Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
An epileptic seizure originating at some point within, and rapidly engaging, bilaterally distributed hemispheric networks. |
Is a |
False |
Seizure |
Inferred relationship |
Some |
|
anfald, ikke fastslået om fokalt eller generaliseret |
Is a |
False |
Seizure |
Inferred relationship |
Some |
|
Partielt anfald med nedsat bevidsthed |
Is a |
False |
Seizure |
Inferred relationship |
Some |
|
Musicogenic seizure |
Is a |
True |
Seizure |
Inferred relationship |
Some |
|
Alcohol-related fit |
Is a |
True |
Seizure |
Inferred relationship |
Some |
|
Stress seizure (finding) |
Is a |
True |
Seizure |
Inferred relationship |
Some |
|
Partielt anfald ved bevægelse |
Is a |
False |
Seizure |
Inferred relationship |
Some |
|
Post-ictal state |
Is a |
False |
Seizure |
Inferred relationship |
Some |
|
Akinetisk anfald uden atoni |
Is a |
False |
Seizure |
Inferred relationship |
Some |
|
Febrile convulsion |
Is a |
True |
Seizure |
Inferred relationship |
Some |
|
Anoxic seizure |
Is a |
True |
Seizure |
Inferred relationship |
Some |
|
anfald ved ophør af indtagelse af afhængighedsskabende stof |
Is a |
False |
Seizure |
Inferred relationship |
Some |
|
Partielt anfald med illusioner og hallucinationer |
Is a |
False |
Seizure |
Inferred relationship |
Some |
|
Postseizure confusion |
Is a |
False |
Seizure |
Inferred relationship |
Some |
|
Raised convulsive threshold |
Is a |
False |
Seizure |
Inferred relationship |
Some |
|
Uremic convulsion |
Is a |
True |
Seizure |
Inferred relationship |
Some |
|
Postseizure delirium |
Is a |
False |
Seizure |
Inferred relationship |
Some |
|
Startle partial seizure |
Is a |
True |
Seizure |
Inferred relationship |
Some |
|
Epileptisk aura |
Is a |
False |
Seizure |
Inferred relationship |
Some |
|
Central convulsion |
Is a |
True |
Seizure |
Inferred relationship |
Some |
|
Kortvarigt atonisk anfald |
Is a |
False |
Seizure |
Inferred relationship |
Some |
|
Pattern sensitive seizure |
Is a |
True |
Seizure |
Inferred relationship |
Some |
|
partielt anfald med multiple symptomer |
Is a |
False |
Seizure |
Inferred relationship |
Some |
|
Todd's paresis |
Is a |
True |
Seizure |
Inferred relationship |
Some |
|
Tetanic convulsion |
Is a |
True |
Seizure |
Inferred relationship |
Some |
|
Epileptic cry |
Is a |
True |
Seizure |
Inferred relationship |
Some |
|
Idémæssigt partielt anfald |
Is a |
False |
Seizure |
Inferred relationship |
Some |
|
Reading seizure |
Is a |
True |
Seizure |
Inferred relationship |
Some |
|
Generalized convulsion |
Is a |
False |
Seizure |
Inferred relationship |
Some |
|
Abdominalt anfald |
Is a |
False |
Seizure |
Inferred relationship |
Some |
|
Langvarigt atonisk anfald |
Is a |
False |
Seizure |
Inferred relationship |
Some |
|
Convulsion threshold |
Is a |
False |
Seizure |
Inferred relationship |
Some |
|
Puerperal convulsion |
Is a |
True |
Seizure |
Inferred relationship |
Some |
|
Havde et anfald |
Is a |
False |
Seizure |
Inferred relationship |
Some |
|
A transient occurrence of signs and/or symptoms due to abnormal excessive or synchronous neuronal activity in the brain, regardless of whether focal, generalized, or unknown onset, whether aware or impaired awareness, and whether motor or nonmotor. |
Is a |
True |
Seizure |
Inferred relationship |
Some |
|
Partial seizure |
Is a |
False |
Seizure |
Inferred relationship |
Some |
|
objektivt: anfald/krampe |
Associated finding |
False |
Seizure |
Inferred relationship |
Some |
1 |
objektivt: petit mal-anfald |
Associated finding |
False |
Seizure |
Inferred relationship |
Some |
|
objektivt: psykomotorisk anfald |
Associated finding |
False |
Seizure |
Inferred relationship |
Some |
|
objektivt: salaamanfald |
Associated finding |
False |
Seizure |
Inferred relationship |
Some |
|
objektivt: fokalt (Jackson-) anfald |
Associated finding |
False |
Seizure |
Inferred relationship |
Some |
1 |
On examination - fit/convulsion NOS |
Associated finding |
False |
Seizure |
Inferred relationship |
Some |
1 |
Post-ictal coma |
Temporally follows |
