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Inborn Errors Lipid Metabolism
Subscribe to New Research on Inborn Errors Lipid Metabolism
Errors in the metabolism of LIPIDS resulting from inborn genetic MUTATIONS that are heritable.
Also Known As:
Lipid Metabolism, Inborn Errors; Lipid Metabolism, Inborn Error
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Disease Context: Research Results
Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 668
Inborn Genetic Diseases: 842
Inborn Errors Metabolism: 588
Inborn Errors Lipid Metabolism
Hyperlipoproteinemia Type II: 2611
Lipidoses: 479
Smith-Lemli-Opitz Syndrome: 363
Familial Combined Hyperlipidemia: 312
Cerebrotendinous Xanthomatosis: 285
Hyperlipoproteinemia Type IV: 192
Hyperlipoproteinemia Type III: 147
Sitosterolemia: 128
Barth Syndrome: 116
Medium chain acyl CoA dehydrogenase deficiency: 92
Hyperlipoproteinemia Type I: 66
Hypolipoproteinemias: 23
Triglyceride storage disease with impaired long-chain fatty acid oxidation: 20
Lathosterolosis: 16
Long-chain acyl-CoA dehydrogenase deficiency: 11
Short chain Acyl CoA dehydrogenase deficiency: 11
Hyperlipoproteinemia Type V: 3
Carnitine palmitoyl transferase 1A deficiency: 2
Cytosolic acetoacetyl-CoA thiolase deficiency
Lipase deficiency combined
Nutritional and Metabolic Diseases: 2
Metabolic Diseases: 3200
Inborn Errors Metabolism: 588
Inborn Errors Lipid Metabolism
Hyperlipoproteinemia Type II: 2611
Lipidoses: 479
Smith-Lemli-Opitz Syndrome: 363
Familial Combined Hyperlipidemia: 312
Cerebrotendinous Xanthomatosis: 285
Hyperlipoproteinemia Type IV: 192
Hyperlipoproteinemia Type III: 147
Sitosterolemia: 128
Barth Syndrome: 116
Medium chain acyl CoA dehydrogenase deficiency: 92
Hyperlipoproteinemia Type I: 66
Hypolipoproteinemias: 23
Triglyceride storage disease with impaired long-chain fatty acid oxidation: 20
Lathosterolosis: 16
Long-chain acyl-CoA dehydrogenase deficiency: 11
Short chain Acyl CoA dehydrogenase deficiency: 11
Hyperlipoproteinemia Type V: 3
Carnitine palmitoyl transferase 1A deficiency: 2
Cytosolic acetoacetyl-CoA thiolase deficiency
Lipase deficiency combined
Lipid Metabolism Disorders: 167
Inborn Errors Lipid Metabolism
Sitosterolemia: 128
Medium chain acyl CoA dehydrogenase deficiency: 92
Triglyceride storage disease with impaired long-chain fatty acid oxidation: 20
Lathosterolosis: 16
Long-chain acyl-CoA dehydrogenase deficiency: 11
Short chain Acyl CoA dehydrogenase deficiency: 11
Carnitine palmitoyl transferase 1A deficiency: 2
Cytosolic acetoacetyl-CoA thiolase deficiency
Lipase deficiency combined