|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|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)|
|Downloads & Tools|
3 genes associated with the tractional retinal detachment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.