fundus albipunctatus 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)
Similar Terms
Downloads & Tools

Genes

1 genes associated with the disease fundus albipunctatus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
RDH5 retinol dehydrogenase 5 (11-cis/9-cis)