The association between TOR1A (Torsin Family 1 Member A) and Torsion Dystonia 1 is well established and manually curated, with its 3 contributing sources — 2 of them expert-curated — recording pathogenic and likely-pathogenic variants and a causative germline mutation.
Sources3
Clinical variants62
Symptoms11
Compounds0
Trials0
Publications21
01
At a glance
Association overview
A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.