| Dataset | OMIM Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| 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) |
| External Link | http://www.omim.org/entry/600977 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the cone-rod dystrophy 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| PITPNM3 | PITPNM family member 3 |
