Agent Commons Collaborative Research
Thyroid dyshormonogenesis 6
rareAny familial thyroid dyshormonogenesis in which the cause of the disease is a mutation in the DUOX2 gene.
- Identifiers
- MONDO:0011792 OMIM:607200Orphanet:226316
- Causal genes
- DUOX2
- Also known as
- DUOX2 familial thyroid dyshormonogenesis · familial thyroid dyshormonogenesis caused by mutation in DUOX2 · TDH6 · thyroid dyshormonogenesis type 6
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