Registry of Patients Diagnosed With Lysosomal Storage Diseases | ClinicalTrials HQ

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Trial	Conditions	Status	Phase	Updated	More info	NCT ID
Registry of Patients Diagnosed With Lysosomal Storage Diseases	Brain Diseases, Metabolic, Brain Diseases, Metabolic, Inborn, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Gaucher Disease, Type 3, Gaucher disease, Infant, Newborn, Diseases, Lipid Metabolism Disorders, Lipid Metabolism, Inborn Errors, Lysosomal Storage Diseases, Nervous System, Mucopolysaccharidosis I, Neurobehavioral Manifestations, Neurologic Manifestations, Nutritional and Metabolic Diseases, Skin and Connective Tissue Diseases, Wolman disease, X-linked disease, brain disorder, central nervous system disorder, cholesteryl ester storage disease, connective tissue disorder, cutaneous mucinosis, hereditary disease, inborn carbohydrate metabolic disorder, inborn errors of metabolism, inherited neurodegenerative disorder, intellectual disability, lysosomal lipid storage disorder, lysosomal storage disease, metabolic disease, mucopolysaccharidosis, mucopolysaccharidosis type 2, mucopolysaccharidosis type 4, mucopolysaccharidosis type 6, mucopolysaccharidosis type 7, nervous system disorder, sphingolipidosis	Recruiting	Not stated	2026-04-08		NCT05619900

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Organizations	Linked trials
University of California, San Francisco	637

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Research sites	City	Country	Linked trials
University of California San Francisco	San Francisco	United States	144