Natural History of Glycosphingolipid Storage Disorders and Glycoprotein Disorders | ClinicalTrials HQ

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Trial	Conditions	Status	Phase	Updated	More info	NCT ID
Natural History of Glycosphingolipid Storage Disorders and Glycoprotein Disorders	Bone Diseases, Metabolic, Brain Diseases, Metabolic, Brain Diseases, Metabolic, Inborn, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Dyskinesias, GM1 gangliosidosis, GM2 gangliosidosis, Gangliosidoses, Lipid Metabolism Disorders, Lipid Metabolism, Inborn Errors, Lysosomal Storage Diseases, Nervous System, Myoclonus, Neurologic Manifestations, Nutritional and Metabolic Diseases, Pathological Conditions, Signs and Symptoms, Signs and Symptoms, bone disorder, brain disorder, central nervous system disorder, hereditary disease, inborn carbohydrate metabolic disorder, inborn errors of metabolism, lysosomal lipid storage disorder, lysosomal storage disease, metabolic disease, mucolipidosis, musculoskeletal system disorder, nervous system disorder, sphingolipidosis	Recruiting	Not stated	2026-10-02		NCT00029965

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Organizations	Linked trials
National Human Genome Research Institute (NHGRI)	54

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Research sites	City	Country	Linked trials
National Institutes of Health Clinical Center	Bethesda	United States	800