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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 +
C16.320.565.202.303 Fucosidosis D005645
C16.320.565.202.355 Galactosemias D005693
C16.320.565.202.449 Glycogen Storage Disease D006008 +
C16.320.565.202.460 Hyperoxaluria, Primary D006960
C16.320.565.202.589 Lactose Intolerance D007787
C16.320.565.202.670 Mucolipidoses D009081
C16.320.565.202.715 Mucopolysaccharidoses D009083 +
C16.320.565.202.720 Multiple Carboxylase Deficiency D009100 +
C16.320.565.202.251 Fructose Metabolism, Inborn Errors D015318 +
C16.320.565.202.810 Pyruvate Metabolism, Inborn Errors D015323 +
C16.320.565.202.125 Carbohydrate-Deficient Glycoprotein Syndrome D018981
C16.320.565.202.765 Persistent Hyperinsulinemia Hypoglycemia of Infancy D044903
C16.320.565.202.607 Mannosidase Deficiency Diseases D044904 +
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 +
C18.452.648.202.303 Fucosidosis D005645
C18.452.648.202.355 Galactosemias D005693
C18.452.648.202.449 Glycogen Storage Disease D006008 +
C18.452.648.202.460 Hyperoxaluria, Primary D006960
C18.452.648.202.589 Lactose Intolerance D007787
C18.452.648.202.670 Mucolipidoses D009081
C18.452.648.202.715 Mucopolysaccharidoses D009083 +
C18.452.648.202.720 Multiple Carboxylase Deficiency D009100 +
C18.452.648.202.251 Fructose Metabolism, Inborn Errors D015318 +
C18.452.648.202.810 Pyruvate Metabolism, Inborn Errors D015323 +
C18.452.648.202.125 Carbohydrate-Deficient Glycoprotein Syndrome D018981
C18.452.648.202.607 Mannosidase Deficiency Diseases D044904 +
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