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Hypercholesterolemia, autosomal dominant, type B

MONDO:0007751

Also known as: hypercholesterolemia, autosomal dominant, type B, hypercholesterolemia, familial, 2, apolipoprotein B-100, familial defective, apolipoprotein B-100, familial ligand-defective, hypercholesterolemia, familial, due to ligand-defective apolipoprotein B

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

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Broader categories

Disease (680) Hyperlipidemia (295) Metabolic disease (233) Inherited lipid metabolism disorder (189) Hereditary disease (176) Familial hypercholesterolemia (56) Inborn errors of metabolism (45) Human disease (14) Familial hyperlipidemia (8) Hyperlipoproteinemia (8)
Not yet finished but already full! 1 Completed 1
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  • Heart attack patients under 60 get genetic screening for hidden cholesterol disorder

    Diagnosis Completed

    This study tested whether offering genetic screening to younger heart attack patients (under 60) can uncover hidden cases of Familial Hypercholesterolemia (FH), an inherited condition causing very high cholesterol. Researchers recruited 140 patients admitted with a heart attack a…

    Phase: NA • Sponsor: University of British Columbia • Aim: Diagnosis

    Last updated Jun 27, 2026 12:28 UTC

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