visual auras Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Auras with sensation of flashing or flickering lights, spots, simple patterns, scotomata, or amaurosis. (Human Phenotype Ontology, HP_0011165)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0011165
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Genes

2 genes associated with the visual auras phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
EPM2A epilepsy, progressive myoclonus type 2A, Lafora disease (laforin)
NHLRC1 NHL repeat containing E3 ubiquitin protein ligase 1