# hereditary spastic paraplegia 2

> hereditary spastic paraplegia that has material basis in mutation in the PLP1 gene on chromosome Xq22.2

**Wikidata**: [Q32142710](https://www.wikidata.org/wiki/Q32142710)  
**Source**: https://4ort.xyz/entity/hereditary-spastic-paraplegia-2


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. X-linked spastic paraplegia and Pelizaeus-Merzbacher disease are allelic disorders at the proteolipid protein locus
5. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000123560/MONDO_0010733)
6. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000123560/Orphanet_99015)
7. [Identifiers.org](https://registry.identifiers.org/registry/doid)