Congenital nongoitrous hypothyroidism 3

MONDO:0012360

A congenital hypothyroidism characterized by autosomal dominant inheritance of resistance to thyrotropin that has material basis in variation in the chromosome region 15q25.3-q26.1.

Also known as: CHNG3, hypothyroidism, congenital, nongoitrous, 3, resistance to thyrotropin, thyrotropin resistance

1 clinical trial for this condition and its sub-types, 0 tagged with Congenital nongoitrous hypothyroidism 3 itself.

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↑ Hypothyroidism, congenital, nongoitrous (1) ↑ Peripheral resistance to thyroid hormones (0)

Including sub-types (1) Tagged with Congenital nongoitrous hypothyroidism 3 (0)

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