|Dataset||CTD Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||Very long-chain acyl-CoA dehydrogenase (VLCAD) deficiency (VLCADD) is an inherited disorder of mitochondrial long-chain fatty acid oxidation with a variable presentation including: cardiomyopathy, hypoketotic hypoglycemia, liver disease, exercise intolerance and rhabdomyolysis. (Orphanet Rare Disease Ontology, Orphanet_26793)|
|Downloads & Tools|
1 genes/proteins associated with the disease VLCAD deficiency from the curated CTD Gene-Disease Associations dataset.
|ACADVL||acyl-CoA dehydrogenase, very long chain||2.88009|