Monarch Disease Ontology id MONDO_0009709 (myopathy, centronuclear, 2) is 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 2, centronuclear myopathy caused by mutation in BIN1, myopathy, centronuclear, type 2.