Hyperlipoproteinemia Type I

"Hyperlipoproteinemia Type I" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure, which enables searching at various levels of specificity.

MeSH information

Definition | Details | More General Concepts | Related Concepts | More Specific Concepts

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.

Descriptor ID	D008072
MeSH Number(s)	C16.320.565.398.465 C18.452.584.500.500.644.237 C18.452.648.398.465
Concept/Terms	Hyperlipoproteinemia Type I Hyperlipoproteinemia Type I Hyperlipoproteinemia Type Is Familial Hyperlipoproteinemia Type 1 Hyperchylomicronemia, Familial Hyperlipemia, Idiopathic, Burger-Grutz Type Lipase D Deficiency Deficiencies, Lipase D Deficiency, Lipase D Lipase D Deficiencies Lipoprotein Lipase Deficiency Deficiencies, Lipoprotein Lipase Deficiency, Lipoprotein Lipase Lipase Deficiencies, Lipoprotein Lipoprotein Lipase Deficiencies Hyperlipemia, Essential Familial Essential Familial Hyperlipemia Essential Familial Hyperlipemias Familial Hyperlipemia, Essential Familial Hyperlipemias, Essential Hyperlipemias, Essential Familial Familial Hyperchylomicronemia Familial Hyperchylomicronemias Hyperchylomicronemias, Familial Hyperlipoproteinemia, Type I Hyperlipoproteinemias, Type I Type I Hyperlipoproteinemia Type I Hyperlipoproteinemias Apolipoprotein C-II Deficiency Apolipoprotein C-II Deficiency Apolipoprotein C II Deficiency Apolipoprotein C-II Deficiencies Deficiencies, Apolipoprotein C-II Deficiency, Apolipoprotein C-II Hyperlipoproteinemia Type Ib Hyperlipoproteinemia Type Ibs Hyperlipoproteinemia, Type Ib Hyperlipoproteinemias, Type Ib Type Ib Hyperlipoproteinemia Type Ib Hyperlipoproteinemias C-II Anapolipoproteinemia Anapolipoproteinemia, C-II Anapolipoproteinemias, C-II C-II Anapolipoproteinemias Lipoprotein Lipase Deficiency, Familial Lipoprotein Lipase Deficiency, Familial Hyperlipoproteinemia, Type Ia Hyperlipoproteinemias, Type Ia Type Ia Hyperlipoproteinemia Type Ia Hyperlipoproteinemias Hyperlipoproteinemia Type Ia Hyperlipoproteinemia Type Ias Chylomicronemia, Familial Chylomicronemias, Familial Familial Chylomicronemia Familial Chylomicronemias Familial Lipoprotein Lipase Deficiency

Below are MeSH descriptors whose meaning is more general than "Hyperlipoproteinemia Type I".

Diseases [C]
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Genetic Diseases, Inborn [C16.320]
Metabolism, Inborn Errors [C16.320.565]
Lipid Metabolism, Inborn Errors [C16.320.565.398]
Hyperlipoproteinemia Type I [C16.320.565.398.465]
Nutritional and Metabolic Diseases [C18]
Metabolic Diseases [C18.452]
Lipid Metabolism Disorders [C18.452.584]
Dyslipidemias [C18.452.584.500]
Hyperlipidemias [C18.452.584.500.500]
Hyperlipoproteinemias [C18.452.584.500.500.644]
Hyperlipoproteinemia Type I [C18.452.584.500.500.644.237]
Metabolism, Inborn Errors [C18.452.648]
Lipid Metabolism, Inborn Errors [C18.452.648.398]
Hyperlipoproteinemia Type I [C18.452.648.398.465]

Below are MeSH descriptors whose meaning is related to "Hyperlipoproteinemia Type I".

Below are MeSH descriptors whose meaning is more specific than "Hyperlipoproteinemia Type I".

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