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Genopedia


SCN1A

33 disease terms (MeSH) has been reported with SCN1A gene.

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Disease Term (MeSH)
Total Publication
Meta-analysis Publications
    Epilepsy Phenopedia 42 2
    Seizures, Febrile Phenopedia 13 0
    Epilepsies, Myoclonic Phenopedia 12 1
    Epilepsy, Generalized Phenopedia 8 0
    Epilepsies, Partial Phenopedia 5 0
    Spasms, Infantile Phenopedia 4 0
    Syndrome Phenopedia 4 0
    Seizures Phenopedia 4 0
    Neuropsychological Tests Phenopedia 2 0
    Sclerosis Phenopedia 2 0
    Migraine Disorders Phenopedia 2 0
    Myoclonic Epilepsy, Juvenile Phenopedia 2 0
    Epilepsy, Absence Phenopedia 2 0
    Epilepsy, Temporal Lobe Phenopedia 2 0
    Fever Phenopedia 2 0
    Memory, Short-Term Phenopedia 2 0
    Mental Retardation Phenopedia 1 0
    Headache Disorders, Primary Phenopedia 1 0
    Infection Phenopedia 1 0
    Intellectual Disability Phenopedia 1 0
    Atrial Fibrillation Phenopedia 1 0
    Carbohydrate Metabolism, Inborn Errors Phenopedia 1 0
    Chromosome Aberrations Phenopedia 1 0
    Chromosome Deletion Phenopedia 1 0
    Colorectal Neoplasms Phenopedia 1 0
    Disease Models, Animal Phenopedia 1 0
    Encephalitis, Viral Phenopedia 1 0
    Neurodegenerative Diseases Phenopedia 1 0
    Migraine with Aura Phenopedia 1 0
    Stevens-Johnson Syndrome Phenopedia 1 0
    Temporomandibular Joint Disorders Phenopedia 1 0
    Wechsler Scales Phenopedia 1 0
    West Nile Fever Phenopedia 1 0
Note: The number of publications displayed in this table will differ from the number displayed in the HuGE Literature Finder as the number in Genopedia reflects only the indexed disease term without children terms, but the number in the HuGE Literature Finder reflects all text searches of the disease term including the indexed term and corresponding children terms.
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