# hereditary spastic paraplegia 13

> hereditary spastic paraplegia that is characterized by a pure form of the disease with late onset and has material basis in mutation in the HSPD1 on chromosome 2q33

**Wikidata**: [Q32142594](https://www.wikidata.org/wiki/Q32142594)  
**Source**: https://4ort.xyz/entity/hereditary-spastic-paraplegia-13


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Hereditary spastic paraplegia SPG13 is associated with a mutation in the gene encoding the mitochondrial chaperonin Hsp60
5. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000144381/MONDO_0011532)
6. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000144381/Orphanet_100994)
7. [Identifiers.org](http://www.ebi.ac.uk/miriam/main/collections/MIR:00000233)