# autosomal dominant nonsyndromic deafness 15

> autosomal dominant nonsyndromic deafness that is characterized by postlingual onset with high frequency progressive hearing loss and has material basis in mutation in the POU4F3 gene on chromosome 5q32

**Wikidata**: [Q28024673](https://www.wikidata.org/wiki/Q28024673)  
**Source**: https://4ort.xyz/entity/autosomal-dominant-nonsyndromic-deafness-15


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. Mutation in transcription factor POU4F3 associated with inherited progressive hearing loss in humans
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)