Template:Lipid metabolism disorders

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Lipid metabolism disorders / Inborn error of lipid metabolism - dyslipidemia (E78 and E71.3, 272)
Hyperlipidemia
Hypercholesterolemia/Hypertriglyceridemia (Familial hypercholesterolemia, Combined hyperlipidemia) - Xanthoma
Hypolipoproteinemia
Hypoalphalipoproteinemia/HDL (Lecithin cholesterol acyltransferase deficiency, Tangier disease)
Hypobetalipoproteinemia/LDL (Abetalipoproteinemia, Apolipoprotein B deficiency)
Lipodystrophy
Barraquer-Simons syndrome
Fatty acid metabolism deficiency
transport: Carnitine (Primary, I, II, -acylcarnitine) - Adrenoleukodystrophy

beta oxidation: Acyl CoA dehydrogenase (Short-chain, Medium-chain, Long-chain 3-hydroxy, Very long-chain) - Mitochondrial trifunctional protein deficiency

to acetyl-CoA: Malonic aciduria
Cholesterol synthesis
Smith-Lemli-Opitz syndrome
Other
Sjögren-Larsson syndrome - Lipomatosis - Adiposis dolorosa
see also lipid metabolism enzymes, lipoprotein metabolism
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  • This page was last modified 21:34, 3 June 2008 by Wikipedia user Arcadian. Based on work by Wikipedia user(s) Rcej and Sardanaphalus.
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