Aarskog-Scott Syndrome

About the Disease
Aarskog-Scott Syndrome, also known as aarskog syndrome, is related to unilateral focal polymicrogyria and aarskog syndrome, autosomal dominant. An important gene associated with Aarskog-Scott Syndrome is FGD1 (FYVE, RhoGEF And PH Domain Containing 1), and among its related pathways/superpathways are Signal Transduction and GPCR downstream signalling. Affiliated tissues include testes, heart and skin, and related phenotypes are hypertelorism and umbilical hernia

Common Targets
MCF2 | FGD1

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