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. . 1.00
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. . 0.83
