Mitochondrial myopathy, episodic, with optic atrophy and reversible leukoencephalopathy

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Subtype of: Mitochondrial myopathy
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Mitochondrial myopathy, episodic, with optic atrophy and reversible leukoencephalopathy
MONDO_0009637
FDX2 Unknown
34905296 30010796 24281368 28803783
Open Targets
All1 Causal0 Unknown1
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Mitochondrial myopathy 1 shared geneFDX2 Related via 1 shared gene including FDX2. Systemic lupus erythematosus 1 shared geneFDX2 Related via 1 shared gene including FDX2. Psoriasis 1 shared geneFDX2 Related via 1 shared gene including FDX2.