{"orpha":434786,"name":"Rare genetic autonomic nervous system 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-434786/","orphanet_url":"https://www.orpha.net/en/disease/detail/434786","names":{"fr":{"name":"Maladie génétique rare du système nerveux autonome"},"de":{"name":"Seltene genetische Krankheit des autonomen Nervensystems"},"es":{"name":"Trastorno genético raro del sistema nervioso autónomo"},"it":{"name":"Malattia genetica rara del sistema nervoso autonomo"},"nl":{"name":"Zeldzame genetische aandoening van autonoom zenuwstelsel"},"pt":{"name":"Doença genética do sistema nervoso autónomo"},"pl":{"name":"Rzadkie zaburzenia autonomicznego układu nerwowego uwarunkowane genetycznie"},"cs":{"name":"Vzácná genetická porucha autonomního nervového systému"},"uk":{"name":"Рідкісний генетично обумовлений розлад вегетативної нервової системи"},"zh":{"name":"罕见的遗传性植物神经系统疾病"},"tr":{"name":"Nadir genetik otonom sinir sistemi bozukluğu"}},"xrefs":[{"source":"MONDO","code":"18557","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5681212","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":98006,"name":"Rare neurologic disease"},"parents":[{"orpha":71859,"name":"Rare genetic neurological disorder","classifications":[156]}],"children":[{"orpha":661,"name":"Congenital central hypoventilation syndrome","type":"Disease"},{"orpha":581271,"name":"Cramp-fasciculation syndrome","type":"Disease"},{"orpha":99803,"name":"Haddad syndrome","type":"Malformation syndrome"},{"orpha":199282,"name":"Harlequin syndrome","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}