All diseases

OMIM ID
118800
OMIM term:
PAROXYSMAL NONKINESIGENIC DYSKINESIA 1; PNKD1
Alternative terms:
PAROXYSMAL DYSTONIC CHOREOATHETOSIS; PDC
CHOREOATHETOSIS, FAMILIAL PAROXYSMAL; FPD1
MOUNT-REBACK SYNDROME
CHOREOATHETOSIS, NONKINESIGENIC
DYSTONIA 8; DYT8
(∗) Location:
2q35  
(†) Associated OMIM genes:
MYOFIBRILLOGENESIS REGULATOR 1  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/rkc5tw9r