rhegmatogenous retinal detachment Gene Set

Dataset HPO Gene-Disease 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://compbio.charite.de/hpoweb/showterm?id=HP:0012230
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Genes

1 genes associated with the rhegmatogenous retinal detachment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
COL2A1 collagen, type II, alpha 1