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

13 clinical trials for this condition and its sub-types, 0 tagged with Cardiofaciocutaneous syndrome 3 itself.

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↑ Cardiofaciocutaneous syndrome (7)

Including sub-types (13) Tagged with Cardiofaciocutaneous syndrome 3 (0)

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