Hypothyroidism, congenital, nongoitrous, 2

A congenital hypothyroidism that has material basis in heterozygous mutation in the PAX8 gene on chromosome 2q13.

Also known as: CHNG2, hypothyroidism, congenital, due to thyroid dysgenesis or hypoplasia, hypothyroidism, congenital, nongoitrous, 2, athyreotic hypothyroidism, congenital nongoitrous hypothyroidism 2, hypothyroidism, athyreotic, hypothyroidism, congenital, due to thyroid dysgenesis, resistance to thyrotropin

0 clinical trials for this condition and its sub-types.