# autosomal recessive nonsyndromic deafness 103

> autosomal recessive nonsyndromic deafness that has material basis in mutation in the CLIC5 gene on chromosome 6p21

**Wikidata**: [Q28024589](https://www.wikidata.org/wiki/Q28024589)  
**Source**: https://4ort.xyz/entity/autosomal-recessive-nonsyndromic-deafness-103


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. Progressive hearing loss and vestibular dysfunction caused by a homozygous nonsense mutation in CLIC5
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)