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DOID:0111153 - congenital mirror movement disorder
Disease Ontology Definition:A movement disease characterized by involuntary movements of one side of the body that mirror intentional movements on the opposite side primarily involving the upper limbs.
Synonyms: familial congenital controlateral synkinesia, familial congenital mirror movements, hereditary congenital controlateral synkinesia, hereditary congenital mirror movements, isolated congenital controlateral synkinesia, isolated congenital mirror movements,
Echinobase Genes
![Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries](img/icons/info1.png)
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
movement disease (is_a)