# autosomal dominant nonsyndromic deafness 4A

> autosomal dominant nonsyndromic deafness that is characterized by postlingual onset with flat or gently sloping hearing audioprofiles and has material basis in mutation in the MYH14 gene on chromosome 19q13.33

**Wikidata**: [Q28024702](https://www.wikidata.org/wiki/Q28024702)  
**Source**: https://4ort.xyz/entity/autosomal-dominant-nonsyndromic-deafness-4a


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. Nonmuscle myosin heavy-chain gene MYH14 is expressed in cochlea and mutated in patients affected by autosomal dominant hearing impairment (DFNA4)
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)