peripheral visual field loss Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Loss of peripheral vision with retention of central vision, resulting in a constricted circular tunnel-like field of vision. (Human Phenotype Ontology, HP_0007994)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0007994
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Genes

6 genes associated with the peripheral visual field loss phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CNGB1 cyclic nucleotide gated channel beta 1
CRX cone-rod homeobox
GUCY2D guanylate cyclase 2D, membrane (retina-specific)
PDE6A phosphodiesterase 6A, cGMP-specific, rod, alpha
PRPH2 peripherin 2 (retinal degeneration, slow)
ROM1 retinal outer segment membrane protein 1