disease has basis in dysfunction of LCAT fish eye disease Fish eye disease (FED) is a form of genetic LCAT (lecithin-cholesterol acyltransferase) deficiency characterized clinically by corneal opacifications, and biochemically by significantly reduced HDL cholesterol and partial LCAT enzyme deficiency. GARD:0006450 ICD10:E78.6 LCATA deficiency MONDO:0007620 OMIM:136120 Orphanet:79292 SCTID:238092004 UMLS:C0342895 alpha-LCAT deficiency alpha-lecithin cholesterol acyltransferase deficiency alpha-lecithin:cholesterol acyltransferase deficiency dyslipoproteinemic corneal dystrophy fed fish eye disease fish-eye disease https://rarediseases.info.nih.gov/diseases/6450/fish-eye-disease partial LCAT deficiency LCAT deficiency