False |
Seizure |
Inferred relationship |
Some |
|
Seizure management |
Has focus |
True |
Seizure |
Inferred relationship |
Some |
1 |
Seizure precautions |
Has focus |
True |
Seizure |
Inferred relationship |
Some |
1 |
A type of epilepsy that presents with myoclonic epileptic seizures between 4 months and 3 years of age, in an otherwise normal infant. The myoclonic epileptic seizures may be activated by sudden noise, startle, or touch, and less commonly by photic stimulation. The electroencephalogram must capture generalised epileptiform discharges or myoclonic epileptic seizures and have a normal background. |
Has definitional manifestation |
False |
Seizure |
Inferred relationship |
Some |
|
A type of focal epilepsy where all the seizures originate within the temporal lobe. |
Has definitional manifestation |
False |
Seizure |
Inferred relationship |
Some |
|
A type of focal epilepsy where all the seizures originate within the mesiobasal limbic area of the temporal lobe. |
Has definitional manifestation |
False |
Seizure |
Inferred relationship |
Some |
|
Kohlschutter's syndrome |
Has definitional manifestation |
False |
Seizure |
Inferred relationship |
Some |
|
Rasmussen syndrome |
Has definitional manifestation |
False |
Seizure |
Inferred relationship |
Some |
|
Post-anoxic myoclonus |
Has definitional manifestation |
False |
Seizure |
Inferred relationship |
Some |
|
A type of epilepsy with only focal onset epileptic seizures. Seizures can arise from a single location or multiple locations. |
Has definitional manifestation |
False |
Seizure |
Inferred relationship |
Some |
|
Primary inherited reading epilepsy |
Has definitional manifestation |
False |
Seizure |
Inferred relationship |
Some |
|
lokalisationsrelateret symptomgivende epilepsi |
Has definitional manifestation |
False |
Seizure |
Inferred relationship |
Some |
|
A type of focal epilepsy where all the seizures originate within the amygdalo-hippocampal area of the temporal lobe. |
Has definitional manifestation |
False |
Seizure |
Inferred relationship |
Some |
|
rinencefal epilepsi |
Has definitional manifestation |
False |
Seizure |
Inferred relationship |
Some |
|
A type of focal epilepsy where all the seizures originate within the lateral area of the temporal lobe. |
Has definitional manifestation |
False |
Seizure |
Inferred relationship |
Some |
|
A type of focal epilepsy where all the seizures originate within the frontal lobe. |
Has definitional manifestation |
False |
Seizure |
Inferred relationship |
Some |
|
A type of focal epilepsy where all the seizures originate within the supplementary motor cortex area of the frontal lobe. |
Has definitional manifestation |
False |
Seizure |
Inferred relationship |
Some |
|
A type of focal epilepsy where all the seizures originate within the cingulate area of the frontal lobe. |
Has definitional manifestation |
False |
Seizure |
Inferred relationship |
Some |
|
A type of focal epilepsy where all the seizures originate within the anterior frontopolar area of the frontal lobe. |
Has definitional manifestation |
False |
Seizure |
Inferred relationship |
Some |
|
A type of focal epilepsy where all the seizures originate within the orbitofrontal area of the frontal lobe. |
Has definitional manifestation |
False |
Seizure |
Inferred relationship |
Some |
|
A type of focal epilepsy where all the seizures originate within the dorsolateral area of the frontal lobe. |
Has definitional manifestation |
False |
Seizure |
Inferred relationship |
Some |
|
A type of focal epilepsy where all the seizures originate within the opercular area of the frontal lobe. |
Has definitional manifestation |
False |
Seizure |
Inferred relationship |
Some |
|
ikke-progressiv kontinuerlig partiel epilepsi |
Has definitional manifestation |
False |
Seizure |
Inferred relationship |
Some |
|
A type of focal epilepsy where all the seizures originate within the parietal lobe. |
Has definitional manifestation |
False |
Seizure |
Inferred relationship |
Some |
|
Occipital lobe epilepsy |
Has definitional manifestation |
False |
