All diseases

OMIM ID
125250
OMIM term:
OPTIC ATROPHY WITH OR WITHOUT DEAFNESS, OPHTHALMOPLEGIA, MYOPATHY, ATAXIA, AND NEUROPATHY
Alternative terms:

(∗) Location:
3q29  
(†) Associated OMIM genes:
OPA1  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/ry6jecaa