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Disease Lipid Metabolism, Inborn Errors

Name Lipid Metabolism, Inborn Errors
Synonym Lipid Metabolism, Inborn Error
Definition Errors in the metabolism of LIPIDS resulting from inborn genetic MUTATIONS that are heritable.
Categories Genetic disease (inborn) | Metabolic disease
MeSH® ID D008052
External Links

Top ↑ Ancestors

1. DiseasesCongenital, Hereditary, and Neonatal Diseases and Abnormalities Has associated chemicals Has associated genes Has associated phenotype references Has associated exposure references Genetic Diseases, Inborn Has associated chemicals Has associated genes Has associated phenotype references Has associated exposure references Metabolism, Inborn Errors Has associated chemicals Has associated genes Has associated phenotype references Has associated exposure references Lipid Metabolism, Inborn Errors Has associated chemicals Has associated genes Has associated phenotype references
2. DiseasesNutritional and Metabolic Diseases Has associated chemicals Has associated genes Has associated phenotype references Has associated exposure references Metabolic Diseases Has associated chemicals Has associated genes Has associated phenotype references Has associated exposure references Lipid Metabolism Disorders Has associated chemicals Has associated genes Has associated phenotype references Has associated exposure references Lipid Metabolism, Inborn Errors Has associated chemicals Has associated genes Has associated phenotype references
3. DiseasesNutritional and Metabolic Diseases Has associated chemicals Has associated genes Has associated phenotype references Has associated exposure references Metabolic Diseases Has associated chemicals Has associated genes Has associated phenotype references Has associated exposure references Metabolism, Inborn Errors Has associated chemicals Has associated genes Has associated phenotype references Has associated exposure references Lipid Metabolism, Inborn Errors Has associated chemicals Has associated genes Has associated phenotype references

Top ↑ Descendants

Lipid Metabolism, Inborn Errors Has associated chemicals Has associated genes Has associated phenotype references
  2,4-Dienoyl-CoA Reductase Deficiency Has associated chemicals Has associated genes Has associated phenotype references
  Acetyl-Coa Carboxylase Deficiency Has associated chemicals Has associated genes Has associated phenotype references
  Alpha-Methylacyl-CoA Racemase Deficiency Has associated chemicals Has associated genes Has associated phenotype references
  Apolipoprotein E, Deficiency or Defect of
View node Barth Syndrome Has associated chemicals Has associated genes Has associated phenotype references
  Carnitine-Acylcarnitine Translocase Deficiency Has associated chemicals Has associated genes Has associated phenotype references
  Carnitine palmitoyl transferase 1A deficiency Has associated chemicals Has associated genes Has associated phenotype references
  Carnitine Palmitoyltransferase II Deficiency, Infantile Has associated chemicals Has associated genes Has associated phenotype references
  Carnitine Palmitoyltransferase II Deficiency, Late-Onset Has associated chemicals Has associated genes Has associated phenotype references
  Chanarin-Dorfman Syndrome Has associated chemicals Has associated genes Has associated phenotype references
  Cholesteryl Ester Transfer Protein Deficiency
  Cytosolic acetoacetyl-CoA thiolase deficiency Has associated chemicals Has associated genes Has associated phenotype references
  Desmosterolosis Has associated chemicals Has associated genes Has associated phenotype references
  GLYCOSYLPHOSPHATIDYLINOSITOL DEFICIENCY Has associated chemicals Has associated genes Has associated phenotype references
  HEPATIC LIPASE DEFICIENCY Has associated chemicals Has associated genes Has associated phenotype references
View node Hyperlipidemia, Familial Combined Has associated chemicals Has associated genes Has associated phenotype references
View node Hyperlipoproteinemia Type I Has associated chemicals Has associated genes Has associated phenotype references
View node Hyperlipoproteinemia Type II Has associated chemicals Has associated genes Has associated phenotype references
  Hyperlipoproteinemia Type III Has associated chemicals Has associated genes Has associated phenotype references
  Hyperlipoproteinemia Type IV Has associated chemicals Has associated genes Has associated phenotype references
  Hyperlipoproteinemia Type V Has associated chemicals Has associated genes Has associated phenotype references
View node Hypolipoproteinemias Has associated chemicals Has associated genes Has associated phenotype references
  Lipase deficiency combined Has associated chemicals Has associated genes Has associated phenotype references
View node Lipidoses Has associated chemicals Has associated genes Has associated phenotype references
View node Lipodystrophy, Congenital Generalized Has associated chemicals Has associated genes Has associated phenotype references
  Long-chain acyl-CoA dehydrogenase deficiency
  Lp(A) Deficiency, Congenital
  Medium chain acyl CoA dehydrogenase deficiency Has associated chemicals Has associated genes Has associated phenotype references
  Myopathy with Abnormal Lipid Metabolism Has associated chemicals Has associated genes Has associated phenotype references
  Neutral Lipid Storage Disease with Myopathy Has associated chemicals Has associated genes Has associated phenotype references
  PANCREATIC LIPASE DEFICIENCY Has associated chemicals Has associated genes Has associated phenotype references
  Peroxisomal ACYL-COA oxidase deficiency Has associated chemicals Has associated genes Has associated phenotype references
  Short chain Acyl CoA dehydrogenase deficiency Has associated chemicals Has associated genes Has associated phenotype references
  Sitosterolemia Has associated chemicals Has associated genes Has associated phenotype references
View node Smith-Lemli-Opitz Syndrome Has associated chemicals Has associated genes Has associated phenotype references
  Trifunctional Protein Deficiency With Myopathy And Neuropathy Has associated chemicals Has associated genes Has associated phenotype references
  Triglyceride Storage Disease, Type I
  Triglyceride Storage Disease, Type II
  VLCAD deficiency Has associated chemicals Has associated genes Has associated phenotype references
  Xanthomatosis, Cerebrotendinous Has associated chemicals Has associated genes Has associated phenotype references