# autosomal recessive nonsyndromic deafness 77

> autosomal recessive nonsyndromic deafness that is characterized by postlingual onset with moderate to profound, progressive hearing loss and has material basis in mutation in the LOXHD1 gene on chromosome 18q21

**Wikidata**: [Q28024652](https://www.wikidata.org/wiki/Q28024652)  
**Source**: https://4ort.xyz/entity/autosomal-recessive-nonsyndromic-deafness-77


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. Mutations in LOXHD1, an evolutionarily conserved stereociliary protein, disrupt hair cell function in mice and cause progressive hearing loss in humans
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)