying-essential tremor syndrome","type":"Disease"},{"orpha":905,"name":"Wilson disease","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}