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acyl-CoA dehydrogenase family member type 9 (ACAD9) deficiency
Genetics:
- associated with defects in ACAD9
Clinical manifestations:
- episodic liver dysfunction during otherwise mild illnesses
- cardiomyopathy, along with chronic neurologic dysfunction
General
inborn error of metabolism
Database Correlations
OMIM 611126
References
OMIM :accession 611126