ONKI3 | Medical Subject Headings

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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 ∟ Lipidoses 13 coordinate concepts 4 subordinate concepts ∟ Cholesterol Ester Storage Disease \| ∟ Neuronal Ceroid-Lipofuscinoses \| ∟ Sjogren-Larsson Syndrome \| ∟ Sphingolipidoses ∟ Hyperlipidemia, Familial Combined \| ∟ Hyperlipoproteinemia Type I \| ∟ Hyperlipoproteinemia Type II \| ∟ Hyperlipoproteinemia Type III \| ∟ Hyperlipoproteinemia Type IV \| ∟ Hyperlipoproteinemia Type V \| ∟ Hypolipoproteinemias \| ∟ Smith-Lemli-Opitz Syndrome \| ∟ Xanthomatosis, Cerebrotendinous \| ∟ Dyslipidemias \| ∟ Lipodystrophy \| ∟ Lipomatosis \| ∟ Xanthomatosis Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Lipid Metabolism Disorders ∟ Lipidoses 13 coordinate concepts 4 subordinate concepts ∟ Cholesterol Ester Storage Disease \| ∟ Neuronal Ceroid-Lipofuscinoses \| ∟ Sjogren-Larsson Syndrome \| ∟ Sphingolipidoses ∟ Hyperlipidemia, Familial Combined \| ∟ Hyperlipoproteinemia Type I \| ∟ Hyperlipoproteinemia Type II \| ∟ Hyperlipoproteinemia Type III \| ∟ Hyperlipoproteinemia Type IV \| ∟ Hyperlipoproteinemia Type V \| ∟ Hypolipoproteinemias \| ∟ Smith-Lemli-Opitz Syndrome \| ∟ Xanthomatosis, Cerebrotendinous \| ∟ Dyslipidemias \| ∟ Lipodystrophy \| ∟ Lipomatosis \| ∟ Xanthomatosis Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Metabolism, Inborn Errors ∟ Lipid Metabolism, Inborn Errors ∟ Lipidoses 13 coordinate concepts 4 subordinate concepts ∟ Cholesterol Ester Storage Disease \| ∟ Neuronal Ceroid-Lipofuscinoses \| ∟ Sjogren-Larsson Syndrome \| ∟ Sphingolipidoses ∟ Hyperlipidemia, Familial Combined \| ∟ Hyperlipoproteinemia Type I \| ∟ Hyperlipoproteinemia Type II \| ∟ Hyperlipoproteinemia Type III \| ∟ Hyperlipoproteinemia Type IV \| ∟ Hyperlipoproteinemia Type V \| ∟ Hypolipoproteinemias \| ∟ Smith-Lemli-Opitz Syndrome \| ∟ Xanthomatosis, Cerebrotendinous \| ∟ Dyslipidemias \| ∟ Lipodystrophy \| ∟ Lipomatosis \| ∟ Xanthomatosis X
Broader terms:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Metabolism, Inborn Errors ∟ Lipid Metabolism, Inborn Errors ∟ Lipidoses Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Lipid Metabolism Disorders ∟ Lipidoses Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Metabolism, Inborn Errors ∟ Lipid Metabolism, Inborn Errors ∟ Lipidoses Lipid Metabolism, Inborn Errors > Metabolism, Inborn Errors > Genetic Diseases, Inborn > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) 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
Narrower terms:	Cholesterol Ester Storage Disease \| Neuronal Ceroid-Lipofuscinoses \| Sjogren-Larsson Syndrome \| Sphingolipidoses X
Annotation:	general or unspecified; prefer specifics X
historyNote*:	2007 (1966) X
publicMeSHNote*:	2007; see LIPOIDOSIS 1966-2006 X
Scope note:	Conditions characterized by abnormal lipid deposition due to disturbance in lipid metabolism, such as hereditary diseases involving lysosomal enzymes required for lipid breakdown. They are classified either by the enzyme defect or by the type of lipid involved. X
activeMeSHYear*:	2007X
dateCreated*:	1999-01-01X
dateRevised*:	2006-07-05X
recordAuthorizer*:	sjnX
recordMaintainer*:	lktX
recordOriginator*:	NLMX
Type:	Concept X
Coordinate terms:	Hyperlipidemia, Familial Combined \| Hyperlipoproteinemia Type I \| Hyperlipoproteinemia Type II \| Hyperlipoproteinemia Type III \| Hyperlipoproteinemia Type IV \| Hyperlipoproteinemia Type V \| Hypolipoproteinemias \| Smith-Lemli-Opitz Syndrome \| Xanthomatosis, Cerebrotendinous \| Dyslipidemias \| Lipodystrophy \| Lipomatosis \| Xanthomatosis X
URI:	X
Labels and equivalent concepts:	Lipidoosit (fi) Rasva-aineenvaihduntahäiriö (fi, replaced) Lipoidoosi (fi, replaced) Lipidoosi (fi, replaced) Lipoidosis (en, replaced) Lipidosis (en, replaced) Lipidosis (la-FI, replaced) Lipoidosis (la-FI, replaced) X
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