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Myopathy, centronuclear, 5

MONDO:0014418

Any autosomal recessive centronuclear myopathy in which the cause of the disease is a mutation in the SPEG gene.

Also known as: SPEG autosomal recessive centronuclear myopathy, autosomal recessive centronuclear myopathy caused by mutation in SPEG, myopathy, centronuclear, 5, myopathy, centronuclear, type 5, CNM5

4 clinical trials for this condition and its sub-types, 0 tagged with Myopathy, centronuclear, 5 itself.

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↑ Autosomal recessive centronuclear myopathy (0)

Including sub-types (4) Tagged with Myopathy, centronuclear, 5 (0)

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