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Summary Literature (2)
DOID:10969 - hemiplegia

Disease Ontology Definition:A central nervous system disease that is characterized by the complete paralysis of half of the body.

Synonyms: Infantile hemiplegia, Postnatal infantile hemiplegia,

Xenbase Genes : atp1a3, atp1a2

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0001170 - hemiplegia


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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): central nervous system disease (is_a)