# autosomal dominant nonsyndromic deafness 22

> autosomal dominant nonsyndromic deafness that is characterized by postlingual onset with high frequency progressive hearing loss and has material basis in mutation in the MYO6 gene on chromosome 6q14

**Wikidata**: [Q28024680](https://www.wikidata.org/wiki/Q28024680)  
**Source**: https://4ort.xyz/entity/autosomal-dominant-nonsyndromic-deafness-22


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. Novel association of hypertrophic cardiomyopathy, sensorineural deafness, and a mutation in unconventional myosin VI (MYO6).
4. MYO6, the human homologue of the gene responsible for deafness in Snell's waltzer mice, is mutated in autosomal dominant nonsyndromic hearing loss
5. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000196586/Orphanet_228012)
6. [Identifiers.org](https://registry.identifiers.org/registry/doid)
7. UMLS 2023