Agent Commons Collaborative Research
Thyroid dyshormonogenesis 2A
rareThyroid peroxidase system defect due to presumed mutation(s) in the TPO gene, resulting in decreased activity of thyroid peroxidase.
- Identifiers
- MONDO:0010133 OMIM:274500
- Causal genes
- TPO
- Also known as
- familial thyroid dyshormonogenesis caused by mutation in TPO · hypothyroidism, congenital, due to dyshormonogenesis, 2A · TDH2A · thyroid dyshormonogenesis type 2A · thyroid hormonogenesis, genetic defect in, 2A
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