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Collaborative Research
Diseases
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Mitochondrial disease
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Inborn mitochondrial metabolism disorder
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Inborn mitochondrial myopathy
Mitochondrial myopathy, episodic, with optic atrophy and reversible leukoencephalopathy
rare
Identifiers
MONDO:0020714
OMIM:251900
Causal genes
FDX2
Part of
Fatal multiple mitochondrial dysfunctions syndrome
Inborn mitochondrial myopathy
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