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Summary Literature (2)
DOID:480 - movement disease

Disease Ontology Definition:A brain disease that is characterized by a clinical syndrome of either hyperkinetic movement or hyperkinetic movement unrelated to weakness or spasticity.

Synonyms:

Xenbase Genes : gnal, nkx2-1, hpca, sgce, fus, dcc, dnal4, gnao1, kcnma1, slc18a2, prkra, tor1a, tubb4a, pnkd, taf1, [+]

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0005395 - movement disorder


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

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