FDXR-related optic atrophy mitochondrial dysfunction syndrome

rare

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

Subtypes

Disease	ID	Subtypes
Auditory neuropathy-optic atrophy syndrome	MONDO:0060582
Multiple mitochondrial dysfunctions syndrome 9b	MONDO:0971174
Optic atrophy-ataxia-peripheral neuropathy-global developmental delay syndrome	MONDO:0034092

Rare disease

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