# autosomal dominant nonsyndromic deafness 40

> autosomal dominant nonsyndromic deafness that has material basis in mutation in the CRYM gene on chromosome 16p12

**Wikidata**: [Q28024694](https://www.wikidata.org/wiki/Q28024694)  
**Source**: https://4ort.xyz/entity/autosomal-dominant-nonsyndromic-deafness-40


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. Identification of CRYM as a Candidate Responsible for Nonsyndromic Deafness, through cDNA Microarray Analysis of Human Cochlear and Vestibular Tissues**Nucleotide sequence data reported herein are available in the DDBJ/EMBL/GenBank databases; for details, see the Electronic-Database Information section of this article.
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)