# retinitis pigmentosa 10

> retinitis pigmentosa that has material basis in mutation in the IMPDH1 gene on chromosome 7q32

**Wikidata**: [Q27677787](https://www.wikidata.org/wiki/Q27677787)  
**Source**: https://4ort.xyz/entity/retinitis-pigmentosa-10


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Mutations in the inosine monophosphate dehydrogenase 1 gene (IMPDH1) cause the RP10 form of autosomal dominant retinitis pigmentosa
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)