Thyroid dyshormonogenesis 5

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

1 clinical trial for this condition and its sub-types.