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Differential Diagnosis For Lactic acid/Lactate (Lab) - Increased: Metabolic, Storage Disorders


List of current finding(s):

Metabolic, Storage Disorders: next: Biochemical Causes
Diabetes mellitus, poorly controlled
Diabetic ketoacidosis/coma
Diabetes mellitus
Primary lactic acidemia/children
Glucose 6 PD deficiency
Metabolic disorders
Combined carboxylase/Biotinidase deficiency
Cytochrome C Oxidase Deficiency/COX Complex Defect
French-Canadian type COX mitochondrial defect
Mitochondrial respiratory chain defects
Propionicacidemia/ketotic glycinemia
Pyruvate carboxylase enzyme deficiency/PCD
Pyruvate Dehydrogenase Complex Deficiency/PDCD
Infantile mitochondrial myopathy/Cox defect
Acyl-CoA Dehydrogenase/short chain def
Krebs cycle/EM cycle metabolic disorder
Amylopectinosis (Andersen's) disease (GSD IV)
Forbes disease (Cori disease, III)
Fructose 1,6 diphosphatase deficiency
Fructose intolerance, hereditary
Fructosuria, essential
Hepatophosphorylase def. glycogenosis
Phosphoenolpyruvate carboxykinase defic (PEPCK)
Tricarboxylic acid metabolic deficiency
Von Gierke's disease/glycogenosis I