# autosomal recessive nonsyndromic deafness 8

> autosomal recessive nonsyndromic deafness that has material basis in mutation in the TMPRSS3 gene on chromosome 21q22

**Wikidata**: [Q28024654](https://www.wikidata.org/wiki/Q28024654)  
**Source**: https://4ort.xyz/entity/autosomal-recessive-nonsyndromic-deafness-8


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. Insertion of beta-satellite repeats identifies a transmembrane protease causing both congenital and childhood onset autosomal recessive deafness
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)