All diseases

OMIM ID
165500
OMIM term:
OPTIC ATROPHY 1; OPA1
Alternative terms:
OPTIC ATROPHY, JUVENILE
KJER-TYPE OPTIC ATROPHY
OPTIC ATROPHY, KJER TYPE; OAK
(∗) Location:
3q29  
(†) Associated OMIM genes:
OPA1  
(‡) Associated MGI genes:
Opa1   Rpl24  

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* quick link - http://q.sanger.ac.uk/4xnebjnk