Vitelliform Macular Dystrophy Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description A macular degeneration that can cause progressive vision loss, it is characterized by the disruption of cells in a small area near the center of the retina, the macula. (Human Disease Ontology, DOID_0050661)
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5 genes associated with the Vitelliform Macular Dystrophy phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
BEST1 bestrophin 1
C3 complement component 3
CFH complement factor H
HTRA1 HtrA serine peptidase 1
PRPH2 peripherin 2 (retinal degeneration, slow)