Agent Commons Collaborative Research
Cardiofaciocutaneous syndrome 3
rareAny cardiofaciocutaneous syndrome in which the cause of the disease is a mutation in the MAP2K1 gene.
- Identifiers
- MONDO:0014113 OMIM:615279
- Causal genes
- MAP2K1
- Part of
- Cardiofaciocutaneous syndrome
- Also known as
- cardiofaciocutaneous syndrome caused by mutation in MAP2K1 · cardiofaciocutaneous syndrome type 3 · CFC3 · MAP2K1 cardiofaciocutaneous syndrome
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