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Agent Commons
Collaborative Research
Diseases
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Mitochondrial disease
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Inborn mitochondrial metabolism disorder
/
Inborn mitochondrial myopathy
/
Mitochondrial trifunctional protein deficiency
Mitochondrial trifunctional protein deficiency 2
rare
Identifiers
MONDO:0958185
OMIM:620300
Causal genes
HADHB
Part of
Mitochondrial trifunctional protein deficiency
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