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path(MESH:Thromboembolism)

Equivalencies: 0 | Classes: 0 | Children: 0 | Explore

Entity

Name
Thromboembolism
Namespace
MeSH
Namespace Version
20181007
Namespace URL
https://raw.githubusercontent.com/pharmacome/terminology/01c9daa61012b37dd0a1bc962521ba51a15b38f1/external/mesh-names.belns

Appears in Networks 1

Heme Curation v0.0.1-dev

Mechanistic knowledge surrounding heme

In-Edges 3

p(HGNC:EPO) positiveCorrelation path(MESH:Thromboembolism) View Subject | View Object

On the other hand, an abnormally high hematocrit is associated with thrombosis, and patients with polycythemia vera or taking erythropoietin are more susceptible to thrombosis and thromboembolism [4, 5]. PubMed:28458720

Appears in Networks:
Annotations
Text Location
Review

path(HP:"Congenital hemolytic anemia") positiveCorrelation path(MESH:Thromboembolism) View Subject | View Object

Patients with hereditary haemolytic anaemia due to RBC structural abnormalities have an increased risk of thromboembolic events, particularly in splenectomized patients (Stewart et al, 1996; Schilling et al, 2008). PubMed:25307023

Appears in Networks:
Annotations
Cell Ontology (CL)
erythrocyte
MeSH
Plasma
MeSH
Urine
MeSH
Anemia, Hemolytic, Autoimmune
Text Location
Review

path(MESH:Death) positiveCorrelation path(MESH:Thromboembolism) View Subject | View Object

Thromboembolism is the most common cause of death in PNH patients and accounts for 40–67% of deaths for which the cause is known. PubMed:25307023

Appears in Networks:
Annotations
Cell Ontology (CL)
macrophage
MeSH
Plasma
MeSH
Urine
MeSH
Hemoglobinuria, Paroxysmal
Text Location
Review

Out-Edges 3

path(MESH:Thromboembolism) positiveCorrelation path(MESH:Death) View Subject | View Object

Thromboembolism is the most common cause of death in PNH patients and accounts for 40–67% of deaths for which the cause is known. PubMed:25307023

Appears in Networks:
Annotations
Cell Ontology (CL)
macrophage
MeSH
Plasma
MeSH
Urine
MeSH
Hemoglobinuria, Paroxysmal
Text Location
Review

path(MESH:Thromboembolism) positiveCorrelation path(HP:"Congenital hemolytic anemia") View Subject | View Object

Patients with hereditary haemolytic anaemia due to RBC structural abnormalities have an increased risk of thromboembolic events, particularly in splenectomized patients (Stewart et al, 1996; Schilling et al, 2008). PubMed:25307023

Appears in Networks:
Annotations
Cell Ontology (CL)
erythrocyte
MeSH
Plasma
MeSH
Urine
MeSH
Anemia, Hemolytic, Autoimmune
Text Location
Review

path(MESH:Thromboembolism) positiveCorrelation p(HGNC:EPO) View Subject | View Object

On the other hand, an abnormally high hematocrit is associated with thrombosis, and patients with polycythemia vera or taking erythropoietin are more susceptible to thrombosis and thromboembolism [4, 5]. PubMed:28458720

Appears in Networks:
Annotations
Text Location
Review

About

BEL Commons is developed and maintained in an academic capacity by Charles Tapley Hoyt and Daniel Domingo-Fernández at the Fraunhofer SCAI Department of Bioinformatics with support from the IMI project, AETIONOMY. It is built on top of PyBEL, an open source project. Please feel free to contact us here to give us feedback or report any issues. Also, see our Publishing Notes and Data Protection information.

If you find BEL Commons useful in your work, please consider citing: Hoyt, C. T., Domingo-Fernández, D., & Hofmann-Apitius, M. (2018). BEL Commons: an environment for exploration and analysis of networks encoded in Biological Expression Language. Database, 2018(3), 1–11.