Svensk definition
Ärftlig tillstånd som följd av lipoproteinlipas- eller apolipoprotein C-II brist.
Hyperlipoproteinemia Type I
Hyperlipoproteinemi typ I
Engelsk definition
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.
Svenska synonymer
Familjär lipoproteinlipasbrist — Familjär hyperkylomikronemi — Familjär LPL-brist — Buerger-Gruetz syndrom — Apolipoprotein C-II brist — Typ 1b hyperlipoproteinemi — Hyperlipoproteinemi typ 1b
Engelska synonymer
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