Thyroid dyshormonogenesis 6

Definition

Any familial thyroid dyshormonogenesis in which the cause of the disease is a mutation in the DUOX2 gene.

Also known as DUOX2 familial thyroid dyshormonogenesis, familial thyroid dyshormonogenesis caused by mutation in DUOX2, thyroid dyshormonogenesis 6, thyroid dyshormonogenesis type 6 — per MONDO

Also identified as

• DOID 0112189 per MONDO
• MESH C564608 per MONDO
• OMIM 607200 per MONDO
• Orphanet 226316 per MONDO
• UMLS C1846632 per MONDO