# autosomal recessive nonsyndromic deafness 37

> autosomal recessive nonsyndromic deafness that is characterized by prelingual onset and has material basis in mutation in the MYO6 gene on chromosome 6q14

**Wikidata**: [Q28024622](https://www.wikidata.org/wiki/Q28024622)  
**Source**: https://4ort.xyz/entity/autosomal-recessive-nonsyndromic-deafness-37


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. Mutations of MYO6 are associated with recessive deafness, DFNB37
5. [Identifiers.org](http://www.ebi.ac.uk/miriam/main/collections/MIR:00000233)