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familial congenital mirror movements

Disease Summary
Associated Targets (3)
Tbio

2

Tchem

1


Explore Associated Targets
Mondo Description Congenital mirror movement disorder is a condition in which intentional movements of one side of the body are mirrored by involuntary movements of the other side. For example, when an affected individual makes a fist with the right hand, the left hand makes a similar movement. The mirror movements in this disorder primarily involve the upper limbs, especially the hands and fingers. This pattern of movements is present from infancy or early childhood and usually persists throughout life, without other associated signs and symptoms. Intelligence and lifespan are not affected.
Disease Ontology Description 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.
Mondo Term and Equivalent IDs
MONDO:0016558:  familial congenital mirror movements
DC:0000563: 
GARD:0012551: 
OMIMPS:157600: 
Orphanet:238722: 
SCTID:229247004: 
GWAS Targets (0)
No GWAS traits found
Target Novelty (Tin-x)