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Lennox Gastaut Syndrome
MeSH Descriptor Data 2025
Details
Qualifiers
MeSH Tree Structures
Concepts
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]
Adrenal Hyperplasia, Congenital [C16.320.033]
Alagille Syndrome [C16.320.051]
alpha 1-Antitrypsin Deficiency [C16.320.060]
Anemia, Hemolytic, Congenital [C16.320.070]
Anemia, Hypoplastic, Congenital [C16.320.077]
Ataxia Telangiectasia [C16.320.080]
Autoimmune Lymphoproliferative Syndrome [C16.320.089]
Blood Coagulation Disorders, Inherited [C16.320.099]
Brugada Syndrome [C16.320.100]
CADASIL [C16.320.129]
Camurati-Engelmann Syndrome [C16.320.144]
Cardiomyopathy, Hypertrophic, Familial [C16.320.160]
CHARGE Syndrome [C16.320.165]
Cherubism [C16.320.170]
Chromosome Disorders [C16.320.180]
Ciliopathies [C16.320.184]
Costello Syndrome [C16.320.188]
Cystic Fibrosis [C16.320.190]
Donohue Syndrome [C16.320.215]
Dwarfism [C16.320.240]
Eye Diseases, Hereditary [C16.320.290]
Familial Multiple Lipomatosis [C16.320.298]
Frasier Syndrome [C16.320.306]
GATA2 Deficiency [C16.320.314]
Genetic Diseases, X-Linked [C16.320.322]
Genetic Diseases, Y-Linked [C16.320.338]
Hajdu-Cheney Syndrome [C16.320.355]
Hemoglobinopathies [C16.320.365]
Hereditary Autoinflammatory Diseases [C16.320.382]
Heredodegenerative Disorders, Nervous System [C16.320.400]
Hyper-IgM Immunodeficiency Syndrome [C16.320.413]
Hyperthyroxinemia, Familial Dysalbuminemic [C16.320.427]
Imprinting Disorders [C16.320.447]
Kallmann Syndrome [C16.320.467]
Kartagener Syndrome [C16.320.480]
Laminopathies [C16.320.488]
Lennox Gastaut Syndrome [C16.320.495]
Loeys-Dietz Syndrome [C16.320.510]
Marfan Syndrome [C16.320.540]
Metabolism, Inborn Errors [C16.320.565]
Muscular Dystrophies [C16.320.577]
Myasthenic Syndromes, Congenital [C16.320.590]
Nail-Patella Syndrome [C16.320.600]
Neoplastic Syndromes, Hereditary [C16.320.700]
Oculocerebrorenal Syndrome [C16.320.709]
Orofaciodigital Syndromes [C16.320.714]
Osteoarthropathy, Primary Hypertrophic [C16.320.718]
Osteochondrodysplasias [C16.320.728]
Osteogenesis Imperfecta [C16.320.737]
Pain Insensitivity, Congenital [C16.320.775]
Pelger-Huet Anomaly [C16.320.784]
Primary Immunodeficiency Diseases [C16.320.798]
Pycnodysostosis [C16.320.812]
Renal Tubular Transport, Inborn Errors [C16.320.831]
Skin Diseases, Genetic [C16.320.850]
Werner Syndrome [C16.320.925]
Yellow Nail Syndrome [C16.320.962]
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Lennox Gastaut Syndrome
Preferred
Concept UI
M0590747
Scope Note
A childhood-onset epilepsy syndrome.
Terms
Lennox Gastaut Syndrome
Preferred Term
Term UI
T854035
Date
01/23/2014
LexicalTag
NON
ThesaurusID
NLM (2015)
Lennox-Gastaut Syndrome
Term UI
T000997686
Date
11/19/2019
LexicalTag
EPO
ThesaurusID
NLM (2021)
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