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