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 21 - 30 of 89 in total
Gene ID Gene Symbol Description Source
1738 DLD dihydrolipoamide dehydrogenase
2026 ENO2 enolase 2
2220 FCN2 ficolin 2
2571 GAD1 glutamate decarboxylase 1
2572 GAD2 glutamate decarboxylase 2
2583 B4GALNT1 beta-1,4-N-acetyl-galactosaminyltransferase 1
2629 GBA1 glucosylceramidase beta 1
2639 GCDH glutaryl-CoA dehydrogenase
2752 GLUL glutamate-ammonia ligase
2821 GPI glucose-6-phosphate isomerase
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