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 DeCS Categories

C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.320 Genetic Diseases, Inborn .
C16.320.565 Metabolism, Inborn Errors .
C16.320.565.398 Lipid Metabolism, Inborn Errors .
C16.320.565.398.500 Hypolipoproteinemias .
C16.320.565.398.500.330 Hypoalphalipoproteinemias .
C16.320.565.398.500.330.500 Lecithin Cholesterol Acyltransferase Deficiency .
C18 Nutritional and Metabolic Diseases .
C18.452 Metabolic Diseases .
C18.452.584 Lipid Metabolism Disorders .
C18.452.584.500 Dyslipidemias .
C18.452.584.500.875 Hypolipoproteinemias .
C18.452.584.500.875.330 Hypoalphalipoproteinemias .
C18.452.584.500.875.330.500 Lecithin Cholesterol Acyltransferase Deficiency .
C18.452.648 Metabolism, Inborn Errors .
C18.452.648.398 Lipid Metabolism, Inborn Errors .
C18.452.648.398.500 Hypolipoproteinemias .
C18.452.648.398.500.330 Hypoalphalipoproteinemias .
C18.452.648.398.500.330.500 Lecithin Cholesterol Acyltransferase Deficiency .
D08 Enzymes and Coenzymes .
D08.811 Enzymes .
D08.811.913 Transferases .
D08.811.913.050 Acyltransferases .
D08.811.913.050.625 Phosphatidylcholine-Sterol O-Acyltransferase .
D08.811.913.050.799 Sterol O-Acyltransferase .
 Synonyms & Historicals
Lecithin Cholesterol Acyltransferase Deficiency .
Dyslipoproteinemic Corneal Dystrophy .
Fish-Eye Disease .
LCAT Deficiency .
LCATA Deficiency .
Lecithin:Cholesterol Acyltransferase Deficiency .
Norum Disease .
alpha-LCAT Deficiency .
alpha-Lecithin-Cholesterol Acyltransferase Deficiency .
alpha-Lecithin:Cholesterol Acyltransferase Deficiency .
Acyltransferase Deficiency, Lecithin:Cholesterol .
Corneal Dystrophy, Dyslipoproteinemic .
Deficiency, LCAT .
Deficiency, alpha-LCAT .
Fish Eye Disease .
LCATA Deficiencies .
alpha LCAT Deficiency .
Lecithin Acyltransferase Deficiency .
An autosomal recessive disorder of lipoprotein metabolism caused by mutation of LECITHIN CHOLESTEROL ACYLTRANSFERASE gene. It is characterized by low HDL-cholesterol levels, and the triad of CORNEAL OPACITIES; HEMOLYTIC ANEMIA; and PROTEINURIA with renal failure. .
Phosphatidylcholine-Sterol O-Acyltransferase .
Cholesterol Ester Lysolecithin Acyltransferase .
Lecithin Acyltransferase .
Phosophatidylcholine-Sterol Acyltransferase .
Acyltransferase, Lecithin .
Acyltransferase, Lecithin Cholesterol .
Acyltransferase, Phosophatidylcholine-Sterol .
Cholesterol Acyltransferase, Lecithin .
O-Acyltransferase, Phosphatidylcholine-Sterol .
Phosophatidylcholine Sterol Acyltransferase .
Phosphatidylcholine Sterol O Acyltransferase .
Lecithin Cholesterol Acyltransferase .
An enzyme secreted from the liver into the plasma of many mammalian species. It catalyzes the esterification of the hydroxyl group of lipoprotein cholesterol by the transfer of a fatty acid from the C-2 position of lecithin. In familial lecithin:cholesterol acyltransferase deficiency disease, the absence of the enzyme results in an excess of unesterified cholesterol in plasma. .
Sterol O-Acyltransferase .
Cholesterol Esterifying Enzyme .
Acyl CoA Cholesterol Acyltransferase .
Acyltransferase, Acyl-CoA-Cholesterol .
Acyltransferase, Cholesterol .
Enzyme, Cholesterol Esterifying .
Esterifying Enzyme, Cholesterol .
O-Acyltransferase, Sterol .
Sterol O Acyltransferase .
Acyl-CoA-Cholesterol Acyltransferase .
Cholesterol Acyltransferase .
An enzyme that catalyzes the formation of cholesterol esters by the direct transfer of the fatty acid group from a fatty acyl CoA derivative. This enzyme has been found in the adrenal gland, gonads, liver, intestinal mucosa, and aorta of many mammalian species. EC .