VLCAD deficiency Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
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)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:C536353
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Genes

1 genes/proteins associated with the disease VLCAD deficiency from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
ACADVL acyl-CoA dehydrogenase, very long chain 2.88009