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Disease Ontology Browser
congenital mirror movement disorder (DOID:0111153)
Alliance: disease page
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
Alt IDs: ORDO:238722
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.

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
12/17/2024
MGI 6.24 		The Jackson Laboratory