# autosomal recessive nonsyndromic deafness 97

> autosomal recessive nonsyndromic deafness that has material basis in mutation in the MET gene on chromosome 7q31

**Wikidata**: [Q28024666](https://www.wikidata.org/wiki/Q28024666)  
**Source**: https://4ort.xyz/entity/autosomal-recessive-nonsyndromic-deafness-97


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. A mutation of MET, encoding hepatocyte growth factor receptor, is associated with human DFNB97 hearing loss.
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)