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C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities D009358 + C16.320 Genetic Diseases, Inborn D030342 + C16.320.565 Metabolism, Inborn Errors D008661 + C16.320.565.202 Carbohydrate Metabolism, Inborn Errors D002239 + C16.320.565.202.810 Pyruvate Metabolism, Inborn Errors D015323 + C16.320.565.202.810.444 Leigh Disease D007888 C16.320.565.202.810.666 Pyruvate Carboxylase Deficiency Disease D015324 C16.320.565.202.810.766 Pyruvate Dehydrogenase Complex Deficiency Disease D015325
C18 Nutritional and Metabolic Diseases D009750 + C18.452 Metabolic Diseases D008659 + C18.452.648 Metabolism, Inborn Errors D008661 + C18.452.648.202 Carbohydrate Metabolism, Inborn Errors D002239 + C18.452.648.202.810 Pyruvate Metabolism, Inborn Errors D015323 + C18.452.648.202.810.444 Leigh Disease D007888 C18.452.648.202.810.666 Pyruvate Carboxylase Deficiency Disease D015324 C18.452.648.202.810.766 Pyruvate Dehydrogenase Complex Deficiency Disease D015325