# autosomal dominant nonsyndromic deafness 3B

> autosomal dominant nonsyndromic deafness that has material basis in mutation in the GJB6 gene on chromosome 13q12

**Wikidata**: [Q28024693](https://www.wikidata.org/wiki/Q28024693)  
**Source**: https://4ort.xyz/entity/autosomal-dominant-nonsyndromic-deafness-3b


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. Mutations in GJB6 cause nonsyndromic autosomal dominant deafness at DFNA3 locus
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)