# autosomal recessive nonsyndromic deafness 23

> 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 PCDH15 gene on chromosome 10q21

**Wikidata**: [Q28024606](https://www.wikidata.org/wiki/Q28024606)  
**Source**: https://4ort.xyz/entity/autosomal-recessive-nonsyndromic-deafness-23


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. PCDH15 is expressed in the neurosensory epithelium of the eye and ear and mutant alleles are responsible for both USH1F and DFNB23
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)