# autosomal dominant nonsyndromic deafness 6

> autosomal dominant nonsyndromic deafness that is characterized by prelingual onset and low frequency progressive hearing loss and has material basis in mutation in the WFS1 gene on chromosome 4p16

**Wikidata**: [Q28024714](https://www.wikidata.org/wiki/Q28024714)  
**Source**: https://4ort.xyz/entity/autosomal-dominant-nonsyndromic-deafness-6


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Mutations in the Wolfram syndrome 1 gene (WFS1) are a common cause of low frequency sensorineural hearing loss
5. [Identifiers.org](http://www.ebi.ac.uk/miriam/main/collections/MIR:00000233)