Related MeSH Hierarchy (4)
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Genetic Diseases, Inborn » Metabolism, Inborn Errors » Lipid Metabolism, Inborn Errors » Hyperlipoproteinemia Type II » Homozygous Familial Hypercholesterolemia
Diseases [C] » Nutritional and Metabolic Diseases [C18] » Metabolic Diseases » Lipid Metabolism Disorders » Dyslipidemias » Hyperlipidemias » Hyperlipoproteinemias » Hyperlipoproteinemia Type II » Homozygous Familial Hypercholesterolemia
Diseases [C] » Nutritional and Metabolic Diseases [C18] » Metabolic Diseases » Lipid Metabolism Disorders » Lipid Metabolism, Inborn Errors » Hyperlipoproteinemia Type II » Homozygous Familial Hypercholesterolemia
Diseases [C] » Nutritional and Metabolic Diseases [C18] » Metabolic Diseases » Metabolism, Inborn Errors » Lipid Metabolism, Inborn Errors » Hyperlipoproteinemia Type II » Homozygous Familial Hypercholesterolemia
Description
A rare inherited genetic disorder, one form of HYPERLIPOPROTEINEMIA TYPE II, characterized by high level of LOW-DENSITY LIPOPROTEIN (LDL) which if not treated could elevate the chance of heart attack at an early age. MeSH
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Approved Indicated Drugs (1)
Phase 4 Indicated Drugs (2)
Phase 2 Indicated Drugs (7)
Phase 1 Indicated Drugs (3)
Other Experimental Indicated Drugs (1)
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