retinal pigment epithelial atrophy Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0007698
Similar Terms
Downloads & Tools

Genes

3 genes associated with the retinal pigment epithelial atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
MFRP membrane frizzled-related protein
SNRNP200 small nuclear ribonucleoprotein 200kDa (U5)
TOPORS topoisomerase I binding, arginine/serine-rich, E3 ubiquitin protein ligase