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Hypercholesterolemia, autosomal dominant, 3

MONDO:0011369

Any familial hypercholesterolemia in which the cause of the disease is a mutation in the PCSK9 gene.

Also known as: PCSK9 familial hypercholesterolemia, familial hypercholesterolemia caused by mutation in PCSK9, hypercholesterolemia, autosomal dominant, 3, hypercholesterolemia, autosomal dominant, type 3, hypercholesterolemia, familial, 3, low density lipoprotein cholesterol level QTL 1, Fh3, HCHOLA3

5 clinical trials for this condition and its sub-types, 4 tagged with Hypercholesterolemia, autosomal dominant, 3 itself.

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