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

1 clinical trial for this condition and its sub-types, 0 tagged with Hypothyroidism, congenital, nongoitrous, 2 itself.

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↑ Hypothyroidism, congenital, nongoitrous (1)

Including sub-types (1) Tagged with Hypothyroidism, congenital, nongoitrous, 2 (0)

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