| Term Name: | autosomal dominant nonsyndromic deafness 50 |
|---|---|
| Synonyms: | autosomal dominant deafness 50, DFNA50 |
| Definition: | An autosomal dominant nonsyndromic deafness that is characterized postlingual onset in the second decade of life with flat progressive hearing loss and has_material_basis_in mutation in the MIRN96 gene on chromosome 7q32. |
| Ontology: | Human Disease [DOID:0110576] ( DOID:0110576 ) |