Lennox-Gastaut syndrome

ICD-11 code : 8A62.1;

Preferred Label : Lennox-Gastaut syndrome;

ICD-11 definition : Syndrome defined as a cryptogenic or symptomatic generalized epilepsy, which is characterized by the following symptomatic triad: several epileptic seizures (atypical absences, axial tonic seizures and sudden atonic or myoclonic falls); diffuse slow interictal spike waves in the waking EEG ( 3 Hz) and fast rhythmic bursts (10 Hz) during sleep; slow mental development associated with personality disturbances.;

Details

Origin ID

651135242;

Automatic exact mappings (from CISMeF team)
- Cutis verticis gyrata (disorder) [SNOMED CT concept]
Currated CISMeF NLP mapping
- Lennox Gastaut Syndrome [MeSH concept]
- Lennox Gastaut Syndrome [MeSH Descriptor]
- Lennox syndrome [PASCAL descriptor]
- Lennox-Gastaut Syndrome [NCIt concept]
- Lennox-Gastaut syndrome [ORDO Disease]
- Lennox-Gastaut syndrome [DO Concept]
- Lennox-Gastaut syndrome [MedDRA Preferred Term]
- Lennox-Gastaut syndrome (disorder) [SNOMED CT concept]
- lennox-gastaut syndrome [SNOMED Notion]
ICD-10 Mapping
- Other generalized epilepsy and epileptic syndromes [ICD-10 Sub-category]

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