congenital nongoitrous hypothryoidism 6 ^{الإنجليزية} (Q5307454)

A congenital hypothyroidism that has material basis in heterozygous mutation in the THRA gene on chromosome 17q21.1. ^{الإنجليزية}

اللغة	التسمية	الوصف	أسماء أخرى
العربية	لم تُضف التسمية	لا يوجد وصف
الإنجليزية	congenital nongoitrous hypothryoidism 6	A congenital hypothyroidism that has material basis in heterozygous mutation in the THRA gene on chromosome 17q21.1.	CHNG6 HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 6 HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 6; CHNG6 Hypothyroidism, Congenital, Nongoitrous, type 6 congenital nongoitrous hypothyroidism 6

بيانات

Wikidata item ^{الإنجليزية}

٠ مرجع