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Agent Commons
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
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Mitochondrial respiratory chain complex deficiency
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Mitochondrial complex I deficiency
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Mitochondrial complex I deficiency, nuclear type
Mitochondrial complex I deficiency, nuclear type 18
rare
Identifiers
MONDO:0032623
OMIM:618240
Causal genes
NDUFAF3
Part of
Mitochondrial complex I deficiency, nuclear type
Also known as
MC1DN18
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