ONKI3 | MedIEQ: Medical Subject Headings

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Hyperlipoproteinemia Type III

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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 III 9 coordinate concepts ∟ Hyperlipoproteinemia Type I \| ∟ Hyperlipoproteinemia Type II \| ∟ 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 III 9 coordinate concepts ∟ Hyperlipoproteinemia Type I \| ∟ Hyperlipoproteinemia Type II \| ∟ 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 III 9 coordinate concepts ∟ Hyperlipoproteinemia Type I \| ∟ Hyperlipoproteinemia Type II \| ∟ 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 III Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Lipid Metabolism Disorders ∟ Dyslipidemias ∟ Hyperlipidemias ∟ Hyperlipoproteinemias ∟ Hyperlipoproteinemia Type III Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Metabolism, Inborn Errors ∟ Lipid Metabolism, Inborn Errors ∟ Hyperlipoproteinemia Type III 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:	Hyperlipidemia/familial & genetic (1966-1979)X
historyNote*:	80 X
publicMeSHNote*:	80 X
Scope note:	An autosomal recessively inherited disorder characterized by the accumulation of intermediate-density lipoprotein (IDL or broad-beta-lipoprotein). IDL has a CHOLESTEROL to TRIGLYCERIDES ratio greater than that of VERY-LOW-DENSITY LIPOPROTEINS. This disorder is due to mutation of APOLIPOPROTEIN E, a receptor-binding component of VLDL and CHYLOMICRONS, resulting in their reduced clearance and high plasma levels of both cholesterol and triglycerides. 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 II \| 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 III hyperlipoproteinemia (fi) Hyperlipoproteinemia, Broad-beta (en, replaced) Familial Hypercholesterolemia with Hyperlipemia (en, replaced) Familial Dysbetalipoproteinemia (en, replaced) Broad Beta Disease (en, replaced) Dysbetalipoproteinemia (en, replaced) Dysbetalipoproteinemia, Familial (en, replaced) Hiperlipoproteinemia Tipo III (es) υπερλιποπρωτεϊναιμία τύπου III (el) Hyperlipoproteinämie Typ III (de) hyperlipoproteinémie typ III (cs) Disbetalipoproteinemia (es, replaced) Disbetalipoproteinemia Familiar (es, replaced) Enfermedad beta-Ancha (es, replaced) Dysbetalipoproteinämie (de, replaced) Broad-Beta-Krankheit (de, replaced) X
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