All diseases

OMIM ID
600996
OMIM term:
ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 2; ARVD2
Alternative terms:

(∗) Location:
1q43  
(†) Associated OMIM genes:
RYR2  
(‡) Associated MGI genes:
Ryr2  

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* quick link - http://q.sanger.ac.uk/jxdj42bn