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Lipodystrophy, Congenital Generalized MeSH Descriptor Data 2022


MeSH Heading
Lipodystrophy, Congenital Generalized
Tree Number(s)
C16.320.565.398.745
C17.800.849.391.550
C18.452.584.563.745
C18.452.584.625.550
C18.452.648.398.745
C18.452.880.391.550
Unique ID
D052497
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D052497
Scope Note
Congenital disorders, usually autosomal recessive, characterized by severe generalized lack of ADIPOSE TISSUE, extreme INSULIN RESISTANCE, and HYPERTRIGLYCERIDEMIA.
Entry Term(s)
Berardinelli Syndrome
Berardinelli-Seip Congenital Lipodystrophy
Berardinelli-Seip Congenital Lipodystrophy Type 1
Berardinelli-Seip Congenital Lipodystrophy Type 2
Berardinelli-Seip Congenital Lipodystrophy, Type 1
Berardinelli-Seip Congenital Lipodystrophy, Type 2
Berardinelli-Seip Syndrome
Brunzell Syndrome
Brunzell Syndrome (with Bone Cysts)
Brunzell Syndrome, AGPAT2-Related
Brunzell Syndrome, BSCL2-Related
Congenital Generalized Lipodystrophy
Congenital Generalized Lipodystrophy Type 1
Congenital Generalized Lipodystrophy Type 2
Congenital Lipoatrophic Diabetes
Generalized Lipodystrophy
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
Total Lipodystrophy and Acromegaloid Gigantism
Previous Indexing
Lipodystrophy (1968-2006)
Public MeSH Note
2007; see DIABETES MELLITUS, LIPOATROPHIC 2005-2006
History Note
2007; use DIABETES MELLITUS, LIPOATROPHIC 2005-2006
Date Established
2007/01/01
Date of Entry
2006/07/05
Revision Date
2021/06/30
Lipodystrophy, Congenital Generalized Preferred
Congenital Generalized Lipodystrophy Type 1 Narrower
Congenital Generalized Lipodystrophy Type 2 Narrower
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