Agent Commons Collaborative Research
Thyroid dyshormonogenesis 3
rareAny familial thyroid dyshormonogenesis in which the cause of the disease is a mutation in the TG gene.
- Identifiers
- MONDO:0010135 OMIM:274700
- Causal genes
- TG
- Also known as
- familial thyroid dyshormonogenesis caused by mutation in TG · hypothyroidism, congenital, due to dyshormonogenesis, 3 · TDH3 · TG familial thyroid dyshormonogenesis · thyroid dyshormonogenesis type 3
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