# 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

**Wikidata**: [Q32140451](https://www.wikidata.org/wiki/Q32140451)  
**Source**: https://4ort.xyz/entity/congenital-stationary-night-blindness-autosomal-dominant-3


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Missense mutation in the gene encoding the alpha subunit of rod transducin in the Nougaret form of congenital stationary night blindness
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)