{"orpha":238696,"name":"Transient congenital hypothyroidism due to maternal 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-238696/","orphanet_url":"https://www.orpha.net/en/disease/detail/238696","names":{"fr":{"name":"Hypothyroïdie congénitale transitoire de cause maternelle"},"de":{"name":"Hypothyreose, kongenitale transiente, durch maternalen Faktor"},"es":{"name":"Hipotiroidimo congénito transitorio por causa materna"},"it":{"name":"Ipotiroidismo congenito transitorio di origine materna"},"nl":{"name":"Tijdelijke congenitale hypothyreoïdie als gevolg van maternale factor"},"pt":{"name":"Hipotiroidismo transitório congénito por fator materno"},"pl":{"name":"Przejściowa wrodzona niedoczynność tarczycy z powodu czynnika matczynego"},"cs":{"name":"Tranzientní vrozená hypotyreóza způsobená faktorem ze strany matky"},"uk":{"name":"Транзиторний вроджений гіпотиреоз через материнський фактор"},"zh":{"name":"妊娠期因素所致短暂性先天性甲状腺功能减退"},"tr":{"name":"Maternal faktöre bağlı geçici doğumsal hipotiroidi"}},"xrefs":[{"source":"MONDO","code":"0016555","qualifier":"E","icd_relation":null,"validated":true},{"source":"MONDO","code":"16555","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5680929","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":226313,"name":"Congenital hypothyroidism due to maternal intake of antithyroid drugs","type":"Disease"},{"orpha":95715,"name":"Congenital hypothyroidism due to transplacental passage of TSH-binding inhibitory antibodies","type":"Disease"},{"orpha":1910,"name":"Fetal iodine syndrome","type":"Malformation syndrome"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}