# hereditary spastic paraplegia 15

> hereditary spastic paraplegia that has material basis in mutation in the ZFYVE26 gene on chromosome 14q24.1

**Wikidata**: [Q32142628](https://www.wikidata.org/wiki/Q32142628)  
**Wikipedia**: [English](https://en.wikipedia.org/wiki/SPG15_(disease))  
**Source**: https://4ort.xyz/entity/hereditary-spastic-paraplegia-15


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Identification of the SPG15 gene, encoding spastizin, as a frequent cause of complicated autosomal-recessive spastic paraplegia, including Kjellin syndrome
5. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000072121/MONDO_0010044)
6. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000072121/Orphanet_100996)
7. [Identifiers.org](https://registry.identifiers.org/registry/doid)