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DO Term : torsion dystonia 1 [DOID:0060730] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A generalized dystomia characterized by autosomal dominant inheritance of dystonia usually presenting initially as focal, typically in the limbs, but often generalizes with age that has_material_basis_in heterozygous mutation in the TOR1A gene on chromosome 9q34.
  • synonyms:
  • ORDO:256,
  • ICD10CM:G24.1,
  • 128100,
  • OMIM:128100,
  • dystonia musculorum deformans
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Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents