Search Ontology:
Human Disease

congenital mirror movement disorder

Term ID
DOID:0111153
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
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. (2)
References
  • ORDO:238722
Ontology
Human Disease   ( DOID:0111153 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models