# autosomal recessive nonsyndromic deafness 79

> 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 TPRN gene on chromosome 9q34

**Wikidata**: [Q28024653](https://www.wikidata.org/wiki/Q28024653)  
**Source**: https://4ort.xyz/entity/autosomal-recessive-nonsyndromic-deafness-79


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. Targeted capture and next-generation sequencing identifies C9orf75, encoding taperin, as the mutated gene in nonsyndromic deafness DFNB79
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)