# hereditary spastic paraplegia 56

> hereditary spastic paraplegia that has material basis in mutation in the CYP2U1 gene on chromosome 4q25

**Wikidata**: [Q32143203](https://www.wikidata.org/wiki/Q32143203)  
**Source**: https://4ort.xyz/entity/hereditary-spastic-paraplegia-56


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Alteration of fatty-acid-metabolizing enzymes affects mitochondrial form and function in hereditary spastic paraplegia
5. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000155016/MONDO_0014015)
6. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000155016/Orphanet_320411)
7. [Identifiers.org](https://registry.identifiers.org/registry/doid)