epileptic encephalopathy, early infantile, 15 Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A neonatoal period electroclinical syndrome that is characterized by tonic spasms and partial seizures. (Human Disease Ontology, DOID_0050709)
External Link http://www.omim.org/entry/615006
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Genes

1 genes associated with the epileptic encephalopathy, early infantile, 15 phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
ST3GAL3 ST3 beta-galactoside alpha-2,3-sialyltransferase 3