# autosomal recessive nonsyndromic deafness 18A

> human disease

**Wikidata**: [Q28024598](https://www.wikidata.org/wiki/Q28024598)  
**Source**: https://4ort.xyz/entity/autosomal-recessive-nonsyndromic-deafness-18a


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. A defect in harmonin, a PDZ domain-containing protein expressed in the inner ear sensory hair cells, underlies Usher syndrome type 1C
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)