Congenital nongoitrous hypothyroidism 6

MONDO:0013757

Any hypothyroidism, congenital, nongoitrous in which the cause of the disease is a mutation in the THRA gene.

Also known as: CHNG6, THRA hypothyroidism, congenital, nongoitrous, hypothyroidism, congenital, nongoitrous caused by mutation in THRA, hypothyroidism, congenital, nongoitrous, 6, hypothyroidism, congenital, nongoitrous, type 6

1 clinical trial for this condition and its sub-types, 0 tagged with Congenital nongoitrous hypothyroidism 6 itself.

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

Including sub-types (1) Tagged with Congenital nongoitrous hypothyroidism 6 (0)

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