# autosomal recessive nonsyndromic deafness 101

> autosomal recessive nonsyndromic deafness that has material basis in mutation in the GRXCR2 gene on chromosome 5q32

**Wikidata**: [Q28024587](https://www.wikidata.org/wiki/Q28024587)  
**Source**: https://4ort.xyz/entity/autosomal-recessive-nonsyndromic-deafness-101


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. A Frameshift Mutation inGRXCR2Causes Recessively Inherited Hearing Loss
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)