TOR1A, torsin family 1 member A, 1861

N. diseases: 115; N. variants: 14
Disease: Tardive Dyskinesia ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0686347
Disease: Tardive Dyskinesia
Tardive Dyskinesia 		0.010 GeneticVariation disease BEFREE Our findings indicate that clinical diagnostic criteria that include historical information to detect tardive dystonia and perinatal asphyxia discriminate primary dystonia due to the DYT1 founder mutation. 9191768 1997