Acyl-CoA dehydrogenase 9 deficiency
MONDO:0012624A rare disorder leading to a deficiency of complex I of the respiratory chain and is characterized by neurological dysfunction, hepatic failure and cardiomyopathy.
Also known as: ACAD9 deficiency, acyl-CoA dehydrogenase 9 deficiency, mitochondrial complex I deficiency due to ACAD9 deficiency, mitochondrial complex I deficiency, nuclear type 20
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Disease
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Metabolic disease
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Inherited lipid metabolism disorder
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Hereditary disease
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Inborn errors of metabolism
(45)
Human disease
(14)
Inherited fatty acid metabolism disorder
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Disorder of fatty acid and ketone body metabolism
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Disease of genetic or genomic mechanism
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Disorder of fatty acid oxidation and ketogenesis
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