Myopathy caused by variation in POMT1

MONDO:0700070

Any myopathy in which the cause of the disease is a variation in the POMT1 gene.

Also known as: POMT1 myopathy, POMT1-related myopathy, myopathy caused by mutation in POMT1

3 clinical trials for this condition and its sub-types, 0 tagged with Myopathy caused by variation in POMT1 itself.

Where it sits in the disease tree

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Sub-types of Myopathy caused by variation in POMT1

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