# dystonia 25

> multifocal dystonia characterized by autosomal dominant inheritance of cervical, laryngeal and hand-forearm dystonia that has material basis in heterozygous mutation in the GNAL gene on chromosome 18p11

**Wikidata**: [Q30989665](https://www.wikidata.org/wiki/Q30989665)  
**Source**: https://4ort.xyz/entity/dystonia-25


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Mutations in GNAL cause primary torsion dystonia
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)
6. UMLS 2023