# autosomal recessive nonsyndromic deafness 2

> autosomal recessive nonsyndromic deafness that has material basis in mutation in the MYO7A gene on chromosome 11q13

**Wikidata**: [Q28024602](https://www.wikidata.org/wiki/Q28024602)  
**Source**: https://4ort.xyz/entity/autosomal-recessive-nonsyndromic-deafness-2


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. The autosomal recessive isolated deafness, DFNB2, and the Usher 1B syndrome are allelic defects of the myosin-VIIA gene
5. [Identifiers.org](http://www.ebi.ac.uk/miriam/main/collections/MIR:00000233)