All diseases

OMIM ID
311050
OMIM term:
OPTIC ATROPHY 2; OPA2
Alternative terms:
OPTIC ATROPHY, X-LINKED
OPTIC ATROPHY, NON-LEBER TYPE, WITH EARLY ONSET
(∗) Location:
Xp11.4-p11.21  
(†) Associated OMIM genes:
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/gda5g9wu