# autosomal recessive nonsyndromic deafness 35

> autosomal recessive nonsyndromic deafness that is characterized severe to profound hearing loss and has material basis in mutation in the ESRRB gene on chromosome 14q24

**Wikidata**: [Q28024620](https://www.wikidata.org/wiki/Q28024620)  
**Source**: https://4ort.xyz/entity/autosomal-recessive-nonsyndromic-deafness-35


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. Mutations of ESRRB encoding estrogen-related receptor beta cause autosomal-recessive nonsyndromic hearing impairment DFNB35.
5. [Identifiers.org](http://www.ebi.ac.uk/miriam/main/collections/MIR:00000233)