# autosomal recessive nonsyndromic deafness 93

> human disease

**Wikidata**: [Q28024664](https://www.wikidata.org/wiki/Q28024664)  
**Source**: https://4ort.xyz/entity/autosomal-recessive-nonsyndromic-deafness-93


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. A mutation in CABP2, expressed in cochlear hair cells, causes autosomal-recessive hearing impairment
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)