Familial idiopathic torsion dystonia

MONDO:0044816

An instance of idiopathic torsion dystonia that is caused by an inherited modification of the individual's genome.

Also known as: familial Idiopathic dystonia, hereditary idiopathic torsion dystonia, idiopathic familial dystonia, genetic torsion dystonia

13 clinical trials for this condition and its sub-types.

Follow this condition — get notified about new trials

Broader categories

Sort by