Lipodystrophy, Congenital Generalized

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Lipodystrophy, Congenital Generalized

"Lipodystrophy, Congenital Generalized" 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

Congenital disorders, usually autosomal recessive, characterized by severe generalized lack of ADIPOSE TISSUE, extreme INSULIN RESISTANCE, and HYPERTRIGLYCERIDEMIA.

Descriptor ID	D052497
MeSH Number(s)	C16.320.565.398.745 C17.800.849.391.550 C18.452.584.625.550 C18.452.648.398.745 C18.452.880.391.550
Concept/Terms	Lipodystrophy, Congenital Generalized Lipodystrophy, Congenital Generalized Congenital Generalized Lipodystrophies Generalized Lipodystrophies, Congenital Generalized Lipodystrophy, Congenital Lipodystrophies, Congenital Generalized Congenital Generalized Lipodystrophy Berardinelli-Seip Congenital Lipodystrophy Berardinelli Seip Congenital Lipodystrophy Congenital Lipodystrophy, Berardinelli-Seip Lipodystrophy, Berardinelli-Seip Congenital Congenital Generalized Lipodystrophy Type 2 Congenital Generalized Lipodystrophy Type 2 Berardinelli-Seip Congenital Lipodystrophy Type 2 Berardinelli Seip Congenital Lipodystrophy Type 2 Berardinelli-Seip Congenital Lipodystrophy, Type 2 Berardinelli Seip Congenital Lipodystrophy, Type 2 Brunzell Syndrome Syndrome, Brunzell Brunzell Syndrome, Bscl2-Related Brunzell Syndrome, Bscl2 Related Brunzell Syndromes, Bscl2-Related Bscl2-Related Brunzell Syndrome Bscl2-Related Brunzell Syndromes Syndrome, Bscl2-Related Brunzell Syndromes, Bscl2-Related Brunzell Total Lipodystrophy and Acromegaloid Gigantism Lipoatrophic Diabetes, Congenital Lipodystrophy, Berardinelli-Seip Congenital, Type 2 Lipodystrophy, Congenital Generalized, Type 2 Lipodystrophy, Total, And Acromegaloid Gigantism Seip Syndrome Syndrome, Seip Berardinelli Syndrome Syndrome, Berardinelli Congenital Lipoatrophic Diabetes Congenital Lipoatrophic Diabete Diabete, Congenital Lipoatrophic Diabetes, Congenital Lipoatrophic Lipoatrophic Diabete, Congenital Congenital Generalized Lipodystrophy Type 1 Congenital Generalized Lipodystrophy Type 1 Lipodystrophy, Congenital Generalized, Type 1 Brunzell Syndrome, Agpat2-Related Agpat2-Related Brunzell Syndrome Agpat2-Related Brunzell Syndromes Brunzell Syndrome, Agpat2 Related Brunzell Syndromes, Agpat2-Related Syndrome, Agpat2-Related Brunzell Syndromes, Agpat2-Related Brunzell Lipodystrophy, Berardinelli-Seip Congenital, Type 1 Berardinelli-Seip Congenital Lipodystrophy Type 1 Berardinelli Seip Congenital Lipodystrophy Type 1 Berardinelli-Seip Congenital Lipodystrophy, Type 1 Berardinelli Seip Congenital Lipodystrophy, Type 1

Below are MeSH descriptors whose meaning is more general than "Lipodystrophy, Congenital Generalized".

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]
Lipodystrophy, Congenital Generalized [C16.320.565.398.745]
Skin and Connective Tissue Diseases [C17]
Skin Diseases [C17.800]
Skin Diseases, Metabolic [C17.800.849]
Lipodystrophy [C17.800.849.391]
Lipodystrophy, Congenital Generalized [C17.800.849.391.550]
Nutritional and Metabolic Diseases [C18]
Metabolic Diseases [C18.452]
Lipid Metabolism Disorders [C18.452.584]
Lipodystrophy [C18.452.584.625]
Lipodystrophy, Congenital Generalized [C18.452.584.625.550]
Metabolism, Inborn Errors [C18.452.648]
Lipid Metabolism, Inborn Errors [C18.452.648.398]
Lipodystrophy, Congenital Generalized [C18.452.648.398.745]
Skin Diseases, Metabolic [C18.452.880]
Lipodystrophy [C18.452.880.391]
Lipodystrophy, Congenital Generalized [C18.452.880.391.550]

Below are MeSH descriptors whose meaning is related to "Lipodystrophy, Congenital Generalized".

Below are MeSH descriptors whose meaning is more specific than "Lipodystrophy, Congenital Generalized".

publications

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