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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 17
rare
Identifiers
MONDO:0032622
OMIM:618239
Causal genes
NDUFAF6
Part of
Mitochondrial complex I deficiency, nuclear type
Also known as
MC1DN17
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