# autosomal dominant nonsyndromic deafness 67

> autosomal dominant nonsyndromic deafness that has material basis in mutation in the OSBPL2 gene on chromosome 20q13

**Wikidata**: [Q28024718](https://www.wikidata.org/wiki/Q28024718)  
**Source**: https://4ort.xyz/entity/autosomal-dominant-nonsyndromic-deafness-67


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. Identification of OSBPL2 as a novel candidate gene for progressive nonsyndromic hearing loss by whole-exome sequencing
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)