All diseases

OMIM ID
165300
OMIM term:
OPTIC ATROPHY 3, AUTOSOMAL DOMINANT
Alternative terms:
OPA3, AUTOSOMAL DOMINANT
OPTIC ATROPHY AND CATARACT, AUTOSOMAL DOMINANT
(∗) Location:
19q13.32  
(†) Associated OMIM genes:
OPA3  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/ciqz2e23