| Disease Browser
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Parent Node:
 Lipid Metabolism, Inborn Errors (D008052) |
..Starting node
.. Triglyceride Storage Disease, Type I (C566031)
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Child Nodes:
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Sister Nodes: |
..2,4-Dienoyl-CoA Reductase Deficiency (C565624)
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..Acetyl-Coa Carboxylase Deficiency (C562678)
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..Alpha-Methylacyl-CoA Racemase Deficiency (C565768)
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..Apolipoprotein E, Deficiency or Defect of (C566260)
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..Barth Syndrome (D056889)  2
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..Carnitine palmitoyl transferase 1A deficiency (C535588)
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..Carnitine Palmitoyltransferase II Deficiency, Infantile (C563462)
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..Carnitine Palmitoyltransferase II Deficiency, Late-Onset (C563461)
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..Carnitine-Acylcarnitine Translocase Deficiency (C562812)
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..Cholesteryl Ester Transfer Protein Deficiency (C564591)
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..Cytosolic acetoacetyl-CoA thiolase deficiency (C536005)
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..Desmosterolosis (C566555)
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..Hydroxyacyl-CoA Dehydrogenase, Type 2, Deficiency (C536080)
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..Hyperlipidemia, Familial Combined (D006950) 2
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..Hyperlipoproteinemia Type I (D008072) 1
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..Hyperlipoproteinemia Type II (D006938) 4
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..Hyperlipoproteinemia Type III (D006952)
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..Hyperlipoproteinemia Type IV (D006953)
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..Hyperlipoproteinemia Type V (D006954)
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..Hypolipoproteinemias (D007009) 14
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..Lipase deficiency combined (C535904)
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..Lipidoses (D008064) 71
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..Lipodystrophy, Congenital Generalized (D052497) 3
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..Long-chain acyl-CoA dehydrogenase deficiency (C535690)
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..Lp(A) Deficiency, Congenital (C563618)
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..Medium chain acyl CoA dehydrogenase deficiency (C536038)
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..Myopathy with Abnormal Lipid Metabolism (C562935)
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..Neutral Lipid Storage Disease with Myopathy (C565192)
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..Peroxisomal ACYL-COA oxidase deficiency (C536662)
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..Short chain Acyl CoA dehydrogenase deficiency (C537596)
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..Sitosterolemia (C537345)
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..Smith-Lemli-Opitz Syndrome (D019082) 1
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..Trifunctional Protein Deficiency With Myopathy And Neuropathy (C566945)
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..Triglyceride storage disease with impaired long-chain fatty acid oxidation (C536560)
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..Triglyceride Storage Disease, Type I (C566031)
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..Triglyceride Storage Disease, Type II (C566030)
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..VLCAD deficiency (C536353)
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..Xanthomatosis, Cerebrotendinous (D019294)
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Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
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