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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 +
C16.320.565.066 Amino Acid Metabolism, Inborn Errors D000592 +
C16.320.565.066.620 Multiple Carboxylase Deficiency D009100 +
C16.320.565.066.620.100 Biotinidase Deficiency D028921
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 +
C16.320.565.202.720 Multiple Carboxylase Deficiency D009100 +
C16.320.565.202.720.100 Biotinidase Deficiency D028921
C18 Nutritional and Metabolic Diseases D009750 +
C18.452 Metabolic Diseases D008659 +
C18.452.648 Metabolism, Inborn Errors D008661 +
C18.452.648.066 Amino Acid Metabolism, Inborn Errors D000592 +
C18.452.648.066.620 Multiple Carboxylase Deficiency D009100 +
C18.452.648.066.620.100 Biotinidase Deficiency D028921
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 +
C18.452.648.202.720 Multiple Carboxylase Deficiency D009100 +
C18.452.648.202.720.100 Biotinidase Deficiency D028921