Central Retinal Artery Occlusion Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A retinal artery occlusion characterized by blockage of blood flow through the central retinal artery. (Human Disease Ontology, DOID_13098)
External Link https://www.disgenet.org/browser/0/1/0/C0007688
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Genes

6 genes associated with the disease Central Retinal Artery Occlusion in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
COX8A cytochrome c oxidase subunit VIIIA (ubiquitous)
F5 coagulation factor V (proaccelerin, labile factor)
LPA lipoprotein, Lp(a)
MTHFR methylenetetrahydrofolate reductase (NAD(P)H)
PLAT plasminogen activator, tissue
SERPINC1 serpin peptidase inhibitor, clade C (antithrombin), member 1