# autosomal dominant nonsyndromic deafness 28

> autosomal dominant nonsyndromic deafness that is characterized by postlingual onset with flat or gently downsloping audioprofiles and has material basis in mutation in the GRHL2 gene on chromosome 8q22

**Wikidata**: [Q28024685](https://www.wikidata.org/wiki/Q28024685)  
**Source**: https://4ort.xyz/entity/autosomal-dominant-nonsyndromic-deafness-28


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Mutation of a transcription factor, TFCP2L3, causes progressive autosomal dominant hearing loss, DFNA28
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)