| FEL | familial erythrophagocytic lymphohistiocytosis |
|---|---|
| FEO | familial expansile osteolysis |
| FEV | familial exudative vitreoretinopathy; forced expiratory volume |
| FEVR | familial exudative vitreoretinopathy |
| FH | facial hemihyperplasia; familial hypercholesterolemia; family history; fasting hyperbilirubinemia; f... |
| lipoprotein lipase deficiency, familial | A rare familial condition characterised by massive chylomicronaemia and decreased levels of other lipoproteins. It is due to deficiency of lipoprotein lipase, an alkaline triglyceride hydrolase which catalyses an important step in the extrahepatic removal of triglyceride-rich lipoproteins from the blood. (12 Dec 1998) |
|---|