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