DextrinosisGlycogenosisGsdOther Metabolites Mapped to 'Glycogen storage disease'HMDB0000138 (Glycocholic acid) HMDB0000190 (L-Lactic acid)
- HMDB0000190 (L-Lactic acid)
- Glycogen storage disease
- A glycogen metabolism disorder that has material basis in enzymes deficiencies necessary in the processing of glycogen synthesis or breakdown within muscles, liver, and other cell types. (do).
- Parent Term
- Metabolism and nutrition disorders
- Parent Definition
- A group of disorders, inherited or not, that result in a metabolic malfunction.