# autosomal recessive nonsyndromic deafness 9

> autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with usually severe to profound, stable hearing loss and has material basis in mutation in the OTOF gene on chromosome 2p23

**Wikidata**: [Q28024662](https://www.wikidata.org/wiki/Q28024662)  
**Source**: https://4ort.xyz/entity/autosomal-recessive-nonsyndromic-deafness-9


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafness
5. [ClinGen](https://search.clinicalgenome.org/kb/gene-validity/5613)
6. [ClinGen](https://search.clinicalgenome.org/kb/gene-validity/CGGCIEX:assertion_5613)
7. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000115155/MONDO_0010986)
8. [Identifiers.org](https://registry.identifiers.org/registry/doid)