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.
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
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| 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
- Chylomicronemia, Familial
- Chylomicronemias, Familial
- Familial Chylomicronemia
- Familial Chylomicronemias
- Familial Hyperchylomicronemia
- Familial Hyperchylomicronemias
- Hyperchylomicronemias, Familial
- Familial Hyperlipoproteinemia Type 1
- Familial Lipoprotein Lipase Deficiency
- Familial LPL Deficiency
- Deficiencies, Familial LPL
- Deficiency, Familial LPL
- Familial LPL Deficiencies
- LPL Deficiencies, Familial
- LPL Deficiency, Familial
- Hyperchylomicronemia, Familial
- Hyperlipemia, Essential Familial
- Essential Familial Hyperlipemia
- Essential Familial Hyperlipemias
- Familial Hyperlipemia, Essential
- Familial Hyperlipemias, Essential
- Hyperlipemias, Essential Familial
- Hyperlipemia, Idiopathic, Burger-Grutz Type
- Hyperlipoproteinemia Type Ia
- Hyperlipoproteinemia Type Ias
- Hyperlipoproteinemia, Type I
- Hyperlipoproteinemias, Type I
- Type I Hyperlipoproteinemia
- Type I Hyperlipoproteinemias
- Hyperlipoproteinemia, Type Ia
- Hyperlipoproteinemias, Type Ia
- Type Ia Hyperlipoproteinemia
- Type Ia Hyperlipoproteinemias
- Lipase D Deficiency
- Deficiencies, Lipase D
- Deficiency, Lipase D
- Lipase D Deficiencies
- LIPD Deficiency
- Deficiencies, LIPD
- Deficiency, LIPD
- LIPD Deficiencies
- Lipoprotein Lipase Deficiency
- Deficiencies, Lipoprotein Lipase
- Deficiency, Lipoprotein Lipase
- Lipase Deficiencies, Lipoprotein
- Lipoprotein Lipase Deficiencies
- Lipoprotein Lipase Deficiency, Familial
- Burger-Grutz Syndrome
- Burger Grutz Syndrome
- Burger-Grutz Syndromes
- Syndrome, Burger-Grutz
- Syndromes, Burger-Grutz
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
- Hyperlipoproteinemias, Type Ib
- Type Ib Hyperlipoproteinemia
- Type Ib Hyperlipoproteinemias
- Hyperlipoproteinemia Type Ib
- Hyperlipoproteinemia Type Ibs
- C-II Anapolipoproteinemia
- Anapolipoproteinemia, C-II
- Anapolipoproteinemias, C-II
- C-II Anapolipoproteinemias
- Familial Fat-Induced Hypertriglyceridemia
- Familial Fat Induced Hypertriglyceridemia
- Familial Fat-Induced Hypertriglyceridemias
- Fat-Induced Hypertriglyceridemia, Familial
- Fat-Induced Hypertriglyceridemias, Familial
- Hypertriglyceridemia, Familial Fat-Induced
- Hypertriglyceridemias, Familial Fat-Induced
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Below are MeSH descriptors whose meaning is more general than "Hyperlipoproteinemia Type I".
Below are MeSH descriptors whose meaning is more specific than "Hyperlipoproteinemia Type I".
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