Hypothyroidism, congenital, nongoitrous, 5

Definition

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

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

Also identified as

• DOID 0070125 per MONDO
• MESH C567123 per MONDO
• OMIM 225250 per MONDO
• UMLS C2673630 per MONDO