vitreoretinal degeneration Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Gradual deterioration of the vitreous humor and retina. (Human Phenotype Ontology, HP_0000655)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000655
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Genes

8 genes associated with the vitreoretinal degeneration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
COL11A1 collagen, type XI, alpha 1
COL18A1 collagen, type XVIII, alpha 1
COL2A1 collagen, type II, alpha 1
COL9A2 collagen, type IX, alpha 2
CRB1 crumbs family member 1, photoreceptor morphogenesis associated
NR2E3 nuclear receptor subfamily 2, group E, member 3
P3H2 prolyl 3-hydroxylase 2
VCAN versican