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mirror movements 1

Disease Summary
Associated Targets (1)
Tbio

1


Mondo Description Any familial congenital mirror movements in which the cause of the disease is a mutation in the DCC gene.
Uniprot Description A disorder characterized by contralateral involuntary movements that mirror voluntary ones. While mirror movements are occasionally found in young children, persistence beyond the age of 10 is abnormal. Mirror movements occur more commonly in the upper extremities. Some MRMV1 patients have agenesis of the corpus callosum.
Mondo Term and Equivalent IDs
MONDO:0008002:  mirror movements 1