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DO Term : episodic kinesigenic dyskinesia 2 [DOID:0090054] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A dystonia that is characterized by recurrent brief involuntary hyperkinesias triggered by sudden movements that has_material_basis_in autosomal dominant inheritance of variation in the chromosome region 16q13-q22.1.
  • synonyms:
  • ICD10CM:G24.8,
  • 611031,
  • ORDO:98809,
  • OMIM:611031,
  • MESH:C567026
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Disease

Diseases --> Human genes

Diseases --> Mouse genes

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Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents