# hereditary spastic paraplegia 43

> hereditary spastic paraplegia that has material basis in mutation in the C19ORF12 gene on chromosome 19q12

**Wikidata**: [Q32143030](https://www.wikidata.org/wiki/Q32143030)  
**Source**: https://4ort.xyz/entity/hereditary-spastic-paraplegia-43


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Hereditary spastic paraplegia type 43 (SPG43) is caused by mutation in C19orf12
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)