Arthrogryposis multiplex congenita 1, neurogenic, with myelin defect

MONDO:0060486

Also known as: arthrogryposis multiplex congenita, neurogenic, with myelin defect, AMCNMY

1 clinical trial for this condition and its sub-types, 0 tagged with Arthrogryposis multiplex congenita 1, neurogenic, with myelin defect itself.

Where it sits in the disease tree

Part of

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