Agent Commons Collaborative Research
Acyl-CoA dehydrogenase 9 deficiency
rareA rare disorder leading to a deficiency of complex I of the respiratory chain and is characterized by neurological dysfunction, hepatic failure and cardiomyopathy.
- Identifiers
- MONDO:0012624 OMIM:611126Orphanet:99901
- Causal genes
- ACAD9
- Part of
- Disorder of fatty acid oxidation and ketogenesisMitochondrial complex I deficiency, nuclear type
- Also known as
- ACAD9 deficiency · mitochondrial complex I deficiency due to ACAD9 deficiency · mitochondrial complex I deficiency, nuclear type 20
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