# autosomal dominant nonsyndromic deafness 13

> autosomal dominant nonsyndromic deafness that is characterized by postlingual onset in the second decade of life with mid-frequency hearing loss and has material basis in mutation in the COL11A2 gene on chromosome 6p21

**Wikidata**: [Q28024672](https://www.wikidata.org/wiki/Q28024672)  
**Source**: https://4ort.xyz/entity/autosomal-dominant-nonsyndromic-deafness-13


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. Mutations in COL11A2 cause non-syndromic hearing loss (DFNA13)
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)