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DO Term : torsion dystonia 13 [DOID:0090037] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A dystonia that is characterized by focal or segmental dystonia with cranial, cervical, or upper limb involvement that has_material_basis_in autosomal dominant inheritance of variation in the chromosome region 1p36.32-p36.13.
  • synonyms:
  • ICD10CM:G24.1,
  • 607671,
  • ORDO:98807,
  • OMIM:607671
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