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Malonic Aciduria
Malonic aciduria
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Inborn errors of metabolism
Mitochondrial trifunctional protein deficiency
Lecithin cholesterol acyltransferase deficiency
Tangier disease
3-hydroxy-- 3-methylglutaryl-CoA lyase deficiency
Autosomal recessive disorders
Lipoid proteinosis
Abetalipop- roteinemia
Mitochondrial trifunctional protein deficiency
Lecithin cholesterol acyltransferase deficiency
Tangier disease
Genetic disorder
Hypoalphal- ipoproteinemia
Mitochondrial trifunctional protein deficiency
Genetic disorders
(8)
Barraquer-Simons Syndrome
Adrenoleuk- odystrophy
Mitochondrial trifunctional protein deficiency
Lecithin cholesterol acyltransferase deficiency
Hypoalphal- ipoproteinemia
Hypoalphal- ipoproteinemia
Abetalipop- roteinemia
Tangier disease
3-hydroxy-- 3-methylglutaryl-CoA lyase deficiency
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Diseases and disorders
Adiposis dolorosa
Hypolipoproteinemia
Xanthoma
Mitochondrial trifunctional protein deficiency
Lecithin cholesterol acyltransferase deficiency
Abetalipop- roteinemia
Tangier disease
Skin conditions resulting from errors in metabolism
Apolipoprotein B deficiency
Combined hyperlipidemia
Lipoid proteinosis
Adrenoleuk- odystrophy
Tangier disease
Xanthoma
Lipid disorders
(15)
Familial hyperchole- sterolemia
Hypertrigl- yceridemia
Blood lipids
Cholesterol
Cholesterol Depletion
Cholesterol Depletion
Combined hyperlipidemia
High-density lipoprotein
Hyperchole- sterolemia
Hyperlipidemia
Hypocholesterolemia
Lipoprotein lipase deficiency
Lipoprotein(a)
Low-density lipoprotein
Mevalonate inhibition
Triglyceride
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Rare diseases
Barraquer-Simons Syndrome
See also
(11)
Hypobetali- poproteinemia
Acyl CoA dehydrogenase
Enzymes
Lipoprotein
Beta oxidation
Beta oxidation
Malonyl-CoA
Long-chain fatty acids
Metabolism
Carnitine
PMID
Autosomal recessive
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