|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|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)|
|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.