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Autosomal dominant centronuclear myopathy

MONDO:0008048

An inherited neuromuscular disorder defined by numerous centrally placed nuclei on muscle biopsy and clinical features of a congenital myopathy.

Also known as: AD-CNM, CNM1, autosomal dominant centronuclear myopathy, autosomal dominant centronuclear myopathy caused by mutation in MYF6, centronuclear myopathy 1, centronuclear myopathy, autosomal dominant, centronuclear myopathy, autosomal, modifier of, myopathy, centronuclear, 1

4 clinical trials for this condition and its sub-types, 0 tagged with Autosomal dominant centronuclear myopathy itself.

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