disease has basis in dysfunction of LCAT hypolipoproteinemia (disease) familial hemolytic anemia Norum disease DOID:1391 FLD Familial LCAT (lecithin-cholesterol acyltransferase) deficiency (FLD) is a form of lecithin-cholesterol acyltransferase deficiency (LCAT) characterized clinically by corneal opacities, hemolytic anemia, and renal failure, and biochemically by severely decreased HDL cholesterol and complete deficiency of the LCAT enzyme. GARD:0004011 ICD10:E78.6 LCAT deficiency MONDO:0009515 NCIT:C84813 Norum disease OMIM:245900 Orphanet:79293 SCTID:238091006 UMLS:CN205883 complete LCAT deficiency familial LCAT deficiency lecithin acyltransferase deficiency lecithin:cholesterol acyltransferase deficiency LCAT deficiency