Autosomal dominant nonsyndromic hearing loss 36

Definition

Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the TMC1 gene.

Also identified as

• DOID 0110563 per MONDO
• MESH C564675 per MONDO
• OMIM 606705 per MONDO
• UMLS C1847626 per MONDO