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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5 genes associated with the disease fuchs' endothelial dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
COL8A2 collagen, type VIII, alpha 2
IL23R interleukin 23 receptor
SLC4A11 solute carrier family 4, sodium borate transporter, member 11
TCF4 transcription factor 4
ZEB1 zinc finger E-box binding homeobox 1