# retinitis pigmentosa 18

> retinitis pigmentosa that has material basis in mutation in the PRPF3 gene on chromosome 1q21

**Wikidata**: [Q27677756](https://www.wikidata.org/wiki/Q27677756)  
**Source**: https://4ort.xyz/entity/retinitis-pigmentosa-18


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Mutations in HPRP3, a third member ofpre-mRNA splicing factor genes, implicated in autosomal dominant retinitis pigmentosa
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)