Myopathy caused by variation in POMGNT2

MONDO:0700069

Any myopathy in which the cause of the disease is a variation in the POMGNT2 gene.

Also known as: POMGNT2 myopathy, POMGNT2-related myopathy, myopathy caused by mutation in POMGNT2

2 clinical trials for this condition and its sub-types, 0 tagged with Myopathy caused by variation in POMGNT2 itself.

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