Autosomal dominant nonsyndromic hearing loss 20

Definition

Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the ACTG1 gene.

Also identified as

• DOID 0110550 per MONDO
• MESH C565754 per MONDO
• OMIM 604717 per MONDO
• UMLS C1858172 per MONDO