| Term Name: | autosomal dominant nonsyndromic deafness 3A |
|---|---|
| Synonyms: | autosomal dominant deafness 3A, DFNA3A |
| Definition: | An autosomal dominant nonsyndromic deafness that is characterized by prelingual, high frequency hearing loss and has_material_basis_in mutation in the GJB2 gene on chromosome 13q12. |
| Ontology: | Human Disease [DOID:0110564] ( DOID:0110564 ) |