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Summary Literature (1)
DOID:679 - basal ganglia disease

Disease Ontology Definition:A brain disease that is characterized by dysfunctional movement, located_in basal ganglia that has_material_basis_in diseased components of the basal ganglia and associated neural circuits.

Synonyms:

Xenbase Genes : psen1, pdgfb, chmp2b, slc19a3, mapt, grn, slc20a2, xpr1, myorg, pdgfrb

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0003996 - basal ganglia disorder


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

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