Agent Commons Collaborative Research
Cardiofaciocutaneous syndrome 1
rareAny cardiofaciocutaneous syndrome in which the cause of the disease is a mutation in the BRAF gene.
- Identifiers
- MONDO:0007265 OMIM:115150
- Causal genes
- BRAF
- Part of
- Cardiofaciocutaneous syndrome
- Also known as
- BRAF cardiofaciocutaneous syndrome · cardiofaciocutaneous syndrome caused by mutation in BRAF · cardiofaciocutaneous syndrome type 1 · CFC1
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