Vitelliform Macular Dystrophy Gene Set

Dataset CTD Gene-Disease Associations
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)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D057826
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Genes

2 genes/proteins associated with the disease Vitelliform Macular Dystrophy from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
PRPH2 peripherin 2 (retinal degeneration, slow) 2.88009
BEST1 bestrophin 1 2.88009