Template:Lipid metabolism disorders

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v • d • e 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