All diseases

OMIM ID
128200
OMIM term:
EPISODIC KINESIGENIC DYSKINESIA 1; EKD1
Alternative terms:
PAROXYSMAL KINESIGENIC CHOREOATHETOSIS; PKC
PAROXYSMAL KINESIGENIC DYSKINESIA; PKD
DYSTONIA, FAMILIAL PAROXYSMAL
DYSTONIA 10; DYT10
(∗) Location:
16p11.2  
(†) Associated OMIM genes:
PRRT2  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/yhnfg14s