Congenital hemolytic anemia

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

Entity

Name: Congenital hemolytic anemia
Namespace: HP
Namespace Version: 2017-10-05
Namespace URL: https://arty.scai.fraunhofer.de/artifactory/bel/namespace/hp/hp-20171108.belns

Appears in Networks 1

Heme Curation v0.0.1-dev

Mechanistic knowledge surrounding heme

In-Edges 1

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:

Heme Curation v0.0.1-dev

Annotations

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

Out-Edges 1

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

Appears in Networks:

Heme Curation v0.0.1-dev

Annotations

Cell Ontology (CL): erythrocyte
MeSH: Plasma
MeSH: Urine
MeSH: Anemia, Hemolytic, Autoimmune
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.