# autosomal recessive nonsyndromic deafness 25

> autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with moderate to profound, progressive hearing loss and has material basis in mutation in the GRXCR1 gene on chromosome 4p13

**Wikidata**: [Q28024608](https://www.wikidata.org/wiki/Q28024608)  
**Source**: https://4ort.xyz/entity/autosomal-recessive-nonsyndromic-deafness-25


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Homozygosity mapping reveals mutations of GRXCR1 as a cause of autosomal-recessive nonsyndromic hearing impairment
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)