| Dataset | OMIM Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | 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. (Orphanet Rare Disease Ontology, Orphanet_99901) |
| External Link | http://www.omim.org/entry/611126 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the acad9 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| ACAD9 | acyl-CoA dehydrogenase family, member 9 |
