# autosomal recessive nonsyndromic deafness 102

> autosomal recessive nonsyndromic deafness that has material basis in mutation in the EPS8 gene on chromosome 12p12

**Wikidata**: [Q28024588](https://www.wikidata.org/wiki/Q28024588)  
**Source**: https://4ort.xyz/entity/autosomal-recessive-nonsyndromic-deafness-102


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. EPS8, encoding an actin-binding protein of cochlear hair cell stereocilia, is a new causal gene for autosomal recessive profound deafness
5. [Identifiers.org](http://www.ebi.ac.uk/miriam/main/collections/MIR:00000233)