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GENATLAS PHENOTYPE
last update : 21/02/07
Symbol CFC5
Location 12p12.1
Name cardio-facio-cutaneous syndrome
Corresponding gene KRAS
Main clinical features
  • characterized by minor facial anomalies, cardiac defects, ectodermal anomalies and mental retardation
  • Genetic determination autosomal dominant
    Related entries CFC1-4, NS1, COSTS
    Function/system disorder multisystem/generalized
    mental retardation
    Type MCA/MR
    Remark(s)