Autosomal dominant nonsyndromic hearing loss 23

Definition

Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the SIX1 gene.

Also identified as

• DOID 0110553 per MONDO
• MESH C565357 per MONDO
• OMIM 605192 per MONDO
• UMLS C1854594 per MONDO