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Trial	Conditions	Status	Phase	Updated	More info	NCT ID
Lysosomal Acid Lipase (LAL) Deficiency Registry	Acid Cholesteryl Ester Hydrolase Deficiency, Type 2, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Infant, Newborn, Diseases, Lipid Metabolism Disorders, Lipid Metabolism, Inborn Errors, Nutritional and Metabolic Diseases, Wolman disease, cholesteryl ester storage disease, hereditary disease, inborn errors of metabolism, lysosomal lipid storage disorder, lysosomal storage disease, metabolic disease	Recruiting	Not stated	2026-03-06		NCT01633489

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