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 31 - 40 of 89 in total
Gene ID Gene Symbol Description Source
2876 GPX1 glutathione peroxidase 1
2990 GUSB glucuronidase beta
3098 HK1 hexokinase 1
3251 HPRT1 hypoxanthine phosphoribosyltransferase 1
3419 IDH3A isocitrate dehydrogenase (NAD(+)) 3 catalytic subunit alpha
3423 IDS iduronate 2-sulfatase
3636 INPPL1 inositol polyphosphate phosphatase like 1
3897 L1CAM L1 cell adhesion molecule
4069 LYZ lysozyme
4099 MAG myelin associated glycoprotein
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