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Medical Concepts
Diseases
Nutritional and Metabolic Diseases
Metabolic Diseases
Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors
Amino Acid Transport Disorders, Inborn
Amyloidosis, Familial
Brain Diseases, Metabolic, Inborn
Cerebral Amyloid Angiopathy, Familial
Galactosemias
Hartnup Disease
Hepatolenticular Degeneration
Hereditary Central Nervous System Demyelinating Diseases
Homocystinuria
Hyperglycinemia, Nonketotic
Hyperlysinemias
Leigh Disease
Lesch-Nyhan Syndrome
Lysosomal Storage Diseases, Nervous System
Maple Syrup Urine Disease
MELAS Syndrome
Menkes Kinky Hair Syndrome
MERRF Syndrome
Oculocerebrorenal Syndrome
Peroxisomal Disorders
Phenylketonurias
Pyruvate Carboxylase Deficiency Disease
Pyruvate Dehydrogenase Complex Deficiency Disease
Tyrosinemias
Urea Cycle Disorders, Inborn
Carbohydrate Metabolism, Inborn Errors
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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