Hypothyroidism, congenital, nongoitrous, 5

MONDO:0009154

Any hypothyroidism, congenital, nongoitrous in which the cause of the disease is a mutation in the NKX2-5 gene.

Also known as: CHNG5, NKX2-5 hypothyroidism, congenital, nongoitrous, hypothyroidism, congenital nongoitrous, 5, hypothyroidism, congenital, nongoitrous caused by mutation in NKX2-5, hypothyroidism, congenital, nongoitrous, 5, hypothyroidism, congenital, nongoitrous, type 5, congenital nongoitrous hypothyroidism 5

1 clinical trial for this condition and its sub-types, 0 tagged with Hypothyroidism, congenital, nongoitrous, 5 itself.

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↑ Hypothyroidism, congenital, nongoitrous (1)

Including sub-types (1) Tagged with Hypothyroidism, congenital, nongoitrous, 5 (0)

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