|Dataset||CTD 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|
2 genes/proteins associated with the disease Cone-Rod Dystrophy 5 from the curated CTD Gene-Disease Associations dataset.