Autosomal dominant nonsyndromic hearing loss 15

Definition

Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the POU4F3 gene.

Also identified as

• DOID 0110546 per MONDO
• MESH C566545 per MONDO
• OMIM 602459 per MONDO
• UMLS C1865366 per MONDO