Autosomal dominant nonsyndromic hearing loss 1

Definition

Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the DIAPH1 gene.

Also known as Konigsmark syndrome — per MONDO

Also identified as

• DOID 0110541 per MONDO
• MESH C565121 per MONDO
• OMIM 124900 per MONDO
• UMLS C1852282 per MONDO