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Collaborative Research
Diseases
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Mitochondrial disease
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FDXR-related optic atrophy mitochondrial dysfunction syndrome
Optic atrophy-ataxia-peripheral neuropathy-global developmental delay syndrome
rare
Identifiers
MONDO:0034092
Orphanet:543470
Part of
FDXR-related optic atrophy mitochondrial dysfunction syndrome
Autosomal recessive disease
Hereditary peripheral neuropathy
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