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Familial hypobetalipoproteinemia 2

MONDO:0011505

Any hypobetalipoproteinemia in which the cause of the disease is a mutation in the ANGPTL3 gene.

Also known as: ANGPTL3 hypobetalipoproteinemia, FHBL2, familial hypobetalipoproteinemia 2, familial hypobetalipoproteinemia type 2, hypobetalipoproteinemia caused by mutation in ANGPTL3, hypobetalipoproteinemia, familial, type 2, hypobetalipoproteinemia, familial, 2, hypolipidemia, familial, combined

0 clinical trials for this condition and its sub-types, 0 tagged with Familial hypobetalipoproteinemia 2 itself.

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