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GENATLAS PHENOTYPE

last update : 30/06/2006

Symbol	FGS2
Location	Xq28
HGNC id	3699
Name	FG syndrome 2
Corresponding gene	FLNA
Main clinical features	mental retardation, facial anomalies, prominent forehead, hypotonia, failure to thrive, constipation, and anteriorly placed anus . associated with congenital heart disease, anal atresia, inguinal hernia, cryptorchidism
Genetic determination	sex linked
Function/system disorder	mental retardation
Type	disease