adult-onset night blindness Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Inability to see well at night or in poor light with onset in adulthood. (Human Phenotype Ontology, HP_0007830)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0007830
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Genes

3 genes associated with the adult-onset night blindness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
C1QTNF5 C1q and tumor necrosis factor related protein 5
PRPH2 peripherin 2 (retinal degeneration, slow)
ROM1 retinal outer segment membrane protein 1