tractional retinal detachment Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A type of retinal detachment associated with traction exerted by fibrous or fibrovascular tissue. The fibrous tissue is visible in the vitreous and may be the result of injury, inflammation or neovascularization. If such membranes contract, they pull the sensory retina apart from the underlying retinal pigment epithelium. (Human Phenotype Ontology, HP_0007917)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0007917
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Genes

3 genes associated with the tractional retinal detachment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
LRP5 low density lipoprotein receptor-related protein 5
TSPAN12 tetraspanin 12
VCAN versican