# autosomal recessive nonsyndromic deafness 39

> autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, downsloping hearing loss and has material basis in mutation in the HGF gene on chromosome 7q21

**Wikidata**: [Q28024624](https://www.wikidata.org/wiki/Q28024624)  
**Source**: https://4ort.xyz/entity/autosomal-recessive-nonsyndromic-deafness-39


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Noncoding mutations of HGF are associated with nonsyndromic hearing loss, DFNB39.
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)