An autosomal dominant nonsyndromic deafness characterized by preservation of outer hair cell function and abnormal or absent auditory brainstem responses that has_material_basis_in heterozygous mutation in the DIAPH3 gene on chromosome 13q. (DO)
autosomal dominant auditory neuropathy 3
Autosomal Dominant Deafness 39 with Dentinogenesis Imperfecta 1