Lecithin Acyltransferase Deficiency

"Lecithin Acyltransferase Deficiency" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure, which enables searching at various levels of specificity.

MeSH information

Definition | Details | More General Concepts | Related Concepts | More Specific Concepts

An autosomal recessively inherited disorder caused by mutation of LECITHIN CHOLESTEROL ACYLTRANSFERASE that facilitates the esterification of lipoprotein cholesterol and subsequent removal from peripheral tissues to the liver. This defect results in low HDL-cholesterol level in blood and accumulation of free cholesterol in tissue leading to a triad of CORNEAL OPACITY, hemolytic anemia (ANEMIA, HEMOLYTIC), and PROTEINURIA.

Descriptor ID

D007863

MeSH Number(s)

C16.320.565.398.500.330.500

C18.452.584.500.875.330.500

C18.452.648.398.500.330.500

Concept/Terms

Lecithin Acyltransferase Deficiency

Fish-Eye Disease

Below are MeSH descriptors whose meaning is more general than "Lecithin Acyltransferase Deficiency".

Diseases [C]
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Genetic Diseases, Inborn [C16.320]
Metabolism, Inborn Errors [C16.320.565]
Lipid Metabolism, Inborn Errors [C16.320.565.398]
Hypolipoproteinemias [C16.320.565.398.500]
Hypoalphalipoproteinemias [C16.320.565.398.500.330]
Lecithin Acyltransferase Deficiency [C16.320.565.398.500.330.500]
Nutritional and Metabolic Diseases [C18]
Metabolic Diseases [C18.452]
Lipid Metabolism Disorders [C18.452.584]
Dyslipidemias [C18.452.584.500]
Hypolipoproteinemias [C18.452.584.500.875]
Hypoalphalipoproteinemias [C18.452.584.500.875.330]
Lecithin Acyltransferase Deficiency [C18.452.584.500.875.330.500]
Metabolism, Inborn Errors [C18.452.648]
Lipid Metabolism, Inborn Errors [C18.452.648.398]
Hypolipoproteinemias [C18.452.648.398.500]
Hypoalphalipoproteinemias [C18.452.648.398.500.330]
Lecithin Acyltransferase Deficiency [C18.452.648.398.500.330.500]

Below are MeSH descriptors whose meaning is related to "Lecithin Acyltransferase Deficiency".

Below are MeSH descriptors whose meaning is more specific than "Lecithin Acyltransferase Deficiency".

publications

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