Hypothyroidism, congenital, nongoitrous, 2

MONDO:0024264

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

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

Follow this condition — get notified about new trials

Broader categories

Sort by