retinal arteriolar occlusion Gene Set

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
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Genes

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