ONKI3 | Medical Subject Headings

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Hyperlipoproteinemia Type II

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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 ∟ Hyperlipoproteinemia Type II 9 coordinate concepts ∟ Hyperlipoproteinemia Type I \| ∟ Hyperlipoproteinemia Type III \| ∟ Hyperlipoproteinemia Type IV \| ∟ Hyperlipoproteinemia Type V \| ∟ Hyperlipidemia, Familial Combined \| ∟ Hypolipoproteinemias \| ∟ Lipidoses \| ∟ Smith-Lemli-Opitz Syndrome \| ∟ Xanthomatosis, Cerebrotendinous Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Lipid Metabolism Disorders ∟ Dyslipidemias ∟ Hyperlipidemias ∟ Hyperlipoproteinemias ∟ Hyperlipoproteinemia Type II 9 coordinate concepts ∟ Hyperlipoproteinemia Type I \| ∟ Hyperlipoproteinemia Type III \| ∟ Hyperlipoproteinemia Type IV \| ∟ Hyperlipoproteinemia Type V \| ∟ Hyperlipidemia, Familial Combined \| ∟ Hypolipoproteinemias \| ∟ Lipidoses \| ∟ Smith-Lemli-Opitz Syndrome \| ∟ Xanthomatosis, Cerebrotendinous Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Metabolism, Inborn Errors ∟ Lipid Metabolism, Inborn Errors ∟ Hyperlipoproteinemia Type II 9 coordinate concepts ∟ Hyperlipoproteinemia Type I \| ∟ Hyperlipoproteinemia Type III \| ∟ Hyperlipoproteinemia Type IV \| ∟ Hyperlipoproteinemia Type V \| ∟ Hyperlipidemia, Familial Combined \| ∟ Hypolipoproteinemias \| ∟ Lipidoses \| ∟ Smith-Lemli-Opitz Syndrome \| ∟ Xanthomatosis, Cerebrotendinous X
Broader terms:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Metabolism, Inborn Errors ∟ Lipid Metabolism, Inborn Errors ∟ Hyperlipoproteinemia Type II Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Lipid Metabolism Disorders ∟ Dyslipidemias ∟ Hyperlipidemias ∟ Hyperlipoproteinemias ∟ Hyperlipoproteinemia Type II Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Metabolism, Inborn Errors ∟ Lipid Metabolism, Inborn Errors ∟ Hyperlipoproteinemia Type II Lipid Metabolism, Inborn Errors > Metabolism, Inborn Errors > Genetic Diseases, Inborn > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Hyperlipoproteinemias > Hyperlipidemias > Dyslipidemias > Lipid Metabolism Disorders > Metabolic Diseases > Nutritional and Metabolic Diseases > Medical Subject Headings (MeSH) Lipid Metabolism, Inborn Errors > Metabolism, Inborn Errors > Metabolic Diseases > Nutritional and Metabolic Diseases > Medical Subject Headings (MeSH) X
History note:	Hypercholesterolemia (1966-1979) \| Hyperlipidemia/familial & genetic (1966-1979)X
historyNote*:	2007 (1980) X
publicMeSHNote*:	2007; see HYPERCHOLESTEROLEMIA, FAMILIAL 1980-2007 X
Scope note:	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). X
activeMeSHYear*:	2007X
dateCreated*:	1979-04-23X
dateEstablished*:	1980-01-01X
dateRevised*:	2006-07-05X
recordAuthorizer*:	sjnX
recordMaintainer*:	lktX
recordOriginator*:	VDKX
Type:	Concept X
Coordinate terms:	Hyperlipoproteinemia Type I \| Hyperlipoproteinemia Type III \| Hyperlipoproteinemia Type IV \| Hyperlipoproteinemia Type V \| Hyperlipidemia, Familial Combined \| Hypolipoproteinemias \| Lipidoses \| Smith-Lemli-Opitz Syndrome \| Xanthomatosis, Cerebrotendinous X
URI:	X
Labels and equivalent concepts:	Tyypin II hyperlipoproteinemia (fi) FH-tauti (fi, replaced) FH (fi, replaced) Hyperkolesterolemia, familiaalinen (fi, replaced) Hyperlipoproteinemia, tyypin II (fi, replaced) Suvuittainen hyperkolesterolemia (fi, replaced) Familiaalinen hyperkolesterolemia (fi, replaced) LDL Receptor Disorder (en, replaced) Hyper-Low Density Lipoproteinemia (en, replaced) Familial Combined Hyperlipoproteinemia (en, replaced) Hyperbetalipoproteinemia (en, replaced) Hypercholesterolemia, Autosomal Dominant (en, replaced) Hypercholesterolemia, Familial (en, replaced) Hypercholesterolemia, Essential (en, replaced) Apolipoprotein B-100, Familial Ligand-Defective (en, replaced) Hypercholesterolaemia familialis (la-FI, replaced) X
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