# autosomal dominant nonsyndromic deafness 17

> autosomal dominant nonsyndromic deafness that is characterized by postlingual onset with high frequency progressive hearing loss and has material basis in mutation in the MYH9 gene on chromosome 22q12

**Wikidata**: [Q28024676](https://www.wikidata.org/wiki/Q28024676)  
**Source**: https://4ort.xyz/entity/autosomal-dominant-nonsyndromic-deafness-17


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. Human nonsyndromic hereditary deafness DFNA17 is due to a mutation in nonmuscle myosin MYH9
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)