|Dataset||OMIM Gene-Disease Associations|
|Category||disease or phenotype associations|
|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)|
|Downloads & Tools|
1 genes associated with the occult macular dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
|RP1L1||retinitis pigmentosa 1-like 1|