# autosomal recessive nonsyndromic deafness 6

> 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 TMIE gene on chromosome 3p21

**Wikidata**: [Q28024639](https://www.wikidata.org/wiki/Q28024639)  
**Source**: https://4ort.xyz/entity/autosomal-recessive-nonsyndromic-deafness-6


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. Mutations in a novel gene, TMIE, are associated with hearing loss linked to the DFNB6 locus.
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)