Lennox Gastaut Syndrome MeSH Descriptor Data 2024

MeSH Heading: Lennox Gastaut Syndrome
Tree Number(s): C10.228.140.490.493.750; C16.320.495
Unique ID: D065768
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/D065768
Scope Note: A childhood-onset epilepsy syndrome.
Entry Term(s): Lennox-Gastaut Syndrome
Previous Indexing: Spasms, Infantile (1988-2014)
Public MeSH Note: 2015
History Note: 2015
Date Established: 2015/01/01
Date of Entry: 2014/06/26
Revision Date: 2020/02/06

Allowable Qualifiers: blood (BL)

cerebrospinal fluid (CF)

chemically induced (CI)

classification (CL)

complications (CO)

diagnosis (DI)

diagnostic imaging (DG)

diet therapy (DH)

drug therapy (DT)

economics (EC)

embryology (EM)

enzymology (EN)

epidemiology (EP)

ethnology (EH)

etiology (ET)

genetics (GE)

history (HI)

immunology (IM)

metabolism (ME)

microbiology (MI)

mortality (MO)

nursing (NU)

parasitology (PS)

pathology (PA)

physiopathology (PP)

prevention & control (PC)

psychology (PX)

radiotherapy (RT)

rehabilitation (RH)

surgery (SU)

therapy (TH)

urine (UR)

veterinary (VE)

virology (VI)

Nervous System Diseases [C10]
- Central Nervous System Diseases [C10.228]
  - Brain Diseases [C10.228.140]
    - Epilepsy [C10.228.140.490]
      - Epileptic Syndromes [C10.228.140.490.493]
        
        Epilepsies, Myoclonic [C10.228.140.490.493.063]
        
        Epilepsy, Absence [C10.228.140.490.493.125]
        
        Epilepsy, Frontal Lobe [C10.228.140.490.493.188]
        
        Epilepsy, Rolandic [C10.228.140.490.493.250]
        
        Epilepsy, Temporal Lobe [C10.228.140.490.493.375]
        
        Landau-Kleffner Syndrome [C10.228.140.490.493.500]
        
        Lennox Gastaut Syndrome [C10.228.140.490.493.750]
        
        Spasms, Infantile [C10.228.140.490.493.875]

Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
- Genetic Diseases, Inborn [C16.320]

Lennox Gastaut Syndrome Preferred

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