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Summary Literature (2)
DOID:0050635 - alternating hemiplegia of childhood

Disease Ontology Definition:A hemiplegia characterized by recurrent episodes of temporary weakness or complete paralysis on one or both sides of the body.

Synonyms: AHC,

Xenbase Genes : atp1a3, atp1a2

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0016241 - alternating hemiplegia of childhood


Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): hemiplegia (is_a)