decreased plasma carnitine Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A decreased concentration of carnitine in the blood. (Human Phenotype Ontology, HP_0003234)
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6 genes associated with the decreased plasma carnitine 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