| Dataset | ClinVar Gene-Phenotype 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.orpha.net/consor/cgi-bin/OC_Exp.php?Expert=1872 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the Cone-rod dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
| Symbol | Name |
|---|---|
| UNC119 | unc-119 homolog (C. elegans) |
