|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||A decreased concentration of total carnitine in the blood. (Human Phenotype Ontology, HP_0011936)|
|Downloads & Tools|
1 genes associated with the decreased plasma total carnitine phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
|CPT2||carnitine palmitoyltransferase 2|