# congenital stationary night blindness autosomal dominant 1

> congenital stationary night blindness characterized by autosomal dominant inheritance that has material basis in mutations in the RHO gene on chromosome 3q22.1

**Wikidata**: [Q32143975](https://www.wikidata.org/wiki/Q32143975)  
**Source**: https://4ort.xyz/entity/congenital-stationary-night-blindness-autosomal-dominant-1


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Dark-light: model for nightblindness from the human rhodopsin Gly-90-->Asp mutation
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)