# hereditary spastic paraplegia 11

> hereditary spastic paraplegia that has material basis in mutation in the SPG11 gene on chromosome 15q21

**Wikidata**: [Q32142563](https://www.wikidata.org/wiki/Q32142563)  
**Source**: https://4ort.xyz/entity/hereditary-spastic-paraplegia-11


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Mutations in SPG11, encoding spatacsin, are a major cause of spastic paraplegia with thin corpus callosum
5. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000104133/MONDO_0011445)
6. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000104133/Orphanet_2822)
7. [Identifiers.org](https://registry.identifiers.org/registry/doid)