{"orpha":226310,"name":"OBSOLETE: Peripheral hypothyroidism","type":"Clinical group","group":"Group of disorders","status":"inactive","flags":["Obsolete entity"],"synonyms":[],"definition":null,"note":"This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>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.<br/><br/>Instead, consider using Permanent congenital hypothyroidism","url":"https://raremap.alftech.space/d/ORPHA-226310/","orphanet_url":"https://www.orpha.net/en/disease/detail/226310","names":{"fr":{"name":"OBSOLETE : Hypothyroïdie périphérique"},"de":{"name":"OBSOLET: Hypothyreose, periphere"},"es":{"name":"OBSOLETO: Hipotiroidismo periférico"},"it":{"name":"OBSOLETO: Ipotiroidismo periferico"},"nl":{"name":"OBSOLEET: Perifere hypothyreoïdie"},"pt":{"name":"OBSOLETO: Hipotiroidismo periférico"},"pl":{"name":"NIEAKTUALNE: Obwodowa niedoczynność tarczycy"},"cs":{"name":"NEAKTUÁLNÍ: Periferní hypotyreóza"},"uk":{"name":"ЗАСТАРІЛО: Периферичний гіпотиреоз"},"zh":{"name":"外周甲状腺机能减退症","definition":"周围性甲状腺功能减退症是一种永久性先天性甲状腺功能减退症（见该词条），是一种从出生就存在的永久性甲状腺激素缺乏症，由甲状腺激素代谢的外周缺陷所致。"},"tr":{"name":"Periferik hipotiroidi"}},"xrefs":[],"associations":[{"type":"Referred to","orpha":226292,"name":"Permanent congenital hypothyroidism"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}