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MeSH 搜索器

Lipodystrophy, Familial 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.
推出的年份: 2007
副标题
树号: C16.320.488.813, C17.800.849.391.700, C18.452.584.563.798, C18.452.584.625.700, C18.452.880.391.700
MeSH 单一 ID: D052496
进入的组:
  • Familial Partial Lipodystrophies
  • Partial Lipodystrophy, Familial
  • Familial Partial Lipodystrophy
  • Koberling-Dunnigan Syndrome
  • Koberling Dunnigan Syndrome
  • Familial Partial Lipodystrophy, Type 2
  • Lipodystrophy, Familial, of Limbs and Lower Trunk
  • Lipodystrophy, Familial Partial, Dunnigan Type
  • Lipodystrophy, Reverse Partial
  • Partial Lipodystrophies, Reverse
  • Partial Lipodystrophy, Reverse
  • Reverse Partial Lipodystrophies
  • Reverse Partial Lipodystrophy
  • Dunnigan Syndrome
  • Lipodystrophy, Familial Partial, Type 2
  • 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, Kobberling Type
  • Lipodystrophy, Familial Partial, Kobberling Type
  • Lipodystrophy, Familial Partial, Type 1
早前的内容:
  • Lipodystrophy (1975-2006)

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