1 Child Term
| Identifier | Name | Description |
|---|---|---|
| DOID:0111292 | idiopathic generalized epilepsy 10 | An idiopathic generalized epilepsy that has_material_basis_in variation in the GABRD on chromosome 1p36.33. |
1 Parent Term
| Identifier | Name | Description |
|---|---|---|
| DOID:1826 | epilepsy | A brain disease that is characterized by the occurrance of at least two unprovoked seizures resulting from a persistent epileptogenic abnormality of the brain that is able to spontaneously generate paroxysmal activity and typically manifested by sudden brief episodes of altered or diminished consciousness, involuntary movements, or convulsions. |
