Autosomal dominant nonsyndromic hearing loss 44

Definition

Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the CCDC50 gene.

Also identified as

• DOID 0110569 per MONDO
• MESH C564399 per MONDO
• OMIM 607453 per MONDO
• UMLS C1843895 per MONDO