congenital stationary night blindness 1A (Q32144095)
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A congenital stationary night blindness that has material basis in mutation in the NYX gene on chromosome Xp11.4.
- complete CSNB X-linked
- NBMI
- hemeralopia-myopia
- congenital stationary night blindness 1A X-linked
- CSNB1A
- myopia-night blindness
- congenital stationary night blindness with myopia
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | congenital stationary night blindness 1A |
A congenital stationary night blindness that has material basis in mutation in the NYX gene on chromosome Xp11.4. |
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Statements
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Identifiers
1 reference
1 reference