{"orpha":178045,"name":"Transient congenital hypothyroidism","type":"Clinical group","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-178045/","orphanet_url":"https://www.orpha.net/en/disease/detail/178045","names":{"fr":{"name":"Hypothyroïdie congénitale transitoire"},"de":{"name":"Hypothyreose, kongenitale transiente"},"es":{"name":"Hipotiroidismo congénito transitorio"},"it":{"name":"Ipotiroidismo congenito transitorio"},"nl":{"name":"Voorbijgaande congenitale hypothyreoïdie"},"pt":{"name":"Hipotiroidismo congénito transitório"},"pl":{"name":"Wrodzona przejmijająca niedoczynność tarczycy"},"cs":{"name":"Přechodná vrozená hypotyreóza"},"uk":{"name":"Транзиторний вроджений гіпотиреоз"},"zh":{"name":"暂时性先天性甲状腺功能减退症"},"tr":{"name":"Geçici doğumsal hipotiroidi"}},"xrefs":[{"source":"ICD-11","code":"5A00.03","qualifier":"E","icd_relation":"specific","validated":true,"icd11_uri":"592246939"},{"source":"MONDO","code":"0015792","qualifier":"E","icd_relation":null,"validated":true},{"source":"MONDO","code":"15792","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":97978,"name":"Rare endocrine disease"},"parents":[{"orpha":442,"name":"Congenital hypothyroidism","classifications":[193]}],"children":[{"orpha":238696,"name":"Transient congenital hypothyroidism due to maternal factor","type":"Category"},{"orpha":238699,"name":"Transient congenital hypothyroidism due to neonatal factor","type":"Category"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}