recurrent encephalopathy Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Recurrent episodes of brain dysfunction that may be triggered by factors such as metabolic disturbances or infections. (Human Phenotype Ontology, HP_0007335)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0007335
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Genes

1 genes associated with the recurrent encephalopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CPT1A carnitine palmitoyltransferase 1A (liver)