|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||A type of retinal detachment associated with a retinal tear, that is, with a break in the retina that allows fluid to pass from the vitreous space into the subretinal space between the sensory retina and the retinal pigment epithelium. (Human Phenotype Ontology, HP_0012230)|
|Downloads & Tools|
1 genes associated with the rhegmatogenous retinal detachment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
|COL2A1||collagen, type II, alpha 1|