# autosomal recessive nonsyndromic deafness 48

> autosomal recessive nonsyndromic deafness that has material basis in mutation in the CIB2 gene on chromosome 15q25

**Wikidata**: [Q28024632](https://www.wikidata.org/wiki/Q28024632)  
**Source**: https://4ort.xyz/entity/autosomal-recessive-nonsyndromic-deafness-48


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. Alterations of the CIB2 calcium- and integrin-binding protein cause Usher syndrome type 1J and nonsyndromic deafness DFNB48.
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)