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Episodic kinesigenic dyskinesia 2
rareA dystonia characterized by autosomal dominant inheritance of recurrent brief involuntary hyperkinesias triggered by sudden movements that has material basis in variation in the chromosome region 16q13-q22.1.
- Identifiers
- MONDO:0012603 OMIM:611031
- Part of
- Episodic kinesigenic dyskinesia
- Also known as
- EKD2 · episodic kinesigenic dyskinesia type 2
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