Thyroid dyshormonogenesis 2A

MONDO:0010133

Thyroid peroxidase system defect due to presumed mutation(s) in the TPO gene, resulting in decreased activity of thyroid peroxidase.

Also known as: TDH2A, TPO familial thyroid dyshormonogenesis, familial thyroid dyshormonogenesis caused by mutation in TPO, hypothyroidism, congenital, due to dyshormonogenesis, 2A, thyroid dyshormonogenesis 2A, thyroid dyshormonogenesis type 2A, thyroid hormonogenesis, genetic defect in, 2A, iodide peroxidase deficiency

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