DUOXA2 familial thyroid dyshormonogenesisTDH5familial thyroid dyshormonogenesis caused by mutation in DUOXA2hypothyroidism, congenital, due to dyshormonogenesis, 5thyroid dyshormonogenesis 5thyroid dyshormonogenesis type 5thyroid hormonogenesis, genetic defect in, 5
Definition
Any familial thyroid dyshormonogenesis in which the cause of the disease is a mutation in the DUOXA2 gene.
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