| Dataset | GWAS Catalog SNP-Phenotype Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| 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 |
| Similar Terms | |
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3 genes associated with the Rhegmatogenous retinal detachment phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
