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Summary Literature (0)
MIM:125250 - OPTIC ATROPHY WITH OR WITHOUT DEAFNESS, OPHTHALMOPLEGIA, MYOPATHY, ATAXIA, AND NEUROPATHY

Xenbase Genes: opa1

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0007429 - optic atrophy with or without deafness, ophthalmoplegia, myopathy, ataxia, and neuropathy
MONDO:0014720 - interlobar duct

Disease Ontology (DO):
DOID:0111340 - dominant optic atrophy plus syndrome