alternating hemiplegia of childhood

Summary
Synonym
  • AHC
Definition
A hemiplegia characterized by recurrent episodes of temporary weakness or complete paralysis on one or both sides of the body.
Super Class
hemiplegia
External Links
Disease Ontology
DOID:0050635
Mondo Disease Ontology
MeSH
ORDO
OMIM
GARD
MGI genotype (from TogoID)
Related Genes
Displaying entries 61 - 70 of 89 in total
Gene ID Gene Symbol Description Source
6785 ELOVL4 ELOVL fatty acid elongase 4
7167 TPI1 triosephosphate isomerase 1
7903 ST8SIA4 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 4
8398 PLA2G6 phospholipase A2 group VI
8399 PLA2G10 phospholipase A2 group X
8482 SEMA7A semaphorin 7A (JohnMiltonHagen blood group)
8560 DEGS1 delta 4-desaturase, sphingolipid 1
8803 SUCLA2 succinate-CoA ligase ADP-forming subunit beta
9254 CACNA2D2 calcium voltage-gated channel auxiliary subunit alpha2delta 2
9365 KL klotho
Displaying all 2 entries
Gene ID Gene Symbol Description Source
98660 Atp1a2 ATPase, Na+/K+ transporting, alpha 2 polypeptide
232975 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide
Displaying 1 entry
Gene ID Gene Symbol Description Source
24212 Atp1a2 ATPase Na+/K+ transporting subunit alpha 2
Related Glycoprotein
Displaying entry 71 - 71 of 71 in total
UniProt ID Protein Name Source
Q9Y286 Sialic acid-binding Ig-like lectin 7

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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: August 19, 2024