| 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 |
| Similar Terms | |
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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 |
