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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