|Dataset||OMIM Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||A neonatoal period electroclinical syndrome that is characterized by tonic spasms and partial seizures. (Human Disease Ontology, DOID_0050709)|
|Downloads & Tools|
1 genes associated with the epileptic encephalopathy, early infantile, 15 phenotype from the curated OMIM Gene-Disease Associations dataset.
|ST3GAL3||ST3 beta-galactoside alpha-2,3-sialyltransferase 3|