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antithrombin deficiency
(phenotype)
Summary
General Info
Genetic Markers
Most Correlated Genes
Most Correlated SNPs
ATXN3
No SNPs found
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Pathway Enrichment
Most Correlated Biogroups
regulation of blood coagulation, intrinsic pathway
Antithrombin-III
Antithrombin serpin domain
protein localization to cytosolic proteasome complex involved in ERAD pathway
Machado-Joseph disease protein
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Curated Studies
Most Correlated Studies
Mouse Phenotypes - Blood coagulation disorders
OMIM - Thrombophilia
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Literature
Most Relevant Literature
Arterial thrombosis in homozygous antithrombin deficiency.
Perioperative management of a parturient with antithrombin deficiency and the role of thromboelastog…
Laboratory tests for antithrombin deficiency.
Compound heterozygosity involving Antithrombin Cambridge II (p.Ala416Ser) in antithrombin deficiency…
Neuraxial anesthesia for labor and cesarean delivery in a parturient with hereditary antithrombin de…
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Clinical Trials
Most Relevant Clinical Trials
Belgian Antithrombin Deficiency Registry
A Study of KW-3357 in Congenital Antithrombin Deficiency
Efficacy of Atenativ in Patients With Congenital Antithrombin Deficiency Undergoing Surgery or Deliv…
Recombinant Human Antithrombin (rhAT) in Patients With Hereditary Antithrombin Deficiency Undergoing…
Assess Incidence of Deep Vein Thrombosis(DVT)Following Administration of Recombinant Human Antithrom…
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