Concept information
Nutritional and Metabolic Diseases
Metabolic Diseases
Lipid Metabolism Disorders
Lipid Metabolism, Inborn Errors
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Metabolism, Inborn Errors
Lipid Metabolism, Inborn Errors
Término preferido
Hyperlipoproteinemia Type III
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Tipo
-
mesh:Descriptor
Definición
- An autosomal recessively inherited disorder characterized by the accumulation of intermediate-density lipoprotein (IDL or broad-beta-lipoprotein). IDL has a CHOLESTEROL to TRIGLYCERIDES ratio greater than that of VERY-LOW-DENSITY LIPOPROTEINS. This disorder is due to mutation of APOLIPOPROTEINS E, a receptor-binding component of VLDL and CHYLOMICRONS, resulting in their reduced clearance and high plasma levels of both cholesterol and triglycerides.
Concepto genérico
Etiquetas alternativas
- Broad Beta Disease
- Dysbetalipoproteinemia
- Dysbetalipoproteinemia, Familial
- Familial Dysbetalipoproteinemia
- Familial Hypercholesterolemia with Hyperlipemia
- Hyperlipoproteinemia, Broad-beta
- Hyperlipoproteinemia, Type III
En otras lenguas
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francés
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Dysbêtalipoprotéinémie
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Dyslipoprotéinémie à broad-beta
URI
http://data.loterre.fr/ark:/67375/JVR-HV2T5BW7-R
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