← All indications
Lecithin Cholesterol Acyltransferase Deficiency
An autosomal recessive disorder of lipoprotein metabolism caused by mutation of LECITHIN CHOLESTEROL ACYLTRANSFERASE gene. It is characterized by low HDL-cholesterol levels, and the triad of CORNEAL OPACITIES; HEMOLYTIC ANEMIA; and PROTEINURIA with renal failure.
Drugs by status
Other trials (1)
Organizations
Organization Involved with Phase 3 Indications (1)
Organization Involved with Other Experimental Indications (1)