# retinitis pigmentosa 26

> retinitis pigmentosa that has material basis in mutation in the CERKL gene on chromosome 2q31

**Wikidata**: [Q27677765](https://www.wikidata.org/wiki/Q27677765)  
**Source**: https://4ort.xyz/entity/retinitis-pigmentosa-26


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Mutation of CERKL, a novel human ceramide kinase gene, causes autosomal recessive retinitis pigmentosa (RP26).
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)