# retinitis pigmentosa 39

> retinitis pigmentosa that has material basis in mutation in the USH2A gene on chromosome 1q41

**Wikidata**: [Q27674948](https://www.wikidata.org/wiki/Q27674948)  
**Source**: https://4ort.xyz/entity/retinitis-pigmentosa-39


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Paternal uniparental heterodisomy with partial isodisomy of chromosome 1 in a patient with retinitis pigmentosa without hearing loss and a missense mutation in the Usher syndrome type II gene USH2A.
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)