retinitis punctata albescens Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A fundus dystrophy that is characterized by discrete uniform white dots over the entire fundus with greatest density in the midperiphery and no macular involvement. (Human Disease Ontology, DOID_11105)
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Genes

2 genes associated with the disease retinitis punctata albescens in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
RHO rhodopsin
RLBP1 retinaldehyde binding protein 1