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Up to: Inborn carbohydrate metabolic disorder · Inborn disorder of energy metabolism
Disorder of glycogen metabolism
An inherited metabolic disorder characterized either by defects in glycogen synthesis or defects in the breaking down of glycogen. It results either in the creation of abnormal forms of glycogen or accumulation of glycogen in the tissues.
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Glycogen storage disease II 31 trials · 41 incl. sub-types Sub-types →
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Glycogen storage disease I 10 trials · 13 incl. sub-types Sub-types →
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Danon disease 5 trials
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Glycogen storage disease IX 2 trials · 3 incl. sub-types Sub-types →
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Glycogen storage disease III 2 trials
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Glycogen storage disease V 2 trials
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Glycogen storage disease VI 2 trials
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Glycogen storage disease due to liver phosphorylase kinase deficiency 0 trials · 2 incl. sub-types Sub-types →
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Lafora disease 1 trial Sub-types →
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Glycogen storage disease VII 1 trial
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GYG1-related disorder of glycogen metabolism 0 trials · 1 incl. sub-types Sub-types →
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Glycogen storage disease IXd 0 trials