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
|
| MeSH Number(s) |
C16.320.565.398.450 C18.452.584.500.500.438 C18.452.648.398.450
|
| 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
|
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.
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click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2002 | 0 | 1 | 1 |
| 2004 | 1 | 0 | 1 |
| 2005 | 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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Upstream stimulatory factor 1 associated with familial combined hyperlipidemia, LDL cholesterol, and triglycerides. Hum Genet. 2005 Sep; 117(5):444-51.
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TXNIP gene not associated with familial combined hyperlipidemia in the NHLBI Family Heart Study. Atherosclerosis. 2004 Jun; 174(2):357-62.
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Combination therapy for combined dyslipidemia. Am J Cardiol. 2002 Nov 20; 90(10B):21K-29K.
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Genetic basis of familial dyslipidemia and hypertension: 15-year results from Utah. Am J Hypertens. 1993 Nov; 6(11 Pt 2):319S-327S.
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Diagnosing heterozygous familial hypercholesterolemia using new practical criteria validated by molecular genetics. Am J Cardiol. 1993 Jul 15; 72(2):171-6.
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Population-based frequency of dyslipidemia syndromes in coronary-prone families in Utah. Arch Intern Med. 1990 Mar; 150(3):582-8.
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Concordant dyslipidemia, hypertension and early coronary disease in Utah families. Klin Wochenschr. 1990; 68 Suppl 20:53-9.
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Apolipoprotein, low density lipoprotein subfraction, and insulin associations with familial combined hyperlipidemia. Study of Utah patients with familial dyslipidemic hypertension. Arteriosclerosis. 1989 May-Jun; 9(3):335-44.