 Hypobetalipoproteinemia, Familial, Apolipoprotein B
"Hypobetalipoproteinemia, Familial, Apolipoprotein B" 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 autosomal dominant disorder of lipid metabolism. It is caused by mutations of APOLIPOPROTEINS B, main components of CHYLOMICRONS and BETA-LIPOPROTEINS (low density lipoproteins or LDL). Features include abnormally low LDL, normal triglyceride level, and dietary fat malabsorption.
| Descriptor ID |
D052476
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| MeSH Number(s) |
C18.452.584.500.875.440.750
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| Concept/Terms |
Hypobetalipoproteinemia, Familial, Apolipoprotein B- Hypobetalipoproteinemia, Familial, Apolipoprotein B
- Hypobetalipoproteinemia, Familial, Apo B
- Apolipoprotein B Deficiency Disease
- Abetalipoproteinemia, Normotriglyceridemic, Steinbert Type
- Apolipoprotein B Deficiency
- Apolipoprotein B Deficiencies
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Below are MeSH descriptors whose meaning is more general than "Hypobetalipoproteinemia, Familial, Apolipoprotein B".
Below are MeSH descriptors whose meaning is more specific than "Hypobetalipoproteinemia, Familial, Apolipoprotein B".
This graph shows the total number of publications written about "Hypobetalipoproteinemia, Familial, Apolipoprotein B" by people in UAMS Profiles by year, and whether "Hypobetalipoproteinemia, Familial, Apolipoprotein B" was a major or minor topic of these publications.
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Below are the most recent publications written about "Hypobetalipoproteinemia, Familial, Apolipoprotein B" by people in Profiles over the past ten years.
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