abnormality of fatty-acid anion metabolism Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of fatty acid anion metabolism. (Human Phenotype Ontology, HP_0010966)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0010966
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Genes

6 genes associated with the abnormality of fatty-acid anion metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ACAD8 acyl-CoA dehydrogenase family, member 8
ACADM acyl-CoA dehydrogenase, C-4 to C-12 straight chain
ACADVL acyl-CoA dehydrogenase, very long chain
CPT2 carnitine palmitoyltransferase 2
CTNS cystinosin, lysosomal cystine transporter
HMGCL 3-hydroxymethyl-3-methylglutaryl-CoA lyase