paroxysmal involuntary eye movements Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Sudden-onset episode of abnormal, involuntary eye movements. (Human Phenotype Ontology, HP_0007704)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0007704
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Genes

1 genes associated with the paroxysmal involuntary eye movements phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
SLC2A1 solute carrier family 2 (facilitated glucose transporter), member 1