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 ) |