| Term Name: | autosomal dominant nonsyndromic deafness 22 | 
|---|---|
| Synonyms: | autosomal dominant deafness 22, DFNA22 | 
| Definition: | An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset with high frequency progressive hearing loss and has_material_basis_in mutation in the MYO6 gene on chromosome 6q14. | 
| Ontology: | Human Disease [DOID:0110552] ( DOID:0110552 ) |