{"orpha":156629,"name":"Rare genetic cause of hypertension","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-156629/","orphanet_url":"https://www.orpha.net/en/disease/detail/156629","names":{"fr":{"name":"Hypertension artérielle de cause génétique rare"},"de":{"name":"Hypertension, genetisch bedingte"},"es":{"name":"Hipertensión genética"},"it":{"name":"Ipertensione genetica"},"nl":{"name":"Genetische hypertensie"},"pt":{"name":"Hipertensão genética"},"pl":{"name":"Nadciśnienie uwarunkowane genetycznie"},"cs":{"name":"Geneticky podmíněná hypertenze"},"uk":{"name":"Рідкісна генетично обумовлена гіпертонія"},"zh":{"name":"罕见遗传性高血压"},"tr":{"name":"Hipertansiyonun nadir genetik nedeni"}},"xrefs":[{"source":"MONDO","code":"15512","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5680639","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":93626,"name":"Rare renal disease"},"parents":[{"orpha":93618,"name":"Rare cause of hypertension","classifications":[188]},{"orpha":98056,"name":"Rare genetic renal disease","classifications":[156]}],"children":[{"orpha":320,"name":"Apparent mineralocorticoid excess","type":"Disease"},{"orpha":88659,"name":"Autosomal dominant progressive nephropathy with hypertension","type":"Disease"},{"orpha":1276,"name":"Brachydactyly-arterial hypertension syndrome","type":"Malformation syndrome"},{"orpha":235936,"name":"Familial hyperaldosteronism","type":"Clinical group"},{"orpha":88660,"name":"Hypertension due to gain-of-function mutations in the mineralocorticoid receptor","type":"Disease"},{"orpha":526,"name":"Liddle syndrome","type":"Disease"},{"orpha":636,"name":"Neurofibromatosis type 1","type":"Disease"},{"orpha":757,"name":"Pseudohypoaldosteronism type 2","type":"Disease"},{"orpha":758,"name":"Pseudoxanthoma elasticum","type":"Disease"},{"orpha":904,"name":"Williams syndrome","type":"Malformation syndrome"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}