# autosomal recessive nonsyndromic deafness 67

> autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and has material basis in mutation in the LHFPL5 gene on chromosome 6p21

**Wikidata**: [Q28024645](https://www.wikidata.org/wiki/Q28024645)  
**Source**: https://4ort.xyz/entity/autosomal-recessive-nonsyndromic-deafness-67


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. Mutations of human TMHS cause recessively inherited non-syndromic hearing loss
5. [Identifiers.org](http://www.ebi.ac.uk/miriam/main/collections/MIR:00000233)