congenital stationary night blindness autosomal dominant 3 (Q32140451)
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congenital stationary night blindness characterized by autosomal dominant inheritance that has material basis in heterozygous mutation in the GNAT1 gene on chromosome 3p21
- CSNBAD3
- Nougaret type congenital stationary night blindness
- Night Blindness, Congenital Stationary, Nougaret Type
- congenital stationary night blindness autosomal dominant type 3
- NIGHT BLINDNESS, CONGENITAL STATIONARY, AUTOSOMAL DOMINANT 3
- NIGHT BLINDNESS, CONGENITAL STATIONARY, AUTOSOMAL DOMINANT 3; CSNBAD3
- Night Blindness, Congenital Stationary, Autosomal Dominant type 3
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | congenital stationary night blindness autosomal dominant 3 |
congenital stationary night blindness characterized by autosomal dominant inheritance that has material basis in heterozygous mutation in the GNAT1 gene on chromosome 3p21 |
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