fuchs endothelial dystrophy Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A corneal dystrophy characterized by accumulation of focal outgrowths (guttae) and thickening of Descemet's membrane, leading to corneal edema and loss of vision. (Human Disease Ontology, DOID_11555)
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2 genes associated with the disease fuchs endothelial dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
PTPRG protein tyrosine phosphatase, receptor type, G
TCF4 transcription factor 4