Educational Content: This article is for informational purposes only and does not constitute medical advice. Always consult a healthcare provider for diagnosis and treatment.
Definition of FGD1
Medically reviewed by Min Clinic Staff | Updated: January 2026
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.