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Alternative Terms
type-ii-familial-hyperlipoproteinemia hypercholesterolemia familial-hypercholesterolemia icd mendelian-inheritance-in-man diseases-database medlineplus emedicine medical-subject-headings medicine genetic-disorder low-density-lipoprotein cardiovascular-disease cholesterol very-low-density-lipoprotein triglyceride electrophoresis hyperlipidemia angina-pectoris ptca coronary-bypass-surgery myocardial-infarction transient-ischemic-attack stroke peripheral-artery-occlusive-disease family-history-medicine atherosclerosis xanthoma tendon macrophage xanthelasma arcus-cornealis zygosity apolipoprotein-b gene chromosome liver high-density-lipoprotein redox foam-cells dna allele statin hmg-coa-reductase fibrate bile-acid-sequestrant niacin acipimox myopathy rhabdomyolysis acute-renal-failure ldl-apheresis kidney-dialysis goldstein-joseph-leonard michael-stuart-brown science-journal metabolic-disorder-2 pathology inborn-error-of-metabolism-2 list-of-icd-9-codes-240-279-endocrine-nutritional-and-metabolic-diseases-and-immunity-disorders amino-acid aromatic-amino-acids phenylketonuria alkaptonuria ochronosis tyrosinemia albinism histidinemia branched-chain-amino-acids maple-syrup-urine-disease propionic-acidemia methylmalonic-aciduria isovaleric-acidemia 3-methylcrotonyl-coa-carboxylase-deficiency cystinuria cystinosis hartnup-disease fanconi-s-syndrome oculocerebrorenal-syndrome homocystinuria cystathioninuria-2 urea-cycle-disorder n-acetylglutamate-synthase-deficiency carbamoyl-phosphate-synthetase-i-deficiency ornithine-transcarbamylase-deficiency citrullinemia argininosuccinic-aciduria hyperammonemia glutaric-aciduria-type sarcosinemia carbohydrate lactose-intolerance glycogen-storage-disease pompe-s-disease type-3-glycogenosis type-4-glycogenosis mcardle-disease phosphofructokinase-deficiency hereditary-fructose-intolerance fructose-bisphosphatase-deficiency
type-ii-familial-hyperlipoproteinemia hypercholesterolemia familial-hypercholesterolemia icd mendelian-inheritance-in-man diseases-database medlineplus emedicine medical-subject-headings medicine genetic-disorder low-density-lipoprotein cardiovascular-disease cholesterol very-low-density-lipoprotein triglyceride electrophoresis hyperlipidemia angina-pectoris ptca coronary-bypass-surgery myocardial-infarction transient-ischemic-attack stroke peripheral-artery-occlusive-disease family-history-medicine atherosclerosis xanthoma tendon macrophage xanthelasma arcus-cornealis zygosity apolipoprotein-b gene chromosome liver high-density-lipoprotein redox foam-cells dna allele statin hmg-coa-reductase fibrate bile-acid-sequestrant niacin acipimox myopathy rhabdomyolysis acute-renal-failure ldl-apheresis kidney-dialysis goldstein-joseph-leonard michael-stuart-brown science-journal metabolic-disorder-2 pathology inborn-error-of-metabolism-2 list-of-icd-9-codes-240-279-endocrine-nutritional-and-metabolic-diseases-and-immunity-disorders amino-acid aromatic-amino-acids phenylketonuria alkaptonuria ochronosis tyrosinemia albinism histidinemia branched-chain-amino-acids maple-syrup-urine-disease propionic-acidemia methylmalonic-aciduria isovaleric-acidemia 3-methylcrotonyl-coa-carboxylase-deficiency cystinuria cystinosis hartnup-disease fanconi-s-syndrome oculocerebrorenal-syndrome homocystinuria cystathioninuria-2 urea-cycle-disorder n-acetylglutamate-synthase-deficiency carbamoyl-phosphate-synthetase-i-deficiency ornithine-transcarbamylase-deficiency citrullinemia argininosuccinic-aciduria hyperammonemia glutaric-aciduria-type sarcosinemia carbohydrate lactose-intolerance glycogen-storage-disease pompe-s-disease type-3-glycogenosis type-4-glycogenosis mcardle-disease phosphofructokinase-deficiency hereditary-fructose-intolerance fructose-bisphosphatase-deficiency
