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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
Lipoyl transferase 1 deficiency
rare
Identifiers
MONDO:0014576
OMIM:616299
Orphanet:401862
Causal genes
LIPT1
Part of
Inherited lipoic acid biosynthesis defect
Also known as
lipoyltransferase 1 deficiency · LIPT1D
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