# autosomal dominant nonsyndromic deafness 9

> autosomal dominant nonsyndromic deafness that is characterized by postlingual onset in the second decade with high frequency progressive hearing loss and has material basis in mutation in the COCH gene on chromosome 14q12

**Wikidata**: [Q28024723](https://www.wikidata.org/wiki/Q28024723)  
**Source**: https://4ort.xyz/entity/autosomal-dominant-nonsyndromic-deafness-9


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. Mutations in a novel cochlear gene cause DFNA9, a human nonsyndromic deafness with vestibular dysfunction
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)