All diseases

OMIM ID
611528
OMIM term:
ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 12; ARVD12
Alternative terms:

(∗) Location:
17q21.2  
(†) Associated OMIM genes:
JUP  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/ut8fos6k