Hypercholesterolemia

• Lipid disorders (14)

  • Blood lipids
  • Familial combined hyperlipidemia
  • Familial hyperchole- sterolemia
  • High density lipoprotein
  • Hyperlipop- roteinemia
  • Hyperlipop- roteinemia
  • Hypertrigl- yceridemia
  • LDL-C
  • Serum cholesterol
  • Cholesterol Depletion
  • Hypocholesterolemia
  • Lipoprotein lipase deficiency
  • Lipoprotein(a)
  • Mevalonate inhibition
  • Triglyceride
  • more...

• Medical conditions related to obesity

  • Hypertrigl- yceridemia
  • Familial combined hyperlipidemia

• Cardiology

  • Atherosclerosis
  • Familial hyperchole- sterolemia
  • Hypertrigl- yceridemia
  • Hyperlipop- roteinemia
  • LDL-C
  • Familial combined hyperlipidemia
  • High density lipoprotein

• Lipids

  • Lipoprotein
  • Lipid
  • Lipoproteins
  • Triglycerides
  • Lipid disorders

• Coagulation system (34)

  • Factor II deficiency
  • Factor v deficiency
  • Factor vii deficiency
  • Factor x deficiency
  • Antithrombin
  • Antithrombin
  • Bone hemostasis
  • Clot retraction
  • Coagulation
  • Cofact
  • Des-gamma carboxyprothrombin
  • Factor IX
  • Factor VIII
  • Factor XI
  • Factor XII
  • Factor XIII
  • Fibrin
  • Fibrinogenolysis
  • Hemostasis
  • High-molec- ular-weight kininogen
  • Human Activated Protein C
  • Medical Laboratory Scientist
  • Platelet
  • Platelet activation
  • Prekallikrein
  • Protein C
  • Protein S
  • Protein Z
  • Protein Z-related protease inhibitor
  • Prothrombin complex concentrate
  • Prothrombinase
  • Thrombomodulin
  • Tissue factor
  • Tissue factor pathway inhibitor
  • Von Willebrand factor
  • more...

• Genetic disorders (13)

  • Fibromuscular dysplasia
  • Familial spastic paraparesis
  • Hyperimmunoglobulin E syndrome
  • Abetalipop- roteinemia
  • Mitochondrial trifunctional protein deficiency
  • Mitochondrial trifunctional protein deficiency
  • Malonic aciduria
  • Faciocutan- eoskeletal syndrome
  • Adrenoleuk- odystrophy
  • Barraquer-Simons Syndrome
  • Friedreich ataxia
  • Tangier disease
  • Female pseudo-Turner syndrome
  • Lecithin cholesterol acyltransferase deficiency
  • more...

• Lipoproteins (11)

  • Chylomicrons
  • VLDL
  • Apolipoproteins
  • Braun's lipoprotein
  • High density lipoprotein
  • High density lipoprotein
  • Intermedia- te-density lipoprotein
  • LDL-C
  • Lipid anchored protein
  • Lipoprotein
  • Lipoprotein(a)
  • Lipoprotein-X
  • more...

• Skin conditions resulting from errors in metabolism (86)

  • Apolipoprotein B deficiency
  • Familial dysbetalip- oproteinemia
  • Familial hypertrigl- yceridemia
  • Sitosterolemia
  • Xanthelasma palpabrum
  • Xanthelasma palpabrum
  • Xanthoma
  • Xanthoma tuberosum
  • Xanthomatosis
  • Acute intermittent porphyria
  • Adrenoleuk- odystrophy
  • Alkaptonuria
  • Amyloid purpura
  • Amyloidosis
  • B-mannosidase deficiency
  • CADASIL syndrome
  • Calcinosis cutis
  • Carotenosis
  • Cerebrotendineous xanthomatosis
  • Citrullinemia
  • Diabetic bulla
  • Diabetic cheiroarthropathy
  • Diabetic dermopathy
  • Dystrophic calcinosis cutis
  • Eruptive xanthoma
  • Erythropoietic porphyria
  • Erythropoietic protoporphyria
  • Fabry disease
  • Familial apoprotein CII deficiency
  • Familial combined hyperlipidemia
  • Farber disease
  • Fucosidosis
  • Gaucher's disease
  • Gout
  • Gunther disease
  • Hartnup disease
  • Hepatoeryt- hropoietic porphyria
  • Hereditary coproporphyria
  • Heredofamilial amyloidosis
  • Hunter syndrome
  • Hurler syndrome
  • Hyaluronidase deficiency
  • Iatrogenic calcinosis cutis
  • Idiopathic scrotal calcinosis
  • Lafora disease
  • Lesch–Nyhan syndrome
  • Lichen amyloidosis
  • Limited joint mobility
  • Lipoprotein lipase deficiency
  • Macular amyloidosis
  • Medication-induced hyperlipop- roteinemia
  • Metastatic calcinosis cutis
  • Morquio syndrome
  • Myxedema
  • Necrobiosis lipoidica
  • Niemann–Pick disease
  • Nodular amyloidosis
  • Nodular xanthoma
  • Normolipop- roteinemic xanthomatosis
  • Ochronosis
  • Osteoma cutis
  • Palmar xanthoma
  • Phenylketonuria
  • Porphyria
  • Porphyria cutanea tarda
  • Primary cutaneous amyloidosis
  • Primary systemic amyloidosis
  • Prolidase deficiency
  • Pseudoporphyria
  • Secondary cutaneous amyloidosis
  • Secondary systemic amyloidosis
  • Sialidosis
  • Subepidermal calcified nodule
  • Tangier disease
  • Transient erythroporphyria of infancy
  • Traumatic calcinosis cutis
  • Tuberoeruptive xanthoma
  • Tumoral calcinosis
  • Urbach–Wiethe disease
  • Variegate porphyria
  • Verruciform xanthoma
  • Waxy skin
  • Xanthoma diabeticorum
  • Xanthoma planum
  • Xanthoma striatum palmare
  • Xanthoma tendinosum
  • Xanthomatous biliary cirrhosis
  • more...

