hypercholesterolemia, autosomal dominant, type B

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Trial	Conditions	Status	Phase	Updated	More info	NCT ID
Genetic Testing and Motivational Counseling for FH	Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Dyslipidemias, Hypercholesterolemia, Hyperlipoproteinemia Type IIa, Hyperlipoproteinemia Type IIb, Lipid Metabolism Disorders, Lipid Metabolism, Inborn Errors, Nutritional and Metabolic Diseases, familial hypercholesterolemia, hereditary disease, hypercholesterolemia, autosomal dominant, 3, hypercholesterolemia, autosomal dominant, type B, hypercholesterolemia, familial, 1, hypercholesterolemia, familial, 4, hyperlipidemia, hyperlipoproteinemia, hyperlipoproteinemia type 3, inborn errors of metabolism, metabolic disease	Active, not recruiting	Not applicable	2024-12-17		NCT04656028

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