Autosomal dominant nonsyndromic hearing loss 5

Definition

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

Also identified as

• DOID 0110575 per MONDO
• MESH C563410 per MONDO
• OMIM 600994 per MONDO
• UMLS C1832932 per MONDO