| 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 |
| Similar Terms | |
| Downloads & Tools |
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 |
