{"orpha":181405,"name":"Rare 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-181405/","orphanet_url":"https://www.orpha.net/en/disease/detail/181405","names":{"fr":{"name":"Hypoparathyroïdie rare"},"de":{"name":"Hypoparathyreoidismus, seltener"},"es":{"name":"Hipoparatiroidismo raro"},"it":{"name":"Ipoparatiroidismo raro"},"nl":{"name":"Zeldzame hypoparathyreoïdie"},"pt":{"name":"Hipoparatiroidismo raro"},"pl":{"name":"Rzadka niedoczynność przytarczyc"},"cs":{"name":"Vzácný hypoparatyreoidismus"},"uk":{"name":"Рідкісний гіпопаратиреоз"},"zh":{"name":"罕见甲状旁腺功能减退症"},"tr":{"name":"Nadir hipoparatiroidi"}},"xrefs":[{"source":"MONDO","code":"15896","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5680613","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":36913,"name":"Autoimmune hypoparathyroidism","type":"Disease"},{"orpha":3453,"name":"Autoimmune polyendocrinopathy type 1","type":"Disease"},{"orpha":2238,"name":"Familial isolated hypoparathyroidism","type":"Disease"},{"orpha":97593,"name":"Pseudohypoparathyroidism","type":"Category"},{"orpha":140286,"name":"Secondary hypoparathyroidism due to impaired parathormon secretion","type":"Disease"},{"orpha":181402,"name":"Syndrome with hypoparathyroidism","type":"Category"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}