Fuchs Endothelial Dystrophy Gene Set

Dataset dbGAP Gene-Trait Associations
Category disease or phenotype associations
Type trait
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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Genes

2 genes associated with the trait Fuchs Endothelial Dystrophy in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

Symbol Name Standardized Value
TCF4 transcription factor 4 1.34708
PTPRG protein tyrosine phosphatase, receptor type, G 0.50084