# retinitis pigmentosa 23

> retinitis pigmentosa that has material basis in mutation in the OFD1 gene on chromosome Xp22

**Wikidata**: [Q27677810](https://www.wikidata.org/wiki/Q27677810)  
**Source**: https://4ort.xyz/entity/retinitis-pigmentosa-23


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Deep intronic mutation in OFD1, identified by targeted genomic next-generation sequencing, causes a severe form of X-linked retinitis pigmentosa (RP23)
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)