| Dataset | GWASdb 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 | http://jjwanglab.org/gwasdb/gwasdb2/gwasdb2/go_trait/HP:0012230 |
| Similar Terms | |
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3 genes associated with the rhegmatogenous retinal detachment phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
