An inherited neuromuscular disorder defined by numerous centrally placed nuclei on muscle biopsy and clinical features of a congenital myopathy. The disease is autosomal dominant centronuclear myopathy (MONDO_0008048). Also known as: AD-CNM, CNM1, autosomal dominant centronuclear myopathy caused by mutation in MYF6, centronuclear myopathy 1, centronuclear myopathy, autosomal dominant, centronuclear myopathy, autosomal, modifier of, myopathy, centronuclear, 1, myopathy, centronuclear, 3.