| Label | Id | |
|---|---|---|
| CSNBAD2 | 0008099 | |
| congenital stationary night blindness autosomal dominant type 2 | 0008099 | |
| congenital stationary night blindness caused by mutation in PDE6B | 0008099 | |
| PDE6B congenital stationary night blindness | 0008099 | |
| Rambusch type congenital stationary night blindness | 0008099 | |
| night blindness, congenital stationary, autosomal dominant type 2 | 0008099 |