# autosomal recessive nonsyndromic deafness 61

> autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and has material basis in mutation in the SLC26A5 gene on chromosome 7q22

**Wikidata**: [Q28024640](https://www.wikidata.org/wiki/Q28024640)  
**Source**: https://4ort.xyz/entity/autosomal-recessive-nonsyndromic-deafness-61


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. Prestin, a cochlear motor protein, is defective in non-syndromic hearing loss
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)