| Dataset | CTD Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | disease |
| 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://ctdbase.org/detail.go?type=disease&acc=OMIM:613587 |
| Similar Terms | |
| Downloads & Tools |
1 genes/proteins associated with the disease OCCULT MACULAR DYSTROPHY from the curated CTD Gene-Disease Associations dataset.
| Symbol | Name | Standardized Value |
|---|---|---|
| RP1L1 | retinitis pigmentosa 1-like 1 | 2.88009 |
