# autosomal recessive nonsyndromic deafness 42

> autosomal recessive nonsyndromic deafness that has material basis in mutation in the ILDR1 gene on chromosome 3q13

**Wikidata**: [Q28024627](https://www.wikidata.org/wiki/Q28024627)  
**Source**: https://4ort.xyz/entity/autosomal-recessive-nonsyndromic-deafness-42


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. Loss-of-function mutations of ILDR1 cause autosomal-recessive hearing impairment DFNB42
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)