# autosomal recessive nonsyndromic deafness 29

> 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 CLDN14 gene on chromosome 21q22

**Wikidata**: [Q28024614](https://www.wikidata.org/wiki/Q28024614)  
**Source**: https://4ort.xyz/entity/autosomal-recessive-nonsyndromic-deafness-29


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Mutations in the gene encoding tight junction claudin-14 cause autosomal recessive deafness DFNB29.
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)