About: episodic kinesigenic dyskinesia 1

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An Entity of Type : owl:Class, within Data Space : linkeddata.uriburner.com:28898 associated with source document(s)

Attributes	Values
type	Class
subClassOf	autosomal dominant disease dystonia nodeID://b50942170
label	episodic kinesigenic dyskinesia 1
described by	https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl
id	DOID:0090053
database_cross_reference	GARD:8721 ICD10CM:G24.8 OMIM:128200 ORDO:98809
has_exact_synonym	Paroxysmal kinesigenic choreoathetosis (en)
has_obo_namespace	disease_ontology
http://purl.obolib...g/obo/IAO_0000115	A dystonia characterized by recurrent brief involuntary hyperkinesias triggered by sudden movements that has_material_basis_in autosomal dominant inheritance of heterozygous mutation in the proline-rich transmembrane protein 2 gene (PRRT2) on chromosome 16p11.
is topic of	Human Disease Ontology
is annotatedSource of	nodeID://b50942171

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