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Human Disease

episodic kinesigenic dyskinesia 2

Term ID
DOID:0090054
Synonyms
Definition
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. https://ghr.nlm.nih.gov/condition/familial-paroxysmal-kinesigenic-dyskinesia
References
Ontology
Human Disease   ( DOID:0090054 )
Relationships
is a type of
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Genes Involved
Zebrafish Models