Autosomal dominant nonsyndromic hearing loss 13

Definition

Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the COL11A2 gene.

Also identified as

• DOID 0110545 per MONDO
• MESH C566612 per MONDO
• OMIM 601868 per MONDO
• UMLS C1866095 per MONDO