Seizure |
Inferred relationship |
Some |
|
lokalisationsrelateret symptomgivende epilepsi med specifik præcipiterende faktor |
Has definitional manifestation |
False |
Seizure |
Inferred relationship |
Some |
|
Hemiplegia-hemiconvulsion-epilepsy syndrome |
Has definitional manifestation |
False |
Seizure |
Inferred relationship |
Some |
|
lokalisationsrelateret kryptogen epilepsi |
Has definitional manifestation |
False |
Seizure |
Inferred relationship |
Some |
|
A familial type of self-limited focal epilepsy with onset typically between day two and seven of life. Seizures are focal tonic at onset, affecting the head, face, and limbs. Focal clonic or tonic seizures may evolve to bilateral tonic or clonic seizures. Onset may alternate between hemispheres. Autonomic features (apnea and cyanosis) can be seen. Seizure semiology may progress in a sequential pattern with tonic, clonic, myoclonic and autonomic features following each other without a single predominant feature. Clusters of seizures can occur over hours or days with the neonate behaving normally between events. Developmental progress is usually normal. The electroencephalogram (EEG) background is normal or has minor nonspecific abnormalities. Focal interictal epileptiform abnormalities can be seen in the central, centrotemporal or frontotemporal regions. MRI is normal or has nonspecific findings. Pathogenic variants are seen in KCNQ2, KCNQ3 and SCN2A. |
Has definitional manifestation |
False |
Seizure |
Inferred relationship |
Some |
|
Benign non-familial neonatal convulsions |
Has definitional manifestation |
False |
Seizure |
Inferred relationship |
Some |
|
myoklon epilepsi i den tidlige barndom |
Has definitional manifestation |
False |
Seizure |
Inferred relationship |
Some |
|
A type of epilepsy that presents with typical absence seizures between 9 and 13 years of age in an otherwise normal adolescent. The typical absence seizures usually occur less than daily in the untreated state and are provoked by hyperventilation in 87 percent of cases. Generalized tonic-clonic seizures are seen in greater than 90 percent of cases, most commonly beginning shortly after onset of absence seizures. Myoclonic seizures do not occur. Development and cognition are typically normal. Neurological examination is normal. The electroencephalogram shows 3 to 5.5 Hz generalized spike-wave with a normal background. |
Has definitional manifestation |
False |
Seizure |
Inferred relationship |
Some |
|
A type of epilepsy that presents with generalised tonic-clonic seizures usually between 10 and 25 years of age in an otherwise normal adolescent or adult. The generalised tonic-clonic seizures are typically provoked by sleep deprivation. Other seizure types do not occur. Development and cognition are typically normal. Neurological examination is normal. The electroencephalogram must show generalised epileptiform discharges or capture a generalised tonic-clonic seizure and have a normal background. |
Has definitional manifestation |
False |
Seizure |
Inferred relationship |
Some |
|
kryptogen generaliseret epilepsi |
Has definitional manifestation |
False |
Seizure |
Inferred relationship |
Some |
|
Cryptogenic West syndrome |
Has definitional manifestation |
False |
Seizure |
Inferred relationship |
Some |
|
Symptomatic West syndrome |
Has definitional manifestation |
False |
Seizure |
Inferred relationship |
Some |
|
Lennox-Gastaut syndrome (disorder) |
Has definitional manifestation |
False |
Seizure |
Inferred relationship |
Some |
|
Cryptogenic Lennox-Gastaut syndrome |
Has definitional manifestation |
False |
Seizure |
Inferred relationship |
Some |
|
Symptomatic Lennox-Gastaut syndrome |
Has definitional manifestation |
False |
Seizure |
Inferred relationship |
Some |
|
