# autosomal recessive nonsyndromic deafness 36

> autosomal recessive nonsyndromic deafness that is characterized by prelingual onset and has material basis in mutation in the ESPN gene on chromosome 1p36

**Wikidata**: [Q28024621](https://www.wikidata.org/wiki/Q28024621)  
**Source**: https://4ort.xyz/entity/autosomal-recessive-nonsyndromic-deafness-36


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. Mutations of ESPN cause autosomal recessive deafness and vestibular dysfunction
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)
6. UMLS 2023