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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
![Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries](img/icons/info1.png)
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)