retinal flecks Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Presence of multiple yellowish-white lesions of various size and configuration on the retina not related to vascular lesions. (Human Phenotype Ontology, HP_0012045)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0012045
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Genes

7 genes associated with the retinal flecks phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
BEST1 bestrophin 1
PROM1 prominin 1
PRPH2 peripherin 2 (retinal degeneration, slow)
RDH5 retinol dehydrogenase 5 (11-cis/9-cis)
RHO rhodopsin
RIMS1 regulating synaptic membrane exocytosis 1
RLBP1 retinaldehyde binding protein 1