• Medical sign (9)

  • Hutchinson incisors
  • Angina pectoris
  • Arcus senilis
  • Coronary artery disease
  • Myocardial infarction
  • Myocardial infarction
  • Transient ischemic attack
  • Xanthoma
  • Cholesterol
  • Xanthelasma palpabrum
  • more...

• Hepatology

  • Colesevelam
  • Bile acid sequestrant
  • Cholestyramine
  • Xanthoma
  • Xanthelasma palpabrum

• Hypolipidemic agents (20)

  • Ezetimibe
  • Fibrates
  • Hypolipidemic
  • Statins
  • AEGR-733
  • AEGR-733
  • Acipimox
  • Anti-cholesterol
  • ApoA-1 Milano
  • Benfluorex
  • Bile acid sequestrant
  • Cholesterol absorption inhibitor
  • Cholestyramine
  • Colesevelam
  • Lapaquistat
  • Magnesium pyridoxal 5-phosphate glutamate
  • Meglutol
  • Mipomersen
  • Niacin
  • Phytosterol
  • Torcetrapib
  • more...

• Statins (16)

  • Atorvastatin
  • Cerivastatin
  • Fluvastatin
  • HMG-CoA reductase inhibitors
  • Lovastatin
  • Lovastatin
  • Pravastatin
  • Rosuvastatin
  • Caduet
  • Cholesterol Depletion
  • Ezetimibe/- simvastatin
  • Mevalonate inhibition
  • Mevastatin
  • Pitavastatin
  • Scandinavian Simvastatin Survival Study
  • Simvastatin
  • Statin development
  • more...

• Symptoms

  • Hypertrophic scar
  • Fast breathing
  • Spastic paralysis
  • Xanthoma

• Enzymes

  • Acyl CoA dehydrogenase
  • Subtilisin
  • Proprotein convertase
  • Lipoprotei- n-associated phospholipase A2
  • Kexin

• Medical condition (35)

  • Hyperchole- sterolemia autosomal dominant
  • Fish tapeworm
  • Fibrosing alveolitis
  • Hypercalciuria
  • Hypochondriacal neurosis
  • Hypochondriacal neurosis
  • Fasciitis, necrotizing
  • Hypolipoproteinemia
  • Floppy mitral valve
  • Horizontal nystagmus
  • Fibromyoma
  • Fumarylacetoacetase deficiency disease
  • Defective apolipoprotein b-100
  • Funnel chest
  • Rhabdomyolysis
  • Factor v deficiency
  • Factor vii deficiency
  • Fibromuscular dysplasia
  • Fast breathing
  • Hyperlipop- roteinemia
  • Hutchinson incisors
  • Familial spastic paraparesis
  • Hyperimmunoglobulin E syndrome
  • Xanthoma
  • Fibrodysplasia ossificans progressiva
  • Familial dysbetalip- oproteinemia
  • Horners syndrome
  • Factor x deficiency
  • Abetalipop- roteinemia
  • Mitochondrial trifunctional protein deficiency
  • Malonic aciduria
  • Faciocutan- eoskeletal syndrome
  • Friedreich ataxia
  • Tangier disease
  • Female pseudo-Turner syndrome
  • Sitosterolemia
  • more...

• See also (20)

  • Fenestrations
  • Hyperviscosity.
  • LDLR
  • PCSK9
  • Human artificial chromosome
  • Human artificial chromosome
  • Hyperparat- hyroidism, secondary
  • Fibrodysplasia ossificans progressiva
  • Horners syndrome
  • Heterozygous
  • Dyslipidemia
  • Simvastatin
  • HMG CoA reductase
  • Ezetimibe/- simvastatin
  • Apolipoprotein B
  • National Cholesterol Education Program
  • LDL apheresis
  • Homozygous
  • Familial
  • Bile Acid Sequestrants
  • Cholesterol synthesis
  • more...

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