Familial hypobetalipoproteinemia 1

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

Also known as: hypobetalipoproteinemia, APOB hypobetalipoproteinemia, FHBL1, familial hypobetalipoproteinemia 1, familial hypobetalipoproteinemia type 1, hypobetalipoproteinemia caused by mutation in APOB, hypobetalipoproteinemia, familial, type 1, FHBL

1 clinical trial for this condition and its sub-types, 1 tagged with Familial hypobetalipoproteinemia 1 itself.