Library Powered by BSD FreeBSD MySQL Apache PHP PHP
© May 2005 Lorentz JÄNTSCHI && Sorana Daniela BOLBOACĂ

up one level Up


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 +