Hyperlipoproteinemia Type I
Synonyms
Anapolipoproteinemia, C-II
Anapolipoproteinemias, C-II
Apolipoprotein C II Deficiency
Apolipoprotein C-II Deficiencies
Apolipoprotein C-II Deficiency
Burger Grutz Syndrome
Burger-Grutz Syndrome
Burger-Grutz Syndromes
C-II Anapolipoproteinemia
C-II Anapolipoproteinemias
Chylomicronemia, Familial
Chylomicronemias, Familial
Deficiencies, Apolipoprotein C-II
Deficiencies, Familial LPL
Deficiencies, LIPD
Deficiencies, Lipase D
Deficiencies, Lipoprotein Lipase
Deficiency, Apolipoprotein C-II
Deficiency, Familial LPL
Deficiency, LIPD
Deficiency, Lipase D
Deficiency, Lipoprotein Lipase
Essential Familial Hyperlipemia
Essential Familial Hyperlipemias
Familial Chylomicronemia
Familial Chylomicronemias
Familial Fat Induced Hypertriglyceridemia
Familial Fat-Induced Hypertriglyceridemia
Familial Fat-Induced Hypertriglyceridemias
Familial Hyperchylomicronemia
Familial Hyperchylomicronemias
Familial Hyperlipemia, Essential
Familial Hyperlipemias, Essential
Familial Hyperlipoproteinemia Type 1
Familial LPL Deficiencies
Familial LPL Deficiency
Familial Lipoprotein Lipase Deficiency
Fat-Induced Hypertriglyceridemia, Familial
Fat-Induced Hypertriglyceridemias, Familial
Hyperchylomicronemia, Familial
Hyperchylomicronemias, Familial
Hyperlipemia, Essential Familial
Hyperlipemia, Idiopathic, Burger-Grutz Type
Hyperlipemias, Essential Familial
Hyperlipoproteinemia Type Ia
Hyperlipoproteinemia Type Ias
Hyperlipoproteinemia Type Ib
Hyperlipoproteinemia Type Ibs
Hyperlipoproteinemia Type Is
Hyperlipoproteinemia, Type I
Hyperlipoproteinemia, Type Ia
Hyperlipoproteinemia, Type Ib
Hyperlipoproteinemias, Type I
Hyperlipoproteinemias, Type Ia
Hyperlipoproteinemias, Type Ib
Hypertriglyceridemia, Familial Fat-Induced
Hypertriglyceridemias, Familial Fat-Induced
LIPD Deficiencies
LIPD Deficiency
LPL Deficiencies, Familial
LPL Deficiency, Familial
Lipase D Deficiencies
Lipase D Deficiency
Lipase Deficiencies, Lipoprotein
Lipoprotein Lipase Deficiencies
Lipoprotein Lipase Deficiency
Lipoprotein Lipase Deficiency, Familial
Syndrome, Burger-Grutz
Syndromes, Burger-Grutz
Type I Hyperlipoproteinemia
Type I Hyperlipoproteinemias
Type Ia Hyperlipoproteinemia
Type Ia Hyperlipoproteinemias
Type Ib Hyperlipoproteinemia
Type Ib Hyperlipoproteinemias
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.