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.
Apolipoprotein deficiency | ||||
APOA5 | ||||
APOB | ||||
APOC1 | ||||
APOC2 | ||||
APOC3 | ||||
APOE | ||||
APOL1 | ||||
APOM | ||||
Apolipoprotein A1 deficiency | ||||
Apolipoprotein A2 deficiency | ||||
Apolipoprotein F deficiency | ||||
Apolipoprotein H deficiency | ||||
APOH | ||||
CLU | ||||
1. |
Bancsi LF et al. (1992) Beta 2-glycoprotein I deficiency and the risk of thrombosis. |
2. |
Haupt H et al. (1968) [On a hereditary beta-2-glycoprotein I deficiency]. |
3. |
Cleve H et al. (1969) Further family studies on the genetic control of beta 2-glycoprotein I concentration in human serum. |
4. |
OMIM.ORG article Omim 138700 |