# retinitis pigmentosa 30

> retinitis pigmentosa that has material basis in mutation in the FSCN2 gene on chromosome 17q25

**Wikidata**: [Q27677804](https://www.wikidata.org/wiki/Q27677804)  
**Source**: https://4ort.xyz/entity/retinitis-pigmentosa-30


## References

1. Disease Ontology
2. UniProt
3. Mutation of human retinal fascin gene (FSCN2) causes autosomal dominant retinitis pigmentosa
4. [Identifiers.org](https://registry.identifiers.org/registry/doid)
5. Monarch Disease Ontology release 2018-06-29