Aarskog Syndrome Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A monogenic disease affects a person's height, muscles, skeleton, genitals, and appearance of the face. (Human Disease Ontology, DOID_6683)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:C535331
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1 genes/proteins associated with the disease Aarskog Syndrome from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
FGD1 FYVE, RhoGEF and PH domain containing 1 2.88009