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Lipodystrophy, Familial Partial MeSH Descriptor Data 2023


MeSH Heading
Lipodystrophy, Familial Partial
Tree Number(s)
C16.320.488.813
C17.800.849.391.700
C18.452.584.563.798
C18.452.584.625.700
C18.452.880.391.700
Unique ID
D052496
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D052496
Scope Note
Inherited conditions characterized by the partial loss of ADIPOSE TISSUE, either confined to the extremities with normal or increased fat deposits on the face, neck and trunk (type 1), or confined to the loss of SUBCUTANEOUS FAT from the limbs and trunk (type 2). Type 3 is associated with mutation in the gene encoding PEROXISOME PROLIFERATOR-ACTIVATED RECEPTOR GAMMA.
Entry Term(s)
Dunnigan Syndrome
Familial Partial Lipodystrophy
Familial Partial Lipodystrophy, Kobberling Type
Familial Partial Lipodystrophy, Type 1
Familial Partial Lipodystrophy, Type 2
Familial Partial Lipodystrophy, Type 3
Koberling-Dunnigan Syndrome
Lipodystrophy, Familial Partial, Associated With PPARg Mutations
Lipodystrophy, Familial Partial, Dunnigan Type
Lipodystrophy, Familial Partial, Kobberling Type
Lipodystrophy, Familial Partial, Type 1
Lipodystrophy, Familial Partial, Type 2
Lipodystrophy, Familial Partial, Type 3
Lipodystrophy, Familial, of Limbs and Lower Trunk
Lipodystrophy, Reverse Partial
Previous Indexing
Lipodystrophy (1975-2006)
See Also
PPAR gamma
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
2021/07/01
Lipodystrophy, Familial Partial Preferred
Familial Partial Lipodystrophy, Type 2 Narrower
Familial Partial Lipodystrophy, Type 3 Narrower
Familial Partial Lipodystrophy, Type 1 Narrower
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