cystoid macular degeneration Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A form of macular degeneration characterized by the presence of multiple cysts in the macula. (Human Phenotype Ontology, HP_0008028)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0008028
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Genes

2 genes associated with the cystoid macular degeneration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
BEST1 bestrophin 1
NR2E3 nuclear receptor subfamily 2, group E, member 3