# autosomal recessive nonsyndromic deafness 30

> autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and has material basis in mutations in the MYO3A gene on chromosome 10p12.1

**Wikidata**: [Q28024616](https://www.wikidata.org/wiki/Q28024616)  
**Source**: https://4ort.xyz/entity/autosomal-recessive-nonsyndromic-deafness-30


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. From flies' eyes to our ears: mutations in a human class III myosin cause progressive nonsyndromic hearing loss DFNB30
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)