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This Concept Map, created with IHMC CmapTools, has information related to: Fructose Intolerance and Glycogen Storage Disease, Fructose-1-Phosphate via aldolase B, is converted to Dihydroxyacetone phosphate (DHAP), Aldolase B catalyzes conversion of Fructose-1-Phosphate, True enzyme defect characterizes Glycogen storage disease (GSD) type 1a, Lactic acidemia suggests Enzyme deficiency, McArdle's Disease (GSD type V) characterized by No rise in lactate levels, Oxidative phosphorylation occurs in Inner mitochondrial membrane, McArdle's Disease (GSD type V) characterized by Weakness and cramping after exercise, Hypoglycemia (30 mg/dL) stimulates release of Glucagon, Glucose-6-phosphate via G-6 Pase, is converted to Glucose, Low ATP/AMP ratio stimulates Glycogenolysis, Baby 1 7-month old boy presents with Reducing sugar in urine, Baby 1 7-month old boy presents with Hyperuricemia, Reducing sugar in urine suggests Enzyme deficiency, Lactate dehydrogenase (LDH) catalyzes the conversion of Pyruvate, Aldolase B found in Liver, Free blood glucose when lowered, can cause Seizure, Fructosuria is an inherited Autosomal recessive mutation, Gluconeogenesis occurs in Liver, Dihydroxyacetone phosphate (DHAP) via triose P isomerase, converted to Glyceraldehyde- 3-Phosphate, Reducing equivalents provides substrates for Oxidative phosphorylation