# congenital stationary night blindness 1E

> congenital stationary night blindness characterized by autosomal recessive inheritance that has material basis in homozygous or compound heterozygous mutation in the GPR179 gene on chromosome 17q12

**Wikidata**: [Q32144078](https://www.wikidata.org/wiki/Q32144078)  
**Source**: https://4ort.xyz/entity/congenital-stationary-night-blindness-1e


## References

1. Disease Ontology
2. UniProt
3. Whole-Exome Sequencing Identifies Mutations in GPR179 Leading to Autosomal-Recessive Complete Congenital Stationary Night Blindness
4. [Identifiers.org](https://registry.identifiers.org/registry/doid)
5. Monarch Disease Ontology release 2018-06-29