# autosomal recessive nonsyndromic deafness 3

> 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 MYO15A gene on chromosome 17p11

**Wikidata**: [Q28024615](https://www.wikidata.org/wiki/Q28024615)  
**Source**: https://4ort.xyz/entity/autosomal-recessive-nonsyndromic-deafness-3


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. Unexpected genetic heterogeneity in a large consanguineous Brazilian pedigree presenting deafness
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)