# retinitis pigmentosa 71

> retinitis pigmentosa that has material basis in mutation in the IFT172 gene on chromosome 2p23

**Wikidata**: [Q27674950](https://www.wikidata.org/wiki/Q27674950)  
**Source**: https://4ort.xyz/entity/retinitis-pigmentosa-71


## References

1. Disease Ontology
2. UniProt
3. Mutations in IFT172 cause isolated retinal degeneration and Bardet-Biedl syndrome
4. [Identifiers.org](https://registry.identifiers.org/registry/doid)
5. Monarch Disease Ontology release 2018-06-29