# hereditary spastic paraplegia 31

> 30 years). In some cases, it can present as a complex phenotype with additional associated manifestations including peripheral neuropathy, bulbar palsy (with dysarthria and dysphagia), distal amyotrophy, and impaired distal vibration sense.

**Wikidata**: [Q32142846](https://www.wikidata.org/wiki/Q32142846)  
**Wikipedia**: [English](https://en.wikipedia.org/wiki/Spastic_paraplegia_31)  
**Source**: https://4ort.xyz/entity/hereditary-spastic-paraplegia-31


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Mutations in the novel mitochondrial protein REEP1 cause hereditary spastic paraplegia type 31
5. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000068615/MONDO_0012453)
6. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000068615/Orphanet_101011)
7. [Identifiers.org](https://registry.identifiers.org/registry/doid)