Autosomal dominant nonsyndromic hearing loss 22

Definition

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

Also identified as

• DOID 0110552 per MONDO
• MESH C538197 per MONDO
• OMIM 606346 per MONDO
• UMLS C2931767 per MONDO