hemiplegia

Summary
Synonym
  • Infantile hemiplegia
  • Postnatal infantile hemiplegia
Definition
A central nervous system disease that is characterized by the complete paralysis of half of the body.
Super Class
central nervous system disease
External Links
Disease Ontology
DOID:10969
Mondo Disease Ontology
MeSH
UMLS
GARD
Related Genes
Displaying entries 11 - 20 of 37 in total
Gene ID Gene Symbol Description Source
2762 GMDS GDP-mannose 4,6-dehydratase
2876 GPX1 glutathione peroxidase 1
3251 HPRT1 hypoxanthine phosphoribosyltransferase 1
3417 IDH1 isocitrate dehydrogenase (NADP(+)) 1
3418 IDH2 isocitrate dehydrogenase (NADP(+)) 2
3425 IDUA alpha-L-iduronidase
4153 MBL2 mannose binding lectin 2
4360 MRC1 mannose receptor C-type 1
5160 PDHA1 pyruvate dehydrogenase E1 subunit alpha 1
5290 PIK3CA phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha

About Release Notes Help Feedback

Click here to visit the beta site.


International Collaboration

GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

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


Logo License Policies Site Map

Contact: support@glycosmos.org

This work is licensed under Creative Commons Attribution 4.0 International


GlyCosmos Portal v4.0.0

Last updated: August 19, 2024