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FDXR-related optic atrophy mitochondrial dysfunction syndrome

MONDO:1060116

Any mitochondrial disorder in which the cause of the disease is a mutation in the FDXR gene.

Also known as: FDXR-related optic atrophy mitochondrial dysfunction syndrome

13 clinical trials for this condition and its sub-types, 0 tagged with FDXR-related optic atrophy mitochondrial dysfunction syndrome itself.

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