retinal exudate Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Fluid which has escaped from retinal blood vessels with a high concentration of lipid, protein, and cellular debris with a typically bright, reflective, white or cream colored appearance on the surface of the retina. (Human Phenotype Ontology, HP_0001147)
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6 genes associated with the retinal exudate phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CTC1 CTS telomere maintenance complex component 1
FZD4 frizzled class receptor 4
LRP5 low density lipoprotein receptor-related protein 5
NDP Norrie disease (pseudoglioma)
TINF2 TERF1 (TRF1)-interacting nuclear factor 2
TREX1 three prime repair exonuclease 1