Related MeSH Hierarchy (4)
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Genetic Diseases, Inborn » Metabolism, Inborn Errors » Lipid Metabolism, Inborn Errors » Hypolipoproteinemias » Hypoalphalipoproteinemias
Diseases [C] » Nutritional and Metabolic Diseases [C18] » Metabolic Diseases » Lipid Metabolism Disorders » Lipid Metabolism, Inborn Errors » Hypolipoproteinemias » Hypoalphalipoproteinemias
Diseases [C] » Nutritional and Metabolic Diseases [C18] » Metabolic Diseases » Lipid Metabolism Disorders » Dyslipidemias » Hypolipoproteinemias » Hypoalphalipoproteinemias
Diseases [C] » Nutritional and Metabolic Diseases [C18] » Metabolic Diseases » Metabolism, Inborn Errors » Lipid Metabolism, Inborn Errors » Hypolipoproteinemias » Hypoalphalipoproteinemias
Description
Conditions with abnormally low levels of ALPHA-LIPOPROTEINS (high-density lipoproteins) in the blood. Hypoalphalipoproteinemia can be associated with mutations in genes encoding APOLIPOPROTEIN A-I; LECITHIN CHOLESTEROL ACYLTRANSFERASE; and ATP-BINDING CASSETTE TRANSPORTERS. MeSH
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Subtype Terms (2)
Lecithin Cholesterol Acyltransferase Deficiency
1 experimental drug
Tangier Disease
1 experimental drug
Phase 4 Indicated Drugs (1)
Phase 3 Indicated Drugs (1)
Other Experimental Indicated Drugs (5)
Organization Involved with Phase 4 Indications (1)
Organization Involved with Phase 3 Indications (2)
Organization Involved with Other Experimental Indications (4)
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UMLS Data
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