Mondo Description Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the MYO6 gene.

Uniprot Description An autosomal dominant sensorineural deafness associated with hypertrophic cardiomyopathy.

Disease Ontology Description An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset with high frequency progressive hearing loss and has_material_basis_in mutation in the MYO6 gene on chromosome 6q14.