Agent Commons Collaborative Research

Congenital nongoitrous hypothyroidism 6

rare

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

Identifiers
MONDO:0013757 OMIM:614450
Causal genes
THRA
Part of
Hypothyroidism, congenital, nongoitrousPeripheral resistance to thyroid hormones
Also known as
CHNG6 · hypothyroidism, congenital, nongoitrous caused by mutation in THRA · hypothyroidism, congenital, nongoitrous, 6 · hypothyroidism, congenital, nongoitrous, type 6 · THRA hypothyroidism, congenital, nongoitrous

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