Mirror movements 1

MONDO:0008002

Any familial congenital mirror movements in which the cause of the disease is a mutation in the DCC gene.

Also known as: DCC familial congenital mirror movements, familial congenital mirror movements caused by mutation in DCC, mirror movements 1, mirror movements type 1, MRMV1, bimanual synergia, mirror movements 1 and/Or agenesis of the corpus callosum, mirror movements, congenital

12 clinical trials for this condition and its sub-types, 0 tagged with Mirror movements 1 itself.

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Part of

↑ Mirror movements 1 and/or agenesis of the corpus callosum (0)

Including sub-types (12) Tagged with Mirror movements 1 (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.