Other disorders of carbohydrate metabolism
Notes: Type I glycogen storage disease ; Cardiac glycogenosis ; Type II glycogen storage disease ; Forbes disease ; Type III glycogen storage disease ; Type V glycogen storage disease ; Andersen disease ; Hers disease ; Tauri disease ; Glycogen storage disease, types 0, IV, VI-XI ; Liver phosphorylase deficiency ; Muscle phosphofructokinase deficiency ; Fructokinase deficiency ; Fructosemia ; Fructose-1, 6-diphosphatase deficiency ; Galactokinase deficiency ; Disorder of intestinal carbohydrate absorption NOS ; Glucose-galactose malabsorption ; Sucrase deficiency ; Deficiency of phosphoenolpyruvate carboxykinase ; Deficiency of pyruvate carboxylase ; Deficiency of pyruvate dehydrogenase ; De Vivo syndrome ; Glucose transport defect, blood-brain barrier ; Glut1 deficiency ; GLUT1 deficiency syndrome 1, infantile onset ; GLUT1 deficiency syndrome 2, childhood onset ; (Familial) renal glycosuria ; Essential pentosuria ; diabetes mellitus (E08-E13) ; hypoglycemia NOS (E16.2) ; increased secretion of glucagon (E16.3) ; mucopolysaccharidosis (E76.0-E76.3) ; muscle phosphofructokinase deficiency (E74.09) ; disorders of pyruvate metabolism and gluconeogenesis with anemia (D55.-) ; Leigh’s syndrome (G31.82) ; lactose intolerance (E73.-)