# autosomal dominant nonsyndromic deafness 5

> autosomal dominant nonsyndromic deafness that is characterized by postlingual onset in the first decade of life and high frequency progressive hearing loss and has material basis in mutation in the DFNA5 gene on chromosome 7p15

**Wikidata**: [Q28024704](https://www.wikidata.org/wiki/Q28024704)  
**Source**: https://4ort.xyz/entity/autosomal-dominant-nonsyndromic-deafness-5


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. Nonsyndromic hearing impairment is associated with a mutation in DFNA5
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)