All diseases

OMIM ID
610193
OMIM term:
ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 10; ARVD10
Alternative terms:

(∗) Location:
18q12.1  
(†) Associated OMIM genes:
DSG2  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/pue22qxu