| Term Name: | autosomal dominant nonsyndromic deafness 13 | 
|---|---|
| Synonyms: | autosomal dominant deafness 13, DFNA13 | 
| Definition: | An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset in the second decade of life with mid-frequency hearing loss and has_material_basis_in mutation in the COL11A2 gene on chromosome 6p21. | 
| Ontology: | Human Disease [DOID:0110545] ( DOID:0110545 ) |