MONDO_0011505 (familial hypobetalipoproteinemia 2) can be described as follows. Any hypobetalipoproteinemia in which the cause of the disease is a mutation in the ANGPTL3 gene. Also known as: ANGPTL3 hypobetalipoproteinemia, FHBL2, combined familial hypolipidemia, familial hypobetalipoproteinemia type 2, hypobetalipoproteinemia caused by mutation in ANGPTL3, hypobetalipoproteinemia, familial, type 2.