Any myopathy in which the cause of the disease is a variation in the POMT2 gene.
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polyglucosan body myopathy
MONDO:0000192
muscular atrophy
MONDO:0004323
myopathy of extraocular muscle
MONDO:0004746
acute quadriplegic myopathy
MONDO:0004969
myofascial pain syndrome
MONDO:0006862
myopathy with abnormal lipid metabolism
MONDO:0009703