(Q2349695)
English
familial lipoprotein lipase deficiency
familial hyperlipemia characterized by a deficiency of the enzyme lipoprotein lipase and the subsequent build up of chylomicrons and increased plasma concentration of triglycerides
- Fredrickson type I hyperlipoproteinemia (disorder)
- Fredrickson type I lipaemia
- familial LPL deficiency
- familial hyperchylomicronemia (disorder)
- familial hyperlipoproteinemia type I
- familial lipoprotein lipase deficiency (disorder) [Ambiguous]
- familial lipoprotein lipase deficiency with type I phenotype
- hypercholesterinaemic xanthomatosis
- hyperchylomicronemia
- mixed hyperglyceridemia
- Fredrickson type I hyperlipoproteinemia
- familial chylomiconemia syndrome
- Hyperlipemia, Essential Familial
- HYPERLIPOPROTEINEMIA, TYPE I
- Familial fat-induced hypertriglyceridemia
- Lipoprotein Lipase Deficiency
- Lpl Deficiency
- Hyperlipoproteinemia, Type 1A
- Lipd Deficiency
- Familial hyperchylomicronemia
- Endogenous hypertriglyceridaemia
- Type I hyperlipoproteinemia
- Lipoprotein lipase deficiency, familial
- Hyperlipemia, Idiopathic, Burger-Grutz Type
- Chylomicronemia, Familial
- Burger-Grutz syndrome
- Lipase D Deficiency
- Hyperchylomicronemia, Familial
- familial chylomicronemia syndrome
Statements
1 reference
1 reference
2 references
272.3
2 references
1 reference
Identifiers
1 reference
2 references
2 references
1 reference
1 reference
1 reference