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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 +
C16.320.565.066.102 Albinism D000417 +
C16.320.565.066.187 Alkaptonuria D000474
C16.320.565.066.210 Aminoaciduria, Renal D000608 +
C16.320.565.066.470 Homocystinuria D006712
C16.320.565.066.608 Maple Syrup Urine Disease D008375
C16.320.565.066.620 Multiple Carboxylase Deficiency D009100 +
C16.320.565.066.766 Phenylketonurias D010661 +
C16.320.565.066.480 Hyperhomocysteinemia D020138
C16.320.565.066.477 Hyperglycinemia, Nonketotic D020158
C16.320.565.066.340 Citrullinemia D020159
C16.320.565.066.475 Hyperargininemia D020162
C16.320.565.066.729 Ornithine Carbamoyltransferase Deficiency Disease D020163
C16.320.565.066.275 Carbamoyl-Phosphate Synthase I Deficiency Disease D020165
C16.320.565.066.544 Hyperlysinemias D020167
C16.320.565.066.880 Tyrosinemias D020176
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 +
C18.452.648.066.102 Albinism D000417 +
C18.452.648.066.187 Alkaptonuria D000474
C18.452.648.066.210 Aminoaciduria, Renal D000608 +
C18.452.648.066.470 Homocystinuria D006712
C18.452.648.066.608 Maple Syrup Urine Disease D008375
C18.452.648.066.620 Multiple Carboxylase Deficiency D009100 +
C18.452.648.066.766 Phenylketonurias D010661 +
C18.452.648.066.480 Hyperhomocysteinemia D020138
C18.452.648.066.477 Hyperglycinemia, Nonketotic D020158
C18.452.648.066.340 Citrullinemia D020159
C18.452.648.066.475 Hyperargininemia D020162
C18.452.648.066.729 Ornithine Carbamoyltransferase Deficiency Disease D020163
C18.452.648.066.275 Carbamoyl-Phosphate Synthase I Deficiency Disease D020165
C18.452.648.066.544 Hyperlysinemias D020167
C18.452.648.066.880 Tyrosinemias D020176
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