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Summary Literature (0)
MIM:610708 - OPTIC ATROPHY 5; OPA5

Xenbase Genes: dnm1l

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0008134 - autosomal dominant optic atrophy, classic form
MONDO:0012543 - optic atrophy 5

Disease Ontology (DO):
DOID:0111438 - optic atrophy 5