# autosomal dominant nonsyndromic deafness 12

> autosomal dominant nonsyndromic deafness that is characterized by prelingual onset and mid-frequency hearing loss and has material basis in mutation in the TECTA gene on chromosome 11q23

**Wikidata**: [Q28024671](https://www.wikidata.org/wiki/Q28024671)  
**Source**: https://4ort.xyz/entity/autosomal-dominant-nonsyndromic-deafness-12


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. Mutations in the human α-tectorin gene cause autosomal dominant non-syndromic hearing impairment
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)