Autosomal dominant nonsyndromic hearing loss 11

Definition

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

Also identified as

• DOID 0110543 per MONDO
• MESH C563353 per MONDO
• OMIM 601317 per MONDO
• UMLS C1832475 per MONDO