Mitochondrial complex I deficiency, nuclear type 16
MONDO:0032621Also known as: MC1DN16, MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 16
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)