Hyperlipidemia, Familial Combined

Introduction: Hyperlipidemia, Familial Combined

Description of Hyperlipidemia, Familial Combined

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.
Source: MeSH 2007

Hyperlipidemia, Familial Combined: Related Topics

These medical condition or symptom topics may be relevant to medical information for Hyperlipidemia, Familial Combined:

• Hyperlipidemia (28 causes)
• Familial
• Familial disorder

Terms associated with Hyperlipidemia, Familial Combined:

Terms Similar to Hyperlipidemia, Familial Combined:

• Hyperlipidemia, Multiple Lipoprotein-Type

Source - MeSH 2007

Broader terms for Hyperlipidemia, Familial Combined

• Lipid Metabolism, Inborn Errors
• Hyperlipidemias

Source - MeSH 2007

Hierarchical classifications of Hyperlipidemia, Familial Combined

The following list attempts to classify Hyperlipidemia, Familial Combined into categories where each line is subset of the next.

MeSH 2007 Hierarchy:

• Congenital, Hereditary, and Neonatal Diseases and Abnormalities
  • Genetic Diseases, Inborn
    • Metabolism, Inborn Errors
      • Lipid Metabolism, Inborn Errors
        • Hyperlipidemia, Familial Combined

MeSH 2007 Hierarchy

• Nutritional and Metabolic Diseases
  • Metabolic Diseases
    • Lipid Metabolism Disorders
      • Dyslipidemias
        • Hyperlipidemias
          • Hyperlipidemia, Familial Combined

MeSH 2007 Hierarchy

• Nutritional and Metabolic Diseases
  • Metabolic Diseases
    • Metabolism, Inborn Errors
      • Lipid Metabolism, Inborn Errors
        • Hyperlipidemia, Familial Combined

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