Congenital nongoitrous hypothyroidism 6

Definition

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

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 — per MONDO

Also identified as

• DOID 0070128 per MONDO
• OMIM 614450 per MONDO
• UMLS C3280817 per MONDO