Myopathy, centronuclear, 2

Definition

Any centronuclear myopathy in which the cause of the disease is a mutation in the BIN1 gene.

Also known as BIN1 centronuclear myopathy, centronuclear myopathy caused by mutation in BIN1, myopathy, centronuclear, 2, myopathy, centronuclear, type 2 — per MONDO

Also identified as

• DOID 0111220 per MONDO
• MESH C562934 per MONDO
• OMIM 255200 per MONDO
• UMLS C0410204 per MONDO