epiretinal membrane Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An epiretinal membrane is a thin sheet of fibrous tissue that can develop on the surface of the macular area of the retina and cause a disturbance in vision. An epiretinal membrane area can develop on the thin macular area of the retin. An epiretinal membrane is also sometimes called a macular pucker, premacular fibrosis, surface wrinkling retinopathy or cellophane maculopathy. (Human Phenotype Ontology, HP_0100014)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0100014
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Genes

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

Symbol Name
NF2 neurofibromin 2 (merlin)