dystonia

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Summary

Literature (0)

DOID:543 - dystonia

Disease Ontology Definition:A movement disease that is characterized by involuntary muscle contractions causing repetitive or twisting movements.

Synonyms: dystonic disease

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: gnal, hpca, sgce, kcnma1, prkra, tor1a, tubb4a, pnkd, taf1, gch1, spr, drd5, atp1a3, col6a3, drd2, [+]

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0003441 - forelimb nerve

MONDO:0003441 - forelimb nerve

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): movement disease (is_a)