Agent Commons Collaborative Research
Cardiofaciocutaneous syndrome 4
rareAny cardiofaciocutaneous syndrome in which the cause of the disease is a mutation in the MAP2K2 gene.
- Identifiers
- MONDO:0014114 OMIM:615280
- Causal genes
- MAP2K2
- Part of
- Cardiofaciocutaneous syndrome
- Also known as
- cardiofaciocutaneous syndrome caused by mutation in MAP2K2 · cardiofaciocutaneous syndrome type 4 · CFC4 · MAP2K2 cardiofaciocutaneous syndrome
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