vitelliform macular dystrophy Gene Set

Dataset DISEASES Curated Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
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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Genes

2 genes involed in the disease vitelliform macular dystrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

Symbol Name
BEST1 bestrophin 1
PRPH2 peripherin 2 (retinal degeneration, slow)