glycogen storage disease due to glycogen branching enzyme deficiency, childhood combined hepatic and myopathic form

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, fatal perinatal neuromuscular form

MONDO:0017697

glycogen storage disease due to glycogen branching enzyme deficiency, congenital neuromuscular form

MONDO:0017698

glycogen storage disease due to glycogen branching enzyme deficiency, childhood neuromuscular form

MONDO:0017700