Disease #03880 (CFC2 (cardiofaciocutaneous syndrome, type 2 (CFC-2)), OMIM:615278)

Official abbreviation CFC2
Name cardiofaciocutaneous syndrome, type 2 (CFC-2)
OMIM ID 615278
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene KRAS
Associated tissues -
Disease features -
Remarks -