Thyroid dyshormonogenesis 5

Definition

Any familial thyroid dyshormonogenesis in which the cause of the disease is a mutation in the DUOXA2 gene.

Also known as DUOXA2 familial thyroid dyshormonogenesis, familial thyroid dyshormonogenesis caused by mutation in DUOXA2, hypothyroidism, congenital, due to dyshormonogenesis, 5, TDH5, thyroid dyshormonogenesis 5, thyroid dyshormonogenesis type 5, thyroid hormonogenesis, genetic defect in, 5 — per MONDO

Also identified as

• DOID 0112184 per MONDO
• MESH C562771 per MONDO
• OMIM 274900 per MONDO
• SCTID 63127008 per MONDO
• UMLS C0342196 per MONDO