lennox-gastaut syndrome

Preferred Label : lennox-gastaut syndrome;

Origin ID

DA-31580;

UMLS CUI

C0238111;

Automatic exact mappings (from CISMeF team)
- Cutis verticis gyrata (disorder) [SNOMED CT concept]
- Other generalized epilepsy and epileptic syndromes [ICD-10 Sub-category (who)]
Currated CISMeF NLP mapping
- Epileptic encephalopathy, Lennox-Gastaut type [MeSH concept]
- Lennox Gastaut Syndrome [MeSH Descriptor]
- Lennox Gastaut Syndrome [MeSH concept]
- Lennox Gastaut syndrome [Disease (Nov.)]
- Lennox syndrome [PASCAL descriptor]
- Lennox-Gastaut Syndrome [NCIt concept]
- Lennox-Gastaut syndrome [DO Concept]
- Lennox-Gastaut syndrome [ICD-11 Subcategory]
- Lennox-Gastaut syndrome [MedDRA Preferred Term]
- Lennox-Gastaut syndrome [ORDO Disease]
- Lennox-Gastaut syndrome (disorder) [SNOMED CT concept]
ICD-10 exact mapping(s)
- Other generalized epilepsy and epileptic syndromes [ICD-10 Sub-category (who)]
Manual NTBT mappings (CISMeF)
- Childhood-onset epilepsy syndrome [ORDO Disease]
Metaterm(s)
- neurology [CISMeF Metaterm]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Lennox Gastaut Syndrome [MeSH concept]
- Lennox Gastaut Syndrome [MeSH Descriptor]
- Lennox Gastaut syndrome [Disease (Nov.)]
- Lennox-Gastaut Syndrome [NCIt concept]
- Lennox-Gastaut syndrome [ORDO Disease]
- Lennox-Gastaut syndrome [MedDRA Preferred Term]
- Lennox-Gastaut syndrome [DO Concept]
- Lennox-Gastaut syndrome (disorder) [SNOMED CT concept]