# autosomal recessive nonsyndromic deafness 84B

> autosomal recessive nonsyndromic deafness that has material basis in mutation in the OTOGL gene on chromosome 12q21

**Wikidata**: [Q28024657](https://www.wikidata.org/wiki/Q28024657)  
**Source**: https://4ort.xyz/entity/autosomal-recessive-nonsyndromic-deafness-84b


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. Mutations in OTOGL, encoding the inner ear protein otogelin-like, cause moderate sensorineural hearing loss.
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)