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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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Inherited lipoic acid biosynthesis defect
/
Fatal multiple mitochondrial dysfunctions syndrome
Multiple mitochondrial dysfunctions syndrome 10
rare
Identifiers
MONDO:0975806
OMIM:620960
Causal genes
CIAO1
Part of
Fatal multiple mitochondrial dysfunctions syndrome
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