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MIRAGE
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
Disease Ontology
DOID:0050635
Mondo Disease Ontology
MeSH
ORDO
GARD
MGI genotype (from TogoID)
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
477 ATP1A2 ATPase Na+/K+ transporting subunit alpha 2
Displaying 1 entry
Gene ID Gene Symbol Description Source
232975 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide
Related Glycoprotein
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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

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Last updated: December 8, 2025