| 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 |
| Similar Terms | |
| 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.
| Symbol | Name |
|---|---|
| SLC2A1 | solute carrier family 2 (facilitated glucose transporter), member 1 |
