Home Page

References

OMIM

Gene

GeneReviews

HGMD

HGNC

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)