Rhegmatogenous retinal detachment Gene Set

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
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Genes

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

Symbol Name Standardized Value
CERS2 ceramide synthase 2 0.342586
SS18 synovial sarcoma translocation, chromosome 18 0.165905
LDB2 LIM domain binding 2 0.085234