# autosomal recessive nonsyndromic deafness 32

> autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and has material basis in variation in the chromosome region 1p22.1-p13.3

**Wikidata**: [Q28024618](https://www.wikidata.org/wiki/Q28024618)  
**Source**: https://4ort.xyz/entity/autosomal-recessive-nonsyndromic-deafness-32


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. [Identifiers.org](https://registry.identifiers.org/registry/doid)