Description of the disease * EnglishPolish Pobierz sekcję do PDF Definition Central or secondary congenital hypothyroidism is a type of permanent congenital hypothyroidism (see this term) characterized by permanent thyroid hormone deficiency that is present from birth and secondary to a disorder in the thyroid-stimulating hormone (TSH) - thyrotropin-releasing hormone (TRH) system. Disease data Classification Clinical group Synonyms Secondary hypothyroidism Wtórna niedoczynność tarczycy ORPHA code 226298 OMIM code - ICD10 code E03.1 ICD11 code 5A61.41 *Soruce Extended description of the disease Pobierz sekcję do PDF No additional description. Orphanet - interntowa baza danych dotyczących rzadkich chorób i sierochych leków. ©INSERM 1999 - Dostępna na stronie www.orphanet.pl