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Nutritional and Metabolic Diseases > Metabolic Diseases > Lipid Metabolism Disorders > Lipid Metabolism, Inborn Errors > Hyperlipidemia, Familial Combined
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Metabolism, Inborn Errors > Lipid Metabolism, Inborn Errors > Hyperlipidemia, Familial Combined
Nutritional and Metabolic Diseases > Metabolic Diseases > Metabolism, Inborn Errors > Lipid Metabolism, Inborn Errors > Hyperlipidemia, Familial Combined
... > Nutritional and Metabolic Diseases > Metabolic Diseases > Lipid Metabolism Disorders > Dyslipidemias > Hyperlipidemias > Hyperlipidemia, Familial Combined

Preferred term

Hyperlipidemia, Familial Combined  

Type

  • mesh:Descriptor

Definition

  • 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.

Broader concept

Entry terms

  • Familial Combined Hyperlipidemia
  • Hyperlipidemia, Multiple Lipoprotein-Type

Allowable Qualifier(s)

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URI

http://data.loterre.fr/ark:/67375/JVR-MZHG2TH7-M

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RDF/XML TURTLE JSON-LD Created 4/23/79, last modified 6/30/21