| Dataset | HPO Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | Blockage of retinal arteriole, generally associated with interruption of blood flow and oxygen delivery to affected regions of the retina. (Human Phenotype Ontology, HP_0007985) |
| External Link | http://compbio.charite.de/hpoweb/showterm?id=HP:0007985 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the retinal arteriolar occlusion phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| BEST1 | bestrophin 1 |
