has material basis in autosomal dominant nonsyndromic deafness autosomal dominant auditory neuropathy 3 AUNA3 disease_ontology MIM:619832 An autosomal dominant nonsyndromic deafness characterized by progressive hearing loss with inability to discriminate speech but preserved sensitivity to sound, preservation of outer hair cell function and abnormal or absent auditory brainstem responses and that has_material_basis_in heterozygous mutation in the TMEM43 gene on chromosome 3p25.1. DOID:0112373 autosomal dominant inheritance