Monarch Disease Ontology identifier MONDO_0011792 (thyroid dyshormonogenesis 6) is 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 type 6.