 Hyperlipidemia, Familial Combined
"Hyperlipidemia, Familial Combined" 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.
A type of familial lipid metabolism disorder characterized by a variable pattern of elevated plasma CHOLESTEROL and/or TRIGLYCERIDES. Multiple genes on different chromosomes may be involved, such as the major late transcription factor (UPSTREAM STIMULATORY FACTORS) on CHROMOSOME 1.
| Descriptor ID |
D006950
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| MeSH Number(s) |
C16.320.565.398.450 C18.452.584.500.500.438 C18.452.648.398.450
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| Concept/Terms |
Hyperlipidemia, Familial Combined- Hyperlipidemia, Familial Combined
- Combined Hyperlipidemia, Familial
- Combined Hyperlipidemias, Familial
- Familial Combined Hyperlipidemias
- Hyperlipidemias, Familial Combined
- Familial Combined Hyperlipidemia
- Hyperlipidemia, Multiple Lipoprotein-Type
- Hyperlipidemia, Multiple Lipoprotein Type
- Hyperlipidemias, Multiple Lipoprotein-Type
- Lipoprotein-Type Hyperlipidemia, Multiple
- Lipoprotein-Type Hyperlipidemias, Multiple
- Multiple Lipoprotein-Type Hyperlipidemia
- Multiple Lipoprotein-Type Hyperlipidemias
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Below are MeSH descriptors whose meaning is more general than "Hyperlipidemia, Familial Combined".
- 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]
- Hyperlipidemia, Familial Combined [C16.320.565.398.450]
- 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]
- Hyperlipidemia, Familial Combined [C18.452.584.500.500.438]
- Metabolism, Inborn Errors [C18.452.648]
- Lipid Metabolism, Inborn Errors [C18.452.648.398]
- Hyperlipidemia, Familial Combined [C18.452.648.398.450]
Below are MeSH descriptors whose meaning is more specific than "Hyperlipidemia, Familial Combined".
This graph shows the total number of publications written about "Hyperlipidemia, Familial Combined" by people in this website by year, and whether "Hyperlipidemia, Familial Combined" was a major or minor topic of these publications.
To see the data from this visualization as text, click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2008 | 1 | 0 | 1 |
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Below are the most recent publications written about "Hyperlipidemia, Familial Combined" by people in Profiles.
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Mar-Heyming R, Miyazaki M, Weissglas-Volkov D, Kolaitis NA, Sadaat N, Plaisier C, Pajukanta P, Cantor RM, de Bruin TW, Ntambi JM, Lusis AJ. Association of stearoyl-CoA desaturase 1 activity with familial combined hyperlipidemia. Arterioscler Thromb Vasc Biol. 2008 Jun; 28(6):1193-9.
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Bodnar JS, Chatterjee A, Castellani LW, Ross DA, Ohmen J, Cavalcoli J, Wu C, Dains KM, Catanese J, Chu M, Sheth SS, Charugundla K, Demant P, West DB, de Jong P, Lusis AJ. Positional cloning of the combined hyperlipidemia gene Hyplip1. Nat Genet. 2002 Jan; 30(1):110-6.
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Eckel RH. Familial combined hyperlipidemia and insulin resistance : distant relatives linked by intra-abdominal fat? Arterioscler Thromb Vasc Biol. 2001 Apr; 21(4):469-70.
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Hokanson JE, Krauss RM, Albers JJ, Austin MA, Brunzell JD. LDL physical and chemical properties in familial combined hyperlipidemia. Arterioscler Thromb Vasc Biol. 1995 Apr; 15(4):452-9.
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Skovby F, Dyerberg J, Faergeman O, Haghfelt T, Jensen TJ, Leth A, Sigurd B, Stender S, Vittrup MA. [Hyperlipidemia in children]. Ugeskr Laeger. 1993 Mar 15; 155(11):810-4.
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Hokanson JE, Austin MA, Zambon A, Brunzell JD. Plasma triglyceride and LDL heterogeneity in familial combined hyperlipidemia. Arterioscler Thromb. 1993 Mar; 13(3):427-34.
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Hayden MR, Kirk H, Clark C, Frohlich J, Rabkin S, McLeod R, Hewitt J. DNA polymorphisms in and around the Apo-A1-CIII genes and genetic hyperlipidemias. Am J Hum Genet. 1987 May; 40(5):421-30.
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