Epilepsy Ontology
109 terms(s) returned
Term Type: | Record: 51 to 100 of 109 Records | Page: 2 of 3, First Previous Next Last | Show Records Per Page |
- idiopathic hemiconvulsion-hemiplegia syndrome
- idiopathic or cryptogenic familial epilepsy syndrome with identified loci/genes
- inborn errors of metabolism
- infantile epilepsy syndrome
- infectious disease with epilepsy
- infectious encephalitis
- inflammatory and autoimmune disease with epilepsy
- intracerebral hemorrhage
- low grade astrocytic tumor
- low grade glioma
- low-grade astrocytoma
- malignant glioma
- megalencephaly (disease)
- mental disorder
- mesial temporal lobe epilepsy with hippocampal sclerosis
- metastatic neoplasm
- mitochondrial disease
- motor stereotypies
- myoclonic encephalopathy in non-progressive disorder
- myoclonic epilepsy of infancy
- myoclonic-atonic epilepsy
- narcolepsy-cataplexy syndrome
- neonatal epilepsy syndrome
- neonatal/infantile epilepsy syndrome
- neoplasm (disease)
- neoplastic disease or syndrome
- nervous system neoplasm
- neurocutaneous syndrome
- neuroepithelial neoplasm
- new-onset refractory status epilepticus
- nodular neuronal heterotopia
- non-24-hour sleep-wake syndrome
- oligoastrocytic tumor
- oligoastrocytoma
- opsoclonus-myoclonus syndrome
- paraneoplastic neurologic syndrome
- paroxysmal dystonia
- partial epilepsy
- perceptual disorders
- photosensitive occipital lobe epilepsy
- post-traumatic epilepsy
- psychiatric disorder
- pyridoxine-dependent epilepsy
- rare neuroinflammatory or neuroimmunological disease
- rare paroxysmal movement disorder
- ring chromosome 14
- ring chromosome 20
- rolandic epilepsy
- secondary neoplasm
- seizures, benign familial infantile, 2