All

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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 +
     C16.320.565.202 Carbohydrate Metabolism, Inborn Errors D002239 +
     C16.320.565.390 Glucosephosphate Dehydrogenase Deficiency D005955 
     C16.320.565.437 Hyperbilirubinemia, Hereditary D006933 +
     C16.320.565.499 Jaundice, Chronic Idiopathic D007566 
     C16.320.565.556 Lipid Metabolism, Inborn Errors D008052 +
     C16.320.565.618 Metal Metabolism, Inborn Errors D008664 +
     C16.320.565.769 Progeria D011371 
     C16.320.565.798 Purine-Pyrimidine Metabolism, Inborn Errors D011686 +
     C16.320.565.851 Renal Tubular Transport, Inborn Errors D015499 +
     C16.320.565.580 Lysosomal Storage Diseases D016464 +
     C16.320.565.731 Porphyria, Erythropoietic D017092 
     C16.320.565.735 Porphyria, Hepatic D017094 +
     C16.320.565.728 Porphyria, Erythrohepatic D017121 
     C16.320.565.088 Amino Acid Transport Disorders, Inborn D020157 +
     C16.320.565.150 Brain Diseases, Metabolic, Inborn D020739 +
     C16.320.565.100 Amyloidosis, Familial D028226 +
     C16.320.565.240 Cytochrome-c Oxidase Deficiency D030401 
     C16.320.565.925 Steroid Metabolism, Inborn Errors D043202 +
 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 +
     C18.452.648.202 Carbohydrate Metabolism, Inborn Errors D002239 +
     C18.452.648.390 Glucosephosphate Dehydrogenase Deficiency D005955 
     C18.452.648.437 Hyperbilirubinemia, Hereditary D006933 +
     C18.452.648.499 Jaundice, Chronic Idiopathic D007566 
     C18.452.648.556 Lipid Metabolism, Inborn Errors D008052 +
     C18.452.648.618 Metal Metabolism, Inborn Errors D008664 +
     C18.452.648.769 Progeria D011371 
     C18.452.648.798 Purine-Pyrimidine Metabolism, Inborn Errors D011686 +
     C18.452.648.851 Renal Tubular Transport, Inborn Errors D015499 +
     C18.452.648.595 Lysosomal Storage Diseases D016464 +
     C18.452.648.730 Porphyria, Erythropoietic D017092 
     C18.452.648.735 Porphyria, Hepatic D017094 +
     C18.452.648.728 Porphyria, Erythrohepatic D017121 
     C18.452.648.088 Amino Acid Transport Disorders, Inborn D020157 +
     C18.452.648.151 Brain Diseases, Metabolic, Inborn D020739 +
     C18.452.648.100 Amyloidosis, Familial D028226 +
     C18.452.648.240 Cytochrome-c Oxidase Deficiency D030401 
     C18.452.648.925 Steroid Metabolism, Inborn Errors D043202 +