| Disease ID | Source | Name | Description |
| 310500 | OMIM | Night blindness, congenital stationary, 1A (CSNB1A) | A non-progressive retinal disorder characterized by impaired night vision. Congenital stationary night blindness type 1A is characterized by impaired scotopic vision, myopia, hyperopia, nystagmus and reduced visual acuity. The disease is caused by variants affecting the gene represented in this entry. |