{"orpha":208593,"name":"Genetic hypoparathyroidism","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-208593/","orphanet_url":"https://www.orpha.net/en/disease/detail/208593","names":{"fr":{"name":"Hypoparathyroïdie génétique"},"de":{"name":"Hypoparathyreoidismus, genetisch bedingter"},"es":{"name":"Hipoparatiroidismo genético"},"it":{"name":"Ipoparatiroidismo genetico"},"nl":{"name":"Genetische hypoparathyreoïdie"},"pt":{"name":"Hipoparatiroidismo genético"},"pl":{"name":"Niedoczynność przytarczyc uwarunkowana genetycznie"},"cs":{"name":"Genetický hypoparathyreoidismus"},"uk":{"name":"Генетично обумовлений гіпопаратиреоз"},"zh":{"name":"遗传性甲状旁腺机能减退"},"tr":{"name":"Genetik hipoparatiroidi"}},"xrefs":[{"source":"MONDO","code":"16165","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5680825","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":3453,"name":"Autoimmune polyendocrinopathy type 1","type":"Disease"},{"orpha":2238,"name":"Familial isolated hypoparathyroidism","type":"Disease"},{"orpha":97593,"name":"Pseudohypoparathyroidism","type":"Category"},{"orpha":181402,"name":"Syndrome with hypoparathyroidism","type":"Category"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}