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adult polyglucosan body disease
MONDO:0009897
glycogen storage disease due to glycogen branching enzyme deficiency, progressive hepatic form
MONDO:0017695
glycogen storage disease due to glycogen branching enzyme deficiency, non progressive hepatic form
MONDO:0017696
glycogen storage disease due to glycogen branching enzyme deficiency, congenital neuromuscular form
MONDO:0017698
glycogen storage disease due to glycogen branching enzyme deficiency, childhood combined hepatic and myopathic form
MONDO:0017699
glycogen storage disease due to glycogen branching enzyme deficiency, childhood neuromuscular form
MONDO:0017700