|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||A cessation of the development of a child in the areas of motor skills, speech and language, cognitive skills, and social and/or emotional skills, following the onset of epilepsy. (Human Phenotype Ontology, HP_0006834)|
|Downloads & Tools|
1 genes associated with the developmental stagnation at onset of seizures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
|ST3GAL5||ST3 beta-galactoside alpha-2,3-sialyltransferase 5|