# autosomal dominant nonsyndromic deafness 41

> autosomal dominant nonsyndromic deafness that is characterized by postlingual onset with flat progressive hearing loss and has material basis in mutation in the P2RX2 gene on chromosome 12q24

**Wikidata**: [Q28024695](https://www.wikidata.org/wiki/Q28024695)  
**Source**: https://4ort.xyz/entity/autosomal-dominant-nonsyndromic-deafness-41


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. Mutation of the ATP-gated P2X 2 receptor leads to progressive hearing loss and increased susceptibility to noise
5. [Identifiers.org](http://www.ebi.ac.uk/miriam/main/collections/MIR:00000233)