Mitochondrial complex I deficiency, mitochondrial type 1
MONDO:0027068Any mitochondrial complex I deficiency, mitochondrial type, in which the cause of the disease is a mutation in the MTND3 gene.
Also known as: MC1DM1, mitochondrial complex I deficiency, mitochondrial type 1
40 clinical trials for this condition and its sub-types.
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Disease
(618)
Metabolic disease
(215)
Hereditary disease
(172)
Inborn mitochondrial metabolism disorder
(57)
Inborn errors of metabolism
(42)
Mitochondrial disease
(39)
Human disease
(14)
Developmental defect during embryogenesis
(7)
Mitochondrial respiratory chain complex deficiency
(4)
Mitochondrial oxidative phosphorylation disorder
(3)