Localization-related (focal) (partial) idiopathic epilepsy and epileptic syndromes with seizures of localized onset

Preferred Label : Localization-related (focal) (partial) idiopathic epilepsy and epileptic syndromes with seizures of localized onset;

Inclusion CIM-10 : Childhood epilepsy with occipital EEG paroxysms; Benign childhood epilepsy with centrotemporal EEG spikes;

ICD-10 exclusion note : adult onset localization-related epilepsy (G40.1-, G40.2-);

Diag associé à un acte (%) : 84.5;

Source : OMS;

Date de début : 01/01/1997;

Details

Origin ID

G400;

UMLS CUI

C0475521;

CISMeF manual mappings
- Localization-related(focal)(partial)idiopathic epilepsy and epileptic syndromes with seizures of localized onset (disorder) [SNOMED CT concept]
Orphanet concepts
- Autosomal dominant epilepsy with auditory features [ORDO Disease]
- Autosomal dominant nocturnal frontal lobe epilepsy [ORDO Disease]
- Benign childhood occipital epilepsy, Gastaut type [ORDO Disease]
- Benign childhood occipital epilepsy, Panayiotopoulos type [ORDO Disease]
- Benign familial mesial temporal lobe epilepsy [ORDO Disease]
- Benign infantile focal epilepsy with midline spikes and waves during sleep [ORDO Disease]
- Benign occipital epilepsy [ORDO Disease]
- Familial focal epilepsy with variable foci [ORDO Disease]
- Familial mesial temporal lobe epilepsy with febrile seizures [ORDO Disease]
- Malignant migrating focal seizures of infancy [ORDO Disease]
- Mesial temporal lobe epilepsy with hippocampal sclerosis [ORDO Disease]
- Rare epilepsy [ORDO Disease]
- Rolandic epilepsy [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Localization-related(focal)(partial)idiopathic epilepsy and epileptic syndromes with seizures of localized onset (disorder) [SNOMED CT concept]

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