# hereditary spastic paraplegia 50

> hereditary spastic paraplegia that has material basis in mutation in the AP4M1 gene on chromosome 7q22.1

**Wikidata**: [Q32143133](https://www.wikidata.org/wiki/Q32143133)  
**Source**: https://4ort.xyz/entity/hereditary-spastic-paraplegia-50


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Mutation in the AP4M1 gene provides a model for neuroaxonal injury in cerebral palsy
5. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000221838/MONDO_0013048)
6. [Identifiers.org](https://registry.identifiers.org/registry/doid)