ONKI3 | Medical Subject Headings

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Hypoalphalipoproteinemias

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Hierarchy:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Metabolism, Inborn Errors ∟ Lipid Metabolism, Inborn Errors ∟ Hypolipoproteinemias ∟ Hypoalphalipoproteinemias 1 coordinate concept 2 subordinate concepts ∟ Lecithin Acyltransferase Deficiency \| ∟ Tangier Disease ∟ Hypobetalipoproteinemias Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Lipid Metabolism Disorders ∟ Dyslipidemias ∟ Hypolipoproteinemias ∟ Hypoalphalipoproteinemias 1 coordinate concept 2 subordinate concepts ∟ Lecithin Acyltransferase Deficiency \| ∟ Tangier Disease ∟ Hypobetalipoproteinemias Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Metabolism, Inborn Errors ∟ Lipid Metabolism, Inborn Errors ∟ Hypolipoproteinemias ∟ Hypoalphalipoproteinemias 1 coordinate concept 2 subordinate concepts ∟ Lecithin Acyltransferase Deficiency \| ∟ Tangier Disease ∟ Hypobetalipoproteinemias X
Broader terms:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Metabolism, Inborn Errors ∟ Lipid Metabolism, Inborn Errors ∟ Hypolipoproteinemias ∟ Hypoalphalipoproteinemias Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Lipid Metabolism Disorders ∟ Dyslipidemias ∟ Hypolipoproteinemias ∟ Hypoalphalipoproteinemias Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Metabolism, Inborn Errors ∟ Lipid Metabolism, Inborn Errors ∟ Hypolipoproteinemias ∟ Hypoalphalipoproteinemias Hypolipoproteinemias > Lipid Metabolism, Inborn Errors > Metabolism, Inborn Errors > Genetic Diseases, Inborn > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Hypolipoproteinemias > Dyslipidemias > Lipid Metabolism Disorders > Metabolic Diseases > Nutritional and Metabolic Diseases > Medical Subject Headings (MeSH) Hypolipoproteinemias > Lipid Metabolism, Inborn Errors > Metabolism, Inborn Errors > Metabolic Diseases > Nutritional and Metabolic Diseases > Medical Subject Headings (MeSH) X
Narrower terms:	Lecithin Acyltransferase Deficiency \| Tangier Disease X
History note:	Lipoproteins, HDL (1981-2006)X
historyNote*:	2007; for HYPOALPHALIPOPROTEINEMIA, FAMILIAL & LIPOPROTEIN DEFICIENCY DISEASE, HDL, FAMILIAL use TANGIER DISEASE 1995-2006 X
publicMeSHNote*:	2007; for HYPOALPHALIPOPROTEINEMIA, FAMILIAL & LIPOPROTEIN DEFICIENCY DISEASE, HDL, FAMILIAL see TANGIER DISEASE 1995-2006 X
Scope note:	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. X
activeMeSHYear*:	2007X
dateCreated*:	2006-07-05X
dateEstablished*:	2007-01-01X
recordAuthorizer*:	sjnX
recordMaintainer*:	lktX
recordOriginator*:	lktX
Type:	Concept X
Coordinate terms:	Hypobetalipoproteinemias X
URI:	X
Labels and equivalent concepts:	Hypoalfalipoproteinemiat (fi) Hypo alpha Lipoproteinemia (en, replaced) Hypoalphalipoproteinemia (en, replaced) Lipoprotein Deficiency Disease, HDL, Familial (en, replaced) High-Density Lipoprotein Deficiency Disease, Familial (en, replaced) HDL Lipoprotein Deficiency Disease (en, replaced) Familial alpha-Lipoprotein Deficiency Disease (en, replaced) Familial High-Density Lipoprotein Deficiency Disease (en, replaced) alpha-Lipoprotein Deficiency Disease, Familial (en, replaced) X
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