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References OMIM Gene GeneReviews HGMD HGNC
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