All
 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