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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 + C16.320.565.088 Amino Acid Transport Disorders, Inborn D020157 + C16.320.565.088.400 Hartnup Disease D006250 C16.320.565.088.600 Oculocerebrorenal Syndrome D009800
C18 Nutritional and Metabolic Diseases D009750 + C18.452 Metabolic Diseases D008659 + C18.452.648 Metabolism, Inborn Errors D008661 + C18.452.648.088 Amino Acid Transport Disorders, Inborn D020157 + C18.452.648.088.400 Hartnup Disease D006250 C18.452.648.088.600 Oculocerebrorenal Syndrome D009800