| Dataset | HPO Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | EEG discharges recorded in particular areas of the A localized (focal) abnormality in cerebral electrical activity recorded along the scalp by electroencephalography (EEG). (Human Phenotype Ontology, HP_0011185) |
| External Link | http://compbio.charite.de/hpoweb/showterm?id=HP:0011185 |
| Similar Terms | |
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1 genes associated with the eeg with focal epileptiform discharges phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| GRIN2A | glutamate receptor, ionotropic, N-methyl D-aspartate 2A |
