|Dataset||OMIM Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||A retinal degeneration that is an inherited progressive disease that causes deterioration of the cone and rod photoreceptor cells and often results in blindness. (Human Disease Ontology, DOID_0050572)|
|Downloads & Tools|
1 genes associated with the cone-rod dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
|AIPL1||aryl hydrocarbon receptor interacting protein-like 1|