Disease #03881 (CFC3 (cardiofaciocutaneous syndrome, type 3 (CFC-3)), OMIM:615279)

Official abbreviation CFC3
Name cardiofaciocutaneous syndrome, type 3 (CFC-3)
OMIM ID 615279
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene MAP2K1
Associated tissues -
Disease features -
Remarks -