# retinitis pigmentosa 11

> retinitis pigmentosa that has material basis in mutation in the PRPF31 gene on chromosome 19q13

**Wikidata**: [Q27677806](https://www.wikidata.org/wiki/Q27677806)  
**Source**: https://4ort.xyz/entity/retinitis-pigmentosa-11


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. A human homolog of yeast pre-mRNA splicing gene, PRP31, underlies autosomal dominant retinitis pigmentosa on chromosome 19q13.4 (RP11)
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)