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Myopathy, centronuclear, 2

MONDO:0009709

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

4 clinical trials for this condition and its sub-types, 0 tagged with Myopathy, centronuclear, 2 itself.

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Part of

↑ Autosomal recessive centronuclear myopathy (0)

Including sub-types (4) Tagged with Myopathy, centronuclear, 2 (0)

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