Structured Summary
Abstract
Congenital disorders, usually autosomal recessive, characterized by severe generalized lack of ADIPOSE TISSUE, extreme INSULIN RESISTANCE, and HYPERTRIGLYCERIDEMIA.
MeSH Record
Classification
Broader headings
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MeSH Record
Synonyms
58 entry terms
- Berardinelli-Seip Congenital Lipodystrophy
- Berardinelli-Seip Syndrome
- Brunzell Syndrome (with Bone Cysts)
- Generalized Lipodystrophy
- Lipodystrophy, Congenital Generalized
- Total Lipodystrophy
- Berardinelli Seip Congenital Lipodystrophy
- Berardinelli Seip Syndrome
- Congenital Generalized Lipodystrophies
- Congenital Lipodystrophy, Berardinelli-Seip
- Generalized Lipodystrophies
- Generalized Lipodystrophies, Congenital
- Generalized Lipodystrophy, Congenital
- Lipodystrophies, Congenital Generalized
- Lipodystrophies, Generalized
- Lipodystrophies, Total
- Lipodystrophy, Berardinelli-Seip Congenital
- Lipodystrophy, Generalized
- Lipodystrophy, Total
- Syndrome, Berardinelli-Seip
- Syndrome, Brunzell (with Bone Cysts)
- Total Lipodystrophies
- Berardinelli Syndrome
- Berardinelli-Seip Congenital Lipodystrophy Type 1
- Berardinelli-Seip Congenital Lipodystrophy Type 2
- Berardinelli-Seip Congenital Lipodystrophy, Type 1
- Berardinelli-Seip Congenital Lipodystrophy, Type 2
- Brunzell Syndrome
- Brunzell Syndrome, AGPAT2-Related
- Brunzell Syndrome, BSCL2-Related
- Congenital Generalized Lipodystrophy Type 1
- Congenital Generalized Lipodystrophy Type 2
- Congenital Lipoatrophic Diabetes
- Lipoatrophic Diabetes, Congenital
- Lipodystrophy, Berardinelli-Seip Congenital, Type 1
- Lipodystrophy, Berardinelli-Seip Congenital, Type 2
- Lipodystrophy, Congenital Generalized, Type 1
- Lipodystrophy, Congenital Generalized, Type 2
- Lipodystrophy, Total, And Acromegaloid Gigantism
- Seip Syndrome
- Total Lipodystrophy and Acromegaloid Gigantism
- AGPAT2-Related Brunzell Syndrome
- BSCL2-Related Brunzell Syndrome
- Berardinelli Seip Congenital Lipodystrophy Type 1
- Berardinelli Seip Congenital Lipodystrophy Type 2
- Berardinelli Seip Congenital Lipodystrophy, Type 1
- Berardinelli Seip Congenital Lipodystrophy, Type 2
- Brunzell Syndrome, AGPAT2 Related
- Brunzell Syndrome, BSCL2 Related
- Congenital Lipoatrophic Diabete
- Diabete, Congenital Lipoatrophic
- Diabetes, Congenital Lipoatrophic
- Lipoatrophic Diabete, Congenital
- Syndrome, AGPAT2-Related Brunzell
- Syndrome, BSCL2-Related Brunzell
- Syndrome, Berardinelli
- Syndrome, Brunzell
- Syndrome, Seip
MeSH Record
Aspects Covered
34 allowable subheadings
Indexed with the subheadings blood, cerebrospinal fluid, chemically induced, classification, complications, diagnosis, diagnostic imaging, diet therapy, drug therapy, economics, embryology, enzymology, epidemiology, ethnology, etiology, genetics, history, immunology, metabolism, microbiology, mortality, nursing, parasitology, pathology, physiopathology, prevention & control, psychology, radiotherapy, rehabilitation, surgery, therapy, urine, veterinary, virology.
MeSH Record
History Note
2007; use DIABETES MELLITUS, LIPOATROPHIC 2005-2006
MeSH Record
Previous Indexing
- Lipodystrophy (1968-2006)
MeSH Hierarchy
Tree Numbers
AMA Style
References
- National Library of Medicine. Congenital Generalized Lipodystrophy. Medical Subject Headings (MeSH). 2026. Unique ID D052497. http://id.nlm.nih.gov/mesh/2026/D052497
- Congenital Generalized Lipodystrophy. In: Wikipedia. https://en.wikipedia.org/wiki/Congenital_generalized_lipodystrophy
- Congenital Generalized Lipodystrophy. In: Wikidata. https://www.wikidata.org/wiki/Q3242224