Glycogen storage disease due to glycogen branching enzyme deficiency, non progressive hepatic form
ORPHA:308638Danon disease
ORPHA:34587Fanconi-Bickel syndrome
ORPHA:2088Glycogen storage disease due to glycogen branching enzyme deficiency
ORPHA:367Glycogen storage disease due to glycogen branching enzyme deficiency, adult neuromuscular form
ORPHA:308712Glycogen storage disease due to glycogen branching enzyme deficiency, childhood combined hepatic and myopathic form
ORPHA:308684Glycogen storage disease due to glycogen branching enzyme deficiency, childhood neuromuscular form
ORPHA:308698Glycogen storage disease due to glycogen branching enzyme deficiency, congenital neuromuscular form
ORPHA:308670Glycogen storage disease due to glycogen branching enzyme deficiency, fatal perinatal neuromuscular form
ORPHA:308655Glycogen storage disease due to glycogen branching enzyme deficiency, progressive hepatic form
ORPHA:308621Glycogen storage disease due to glycogen debranching enzyme deficiency
ORPHA:366Glycogen storage disease due to glycogen synthase deficiency
ORPHA:308520Glycogen storage disease due to hepatic glycogen synthase deficiency
ORPHA:2089Glycogen storage disease due to liver glycogen phosphorylase deficiency
ORPHA:369Glycogen storage disease due to muscle beta-enolase deficiency
ORPHA:99849