# retinitis pigmentosa 38

> retinitis pigmentosa that has material basis in mutation in the MERTK gene on chromosome 2q13

**Wikidata**: [Q27677764](https://www.wikidata.org/wiki/Q27677764)  
**Source**: https://4ort.xyz/entity/retinitis-pigmentosa-38


## References

1. Disease Ontology
2. UniProt
3. Mutations in MERTK, the human orthologue of the RCS rat retinal dystrophy gene, cause retinitis pigmentosa
4. [Identifiers.org](https://registry.identifiers.org/registry/doid)
5. Monarch Disease Ontology release 2018-06-29