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Familial hypobetalipoproteinemia 2
MONDO:0011505Any 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
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Disease
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Metabolic disease
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Inherited lipid metabolism disorder
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Hereditary disease
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Inborn errors of metabolism
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Human disease
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Disease of genetic or genomic mechanism
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Hypobetalipoproteinemia
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Hypolipoproteinemia
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