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Glycogen storage disease I
Glycogenosis due to glucose-6-phosphatase (G6P) deficiency or glycogen storage disease, (GSD), type 1, is a group of inherited metabolic diseases, including types a and b, and characterized by poor tolerance to fasting, growth retardation and hepatomegaly resulting from accumulation of glycogen and fat in the liver.
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Glycogen storage disease type 1 due to SLC37A4 mutation 0 trials · 3 incl. sub-types Sub-types →
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Glycogen storage disease Id 0 trials