Autosomal dominant nonsyndromic hearing loss 6

Definition

Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the WFS1 gene.

Also identified as

• DOID 0110584 per MONDO
• MESH C563421 per MONDO
• OMIM 600965 per MONDO
• UMLS C1833021 per MONDO