All
 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