# autosomal dominant nonsyndromic deafness 23

> autosomal dominant nonsyndromic deafness that is characterized by prelingual onset with high frequency progressive hearing loss and has material basis in mutation in the SIX1 gene on chromosome 14q23

**Wikidata**: [Q28024681](https://www.wikidata.org/wiki/Q28024681)  
**Source**: https://4ort.xyz/entity/autosomal-dominant-nonsyndromic-deafness-23


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. SIX1 mutations cause branchio-oto-renal syndrome by disruption of EYA1-SIX1-DNA complexes
5. [Identifiers.org](http://www.ebi.ac.uk/miriam/main/collections/MIR:00000233)