Variants
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Familial apolipoprotein C-II deficiency

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Description

Clinically and biochemically, apoC-II deficiency closely simulates lipoprotein lipase deficiency, or hyperlipoproteinemia type I (238600), and is therefore referred to as hyperlipoproteinemia type IB.

OMIM

  • Mode of Inheritance

  • Autosomal recessive inheritance

VARIANTS

28

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Genes

External Links

  • OMIM

    207750

  • Orphanet

    309020

  • HPO
  • Medgen

    C1720779

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