search

MeSH 搜索器

Hyperlipoproteinemia Type I

An inherited condition due to a deficiency of either LIPOPROTEIN LIPASE or APOLIPOPROTEIN C-II (a lipase-activating protein). The lack of lipase activities results in inability to remove CHYLOMICRONS and TRIGLYCERIDES from the blood which has a creamy top layer after standing.
推出的年份: 2007(1980)
副标题
树号: C16.320.565.398.465, C18.452.584.500.500.644.237, C18.452.584.563.465, C18.452.648.398.465
MeSH 单一 ID: D008072
进入的组:
  • Hyperlipoproteinemia Type Is
  • Familial Lipoprotein Lipase Deficiency
  • Lipoprotein Lipase Deficiency, Familial
  • Familial Hyperchylomicronemia
  • Familial Hyperchylomicronemias
  • Hyperchylomicronemias, Familial
  • Hyperlipoproteinemia Type Ia
  • Hyperlipoproteinemia Type Ias
  • Familial Hyperlipoproteinemia Type 1
  • Lipase D Deficiency
  • Deficiencies, Lipase D
  • Deficiency, Lipase D
  • Lipase D Deficiencies
  • Familial LPL Deficiency
  • Deficiencies, Familial LPL
  • Deficiency, Familial LPL
  • Familial LPL Deficiencies
  • LPL Deficiencies, Familial
  • LPL Deficiency, Familial
  • Hyperlipemia, Idiopathic, Burger-Grutz Type
  • Lipoprotein Lipase Deficiency
  • Deficiencies, Lipoprotein Lipase
  • Deficiency, Lipoprotein Lipase
  • Lipase Deficiencies, Lipoprotein
  • Lipoprotein Lipase Deficiencies
  • Chylomicronemia, Familial
  • Chylomicronemias, Familial
  • Familial Chylomicronemia
  • Familial Chylomicronemias
  • Hyperlipoproteinemia, Type Ia
  • Hyperlipoproteinemias, Type Ia
  • Type Ia Hyperlipoproteinemia
  • Type Ia Hyperlipoproteinemias
  • Hyperlipemia, Essential Familial
  • Essential Familial Hyperlipemia
  • Essential Familial Hyperlipemias
  • Familial Hyperlipemia, Essential
  • Familial Hyperlipemias, Essential
  • Hyperlipemias, Essential Familial
  • Burger-Grutz Syndrome
  • Burger Grutz Syndrome
  • Burger-Grutz Syndromes
  • Syndrome, Burger-Grutz
  • Syndromes, Burger-Grutz
  • LIPD Deficiency
  • Deficiencies, LIPD
  • Deficiency, LIPD
  • LIPD Deficiencies
  • Hyperchylomicronemia, Familial
  • Hyperlipoproteinemia, Type I
  • Hyperlipoproteinemias, Type I
  • Type I Hyperlipoproteinemia
  • Type I Hyperlipoproteinemias
  • Apolipoprotein C-II Deficiency
  • Apolipoprotein C II Deficiency
  • Apolipoprotein C-II Deficiencies
  • Deficiencies, Apolipoprotein C-II
  • Deficiency, Apolipoprotein C-II
  • Familial Fat-Induced Hypertriglyceridemia
  • Familial Fat Induced Hypertriglyceridemia
  • Familial Fat-Induced Hypertriglyceridemias
  • Fat-Induced Hypertriglyceridemia, Familial
  • Fat-Induced Hypertriglyceridemias, Familial
  • Hypertriglyceridemia, Familial Fat-Induced
  • Hypertriglyceridemias, Familial Fat-Induced
  • C-II Anapolipoproteinemia
  • Anapolipoproteinemia, C-II
  • Anapolipoproteinemias, C-II
  • C-II Anapolipoproteinemias
  • Hyperlipoproteinemia Type Ib
  • Hyperlipoproteinemia Type Ibs
  • Hyperlipoproteinemia, Type Ib
  • Hyperlipoproteinemias, Type Ib
  • Type Ib Hyperlipoproteinemia
  • Type Ib Hyperlipoproteinemias
早前的内容:
  • Hyperlipidemia/familial & genetic (1966-1979)

留言 (0)

沒有登入
gif