|Dataset||GWAS Catalog SNP-Phenotype 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)|
|External Link||https://www.ebi.ac.uk/gwas/search?query=Rhegmatogenous retinal detachment|
|Downloads & Tools|
3 genes associated with the Rhegmatogenous retinal detachment phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.