lipemia retinalis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A creamy appearance of the retinal blood vessels that occurs when the concentration of lipids in the blood are extremely increased, with pale pink to milky white retinal vessels and altered pale reflexes from choroidal vasculature. (Human Phenotype Ontology, HP_0000660)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000660
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Genes

5 genes associated with the lipemia retinalis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
APOC2 apolipoprotein C-II
G6PC glucose-6-phosphatase, catalytic subunit
GPIHBP1 glycosylphosphatidylinositol anchored high density lipoprotein binding protein 1
LPL lipoprotein lipase
SLC37A4 solute carrier family 37 (glucose-6-phosphate transporter), member 4