dysbetalipoproteinemia
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familial dysbetalipoproteinemia — an inherited disorder of lipoprotein metabolism caused by mutations in the APOE gene (locus: 19q13.2), which encodes apolipoprotein E (apo E), that result in defective binding of apo E to lipoprotein receptors. It is characterized biochemically… … Medical dictionary
Abetalipoproteinemia — Classification and external resources Micrograph showing enterocytes with a clear cytoplasm (due to lipid accumulation) characteristic of abetalipoproteinemia. Duodenal bi … Wikipedia
Lipodystrophy — Classification and external resources ICD 10 E88.1 ICD 9 272.6 … Wikipedia
Xanthoma — Classification and external resources Photograph of patient s hands showing multiple xanthoma tendinosum. Kumar et al. Cases Journal 2008 ICD 10 E … Wikipedia
Combined hyperlipidemia — Classification and external resources ICD 10 E78.4 ICD 9 272.4 In medicine … Wikipedia
Inborn error of metabolism — Classification and external resources ICD 10 E70 E90 ICD 9 … Wikipedia
Hyperlipidemia — DiseasesDB = 6255 MeshID = D006949 Hyperlipidemia, hyperlipoproteinemia or dyslipidemia is the presence of raised or abnormal levels of lipids and/or lipoproteins in the blood. Lipids (fatty molecules) are transported in a protein capsule, and… … Wikipedia
Carnitine palmitoyltransferase II deficiency — Classification and external resources Carnitine ICD 9 … Wikipedia
Lipomatosis — Classification and external resources ICD 10 E88.2 MeSH D008068 Lipomatosis is a … Wikipedia
Apolipoprotein E — (APOE) is an apoprotein found in the chylomicron that binds to a specific receptor on liver cells and peripheral cells. It is essential for the normal catabolism of triglyceride rich lipoprotein constituents.cite web | title = Entrez Gene: APOE… … Wikipedia
