congenital stationary night blindness 1H (Q32144035)
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congenital stationary night blindness characterized by autosomal recessive inheritance that has material basis in homozygous or compound heterozygous mutation in the GNB3 gene on chromosome 12p13
- CSNB1H
- congenital stationary night blindness type 1H
- Night Blindness, Congenital Stationary, Type 1H
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | congenital stationary night blindness 1H |
congenital stationary night blindness characterized by autosomal recessive inheritance that has material basis in homozygous or compound heterozygous mutation in the GNB3 gene on chromosome 12p13 |
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