Autosomal dominant nonsyndromic hearing loss 12

Definition

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

Also known as autosomal dominant nonsyndromic hearing loss 12 — per MONDO

Also identified as

• DOID 0110544 per MONDO
• MESH C563295 per MONDO
• OMIM 601543 per MONDO
• UMLS C1832187 per MONDO