congenital stationary night blindness autosomal dominant 2 (Q32143990)
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congenital stationary night blindness characterized by autosomal dominant inhertance that has material basis in heterozygous mutation in the PDE6B gene on chromosome 4p16
- Rambusch type congenital stationary night blindness
- CSNBAD2
- NIGHT BLINDNESS, CONGENITAL STATIONARY, AUTOSOMAL DOMINANT 2; CSNBAD2
- Night Blindness, Congenital Stationary, Rambusch Type
- congenital stationary night blindness autosomal dominant type 2
- NIGHT BLINDNESS, CONGENITAL STATIONARY, AUTOSOMAL DOMINANT 2
- Night Blindness, Congenital Stationary, Autosomal Dominant type 2
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | congenital stationary night blindness autosomal dominant 2 |
congenital stationary night blindness characterized by autosomal dominant inhertance that has material basis in heterozygous mutation in the PDE6B gene on chromosome 4p16 |
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