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Medical Concepts
Diseases
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors
Albinism
Alkaptonuria
Hyperglycinemia, Nonketotic
Hyperhomocysteinemia
Hyperlysinemias
Maple Syrup Urine Disease
Multiple Acyl Coenzyme A Dehydrogenase Deficiency
Multiple Carboxylase Deficiency
Phenylketonurias
Prolidase Deficiency
Propionic Acidemia
Tyrosinemias
Urea Cycle Disorders, Inborn
Amino Acid Transport Disorders, Inborn
Amyloidosis, Familial
Brain Diseases, Metabolic, Inborn
Carbohydrate Metabolism, Inborn Errors
Cytochrome-c Oxidase Deficiency
Hyperbilirubinemia, Hereditary
Lipid Metabolism, Inborn Errors
Lysosomal Storage Diseases
Metal Metabolism, Inborn Errors
Peroxisomal Disorders
Porphyrias
Progeria
Purine-Pyrimidine Metabolism, Inborn Errors
Renal Tubular Transport, Inborn Errors
Steroid Metabolism, Inborn Errors
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