|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||Sudden-onset episode of abnormal, involuntary eye movements. (Human Phenotype Ontology, HP_0007704)|
|Downloads & Tools|
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.
|SLC2A1||solute carrier family 2 (facilitated glucose transporter), member 1|