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Hyperlipoproteinemia Type I MeSH Descriptor Data 2025


MeSH Heading
Hyperlipoproteinemia Type I
Tree Number(s)
C16.320.565.398.465
C18.452.584.500.500.644.237
C18.452.584.563.465
C18.452.648.398.465
Unique ID
D008072
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D008072
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.
Entry Term(s)
Apolipoprotein C-II Deficiency
Burger-Grutz Syndrome
C-II Anapolipoproteinemia
Chylomicronemia, Familial
Familial Fat-Induced Hypertriglyceridemia
Familial Hyperchylomicronemia
Familial Hyperlipoproteinemia Type 1
Familial LPL Deficiency
Familial Lipoprotein Lipase Deficiency
Hyperchylomicronemia, Familial
Hyperlipemia, Essential Familial
Hyperlipemia, Idiopathic, Burger-Grutz Type
Hyperlipoproteinemia Type Ia
Hyperlipoproteinemia Type Ib
Hyperlipoproteinemia, Type I
Hyperlipoproteinemia, Type Ia
Hyperlipoproteinemia, Type Ib
LIPD Deficiency
Lipase D Deficiency
Lipoprotein Lipase Deficiency
Lipoprotein Lipase Deficiency, Familial
Previous Indexing
Hyperlipidemia/familial & genetic (1966-1979)
See Also
Apolipoprotein C-II
Lipoprotein Lipase
Public MeSH Note
2007; see LIPOPROTEIN LIPASE DEFICIENCY, FAMILIAL 1991-2006, see HYPERLIPOPROTEINEMIA 1980-1990
History Note
2007 (1980)
Date Established
1991/01/01
Date of Entry
1979/04/23
Revision Date
2021/06/30
Hyperlipoproteinemia Type I Preferred
Apolipoprotein C-II Deficiency Narrower
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