Mitochondrial complex I deficiency, nuclear type
MONDO:0100223Any mitochondrial complex I deficiency in which the cause of the disease is a mutation in the nuclear-encoded genes that encode structural subunits or assembly factors of complex I.
40 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsSub-types
Leber hereditary optic neuropathy, autosomal recessive
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Leber-like hereditary optic neuropathy, autosomal recessive 1
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Leber-like hereditary optic neuropathy, autosomal recessive 2
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Mitochondrial complex I deficiency, nuclear type 1
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Mitochondrial complex I deficiency, nuclear type 10
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Mitochondrial complex I deficiency, nuclear type 11
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Mitochondrial complex I deficiency, nuclear type 12
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Mitochondrial complex I deficiency, nuclear type 13
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Mitochondrial complex I deficiency, nuclear type 14
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Mitochondrial complex I deficiency, nuclear type 15
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Mitochondrial complex I deficiency, nuclear type 16
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Mitochondrial complex I deficiency, nuclear type 17
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Mitochondrial complex I deficiency, nuclear type 18
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Mitochondrial complex I deficiency, nuclear type 19
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Mitochondrial complex I deficiency, nuclear type 2
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Mitochondrial complex I deficiency, nuclear type 21
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Mitochondrial complex I deficiency, nuclear type 22
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Mitochondrial complex I deficiency, nuclear type 23
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Mitochondrial complex I deficiency, nuclear type 24
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Mitochondrial complex I deficiency, nuclear type 25
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Broader categories
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)