Lipoyl transferase 1 deficiency
MONDO:0014576Also known as: LIPT1D, lipoyltransferase 1 deficiency
14 clinical trials for this condition and its sub-types.
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Disease
(717)
Metabolic disease
(241)
Inherited lipid metabolism disorder
(199)
Hereditary disease
(188)
Inborn mitochondrial metabolism disorder
(59)
Inborn errors of metabolism
(47)
Mitochondrial disease
(40)
Human disease
(15)
Developmental defect during embryogenesis
(8)
Inherited fatty acid metabolism disorder
(7)