# hereditary spastic paraplegia 6

> hereditary spastic paraplegia that is usually characterized by rapidly progressive and severe spastic paraplegia and has material basis in mutation in the NIPA1 gene on chromosome 15q11.2

**Wikidata**: [Q32143240](https://www.wikidata.org/wiki/Q32143240)  
**Wikipedia**: [English](https://en.wikipedia.org/wiki/Spastic_paraplegia_6)  
**Source**: https://4ort.xyz/entity/hereditary-spastic-paraplegia-6


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. NIPA1 Gene Mutations Cause Autosomal Dominant Hereditary Spastic Paraplegia (SPG6)
5. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000170113/MONDO_0010878)
6. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000170113/Orphanet_100988)
7. [Identifiers.org](https://registry.identifiers.org/registry/doid)