# retinitis pigmentosa 7

> retinitis pigmentosa that has material basis in mutation in the PRPH2 gene on chromosome 6p21

**Wikidata**: [Q27677782](https://www.wikidata.org/wiki/Q27677782)  
**Source**: https://4ort.xyz/entity/retinitis-pigmentosa-7


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Digenic retinitis pigmentosa due to mutations at the unlinked peripherin/RDS and ROM1 loci
5. A three-base-pair deletion in the peripherin–RDS gene in one form of retinitis pigmentosa
6. [Identifiers.org](https://registry.identifiers.org/registry/doid)