An inherited metabolic disease that is has its basis in the disruption of lipoate biosynthetic process.
Comprehensive, easy-to-understand information about this condition
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oxoglutaricaciduria
MONDO:0008759
multiple acyl-CoA dehydrogenase deficiency
MONDO:0009282
pyruvate dehydrogenase E3 deficiency
MONDO:0009529
inborn mitochondrial myopathy
MONDO:0009637
carnitine palmitoyl transferase 1A deficiency
MONDO:0009705
HSD10 mitochondrial disease
MONDO:0010327