Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
A seizure type with focal onset, with awareness or impaired awareness, either motor or non-motor, progressing to bilateral tonic (stiffening) followed by clonic (sustained rhythmic jerking) activity of body and limbs. |
Is a |
False |
Partial seizure |
Inferred relationship |
Some |
|
An epileptic seizure originating within networks limited to one hemisphere that involves musculature of any kind at the onset, regardless of whether aware or with impaired awareness. The motor activity could be an increase (positive) or decrease (negative) in muscle contraction to produce a movement. |
Is a |
False |
Partial seizure |
Inferred relationship |
Some |
|
Komplekst partielt anfald med nedsat bevidsthed |
Is a |
False |
Partial seizure |
Inferred relationship |
Some |
|
Simpelt partielt anfald uden nedsat bevidsthed |
Is a |
False |
Partial seizure |
Inferred relationship |
Some |
|
Benign frontal epilepsi i barndommen |
Has definitional manifestation |
False |
Partial seizure |
Inferred relationship |
Some |
|
Benign psykomotorisk epilepsi i barndommen |
Has definitional manifestation |
False |
Partial seizure |
Inferred relationship |
Some |
|
Benign atypical partial epilepsy in childhood |
Has definitional manifestation |
False |
Partial seizure |
Inferred relationship |
Some |
|
epilepsi med recidiverende unilaterale anfald hos børn |
Has definitional manifestation |
False |
Partial seizure |
Inferred relationship |
Some |
|
epilepsi i barndommen med occipitale paroksysmer |
Has definitional manifestation |
False |
Partial seizure |
Inferred relationship |
Some |
|
A rare genetic neurological disorder characterised by late infancy to early-adolescence onset of prolonged, nocturnal seizures which begin with autonomic features (e.g. vomiting, pallor, sweating) and associate tonic eye deviation, impairment of consciousness and may evolve to a hemi-clonic or generalised convulsion. Autonomic status epilepticus may be the only clinical event in some cases. |
Has definitional manifestation |
False |
Partial seizure |
Inferred relationship |
Some |
|
A rare genetic neurological disorder with characteristics of childhood to mid-adolescence onset of frequent, brief, diurnal simple partial seizures which usually begin with visual hallucinations (e.g. phosphenes) and/or ictal blindness and may associate non visual seizures (such as deviation of the eyes, oculo clonic seizures), forced eyelid closure and blinking and sensory hallucinations. Post-ictal headache is common while impairment of consciousness is rare. |
Has definitional manifestation |
False |
Partial seizure |
Inferred relationship |
Some |
|
kronisk progredierende epilepsia partialis continua i barndommen |
Has definitional manifestation |
False |
Partial seizure |
Inferred relationship |
Some |
|
An absence seizure associated with eyelid myoclonia (myoclonic jerks of the eyelids and upward deviation of the eyes) often precipitated by closing the eyes or by light. |
Has definitional manifestation |
False |
Partial seizure |
Inferred relationship |
Some |
|
Ikke-konvulsiv simpel partiel status epilepticus |
Has definitional manifestation |
False |
Partial seizure |
Inferred relationship |
Some |
|
Kompleks partiel status epilepticus |
Has definitional manifestation |
False |
Partial seizure |
Inferred relationship |
Some |
|
Ekstratemporal epilepsi |
Has definitional manifestation |
False |
Partial seizure |
Inferred relationship |
Some |
|
Psykomotorisk epilepsi |
Has definitional manifestation |
False |
Partial seizure |
Inferred relationship |
Some |
|
A group of epilepsies characterized by age-dependent occurrence of drug responsive focal seizures in otherwise normal children. Seizures are focal motor or sensory with or without impaired awareness and may evolve to bilateral tonic-clonic seizures. Remission usually occurs by puberty. Development and cognition are typically normal. Neurological examination is normal. No significant structural lesions of the brain are present, and presumed genetic factors have an important role. The electroencephalogram (EEG) background activity is normal. Seizure semiology and EEG features are specific for each of the syndromes included in this group. |
Has definitional manifestation |
False |
Partial seizure |
Inferred relationship |
Some |
|
Visceral epilepsi |
Has definitional manifestation |
False |
Partial seizure |
Inferred relationship |
Some |
|
A prolonged focal-onset clonic seizure occurring and limited to specific parts of the body such as the hand, face, arm or leg. |
Has definitional manifestation |
False |
Partial seizure |
Inferred relationship |
Some |
|
An epileptic seizure originating within networks limited to one hemisphere. They may be discretely localised or more widely distributed. Focal seizures may originate in subcortical structures. |
Has definitional manifestation |
False |
Partial seizure |
Inferred relationship |
Some |
|
kronisk progredierende epilepsia partialis continua |
Has definitional manifestation |
False |
Partial seizure |
Inferred relationship |
Some |
|
Centrencefal epilepsi |
Has definitional manifestation |
False |
Partial seizure |
Inferred relationship |
Some |
|
anfald med løben |
Has definitional manifestation |
False |
Partial seizure |
Inferred relationship |
Some |
|
An epileptic seizure originating within networks limited to one hemisphere, initially manifesting as bursts of laughter or giggling, regardless of whether aware or with impaired awareness. |
Has definitional manifestation |
False |
Partial seizure |
Inferred relationship |
Some |
|
Photogenic epilepsy |
Has definitional manifestation |
False |
Partial seizure |
Inferred relationship |
Some |
|
Visual reflex epilepsy |
Has definitional manifestation |
False |
Partial seizure |
Inferred relationship |
Some |
|