| FDH | familial dysalbuminemic hyperthyroxinemia; focal dermal hypoplasia; formaldehyde dehydrogenase |
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| FEL | familial erythrophagocytic lymphohistiocytosis |
| FEO | familial expansile osteolysis |
| FEV | familial exudative vitreoretinopathy; forced expiratory volume |
| FEVR | familial exudative vitreoretinopathy |
| familial white folded dysplasia | An autosomal dominant condition of the oral cavity characterised by soft, white or opalescent, thickened and corrugated folds of mucous membrane; other mucosal sites are occasionally involved simultaneously. Synonym: familial white folded dysplasia, oral epithelial nevus. (05 Mar 2000) |
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| 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) |