Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (0)
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

MIM:
MIM:104290 - ALTERNATING HEMIPLEGIA OF CHILDHOOD 1; AHC1
MIM:614820 - ALTERNATING HEMIPLEGIA OF CHILDHOOD 2; AHC2

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

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