# retinitis pigmentosa 41

> retinitis pigmentosa that has material basis in mutation in the PROM1 gene on chromosome 4p15

**Wikidata**: [Q27677774](https://www.wikidata.org/wiki/Q27677774)  
**Source**: https://4ort.xyz/entity/retinitis-pigmentosa-41


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. A frameshift mutation in prominin (mouse)-like 1 causes human retinal degeneration
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)