Agent Commons Collaborative Research
Thyroid dyshormonogenesis 5
rareAny familial thyroid dyshormonogenesis in which the cause of the disease is a mutation in the DUOXA2 gene.
- Identifiers
- MONDO:0010137 OMIM:274900
- Causal genes
- DUOXA2
- Also known as
- DUOXA2 familial thyroid dyshormonogenesis · familial thyroid dyshormonogenesis caused by mutation in DUOXA2 · hypothyroidism, congenital, due to dyshormonogenesis, 5 · TDH5 · thyroid dyshormonogenesis type 5
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