Hyperlipidemia, Familial Combined

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.

Year introduced: 1980

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Tree Number(s): C16.320.565.398.450, C18.452.584.500.500.438, C18.452.584.563.450, C18.452.648.398.450

MeSH Unique ID: D006950

Entry Terms:

• 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

All MeSH Categories
Diseases Category
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Metabolism, Inborn Errors
Lipid Metabolism, Inborn Errors
Hyperlipidemia, Familial Combined

All MeSH Categories
Diseases Category
Nutritional and Metabolic Diseases
Metabolic Diseases
Lipid Metabolism Disorders
Dyslipidemias
Hyperlipidemias
Hyperlipidemia, Familial Combined

All MeSH Categories
Diseases Category
Nutritional and Metabolic Diseases
Metabolic Diseases
Lipid Metabolism Disorders
Lipid Metabolism, Inborn Errors
Hyperlipidemia, Familial Combined

All MeSH Categories
Diseases Category
Nutritional and Metabolic Diseases
Metabolic Diseases
Metabolism, Inborn Errors
Lipid Metabolism, Inborn Errors
Hyperlipidemia, Familial Combined