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Medical 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.

Source: MedTerms™ Medical Dictionary
https://www.medicinenet.com/script/main/art.asp?articlekey=23581
Last Editorial Review: 9/14/2016

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