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

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