Autosomal dominant nonsyndromic hearing loss 2A

Definition

Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the KCNQ4 gene.

Also identified as

• DOID 0110558 per MONDO
• MESH C567441 per MONDO
• OMIM 600101 per MONDO
• UMLS C2677637 per MONDO