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Lennox Gastaut Syndrome
A childhood-onset epilepsy syndrome.
推出的年份: 2015
副标题
blood
cerebrospinal fluid
chemically induced
classification
complications
diagnosis
diagnostic imaging
diet therapy
drug therapy
economics
embryology
enzymology
epidemiology
ethnology
etiology
genetics
history
immunology
metabolism
microbiology
mortality
nursing
parasitology
pathology
physiopathology
prevention and control
psychology
radiotherapy
rehabilitation
surgery
therapy
urine
veterinary
virology
树号:
C10.228.140.490.493.750, C16.320.495
MeSH 单一 ID:
D065768
进入的组:
Lennox Gastaut Syndromes
Lennox-Gastaut Syndrome
早前的内容:
Spasms, Infantile (1988-2014)
All MeSH Categories
Diseases Category
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]
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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]
All MeSH Categories
Diseases Category
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]
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Anemia, Hypoplastic, Congenital [C16.320.077]
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Ataxia Telangiectasia [C16.320.080]
Autoimmune Lymphoproliferative Syndrome [C16.320.089]
Blood Coagulation Disorders, Inherited [C16.320.099]
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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]
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Ciliopathies [C16.320.184]
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Costello Syndrome [C16.320.188]
Cystic Fibrosis [C16.320.190]
Donohue Syndrome [C16.320.215]
Dwarfism [C16.320.240]
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Eye Diseases, Hereditary [C16.320.290]
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Familial Multiple Lipomatosis [C16.320.298]
Frasier Syndrome [C16.320.306]
GATA2 Deficiency [C16.320.314]
Genetic Diseases, X-Linked [C16.320.322]
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Genetic Diseases, Y-Linked [C16.320.338]
Hajdu-Cheney Syndrome [C16.320.355]
Hemoglobinopathies [C16.320.365]
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Hereditary Autoinflammatory Diseases [C16.320.382]
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Heredodegenerative Disorders, Nervous System [C16.320.400]
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Hyper-IgM Immunodeficiency Syndrome [C16.320.413]
Hyperthyroxinemia, Familial Dysalbuminemic [C16.320.427]
Kallmann Syndrome [C16.320.467]
Kartagener Syndrome [C16.320.184.500.531]
Laminopathies [C16.320.488]
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Lennox Gastaut Syndrome [C16.320.495]
Loeys-Dietz Syndrome [C16.320.510]
Marfan Syndrome [C16.320.540]
Metabolism, Inborn Errors [C16.320.565]
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Muscular Dystrophies [C16.320.577]
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Myasthenic Syndromes, Congenital [C16.320.590]
Nail-Patella Syndrome [C16.320.600]
Neoplastic Syndromes, Hereditary [C16.320.700]
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Oculocerebrorenal Syndrome [C16.320.322.750]
Orofaciodigital Syndromes [C16.320.180.830.670]
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]
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Pycnodysostosis [C16.320.565.595.800]
Renal Tubular Transport, Inborn Errors [C16.320.565.893]
Skin Diseases, Genetic [C16.320.850]
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Werner Syndrome [C16.320.925]
Yellow Nail Syndrome [C16.320.962]
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