Visual Auras Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Auras with sensation of flashing or flickering lights, spots, simple patterns, scotomata, or amaurosis. (Human Phenotype Ontology, HP_0011165)
External Link https://www.disgenet.org/browser/0/1/0/C1850765
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Genes

7 genes associated with the disease Visual Auras in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
CNTN2 contactin 2 (axonal)
CSAD cysteine sulfinic acid decarboxylase
EPM2A epilepsy, progressive myoclonus type 2A, Lafora disease (laforin)
HLA-DRB1 major histocompatibility complex, class II, DR beta 1
LGI1 leucine-rich, glioma inactivated 1
NHLRC1 NHL repeat containing E3 ubiquitin protein ligase 1
TGFBI transforming growth factor, beta-induced, 68kDa