Mirror movements 2

MONDO:0013790

Any familial congenital mirror movements in which the cause of the disease is a mutation in the RAD51 gene.

Also known as: RAD51 familial congenital mirror movements, familial congenital mirror movements caused by mutation in RAD51, mirror movements 2, mirror movements type 2, MRMV2

12 clinical trials for this condition and its sub-types, 0 tagged with Mirror movements 2 itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Familial congenital mirror movements (3)

Including sub-types (12) Tagged with Mirror movements 2 (0)

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