# autosomal recessive nonsyndromic deafness 68

> autosomal recessive nonsyndromic deafness that has material basis in mutation in the S1PR2 gene on chromosome 19p13

**Wikidata**: [Q28024646](https://www.wikidata.org/wiki/Q28024646)  
**Source**: https://4ort.xyz/entity/autosomal-recessive-nonsyndromic-deafness-68


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Autosomal-Recessive Hearing Impairment Due to Rare Missense Variants within S1PR2
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)