# autosomal dominant nonsyndromic deafness 65

> autosomal dominant nonsyndromic deafness that has material basis in mutation in the TBC1D24 gene on chromosome 16p13

**Wikidata**: [Q28024716](https://www.wikidata.org/wiki/Q28024716)  
**Source**: https://4ort.xyz/entity/autosomal-dominant-nonsyndromic-deafness-65


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. A Dominant Mutation in the Stereocilia-Expressing GeneTBC1D24is a Probable Cause for Nonsyndromic Hearing Impairment
5. TBC1D24Mutation Causes Autosomal-Dominant Nonsyndromic Hearing Loss
6. [Identifiers.org](https://registry.identifiers.org/registry/doid)