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Category:Lipid metabolism disorders
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Inborn error
of
lipid metabolism
:
dyslipidemia
(
E78
,
272.0–272.6
)
Hyperlipidemia
Hypercholesterolemia
/
Hypertriglyceridemia
Lipoprotein lipase deficiency/Type Ia
Familial apoprotein CII deficiency/Type Ib
Familial hypercholesterolemia/Type IIa
Combined hyperlipidemia/Type IIb
Familial dysbetalipoproteinemia/Type III
Familial hypertriglyceridemia/Type IV
Xanthoma/Xanthomatosis
Hypolipoproteinemia
Hypoalphalipoproteinemia/HDL
Lecithin cholesterol acyltransferase deficiency
Tangier disease
Hypobetalipoproteinemia/LDL
Abetalipoproteinemia
Apolipoprotein B deficiency
Chylomicron retention disease
Lipodystrophy
Barraquer–Simons syndrome
Other
Lipomatosis
Adiposis dolorosa
Lipoid proteinosis
APOA1 familial renal amyloidosis
v
t
e
Index of
inborn errors of metabolism
Description
Metabolism
Enzymes and pathways:
citric acid cycle
enzymes
pentose phosphate
intermediates
glycoproteins
enzymes
glycosaminoglycans
proteoglycan enzymes
phospholipid
metabolism
cholesterol and steroid
intermediates
sphingolipids
enzymes
eicosanoids
enzymes
amino acid
intermediates
urea cycle
enzymes
nucleotide
intermediates
Disorders
Citric acid cycle and electron transport chain
Glycoprotein
Proteoglycan
Fatty-acid
Phospholipid
Cholesterol and steroid
Eicosanoid
Amino acid
Purine-pyrimidine
Heme metabolism
Symptoms and signs
Treatment
Drugs
other
Pages in category "Lipid metabolism disorders"
The following 12 pages are in this category, out of 12 total.
A
Abetalipoproteinemia
Apolipoprotein B deficiency
C
Chylomicron retention disease
F
Familial hypercholesterolemia
H
Hypercholesterolemia
Hypertriglyceridemia
Hypoalphalipoproteinemia
Hypobetalipoproteinemia
Hypolipoproteinemia
L
Lecithin cholesterol acyltransferase deficiency
Lipomatosis
U
Urbach–Wiethe disease
Categories
:
Lipid disorders
Inborn errors of metabolism
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