cardiovascular system disease

Summary
Synonym
  • disease of subdivision of hemolymphoid system
Definition
A disease of anatomical entity which occurs in the blood, heart, blood vessels or the lymphatic system that passes nutrients (such as amino acids and electrolytes), gases, hormones, blood cells or lymph to and from cells in the body to help fight diseases and help stabilize body temperature and pH to maintain homeostasis.
Super Class
disease of anatomical entity
Disease Ontology
DOID:1287
Mondo Disease Ontology
MeSH
UMLS
NCI Thesaurus
WikiPathways (from TogoID)
Related Genes
Displaying entries 1 - 10 of 16 in total
Gene ID Gene Symbol Description Source
177 AGER advanced glycosylation end-product specific receptor
2244 FGB fibrinogen beta chain
2696 GIPR gastric inhibitory polypeptide receptor
2876 GPX1 glutathione peroxidase 1
2997 GYS1 glycogen synthase 1
3075 CFH complement factor H
4353 MPO myeloperoxidase
5167 ENPP1 ectonucleotide pyrophosphatase/phosphodiesterase 1
5468 PPARG peroxisome proliferator activated receptor gamma
5743 PTGS2 prostaglandin-endoperoxide synthase 2
Displaying 1 entry
Gene ID Gene Symbol Description Source
178014 enpl-1 Endoplasmin homolog

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: April 7, 2025