# retinitis pigmentosa 56

> retinitis pigmentosa that has material basis in mutation in the IMPG2 gene on chromosome 3q12.3

**Wikidata**: [Q27677768](https://www.wikidata.org/wiki/Q27677768)  
**Source**: https://4ort.xyz/entity/retinitis-pigmentosa-56


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Mutations in IMPG2, encoding interphotoreceptor matrix proteoglycan 2, cause autosomal-recessive retinitis pigmentosa.
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)