Lipomatosis

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Lipomatosis Classification and external resources
ICD-10	E88.2
MeSH	D008068

Lipomatosis is a hereditary condition where multiple lipomas present on the body.

[edit] See also

• Pelvic lipomatosis

v • d • e 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