Cholesteryl ester storage disease

MONDO:0019149

A form of lysosomal acid lipase deficiency characterized by progressive cholesterol esters and triglyceride accumulation in tissues and organs typically presenting with hepatosplenomegaly, liver dysfunction and/or dyslipidemia.

Also known as: LAL deficiency, partial, LIPA deficiency, partial, cholesterol ester hydrolase deficiency, partial, cholesterol ester storage disease, lysosomal acid lipase deficiency, partial, CESD, lysosomal and lipase deficiency

36 clinical trials for this condition and its sub-types.

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