{"orpha":238699,"name":"Transient congenital hypothyroidism due to neonatal factor","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-238699/","orphanet_url":"https://www.orpha.net/en/disease/detail/238699","names":{"fr":{"name":"Hypothyroïdie congénital transitoire de cause néonatale"},"de":{"name":"Hypothyreose, kongenitale transiente, durch neonatalen Faktor"},"es":{"name":"Hipotiroidismo congénito transitorio por un factor neonatal"},"it":{"name":"Ipotiroidismo congenito transitorio di origine neonatale"},"nl":{"name":"Tijdelijke congenitale hypothyreoïdie als gevolg van neonatale factor"},"pt":{"name":"Hipotiroidismo transitório congénito por fator neonatal"},"pl":{"name":"Przejściowa wrodzona niedoczynność tarczycy z powodu czynnika noworodkowego"},"cs":{"name":"Tranzientní vrozená hypotyreóza způsobená faktorem ze strany novorozence"},"uk":{"name":"Транзиторний вроджений гіпотиреоз внаслідок неонатального фактору"},"zh":{"name":"新生儿因素所致短暂性先天性甲状腺功能减退"},"tr":{"name":"Yenidoğan faktörüne bağlı geçici doğumsal hipotiroidi"}},"xrefs":[{"source":"ICD-10","code":"P72.2","qualifier":"E","icd_relation":"specific","validated":true},{"source":"MONDO","code":"0016556","qualifier":"E","icd_relation":null,"validated":true},{"source":"MONDO","code":"16556","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5680930","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":97978,"name":"Rare endocrine disease"},"parents":[{"orpha":178045,"name":"Transient congenital hypothyroidism","classifications":[193]}],"children":[{"orpha":226316,"name":"Genetic transient congenital hypothyroidism","type":"Disease"},{"orpha":238688,"name":"Neonatal iodine exposure","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}