# autosomal dominant nonsyndromic deafness 68

> autosomal dominant nonsyndromic deafness that has material basis in mutation in the HOMER2 gene on chromosome 15q25

**Wikidata**: [Q28024719](https://www.wikidata.org/wiki/Q28024719)  
**Source**: https://4ort.xyz/entity/autosomal-dominant-nonsyndromic-deafness-68


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. HOMER2, a Stereociliary Scaffolding Protein, Is Essential for Normal Hearing in Humans and Mice
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)