All diseases

OMIM ID
602086
OMIM term:
ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 3; ARVD3
Alternative terms:

(∗) Location:
14q12-q22  
(†) Associated OMIM genes:
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/1o0z734p