| Dataset | OMIM Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the cone-rod retinal dystrophy-1 phenotype from the curated OMIM Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| CORD1 | cone rod dystrophy 1 (autosomal dominant) |
