# autosomal recessive nonsyndromic deafness 53

> autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and has material basis in mutation in the COL11A2 gene on chromosome 6p21

**Wikidata**: [Q28024636](https://www.wikidata.org/wiki/Q28024636)  
**Source**: https://4ort.xyz/entity/autosomal-recessive-nonsyndromic-deafness-53


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. Mutation of COL11A2 causes autosomal recessive non-syndromic hearing loss at the DFNB53 locus
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)