A type of epilepsy that presents with myoclonic-atonic seizures usually between 2 to 6 years of age. Other generalised seizure types which may be seen in this syndrome include atonic, myoclonic, generalised tonic-clonic seizures, tonic and absence seizures. Nonconvulsive status epilepticus is common. Development prior to seizure onset is normal in two thirds of cases. These children typically show developmental stagnation or even regression during the active seizures (stormy) phase, which improves once seizures are controlled. The electroencephalogram shows generalised 2 to 6 Hz spike-wave or polyspike-and-wave abnormalities, with normal background. |
Has definitional manifestation |
False |
Seizure |
Inferred relationship |
Some |
|
Epilepsy with myoclonic absence presents with daily myoclonic absence seizures between 1 to 12 years of age. Other generalised seizure types which may be seen in this syndrome include generalised tonic-clonic seizures, clonic, atonic and typical absence seizures. Developmental impairment may be present at onset of epilepsy and may become more evident with age. The electroencephalogram shows regular three Hz generalised spike-and-wave pattern time-locked with myoclonic jerks, with a normal background. |
Has definitional manifestation |
False |
Seizure |
Inferred relationship |
Some |
|
Unverricht-Lundborg syndrome |
Has definitional manifestation |
False |
Seizure |
Inferred relationship |
Some |
|
Lafora disease |
Has definitional manifestation |
False |
Seizure |
Inferred relationship |
Some |
|
A mitochondrial encephalomyopathy with characteristics of myoclonic seizures. Patients usually present during adolescence or early adulthood with myoclonic epilepsy, sometimes with neurosensory deafness, optic atrophy, short stature or peripheral neuropathy. The disease is progressive with worsening of the epilepsy and onset of additional symptoms including ataxia, deafness, muscle weakness, and dementia. Caused by mutations in the mitochondrial DNA. |
Has definitional manifestation |
False |
Seizure |
Inferred relationship |
Some |
|
kryptogen myoklon epilepsi |
Has definitional manifestation |
False |
Seizure |
Inferred relationship |
Some |
|
idiopatisk myoklon epilepsi |
Has definitional manifestation |
False |
Seizure |
Inferred relationship |
Some |
|
Early infantile epileptic encephalopathy with suppression bursts |
Has definitional manifestation |
False |
Seizure |
Inferred relationship |
Some |
|
symptomatisk myoklon epilepsi |
Has definitional manifestation |
False |
Seizure |
Inferred relationship |
Some |
|
Situation-related seizures |
Has definitional manifestation |
False |
Seizure |
Inferred relationship |
Some |
|
isolerede anfald |
Has definitional manifestation |
False |
Seizure |
Inferred relationship |
Some |
|
anfald som respons på akut hændelse |
Has definitional manifestation |
False |
Seizure |
Inferred relationship |
Some |
|
epilepsi, ikke fastslået om fokal eller generaliseret |
Has definitional manifestation |
False |
Seizure |
Inferred relationship |
Some |
|
A genetic epilepsy of childhood with characteristics of drug-resistant seizures often induced by fever, presenting in previously healthy children, and which frequently leads to cognitive and motor impairment. Seizures can regress in adulthood but most patients have ongoing seizures that are refractory to medication. Around 85% of cases are due to a mutation or deletion in the SCN1A gene (2q24.3), encoding a voltage-gated sodium channel essential for the excitability of neurons. In families with a known SCN1A mutation, inheritance is autosomal dominant. |
Has definitional manifestation |
False |
Seizure |
Inferred relationship |
Some |
|
Epilepsy with continuous spike wave during slow-wave sleep |
Has definitional manifestation |
False |
Seizure |
Inferred relationship |
Some |
|
Secondary reading epilepsy |
Has definitional manifestation |
False |
Seizure |
Inferred relationship |
Some |
|
Drug-induced epilepsy |
Has definitional manifestation |
False |
Seizure |
Inferred relationship |
Some |
|
Narcotic withdrawal epilepsy |
Has definitional manifestation |
False |
Seizure |
Inferred relationship |
Some |
|
Menstrual epilepsy |
Has definitional manifestation |
False |
Seizure |
Inferred relationship |
Some |
|
natlig epilepsi |
Has definitional manifestation |
False |
Seizure |
Inferred relationship |
Some |
|