# autosomal recessive nonsyndromic deafness 12

> autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and has material basis in mutation in the CDH23 gene on chromosome 10q22

**Wikidata**: [Q28024592](https://www.wikidata.org/wiki/Q28024592)  
**Source**: https://4ort.xyz/entity/autosomal-recessive-nonsyndromic-deafness-12


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)