FDXR-related optic atrophy mitochondrial dysfunction syndrome

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
FDXR-related optic atrophy mitochondrial dysfunction syndrome
FDXR Unknown — ClinGen
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with FDXR-related optic atrophy mitochondrial dysfunction syndrome.
3 View disease cluster →
Auditory neuropathy with optic atrophy 1 shared geneFDXR Related via 1 shared gene including FDXR. Auditory neuropathy 1 shared geneFDXR Related via 1 shared gene including FDXR. Optic atrophy 1 shared geneFDXR Related via 1 shared gene including FDXR.