# autosomal dominant nonsyndromic deafness 44

> autosomal dominant nonsyndromic deafness that is characterized postlingual onset with low to mild frequency progressive hearing loss and has material basis in mutation in the CCDC50 gene on chromosome 3q28

**Wikidata**: [Q28024697](https://www.wikidata.org/wiki/Q28024697)  
**Source**: https://4ort.xyz/entity/autosomal-dominant-nonsyndromic-deafness-44


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. A Mutation in CCDC50, a Gene Encoding an Effector of Epidermal Growth Factor–Mediated Cell Signaling, Causes Progressive Hearing Loss
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)