Myopathy caused by variation in POMT2

MONDO:0700071

Any myopathy in which the cause of the disease is a variation in the POMT2 gene.

Also known as: POMT2 myopathy, POMT2-related myopathy, myopathy caused by mutation in POMT2

3 clinical trials for this condition and its sub-types, 0 tagged with Myopathy caused by variation in POMT2 itself.

Where it sits in the disease tree

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Sub-types of Myopathy caused by variation in POMT2

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