# autosomal dominant nonsyndromic deafness 25

> autosomal dominant nonsyndromic deafness that is characterized by postlingual onset in the second-sixth decade of life with high frequency progressive hearing loss and has material basis in mutation in the SLC17A8 gene on chromosome 12q23

**Wikidata**: [Q28024683](https://www.wikidata.org/wiki/Q28024683)  
**Source**: https://4ort.xyz/entity/autosomal-dominant-nonsyndromic-deafness-25


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Impairment of SLC17A8 Encoding Vesicular Glutamate Transporter-3, VGLUT3, Underlies Nonsyndromic Deafness DFNA25 and Inner Hair Cell Dysfunction in Null Mice
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)