# autosomal recessive nonsyndromic deafness 76

> autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with high frequency, progressive hearing loss and has material basis in mutation in the SYNE4 gene on chromosome 19q13

**Wikidata**: [Q28024651](https://www.wikidata.org/wiki/Q28024651)  
**Source**: https://4ort.xyz/entity/autosomal-recessive-nonsyndromic-deafness-76


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. The LINC complex is essential for hearing
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)