# autosomal recessive nonsyndromic deafness 88

> autosomal recessive nonsyndromic deafness that has material basis in mutation in the ELMOD3 gene on chromosome 2p11

**Wikidata**: [Q28024660](https://www.wikidata.org/wiki/Q28024660)  
**Source**: https://4ort.xyz/entity/autosomal-recessive-nonsyndromic-deafness-88


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. An Alteration in ELMOD3, an Arl2 GTPase-Activating Protein, Is Associated with Hearing Impairment in Humans
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)