| Dataset | OMIM Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | An age related macular degeneration that is characterized by progressive vision loss usually to the point of legal blindness. (Human Disease Ontology, DOID_0050817) |
| External Link | http://www.omim.org/entry/248200 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the stargardt disease 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| ABCA4 | ATP-binding cassette, sub-family A (ABC1), member 4 |
