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Mitochondrial complex IV deficiency, nuclear type 17
MONDO:0033652Any mitochondrial complex IV deficiency in which the cause of the disease is a mutation in the COA8 gene.
Also known as: MC4DN17, mitochondrial complex IV deficiency, nuclear type 17
40 clinical trials for this condition and its sub-types.
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Disease
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Metabolic disease
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Hereditary disease
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Inborn mitochondrial metabolism disorder
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Inborn errors of metabolism
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Mitochondrial disease
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Human disease
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Developmental defect during embryogenesis
(7)
Mitochondrial respiratory chain complex deficiency
(4)
Mitochondrial oxidative phosphorylation disorder
(3)