Autosomal dominant nonsyndromic hearing loss 3B

Definition

Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the GJB6 gene.

Also identified as

• DOID 0110565 per MONDO
• MESH C567215 per MONDO
• OMIM 612643 per MONDO
• UMLS C2675237 per MONDO