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 +
 C16.320.565.202 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 +