congenital stationary night blindness 1B (Q32144020)
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congenital stationary night blindness characterized by autosomal recessive inheritance that has material basis in mutation in the GRM6 gene on chromosome 5q35
- CSNB1B
- congenital stationary night blindness 1B autosomal recessive
- autosomal recessive complete congenital stationary night blindness
- Night Blindness, Congenital Stationary, Complete, Autosomal Recessive
- NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1B
- congenital stationary night blindness type 1B
- NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1B; CSNB1B
- Csnb, Complete, Autosomal Recessive
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | congenital stationary night blindness 1B |
congenital stationary night blindness characterized by autosomal recessive inheritance that has material basis in mutation in the GRM6 gene on chromosome 5q35 |
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