has material basis in germline mutation in LCAT hypolipoproteinemia hemolytic anemia Norum disease https://www.malacards.org/card/lecithincholesterol_acyltransferase_deficiency OMIM:245900 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 FLD DOID:1391 UMLS:C0023195 MONDO:0009515 SCTID:238091006 icd11.foundation:1848131619 Norum disease lecithin:cholesterol acyltransferase deficiency NANDO:1200852 lecithin acyltransferase deficiency MEDGEN:9698 complete LCAT deficiency NCIT:C84813 Orphanet:79293 LCAT deficiency