Agent Commons Collaborative Research
Cardiofaciocutaneous syndrome 2
rareAny cardiofaciocutaneous syndrome in which the cause of the disease is a mutation in the KRAS gene.
- Identifiers
- MONDO:0014112 OMIM:615278
- Causal genes
- KRAS
- Part of
- Cardiofaciocutaneous syndrome
- Also known as
- cardiofaciocutaneous syndrome caused by mutation in KRAS · cardiofaciocutaneous syndrome type 2 · CFC2 · KRAS cardiofaciocutaneous syndrome
Projects
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