# autosomal dominant nonsyndromic deafness 70

> autosomal dominant nonsyndromic deafness that has material basis in mutation in the MCM2 gene on chromosome 3q21

**Wikidata**: [Q28024722](https://www.wikidata.org/wiki/Q28024722)  
**Source**: https://4ort.xyz/entity/autosomal-dominant-nonsyndromic-deafness-70


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. Whole Exome Sequencing Identified MCM2 as a Novel Causative Gene for Autosomal Dominant Nonsyndromic Deafness in a Chinese Family
5. [Identifiers.org](http://www.ebi.ac.uk/miriam/main/collections/MIR:00000233)