# autosomal dominant nonsyndromic deafness 56

> autosomal dominant nonsyndromic deafness that has material basis in mutation in the TNC gene on chromosome 9q33

**Wikidata**: [Q28024710](https://www.wikidata.org/wiki/Q28024710)  
**Source**: https://4ort.xyz/entity/autosomal-dominant-nonsyndromic-deafness-56


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. Exome sequencing and linkage analysis identified tenascin-C (TNC) as a novel causative gene in nonsyndromic hearing loss
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)