# autosomal dominant nonsyndromic deafness 69

> autosomal dominant nonsyndromic deafness that has material basis in mutation in the KITLG gene on chromosome 12q21

**Wikidata**: [Q28024720](https://www.wikidata.org/wiki/Q28024720)  
**Source**: https://4ort.xyz/entity/autosomal-dominant-nonsyndromic-deafness-69


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. Allelic Mutations of KITLG, Encoding KIT Ligand, Cause Asymmetric and Unilateral Hearing Loss and Waardenburg Syndrome Type 2
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)