Lipoyl transferase 1 deficiency
MONDO:0014576Also known as: LIPT1D, lipoyltransferase 1 deficiency
50 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsBroader categories
Disease
(618)
Metabolic disease
(215)
Hereditary disease
(172)
Inherited lipid metabolism disorder
(165)
Inborn mitochondrial metabolism disorder
(57)
Inborn errors of metabolism
(42)
Mitochondrial disease
(39)
Human disease
(14)
Developmental defect during embryogenesis
(7)
Inherited fatty acid metabolism disorder
(6)