ONKI3 | Medical Subject Headings

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Hyperlipoproteinemia Type I

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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 I 9 coordinate concepts ∟ Hyperlipoproteinemia Type II \| ∟ 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 I 9 coordinate concepts ∟ Hyperlipoproteinemia Type II \| ∟ 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 I 9 coordinate concepts ∟ Hyperlipoproteinemia Type II \| ∟ 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 I Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Lipid Metabolism Disorders ∟ Dyslipidemias ∟ Hyperlipidemias ∟ Hyperlipoproteinemias ∟ Hyperlipoproteinemia Type I Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Metabolism, Inborn Errors ∟ Lipid Metabolism, Inborn Errors ∟ Hyperlipoproteinemia Type I 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*:	2007 (1980) X
publicMeSHNote*:	2007; see LIPOPROTEIN LIPASE DEFICIENCY, FAMILIAL 1991-2006, see HYPERLIPOPROTEINEMIA 1980-1990 X
Scope note:	An inherited condition due to a deficiency of either LIPOPROTEIN LIPASE or APOLIPOPROTEIN C-II (a lipase-activating protein). The lack of lipase activities results in inability to remove CHYLOMICRONS and TRIGLYCERIDES from the blood which has a creamy top layer after standing. X
activeMeSHYear*:	2007X
dateCreated*:	1979-04-23X
dateEstablished*:	1991-01-01X
dateRevised*:	2006-07-05X
recordAuthorizer*:	sjnX
recordMaintainer*:	lktX
recordOriginator*:	VDKX
Type:	Concept X
Coordinate terms:	Hyperlipoproteinemia Type II \| 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 I hyperlipoproteinemia (fi) Hyperlipoproteinemia, tyypin I (fi, replaced) Suvuittainen lipoproteiinilipaasin puute (fi, replaced) Suvuittainen lipoproteiinilipaasipuute (fi, replaced) Familiaalinen lipoproteiinilipaasin puutos (fi, replaced) Hyperlipoproteinemia Type Ib (en, replaced) Familial Lipoprotein Lipase Deficiency (en, replaced) Hyperchylomicronemia, Familial (en, replaced) Hyperlipoproteinemia Type Ia (en, replaced) Familial Hyperchylomicronemia (en, replaced) X
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