{"orpha":448426,"name":"Genetic primary orthostatic hypotension","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-448426/","orphanet_url":"https://www.orpha.net/en/disease/detail/448426","names":{"fr":{"name":"Hypotension orthostatique primaire génétique"},"de":{"name":"Primäre orthostatische Hypotension, genetisch bedingte"},"es":{"name":"Hipotensión ortostática primaria genética"},"it":{"name":"Ipotensione ortostatica primitiva genetica"},"nl":{"name":"Genetische primaire orthostatische hypotensie"},"pt":{"name":"Hipotensão ortostática primária genética"},"pl":{"name":"Pierwotne niedociśnienie ortostatyczne uwarunkowane genetycznie"},"cs":{"name":"Geneticky podmíněná primární ortostatická hypotenze"},"uk":{"name":"Генетично обумовлена первинна ортостатична гіпотензія"},"zh":{"name":"遗传原位体位性低血压"},"tr":{"name":"Genetik primer ortostatik hipotansiyon"}},"xrefs":[{"source":"UMLS","code":"C5681106","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":98006,"name":"Rare neurologic disease"},"parents":[{"orpha":521232,"name":"Genetic primary orthostatic disorder","classifications":[156]}],"children":[{"orpha":230,"name":"Dopamine beta-hydroxylase deficiency","type":"Disease"},{"orpha":1764,"name":"Familial dysautonomia","type":"Disease"},{"orpha":411602,"name":"Hereditary late-onset Parkinson disease","type":"Disease"},{"orpha":2400,"name":"Peripheral motor neuropathy-dysautonomia syndrome","type":"Disease"},{"orpha":2828,"name":"Young-onset Parkinson disease","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}