# retinitis pigmentosa 37

> retinitis pigmentosa that has material basis in mutation in the NR2E3 gene on chromosome 15q23

**Wikidata**: [Q27677797](https://www.wikidata.org/wiki/Q27677797)  
**Source**: https://4ort.xyz/entity/retinitis-pigmentosa-37


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Recurrent mutation in the first zinc finger of the orphan nuclear receptor NR2E3 causes autosomal dominant retinitis pigmentosa
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)