{"orpha":371861,"name":"Genetic hyperaldosteronism","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-371861/","orphanet_url":"https://www.orpha.net/en/disease/detail/371861","names":{"fr":{"name":"Hyperaldostéronisme génétique"},"de":{"name":"Hyperaldosteronismus, genetisch bedingter"},"es":{"name":"Hiperaldosteronismo genético"},"it":{"name":"Iperaldosteronismo genetico"},"nl":{"name":"Genetisch hyperaldosteronisme"},"pt":{"name":"Hiperaldosteronismo genético"},"pl":{"name":"Hiperaldosteronizm uwarunkowany genetycznie"},"cs":{"name":"Geneticky podmíněný hyperaldosteronismus"},"uk":{"name":"Генетично обумовлений гіперальдостеронізм"},"zh":{"name":"遗传性醛固酮增多症"},"tr":{"name":"Genetik hiperaldosteronizm"}},"xrefs":[{"source":"MONDO","code":"16525","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5681149","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":97978,"name":"Rare endocrine disease"},"parents":[{"orpha":183637,"name":"Rare genetic adrenal disease","classifications":[156]}],"children":[{"orpha":235936,"name":"Familial hyperaldosteronism","type":"Clinical group"},{"orpha":369929,"name":"Primary hyperaldosteronism-seizures-neurological abnormalities syndrome","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}