# autosomal recessive nonsyndromic deafness 49

> autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with moderate to profound, stable hearing loss and has material basis in mutation in the MARVELD2 gene on chromosome 5q13

**Wikidata**: [Q28024633](https://www.wikidata.org/wiki/Q28024633)  
**Source**: https://4ort.xyz/entity/autosomal-recessive-nonsyndromic-deafness-49


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. Tricellulin is a tight-junction protein necessary for hearing
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)