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Summary Literature (0)
MIM:165300 - OPTIC ATROPHY 3, AUTOSOMAL DOMINANT; OPA3

Xenbase Genes: opa3

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0008133 - optic atrophy 3

Disease Ontology (DO):
DOID:0111433 - optic atrophy 3
DOID:5723 - optic atrophy