# autosomal recessive nonsyndromic deafness 84A

> autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with moderate to profound, progressive hearing loss and has material basis in mutation in the PTPRQ gene on chromosome 12q21

**Wikidata**: [Q28024656](https://www.wikidata.org/wiki/Q28024656)  
**Source**: https://4ort.xyz/entity/autosomal-recessive-nonsyndromic-deafness-84a


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Mutations in PTPRQ Are a Cause of Autosomal-Recessive Nonsyndromic Hearing Impairment DFNB84 and Associated with Vestibular Dysfunction
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)