Thyroid dyshormonogenesis 6

MONDO:0011792

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, TDH6, hypothyroidism, congenital, due to dyshormonogenesis, 6, thyroid hormonogenesis, genetic defect in, 6

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