| Dataset | OMIM Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | A macular degeneration that is characterized by a central cone dysfunction leading to a loss of vision with a normal fundus and normal fluorescein angiography findings. (Human Disease Ontology, DOID_0050578) |
| External Link | http://www.omim.org/entry/613587 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the occult macular dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| RP1L1 | retinitis pigmentosa 1-like 1 |
