{"orpha":181408,"name":"Rare 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-181408/","orphanet_url":"https://www.orpha.net/en/disease/detail/181408","names":{"fr":{"name":"Hyperparathyroïdie rare"},"de":{"name":"Hyperparathyroidismus, seltener"},"es":{"name":"Hiperparatiroidismo raro"},"it":{"name":"Iperparatiroidismo raro"},"nl":{"name":"Zeldzame hyperparathyreoïdie"},"pt":{"name":"Hiperparatiroidismo raro"},"pl":{"name":"Rzadka nadczynność przytarczyc"},"cs":{"name":"Vzácný hyperparatyreoidismus"},"uk":{"name":"Рідкісний гіперпаратиреоз"},"zh":{"name":"罕见甲状旁腺功能亢进症"},"tr":{"name":"Nadir hiperparatiroidi"}},"xrefs":[{"source":"MONDO","code":"15897","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5680614","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":97978,"name":"Rare endocrine disease"},"parents":[{"orpha":68415,"name":"Rare parathyroid disease and phosphocalcic metabolism anomaly","classifications":[193]}],"children":[{"orpha":2207,"name":"Familial primary hyperparathyroidism","type":"Clinical group"},{"orpha":417,"name":"Neonatal severe primary hyperparathyroidism","type":"Disease"},{"orpha":143,"name":"Parathyroid carcinoma","type":"Disease"},{"orpha":300493,"name":"Sagliker syndrome","type":"Particular clinical situation in a disease or syndrome"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}