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
  • GARD:12551
  • MIM:PS157600
  • ORDO:238722
  • SNOMEDCT_US_2025_09_01:784348007
  • UMLS_CUI:C5191311
Ontology
Human Disease   ( DOID:0111153 )
Relationships
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Genes Involved
Zebrafish Models