Cardiofaciocutaneous syndrome 3

MONDO:0014113

Any cardiofaciocutaneous syndrome in which the cause of the disease is a mutation in the MAP2K1 gene.

Also known as: MAP2K1 cardiofaciocutaneous syndrome, cardiofaciocutaneous syndrome 3, cardiofaciocutaneous syndrome caused by mutation in MAP2K1, cardiofaciocutaneous syndrome type 3, CFC3

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