# hereditary spastic paraplegia 35

> hereditary spastic paraplegia that has material basis in mutation in the FA2H gene on chromosome 16q23.1

**Wikidata**: [Q32142909](https://www.wikidata.org/wiki/Q32142909)  
**Source**: https://4ort.xyz/entity/hereditary-spastic-paraplegia-35


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Mutations in the fatty acid 2-hydroxylase gene are associated with leukodystrophy with spastic paraparesis and dystonia
5. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000103089/MONDO_0012866)
6. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000103089/Orphanet_171629)
7. [Identifiers.org](https://registry.identifiers.org/registry/doid)