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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 34
rare
Identifiers
MONDO:0032910
OMIM:618776
Causal genes
NDUFAF8
Part of
Mitochondrial complex I deficiency, nuclear type
Also known as
MC1DN34
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