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 1 - 10 of 89 in total
Gene ID Gene Symbol Description Source
28 ABO ABO, alpha 1-3-N-acetylgalactosaminyltransferase and alpha 1-3-galactosyltransferase
43 ACHE acetylcholinesterase (Yt blood group)
142 PARP1 poly(ADP-ribose) polymerase 1
224 ALDH3A2 aldehyde dehydrogenase 3 family member A2
410 ARSA arylsulfatase A
477 ATP1A2 ATPase Na+/K+ transporting subunit alpha 2
684 BST2 bone marrow stromal cell antigen 2
912 CD1D CD1d molecule
1012 CDH13 cadherin 13
1116 CHI3L1 chitinase 3 like 1
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

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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