Term Name: | autosomal dominant nonsyndromic deafness 2A |
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Synonyms: | autosomal dominant deafness 2A, DFNA2A |
Definition: | An autosomal dominant nonsyndromic deafness that is characterized by high frequency progressive hearing loss and has_material_basis_in mutation in the KCNQ4 gene on chromosome 1p34.2. |
Ontology: | Human Disease [DOID:0110558] ( DOID:0110558 ) |