All diseases

OMIM ID
609286
OMIM term:
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT, 3; PEOA3
Alternative terms:

(∗) Location:
10q24.31  
(†) Associated OMIM genes:
C10ORF2  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/m2op86ym