Related MeSH Hierarchy (4)
Diseases [C] » Nutritional and Metabolic Diseases [C18] » Metabolic Diseases » Lipid Metabolism Disorders » Lipid Metabolism, Inborn Errors » Hyperlipoproteinemia Type II
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Genetic Diseases, Inborn » Metabolism, Inborn Errors » Lipid Metabolism, Inborn Errors » Hyperlipoproteinemia Type II
Diseases [C] » Nutritional and Metabolic Diseases [C18] » Metabolic Diseases » Lipid Metabolism Disorders » Dyslipidemias » Hyperlipidemias » Hyperlipoproteinemias » Hyperlipoproteinemia Type II
Diseases [C] » Nutritional and Metabolic Diseases [C18] » Metabolic Diseases » Metabolism, Inborn Errors » Lipid Metabolism, Inborn Errors » Hyperlipoproteinemia Type II
Description
A group of familial disorders characterized by elevated circulating cholesterol contained in either LOW-DENSITY LIPOPROTEINS alone or also in VERY-LOW-DENSITY LIPOPROTEINS (pre-beta lipoproteins). MeSH
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Subtype Terms (1)
Homozygous Familial Hypercholesterolemia
31 drugs (12 approved, 19 experimental)
Approved Indicated Drugs (16)
Phase 3 Indicated Drugs (9)
Phase 2 Indicated Drugs (4)
Phase 1 Indicated Drugs (3)
Other Experimental Indicated Drugs (5)
Organization Involved with Phase 4 Indications (3)
Organization Involved with Phase 3 Indications (20)
Organization Involved with Phase 2 Indications (19)
Organization Involved with Phase 1 Indications (1)
Organization Involved with Other Experimental Indications (8)
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