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 |
- |
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