Phosphoenolpyruvic acid Pathways

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Displaying pathways 25 – 39 of 39 in total

Sialuria or French Type Sialuria
Sialuria or French Type Sialuria
Salla Disease/Infantile Sialic Acid Storage Disease
Salla Disease/Infantile Sialic Acid Storage Disease
Tay-Sachs Disease
Tay-Sachs Disease
Leigh Syndrome
Leigh Syndrome
Pyruvate Decarboxylase E1 Component Deficiency (PDHE1 Deficiency)
Pyruvate Decarboxylase E1 Component Deficiency (PDHE1 Deficiency)
Pyruvate Dehydrogenase Complex Deficiency
Pyruvate Dehydrogenase Complex Deficiency
Primary Hyperoxaluria II, PH2
Primary Hyperoxaluria II, PH2
Pyruvate Kinase Deficiency
Pyruvate Kinase Deficiency
Glycogen Storage Disease Type 1A (GSD1A) or Von Gierke Disease
Glycogen Storage Disease Type 1A (GSD1A) or Von Gierke Disease
Phosphoenolpyruvate Carboxykinase Deficiency 1 (PEPCK1)
Phosphoenolpyruvate Carboxykinase Deficiency 1 (PEPCK1)
Fructose-1,6-diphosphatase Deficiency
Fructose-1,6-diphosphatase Deficiency
Triosephosphate Isomerase Deficiency
Triosephosphate Isomerase Deficiency
Glycogenosis, Type IB
Glycogenosis, Type IB
Glycogenosis, Type IC
Glycogenosis, Type IC
Glycogenosis, Type IA. Von Gierke Disease
Glycogenosis, Type IA. Von Gierke Disease

Displaying pathways 25 – 39 of 39 in total