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Glucose, Galactose, GABA, glutathione, Heme, NAD, NADP,serotonine,…

- - - - Glyceraldehyde 3-P
        
        1,3-Bisphosphoglycerate
        
        3-Phosphoglycerate
        
        2-Phosphoglycerate
        
        Phosphoenolpyruvate
        
        Pyruvate
        
        5 more items...
      - Dihydroxyacetone-P
        
        Glycerol-P
        
        Triacylglycerol
        
        Glycerol
        
        Fatty acids
        
        Cystic fibrosis (CF)
        This autosomal recessive disorder is caused by mutations to the gene for the CF transmembrane conductance regulator (CFTR) protein that functions as a chloride channel on epithelium.
  - - - Ribulos 5-P
        
        Xylulose 5-P
        
        Sedoheptulose 7-P
        
        Erythrose 4-P
        
        Ribose 5-P
        
        Glyceraldehyde 3-P
- - - - Glyceraldehyde
- - - - Glucogen storage diseases
        TYPE Ia: VON GIERKE DISEASE (GLUCOSE 6-PHOSPHATASE DEFICIENCY)
        TYPE Ib: GLUCOSE 6-PHOSPHATE TRANSLOCASE DEFICIENCY
        TYPE II: POMPE DISEASE (LYSOSOMAL α(1→4)-GLUCOSIDASE DEFICIENCY) TYPE III: CORI DISEASE (4:4 TRANSFERASE and/or 1:6 GLUCOSIDASE DEFICIENCY)
        TYPE V: McARDLE SYNDROME (SKELETAL MUSCLE GLYCOGEN PHOSPHORYLASE OR MYOPHOSPHORYLASE DEFICIENCY)
- - - - GOUT
        This disorder is characterized by hyperuricemia with recurrent attacks of acute arthritic joint inflammation, caused by deposition of mono-sodium urate crystals.
- - - - Arginine
        
        Ornithine
        
        Urea