rhegmatogenous retinal detachment Gene Set

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
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3 genes associated with the rhegmatogenous retinal detachment phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

Symbol Name Standardized Value
CERS2 ceramide synthase 2 1.15352
SS18 synovial sarcoma translocation, chromosome 18 1.00059
LDB2 LIM domain binding 2 0.919744