# autosomal dominant nonsyndromic deafness 36

> autosomal dominant nonsyndromic deafness that is characterized by postlingual onset with flat or gently downsloping audioprofiles and has material basis in mutation in the TMC1 gene on chromosome 9q21

**Wikidata**: [Q28024691](https://www.wikidata.org/wiki/Q28024691)  
**Source**: https://4ort.xyz/entity/autosomal-dominant-nonsyndromic-deafness-36


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. Dominant and recessive deafness caused by mutations of a novel gene, TMC1, required for cochlear hair-cell function
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)