# autosomal recessive nonsyndromic deafness 98

> autosomal recessive nonsyndromic deafness that has material basis in mutation in the TSPEAR gene on chromosome 21q22

**Wikidata**: [Q28024667](https://www.wikidata.org/wiki/Q28024667)  
**Source**: https://4ort.xyz/entity/autosomal-recessive-nonsyndromic-deafness-98


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. Defect in the gene encoding the EAR/EPTP domain-containing protein TSPEAR causes DFNB98 profound deafness
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)