All diseases

OMIM ID
610131
OMIM term:
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT, 4; PEOA4
Alternative terms:

(∗) Location:
17q23.3  
(†) Associated OMIM genes:
POLG2  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/du8z4ts5