{"orpha":208596,"name":"Genetic hyperparathyroidism","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-208596/","orphanet_url":"https://www.orpha.net/en/disease/detail/208596","names":{"fr":{"name":"Hyperparathyroïdie génétique"},"de":{"name":"Hyperparathyreoidismus, genetisch bedingter"},"es":{"name":"Hiperparatiroidismo genético"},"it":{"name":"Iperparatiroidismo genetico"},"nl":{"name":"Genetische hyperparathyreoïdie"},"pt":{"name":"Hiperparatiroidismo genético"},"pl":{"name":"Nadczynność przytarczyc uwarunkowana genetycznie"},"cs":{"name":"Genetický hyperparathyreoidismus"},"uk":{"name":"Генетично обумовлений гіперпаратиреоз"},"zh":{"name":"遗传性甲状旁腺机能亢进"},"tr":{"name":"Genetik hiperparatiroidi"}},"xrefs":[{"source":"MONDO","code":"16166","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5680826","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":97978,"name":"Rare endocrine disease"},"parents":[{"orpha":183634,"name":"Rare genetic parathyroid disease and phosphocalcic metabolism disorder","classifications":[156]}],"children":[{"orpha":2207,"name":"Familial primary hyperparathyroidism","type":"Clinical group"},{"orpha":417,"name":"Neonatal severe primary hyperparathyroidism","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}