Myopathy, centronuclear, 2

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, CNM2, myopathy, centronuclear, autosomal recessive, myotubular myopathy, autosomal recessive

37 clinical trials for this condition and its sub-types.