Exudative Vitreoretinopathy Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A retinal vascular disease characterized by the prevention of blood vessel formation at the edges of the retina and the hemorrhage of the blood vessels in the retina. (Human Disease Ontology, DOID_0050535)
External Link https://www.disgenet.org/browser/0/1/0/C1854002
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Genes

6 genes associated with the disease Exudative Vitreoretinopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
CTNNB1 catenin (cadherin-associated protein), beta 1, 88kDa
FZD4 frizzled class receptor 4
LRP5 low density lipoprotein receptor-related protein 5
NDP Norrie disease (pseudoglioma)
PRSS23 protease, serine, 23
ZNF408 zinc finger protein 408