All diseases

OMIM ID
115150
OMIM term:
CARDIOFACIOCUTANEOUS SYNDROME
Alternative terms:
CFC SYNDROME
CFCS
(∗) Location:
12p12.1   15q22.31   19p13.3   7q34  
(†) Associated OMIM genes:
BRAF   KRAS   MAP2K1   MAP2K2  
(‡) Associated MGI genes:
Braf  

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* quick link - http://q.sanger.ac.uk/acruno9n