{"orpha":181396,"name":"Rare hypothyroidism","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-181396/","orphanet_url":"https://www.orpha.net/en/disease/detail/181396","names":{"fr":{"name":"Hypothyroïdie rare"},"de":{"name":"Hypothyreose, seltene"},"es":{"name":"Hipotiroidismo raro"},"it":{"name":"Ipotiroidismo raro"},"nl":{"name":"Zeldzame hypothyreoïdie"},"pt":{"name":"Hipotiroidismo raro"},"pl":{"name":"Rzadka postać niedoczynności tarczycy"},"cs":{"name":"Vzácný hypotyreoidismus"},"uk":{"name":"Рідкісний гіпотиреоз"},"zh":{"name":"罕见甲状腺功能减退症"},"tr":{"name":"Nadir hipotiroidi"}},"xrefs":[{"source":"MONDO","code":"15893","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5680612","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":97978,"name":"Rare endocrine disease"},"parents":[{"orpha":183631,"name":"Rare genetic thyroid disease","classifications":[156]},{"orpha":101955,"name":"Rare thyroid disease","classifications":[193]}],"children":[{"orpha":442,"name":"Congenital hypothyroidism","type":"Category"},{"orpha":177101,"name":"Rare adult hypothyroidism","type":"Category"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}