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.
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
- Berardinelli-Seip Syndrome
- Berardinelli Seip Syndrome
- Syndrome, Berardinelli-Seip
- Brunzell Syndrome (with Bone Cysts)
- Syndrome, Brunzell (with Bone Cysts)
- Generalized Lipodystrophy
- Generalized Lipodystrophies
- Lipodystrophies, Generalized
- Lipodystrophy, Generalized
- Total Lipodystrophy
- Lipodystrophies, Total
- Lipodystrophy, Total
- Total Lipodystrophies
- Berardinelli-Seip Congenital Lipodystrophy
- Berardinelli Seip Congenital Lipodystrophy
- Congenital Lipodystrophy, Berardinelli-Seip
- Lipodystrophy, Berardinelli-Seip Congenital
- Congenital Generalized Lipodystrophy
Congenital Generalized Lipodystrophy Type 1- Congenital Generalized Lipodystrophy Type 1
- Brunzell Syndrome, AGPAT2-Related
- AGPAT2-Related Brunzell Syndrome
- Brunzell Syndrome, AGPAT2 Related
- Syndrome, AGPAT2-Related Brunzell
- Lipodystrophy, Berardinelli-Seip Congenital, Type 1
- Lipodystrophy, Congenital Generalized, 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
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
- Congenital Lipoatrophic Diabetes
- Congenital Lipoatrophic Diabete
- Diabete, Congenital Lipoatrophic
- Diabetes, Congenital Lipoatrophic
- Lipoatrophic Diabete, Congenital
- Brunzell Syndrome, BSCL2-Related
- BSCL2-Related Brunzell Syndrome
- Brunzell Syndrome, BSCL2 Related
- Syndrome, BSCL2-Related Brunzell
- Lipodystrophy, Berardinelli-Seip Congenital, Type 2
- Lipodystrophy, Congenital Generalized, Type 2
- Lipodystrophy, Total, And Acromegaloid Gigantism
- Seip Syndrome
- Syndrome, Seip
- Total Lipodystrophy and Acromegaloid Gigantism
- Berardinelli Syndrome
- Syndrome, Berardinelli
- Lipoatrophic Diabetes, Congenital
|
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 more specific than "Lipodystrophy, Congenital Generalized".
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