Glycogen Storage Disease Type 1

About the Disease
Glycogen Storage Disease Due to Glucose-6-Phosphatase Deficiency, also known as glycogen storage disease type i, is related to glycogen storage disease ia and glycogen storage disease due to glucose-6-phosphatase deficiency type ib, and has symptoms including intermittent diarrhea The drugs Prednisolone phosphate and Prednisolone acetate have been mentioned in the context of this disorder. Affiliated tissues include liver, kidney and bone marrow, and related phenotypes are recurrent respiratory infections and short stature

Common Targets
SLC37A4 | ACADVL | SLC4A2 | K(ATP) Channel (nonspecified subtype) | G6PC1 | GAA

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