|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||Recurrent episodes of brain dysfunction that may be triggered by factors such as metabolic disturbances or infections. (Human Phenotype Ontology, HP_0007335)|
|Downloads & Tools|
1 genes associated with the recurrent encephalopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
|CPT1A||carnitine palmitoyltransferase 1A (liver)|