# hereditary spastic paraplegia 42

> hereditary spastic paraplegia that has material basis in mutation in the SLC33A1 gene on chromosome 3q25.31

**Wikidata**: [Q32143018](https://www.wikidata.org/wiki/Q32143018)  
**Source**: https://4ort.xyz/entity/hereditary-spastic-paraplegia-42


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. A Missense Mutation in SLC33A1, which Encodes the Acetyl-CoA Transporter, Causes Autosomal-Dominant Spastic Paraplegia (SPG42)
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)