# autosomal dominant nonsyndromic deafness 2B

> autosomal dominant nonsyndromic deafness that is characterized postlingual onset in the fourth decade of life with by high frequency progressive hearing loss and has material basis in mutation in the GJB3 gene on chromosome 1p34.3

**Wikidata**: [Q28024687](https://www.wikidata.org/wiki/Q28024687)  
**Source**: https://4ort.xyz/entity/autosomal-dominant-nonsyndromic-deafness-2b


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. Mutations in the gene encoding gap junction protein beta-3 associated with autosomal dominant hearing impairment
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)