# autosomal dominant nonsyndromic deafness 3A

> autosomal dominant nonsyndromic deafness that is characterized by prelingual, high frequency hearing loss and has material basis in mutation in the GJB2 gene on chromosome 13q12

**Wikidata**: [Q28024692](https://www.wikidata.org/wiki/Q28024692)  
**Source**: https://4ort.xyz/entity/autosomal-dominant-nonsyndromic-deafness-3a


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. Connexin 26 mutations in hereditary non-syndromic sensorineural deafness
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)