occult macular dystrophy Gene Set

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
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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