# hereditary spastic paraplegia 73

> hereditary spastic paraplegia that has material basis in mutation in the CPT1C gene on chromosome 19q13

**Wikidata**: [Q32143335](https://www.wikidata.org/wiki/Q32143335)  
**Source**: https://4ort.xyz/entity/hereditary-spastic-paraplegia-73


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Mutation inCPT1CAssociated With Pure Autosomal Dominant Spastic Paraplegia
5. [Identifiers.org](http://www.ebi.ac.uk/miriam/main/collections/MIR:00000233)