DO_rare_slim has material basis in autosomal dominant disease torsion dystonia 4 disease_ontology ORDO:98805 DOID:0090041 ICD10CM:G24.1 MIM:128101 A dystonia that is characterized by progressive laryngeal and cervical dystonia (onset in the second to third decade of life) followed by involvement of other muscles, such as the neck or limbs that has_material_basis_in autosomal dominant inheritance of heterozygous mutation in the tubulin beta 4A class IVa (TUBB4A) gene on chromosome 19p13. dystonia autosomal dominant inheritance