# hereditary spastic paraplegia 12

> hereditary spastic paraplegia that has material basis in mutation in the RTN2 gene on chromosome 19q13

**Wikidata**: [Q32142578](https://www.wikidata.org/wiki/Q32142578)  
**Source**: https://4ort.xyz/entity/hereditary-spastic-paraplegia-12


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Mutations in the ER-shaping protein reticulon 2 cause the axon-degenerative disorder hereditary spastic paraplegia type 12
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)