# autosomal dominant nonsyndromic deafness 20

> autosomal dominant nonsyndromic deafness that is characterized by postlingual onset with high frequency progressive hearing loss and has material basis in mutation in the ACTG1 gene on chromosome 17q25

**Wikidata**: [Q28024678](https://www.wikidata.org/wiki/Q28024678)  
**Source**: https://4ort.xyz/entity/autosomal-dominant-nonsyndromic-deafness-20


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Mutations in the gamma-actin gene (ACTG1) are associated with dominant progressive deafness (DFNA20/26).
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)