# 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

**Wikidata**: [Q32140436](https://www.wikidata.org/wiki/Q32140436)  
**Source**: https://4ort.xyz/entity/congenital-stationary-night-blindness-1g


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. GNAT1 associated with autosomal recessive congenital stationary night blindness
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)