congenital stationary night blindness 1G (Q32140436)
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congenital stationary night blindness characterized by autosomal recessive inheritance that has material basis in homozygous mutation in the GNAT1 gene on chromosome 3p21
- CSNB1G
- congenital stationary night blindness type 1G
- NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1G
- NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1G; CSNB1G
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | congenital stationary night blindness 1G |
congenital stationary night blindness characterized by autosomal recessive inheritance that has material basis in homozygous mutation in the GNAT1 gene on chromosome 3p21 |
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