Atypical Hemolytic Uremic Syndrome

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

Entity

Name: Atypical Hemolytic Uremic Syndrome
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 1

bp(GO:"complement activation, alternative pathway") positiveCorrelation path(MESH:"Atypical Hemolytic Uremic Syndrome") View Subject | View Object

Atypical hemolytic uremic syndrome (aHUS) is characterized by an over activation of the complement alternative pathway (CAP) due to genetic and acquired abnormalities (Noris and Remuzzi, 2009). PubMed:24904418

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Heme Curation v0.0.1-dev

Annotations

Cell Ontology (CL): macrophage
MeSH: Liver
MeSH: Cerebral Hemorrhage
Text Location: Review

Out-Edges 1

path(MESH:"Atypical Hemolytic Uremic Syndrome") positiveCorrelation bp(GO:"complement activation, alternative pathway") View Subject | View Object

Appears in Networks:

Heme Curation v0.0.1-dev

Annotations

Cell Ontology (CL): macrophage
MeSH: Liver
MeSH: Cerebral Hemorrhage
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.