Laboratory for Molecular Diagnostics
Center for Nephrology and Metabolic Disorders
Moldiag Diseases Genes Support Contact

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.

external link
2.

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

external link
3.

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

external link
4.

OMIM.ORG article

Omim 138700 external link
Update: Aug. 14, 2020
Copyright © 2005-2021 by Center for Nephrology and Metabolic Disorders, Dr. Mato Nagel, MD
Albert-Schweitzer-Ring 32, D-02943 Weißwasser, Germany, Tel.: +49-3576-287922, Fax: +49-3576-287944
Sitemap | Webmail | Disclaimer | Privacy Issues | Website Credits