Disease #00640 (CFC1 (cardiofaciocutaneous syndrome, type 1 (CFC-1)), OMIM:115150)
Official abbreviation |
CFC1 |
Name |
cardiofaciocutaneous syndrome, type 1 (CFC-1) |
OMIM ID |
115150 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
2 |
Phenotype entries for this disease |
2 |
Associated with 4 genes |
BRAF, KRAS, MAP2K1, MAP2K2 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Individuals
|
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