visual hallucinations Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0002367
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Genes

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

Symbol Name
CACNA1A calcium channel, voltage-dependent, P/Q type, alpha 1A subunit
CLN6 ceroid-lipofuscinosis, neuronal 6, late infantile, variant
DNAJC5 DnaJ (Hsp40) homolog, subfamily C, member 5
EPM2A epilepsy, progressive myoclonus type 2A, Lafora disease (laforin)
FIG4 FIG4 phosphoinositide 5-phosphatase
NHLRC1 NHL repeat containing E3 ubiquitin protein ligase 1
SNCA synuclein, alpha (non A4 component of amyloid precursor)
SNCB synuclein, beta