Disease Browser
Parent Node: Dyslipidemias (D050171) Parent Node: Lipid Metabolism, Inborn Errors (D008052) ..Starting node .. Hypolipoproteinemias (D007009) Child Nodes:
........Hypoalphalipoproteinemias (D052456) 4 ........Hypobetalipoproteinemias (D006995) 8 ........Wolman Disease with Hypolipoproteinemia and Acanthocytosis (C564736) Sister Nodes: ..2,4-Dienoyl-CoA Reductase Deficiency (C565624) ..Acetyl-Coa Carboxylase Deficiency (C562678) ..Alpha-Methylacyl-CoA Racemase Deficiency (C565768) ..Apolipoprotein E, Deficiency or Defect of (C566260) ..Barth Syndrome (D056889) 2 ..Carnitine palmitoyl transferase 1A deficiency (C535588) ..Carnitine Palmitoyltransferase II Deficiency, Infantile (C563462) ..Carnitine Palmitoyltransferase II Deficiency, Late-Onset (C563461) ..Carnitine-Acylcarnitine Translocase Deficiency (C562812) ..Cholesteryl Ester Transfer Protein Deficiency (C564591) ..Cytosolic acetoacetyl-CoA thiolase deficiency (C536005) ..Desmosterolosis (C566555) ..Hydroxyacyl-CoA Dehydrogenase, Type 2, Deficiency (C536080) ..Hyperlipidemia, Familial Combined (D006950) 2 ..Hyperlipoproteinemia Type I (D008072) 1 ..Hyperlipoproteinemia Type II (D006938) 4 ..Hyperlipoproteinemia Type III (D006952) ..Hyperlipoproteinemia Type IV (D006953) ..Hyperlipoproteinemia Type V (D006954) ..Hypolipoproteinemias (D007009) 14 ..Lipase deficiency combined (C535904) ..Lipidoses (D008064) 71 ..Lipodystrophy, Congenital Generalized (D052497) 3 ..Long-chain acyl-CoA dehydrogenase deficiency (C535690) ..Lp(A) Deficiency, Congenital (C563618) ..Medium chain acyl CoA dehydrogenase deficiency (C536038) ..Myopathy with Abnormal Lipid Metabolism (C562935) ..Neutral Lipid Storage Disease with Myopathy (C565192) ..Peroxisomal ACYL-COA oxidase deficiency (C536662) ..Short chain Acyl CoA dehydrogenase deficiency (C537596) ..Sitosterolemia (C537345) ..Smith-Lemli-Opitz Syndrome (D019082) 1 ..Trifunctional Protein Deficiency With Myopathy And Neuropathy (C566945) ..Triglyceride storage disease with impaired long-chain fatty acid oxidation (C536560) ..Triglyceride Storage Disease, Type I (C566031) ..Triglyceride Storage Disease, Type II (C566030) ..VLCAD deficiency (C536353) ..Xanthomatosis, Cerebrotendinous (D019294) Human Disease MESH is developed by UMLS . Further data from MedGen , OMIM , CTD