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Disease association ontology term - MONDO:0014113 - cardiofaciocutaneous syndrome 3

Term summary

ID
MONDO:0014113
Name
cardiofaciocutaneous syndrome 3
Ontology or CV name
Disease association
Definition
Any cardiofaciocutaneous syndrome in which the cause of the disease is a mutation in the MAP2K1 gene.

Parents

Annotation

Disease association

MONDO:0014113 - cardiofaciocutaneous syndrome 3

References:

Genes: