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 DeCS Categories

C11 Eye Diseases .
C11.204 Corneal Diseases .
C11.204.236 Corneal Dystrophies, Hereditary .
C11.270 Eye Diseases, Hereditary .
C11.270.162 Corneal Dystrophies, Hereditary .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.320 Genetic Diseases, Inborn .
C16.320.290 Eye Diseases, Hereditary .
C16.320.290.162 Corneal Dystrophies, Hereditary .
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 .
 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. .
Dyslipidemias .
Dyslipidemia .
Dyslipoproteinemia .
Dyslipoproteinemias .
Abnormalities in the serum levels of LIPIDS, including overproduction or deficiency. Abnormal serum lipid profiles may include high total CHOLESTEROL, high TRIGLYCERIDES, low HIGH DENSITY LIPOPROTEIN CHOLESTEROL, and elevated LOW DENSITY LIPOPROTEIN CHOLESTEROL. .
Corneal Dystrophies, Hereditary .
Corneal Dystrophy, Hereditary .
Corneal Granular Dystrophies .
Corneal Granular Dystrophy .
Corneal Macular Dystrophies .
Corneal Macular Dystrophy .
Corneal Stromal Dystrophies .
Corneal Stromal Dystrophy .
Dystrophies, Corneal Granular .
Dystrophies, Corneal Macular .
Dystrophies, Corneal Stromal .
Dystrophies, Groenouw's .
Dystrophies, Hereditary Corneal .
Dystrophy, Corneal Granular .
Dystrophy, Corneal Macular .
Dystrophy, Corneal Stromal .
Dystrophy, Hereditary Corneal .
Granular Dystrophies, Corneal .
Groenouw Dystrophies .
Groenouws Dystrophies .
Hereditary Corneal Dystrophies .
Hereditary Corneal Dystrophy .
Macular Dystrophies, Corneal .
Stromal Dystrophy, Corneal .
Granular Dystrophy, Corneal .
Groenouw's Dystrophies .
Macular Dystrophy, Corneal .
Stromal Dystrophies, Corneal .
Bilateral hereditary disorders of the cornea, usually autosomal dominant, which may be present at birth but more frequently develop during adolescence and progress slowly throughout life. Central macular dystrophy is transmitted as an autosomal recessive defect. .