# autosomal recessive nonsyndromic deafness 21

> autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and has material basis in mutation in the TECTA gene on chromosome 11q23.3

**Wikidata**: [Q28024604](https://www.wikidata.org/wiki/Q28024604)  
**Source**: https://4ort.xyz/entity/autosomal-recessive-nonsyndromic-deafness-21


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. An alpha-tectorin gene defect causes a newly identified autosomal recessive form of sensorineural pre-lingual non-syndromic deafness, DFNB21.
5. [Identifiers.org](http://www.ebi.ac.uk/miriam/main/collections/MIR:00000233)