acyl-CoA dehydrogenase 9 deficiency
Acyl-CoA dehydrogenase 9 (ACAD9) deficiency is a rare disorder leading to a deficiency of complex I of the respiratory chain and is characterized by neurological dysfunction, hepatic failure and cardiomyopathy
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Summary
acyl-CoA dehydrogenase 9 deficiency is a developmental defect during embryogenesis[1]. It is known by 3 alternative names across languages and contexts.[2]
Key Facts
- acyl-CoA dehydrogenase 9 deficiency's instance of is recorded as developmental defect during embryogenesis[3].
- acyl-CoA dehydrogenase 9 deficiency's instance of is recorded as rare disease[4].
- acyl-CoA dehydrogenase 9 deficiency's instance of is recorded as class of disease[5].
- acyl-CoA dehydrogenase 9 deficiency is a type of exercise intolerance with lactic acidosis[6].
- acyl-CoA dehydrogenase 9 deficiency is a type of mitochondrial disease with hypertrophic cardiomyopathy[7].
- acyl-CoA dehydrogenase 9 deficiency is a type of fatty acid oxidation and ketogenesis disorder with hypertrophic cardiomyopathy[8].
- acyl-CoA dehydrogenase 9 deficiency is a type of fatty acid oxidation and ketogenesis disorder with dilated cardiomyopathy[9].
- acyl-CoA dehydrogenase 9 deficiency's genetic association is recorded as ACAD9[10].
- acyl-CoA dehydrogenase 9 deficiency's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_99901[11].
Why It Matters
acyl-CoA dehydrogenase 9 deficiency is known by 3 alternative names across languages and contexts.[2]