Thyroid dyshormonogenesis 5

MONDO:0010137

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, TDH5, familial thyroid dyshormonogenesis caused by mutation in DUOXA2, hypothyroidism, congenital, due to dyshormonogenesis, 5, thyroid dyshormonogenesis 5, thyroid dyshormonogenesis type 5, thyroid hormonogenesis, genetic defect in, 5

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