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.

Descriptor ID	D052496
MeSH Number(s)	C17.800.849.391.700 C18.452.584.625.700 C18.452.880.391.700
Concept/Terms	Lipodystrophy, Familial Partial Lipodystrophy, Familial Partial Familial Partial Lipodystrophies Lipodystrophies, Familial Partial Partial Lipodystrophies, Familial Partial Lipodystrophy, Familial Familial Partial Lipodystrophy Koberling-Dunnigan Syndrome Koberling Dunnigan Syndrome Familial Partial Lipodystrophy, Type 2 Familial Partial Lipodystrophy, Type 2 Lipodystrophy, Familial, of Limbs and Lower Trunk Lipodystrophy, Familial Partial, Type 2 Lipodystrophy, Reverse Partial Lipodystrophies, Reverse Partial Partial Lipodystrophies, Reverse Partial Lipodystrophy, Reverse Reverse Partial Lipodystrophies Reverse Partial Lipodystrophy Dunnigan Syndrome Syndrome, Dunnigan Lipodystrophy, Familial Partial, Dunnigan Type Familial Partial Lipodystrophy, Type 3 Familial Partial Lipodystrophy, Type 3 Lipodystrophy, Familial Partial, Associated With PPARg Mutations Lipodystrophy, Familial Partial, Type 3 Familial Partial Lipodystrophy, Type 1 Familial Partial Lipodystrophy, Type 1 Lipodystrophy, Familial Partial, Kobberling Type Lipodystrophy, Familial Partial, Type 1 Familial Partial Lipodystrophy, Kobberling Type

Below are MeSH descriptors whose meaning is more general than "Lipodystrophy, Familial Partial".

Below are MeSH descriptors whose meaning is related to "Lipodystrophy, Familial Partial".

Below are MeSH descriptors whose meaning is more specific than "Lipodystrophy, Familial Partial".