# retinitis pigmentosa 42

> retinitis pigmentosa that has material basis in mutation in the KLHL7 gene on chromosome 7p15.3

**Wikidata**: [Q27677785](https://www.wikidata.org/wiki/Q27677785)  
**Source**: https://4ort.xyz/entity/retinitis-pigmentosa-42


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Mutations in a BTB-Kelch protein, KLHL7, cause autosomal-dominant retinitis pigmentosa
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)