FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term congenital mirror movement disorder ID (Ontology) DOID:0111153 (Human Disease)
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.
Also Known As "familial congenital controlateral synkinesia" ; "familial congenital mirror movements" ; "hereditary congenital controlateral synkinesia" (for all, see Synonyms field below)
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Spanning Tree (Parents/Children)
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disease
 |__physical disorder__
brain disease          |
 |__movement disease___|
                       congenital mirror movement disorder  6 rec.
                        |__mirror movements 1 2 rec.
                        |__mirror movements 2 1 rec.
                        |__mirror movements 3 1 rec.
                        |__mirror movements 4 2 rec.
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Is a physical disorder
movement disease
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Synonyms
  • "familial congenital controlateral synkinesia" EXACT
    "familial congenital mirror movements" EXACT
    "hereditary congenital controlateral synkinesia" EXACT
    "hereditary congenital mirror movements" EXACT
    "isolated congenital controlateral synkinesia" EXACT
    "isolated congenital mirror movements" EXACT
Secondary IDs
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GARD:12551
MIM:PS157600
ORDO:238722
UMLS_CUI:C5191311