DO_rare_slim has material basis in autosomal dominant disease generalized dystonia torsion dystonia 6 disease_ontology ICD10CM:G24.1 ORDO:98806 A generalized dystonia that is characterized by early-onset generalised dystonia typically involing the craniocervical region with spasmodic dysphonia that has_material_basis_in autosomal dominant inheritance of heterozygous mutation in the THAP domain containing 1 gene (THAP1) on chromosome 8p11. MIM:602629 DOID:0090039 autosomal dominant inheritance