# dystonia 24

> focal dystonia characterized by autosomal dominant inheritance of focal dystonia affecting the neck, laryngeal muscles, and muscles of the upper limbs that has material basis in heterozygous mutation in the ANO3 gene on chromosome 11p14

**Wikidata**: [Q30989523](https://www.wikidata.org/wiki/Q30989523)  
**Source**: https://4ort.xyz/entity/dystonia-24


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Mutations in ANO3 cause dominant craniocervical dystonia: ion channel implicated in pathogenesis
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)