Mondo Description Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the MYO7A gene.

Uniprot Description A form of non-syndromic sensorineural hearing loss. Sensorineural deafness results from damage to the neural receptors of the inner ear, the nerve pathways to the brain, or the area of the brain that receives sound information. DFNA11 is characterized by onset after complete speech acquisition and subsequent gradual progression.