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Collaborative Research
Diseases
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Mitochondrial disease
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Inborn mitochondrial metabolism disorder
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Mitochondrial oxidative phosphorylation disorder
Ataxia neuropathy spectrum
rare
Identifiers
MONDO:0016798
Orphanet:254818
Part of
Mitochondrial oxidative phosphorylation disorder
Subtypes
All diseases
Rare only
Disease
Rare
Not rare
Subtypes
Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis
MONDO:0011835
POLG
1
Recessive mitochondrial ataxia syndrome
MONDO:0019791
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