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Genopedia


ATXN2
52 disease terms (MeSH) has been reported with ATXN2 gene.

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Disease Term (MeSH)
Total Publication
Meta-analysis Publications
    Amyotrophic Lateral Sclerosis Phenopedia 22 1
    Spinocerebellar Ataxias Phenopedia 21 0
    Frontotemporal Dementia Phenopedia 4 1
    Parkinsonian Disorders Phenopedia 3 0
    Parkinson Disease Phenopedia 3 0
    Cerebellar Ataxia Phenopedia 3 0
    Disease Progression Phenopedia 3 0
    Cardiovascular Diseases Phenopedia 3 0
    Coronary Artery Disease Phenopedia 2 0
    Hashimoto Disease Phenopedia 2 0
    Kidney Failure, Chronic Phenopedia 2 0
    Restless Legs Syndrome Phenopedia 2 0
    Schizophrenia Phenopedia 2 0
    Hypertension Phenopedia 2 0
    Obesity Phenopedia 2 0
    Graves Disease Phenopedia 2 0
    Heredodegenerative Disorders, Nervous System Phenopedia 2 0
    Celiac Disease Phenopedia 2 0
    Child Development Disorders, Pervasive Phenopedia 1 0
    Gout Phenopedia 1 0
    Motor Neuron Disease Phenopedia 1 0
    Sleep Disorders Phenopedia 1 0
    Genomic Instability Phenopedia 1 0
    Glaucoma, Open-Angle Phenopedia 1 0
    Chronic Disease Phenopedia 1 0
    Neuropsychological Tests Phenopedia 1 0
    Machado-Joseph Disease Phenopedia 1 0
    Syndrome Phenopedia 1 1
    Supranuclear Palsy, Progressive Phenopedia 1 0
    Cognition Phenopedia 1 0
    Depressive Disorder Phenopedia 1 0
    Diabetes Mellitus, Type 1 Phenopedia 1 0
    Diabetes Mellitus, Type 2 Phenopedia 1 0
    Myoclonic Epilepsies, Progressive Phenopedia 1 0
    Peripheral Nervous System Diseases Phenopedia 1 0
    Metabolic Syndrome X Phenopedia 1 0
    Pancreatic Neoplasms Phenopedia 1 0
    Adenocarcinoma Phenopedia 1 0
    Arthritis, Juvenile Rheumatoid Phenopedia 1 0
    Autoimmune Diseases Phenopedia 1 0
    Central Nervous System Diseases Phenopedia 1 0
    Channelopathies Phenopedia 1 0
    Dyslipidemias Phenopedia 1 0
    Alzheimer Disease Phenopedia 1 0
    Lung Neoplasms Phenopedia 1 0
    Nerve Degeneration Phenopedia 1 0
    Inflammation Phenopedia 1 0
    Multiple System Atrophy Phenopedia 1 0
    Sarcoidosis Phenopedia 1 0
    Antiphospholipid Syndrome Phenopedia 1 0
    Ataxia Phenopedia 1 1
    Multiple Sclerosis 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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