Autosomal dominant nonsyndromic hearing loss 4A

Definition

Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the MYH14 gene.

Also identified as

• DOID 0110573 per MONDO
• MESH C563460 per MONDO
• OMIM 600652 per MONDO
• UMLS C1833503 per MONDO