| Dataset | OMIM Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| External Link | http://www.omim.org/entry/300071 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the night blindness, congenital stationary (incomplete), 2a, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| CACNA1F | calcium channel, voltage-dependent, L type, alpha 1F subunit |
