Lipodystrophy, Familial Partial [familiární parciální lipodystrofie]
- Terms
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familiární parciální lipodystrofie Dunniganova typu
familiární parciální lipodystrofie typ 1
familiární parciální lipodystrofie typ 2
familiární parciální lipodystrofie typ 3
lipodystrofie familiární parciální
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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
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.
- DUI
- D052496 MeSH Browser
- CUI
- M0462327
- Previous indexing
- Lipodystrophy (1975-2006)
- History note
- 2007; use DIABETES MELLITUS, LIPOATROPHIC 2005-2006
- Public note
- 2007; see DIABETES MELLITUS, LIPOATROPHIC 2005-2006
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