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Congenital Disorder

Metabolism, Inborn Errors

AMW:DIS:160071

Errors in metabolic processes resulting from inborn genetic mutations that are inherited or acquired in utero.

Pathology clinical
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Metabolism, Inborn Errors has parent Genetic Diseases, Inborn
Metabolism, Inborn Errors has parent Metabolic Diseases
Brain Diseases, Metabolic, Inborn has parent Metabolism, Inborn Errors
Renal Tubular Transport, Inborn Errors has parent Metabolism, Inborn Errors
Progeria has parent Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors has parent Metabolism, Inborn Errors
Amino Acid Transport Disorders, Inborn has parent Metabolism, Inborn Errors
Amyloidosis, Familial has parent Metabolism, Inborn Errors
Carbohydrate Metabolism, Inborn Errors has parent Metabolism, Inborn Errors
Cytochrome-c Oxidase Deficiency has parent Metabolism, Inborn Errors
Hyperbilirubinemia, Hereditary has parent Metabolism, Inborn Errors
Lipid Metabolism, Inborn Errors has parent Metabolism, Inborn Errors
Lysosomal Storage Diseases has parent Metabolism, Inborn Errors
Metal Metabolism, Inborn Errors has parent Metabolism, Inborn Errors
Peroxisomal Disorders has parent Metabolism, Inborn Errors
Purine-Pyrimidine Metabolism, Inborn Errors has parent Metabolism, Inborn Errors
Steroid Metabolism, Inborn Errors has parent Metabolism, Inborn Errors

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