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Summary Literature (0)
MIM:165500 - OPTIC ATROPHY 1; OPA1

Xenbase Genes: opa1

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0008134 - autosomal dominant optic atrophy, classic form

Disease Ontology (DO):
DOID:0111441 - optic atrophy 1
DOID:5723 - optic atrophy