Laboratory for Molecular Diagnostics
Center for Nephrology and Metabolic Disorders

Apolipoprotein H deficiency

Apolipoprotein H deficiency is a disorder defined by absence of the protein from plasma. It was found in healthy probands. Despite its involvement in clotting, no increased risk of thromboembolic diseases seems to be associated with low values of the protein.

Systematic

Apolipoprotein deficiency
APOA5
APOB
APOC1
APOC2
APOC3
APOE
APOL1
APOM
Apolipoprotein A1 deficiency
Apolipoprotein A2 deficiency
Apolipoprotein F deficiency
Apolipoprotein H deficiency
APOH
CLU

References:

1.

Bancsi LF et al. (1992) Beta 2-glycoprotein I deficiency and the risk of thrombosis.

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2.

Haupt H et al. (1968) [On a hereditary beta-2-glycoprotein I deficiency].

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3.

Cleve H et al. (1969) Further family studies on the genetic control of beta 2-glycoprotein I concentration in human serum.

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Update: Sept. 26, 2018