Structured Summary
Abstract
Conditions with abnormally low levels of BETA-LIPOPROTEINS (low density lipoproteins or LDL) in the blood. It is defined as LDL values equal to or less than the 5th percentile for the population. They include the autosomal dominant form involving mutation of the APOLIPOPROTEINS B gene, and the autosomal recessive form involving mutation of the microsomal triglyceride transfer protein. All are characterized by low LDL and dietary fat malabsorption.
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Synonyms
4 entry terms
- Familial Hypobetalipoproteinemia
- Hypo beta Lipoproteinemia
- Hypobetalipoproteinemia
- Hypo beta Lipoproteinemias
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Aspects Covered
34 allowable subheadings
Indexed with the subheadings blood, cerebrospinal fluid, chemically induced, classification, complications, diagnosis, diagnostic imaging, diet therapy, drug therapy, economics, embryology, enzymology, epidemiology, ethnology, etiology, genetics, history, immunology, metabolism, microbiology, mortality, nursing, parasitology, pathology, physiopathology, prevention & control, psychology, radiotherapy, rehabilitation, surgery, therapy, urine, veterinary, virology.
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History Note
2007 (1978)
MeSH Record
Previous Indexing
- Blood Protein Disorders (1966-1977)
- Lipid Metabolism, Inborn Errors (1966-1977)
- Lipoproteins (1966-1977)
- Lipoproteins, LDL (1972-1977)
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AMA Style
References
- National Library of Medicine. Hypobetalipoproteinemias. Medical Subject Headings (MeSH). 2026. Unique ID D006995. http://id.nlm.nih.gov/mesh/2026/D006995
- Hypobetalipoproteinemias. In: Wikipedia. https://en.wikipedia.org/wiki/Hypobetalipoproteinemia
- Hypobetalipoproteinemias. In: Wikidata. https://www.wikidata.org/wiki/Q3444851