Definition of FGD1

FGD1: The faciodigitogenital dysplasia gene. FGD1 normally plays an essential role in embryonic development. Mutations in FGD1 result in faciodigitogenital dysplasia, which is also called the Aarskog-Scott syndrome.


Last Editorial Review: 6/14/2012

Search MedTerms:


Back to MedTerms online medical dictionary A-Z List
Pill Identifier Tool

Need help identifying pills and medications?
Use the pill finder tool on RxList.


STAY INFORMED

Get the Latest health and medical information delivered direct to your inbox!