ONKI3 | Medical Subject Headings

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Hyperlipoproteinemia Type IV

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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 IV 9 coordinate concepts ∟ Hyperlipoproteinemia Type I \| ∟ Hyperlipoproteinemia Type II \| ∟ Hyperlipoproteinemia Type III \| ∟ 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 IV 9 coordinate concepts ∟ Hyperlipoproteinemia Type I \| ∟ Hyperlipoproteinemia Type II \| ∟ Hyperlipoproteinemia Type III \| ∟ 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 ∟ Hypertriglyceridemia ∟ Hyperlipoproteinemia Type IV 9 coordinate concepts ∟ Hyperlipoproteinemia Type I \| ∟ Hyperlipoproteinemia Type II \| ∟ Hyperlipoproteinemia Type III \| ∟ 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 IV 9 coordinate concepts ∟ Hyperlipoproteinemia Type I \| ∟ Hyperlipoproteinemia Type II \| ∟ Hyperlipoproteinemia Type III \| ∟ 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 IV Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Lipid Metabolism Disorders ∟ Dyslipidemias ∟ Hyperlipidemias ∟ Hyperlipoproteinemias ∟ Hyperlipoproteinemia Type IV Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Lipid Metabolism Disorders ∟ Dyslipidemias ∟ Hyperlipidemias ∟ Hypertriglyceridemia ∟ Hyperlipoproteinemia Type IV Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Metabolism, Inborn Errors ∟ Lipid Metabolism, Inborn Errors ∟ Hyperlipoproteinemia Type IV 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) Hypertriglyceridemia > 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 (1966-1979)X
historyNote*:	80 X
publicMeSHNote*:	80 X
Scope note:	A hypertriglyceridemia disorder, often with autosomal dominant inheritance. It is characterized by the persistent elevations of plasma TRIGLYCERIDES, endogenously synthesized and contained predominantly in VERY-LOW-DENSITY LIPOPROTEINS (pre-beta lipoproteins). In contrast, the plasma CHOLESTEROL and PHOSPHOLIPIDS usually remain within normal limits. 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 III \| Hyperlipoproteinemia Type V \| Hyperlipidemia, Familial Combined \| Hypolipoproteinemias \| Lipidoses \| Smith-Lemli-Opitz Syndrome \| Xanthomatosis, Cerebrotendinous X
URI:	X
Labels and equivalent concepts:	Tyypin IV hyperlipoproteinemia (fi) Hypertriglyseridemia (fi, replaced) VLDL-hyperlipoproteinemia (fi, replaced) Hyperprebeetalipoproteinemia (fi, replaced) Hyperpraebetalipoproteinaemia (fi, replaced) Hyperlipoproteinemia, tyypin IV (fi, replaced) Hyperlipoproteinemi typ IV (sv) Hyperprebetalipoproteinemia (en, replaced) Hypertriglyceridemia, Familial (en, replaced) Hyper prebeta lipoproteinemia (en, replaced) Hypertriglyceridaemia (la-FI, replaced) Hypertriglyceridaemia pura (la-FI, replaced) X
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