episcleritis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Inflammation of the episclera, a thin layer of tissue covering the white part (sclera) of the eye. (Human Phenotype Ontology, HP_0100534)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0100534
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Genes

2 genes associated with the episcleritis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
PSMB8 proteasome (prosome, macropain) subunit, beta type, 8
SLC29A3 solute carrier family 29 (equilibrative nucleoside transporter), member 3