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Genopedia


POLG

73 disease terms (MeSH) has been reported with POLG gene.

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Disease Term (MeSH)
Total Publication
Meta-analysis Publications
    Infertility, Male Phenopedia 12 0
    Parkinson Disease Phenopedia 10 0
    Mitochondrial Diseases Phenopedia 8 0
    Ophthalmoplegia, Chronic Progressive External Phenopedia 6 0
    Breast Neoplasms Phenopedia 5 0
    Peripheral Nervous System Diseases Phenopedia 4 0
    Epilepsy Phenopedia 3 0
    Diffuse Cerebral Sclerosis of Schilder Phenopedia 2 0
    Charcot-Marie-Tooth Disease Phenopedia 2 0
    Urinary Bladder Neoplasms Phenopedia 2 1
    Primary Ovarian Insufficiency Phenopedia 2 0
    Neoplasms Phenopedia 2 0
    Oligospermia Phenopedia 2 0
    HIV Infections Phenopedia 2 0
    Hypertension Phenopedia 1 0
    Hypertrophy, Left Ventricular Phenopedia 1 0
    Infection Phenopedia 1 0
    Mitochondrial Myopathies Phenopedia 1 0
    Multiple Sclerosis Phenopedia 1 0
    Myeloproliferative Disorders Phenopedia 1 0
    Myositis, Inclusion Body Phenopedia 1 0
    Neoplasm Invasiveness Phenopedia 1 0
    Ophthalmoplegia Phenopedia 1 0
    Obesity Phenopedia 1 0
    Optic Nerve Diseases Phenopedia 1 0
    Ovarian Failure, Premature Phenopedia 1 0
    Parkinsonian Disorders Phenopedia 1 0
    Puberty, Delayed Phenopedia 1 0
    Puberty, Precocious Phenopedia 1 0
    Retinal Diseases Phenopedia 1 0
    Seizures Phenopedia 1 0
    Seizures, Febrile Phenopedia 1 0
    Spastic Paraplegia, Hereditary Phenopedia 1 0
    Spinocerebellar Ataxias Phenopedia 1 0
    Spinocerebellar Degenerations Phenopedia 1 0
    Syndrome Phenopedia 1 0
    Thrombophilia Phenopedia 1 0
    Tobacco Use Disorder Phenopedia 1 0
    Polycystic Ovary Syndrome Phenopedia 1 0
    Chromosomal Instability Phenopedia 1 0
    Cognition Disorders Phenopedia 1 0
    Colorectal Neoplasms Phenopedia 1 0
    Cytochrome-c Oxidase Deficiency Phenopedia 1 0
    Diabetes Mellitus, Type 1 Phenopedia 1 0
    Diabetic Neuropathies Phenopedia 1 0
    Cell Transformation, Neoplastic Phenopedia 1 0
    Cerebellar Ataxia Phenopedia 1 0
    Channelopathies Phenopedia 1 0
    46, XX Disorders of Sex Development Phenopedia 1 0
    Abnormalities, Multiple Phenopedia 1 0
    Acidosis, Lactic Phenopedia 1 0
    Acquired Immunodeficiency Syndrome Phenopedia 1 0
    Adenoma Phenopedia 1 0
    Aging, Premature Phenopedia 1 0
    Alzheimer Disease Phenopedia 1 0
    Bipolar Disorder Phenopedia 1 0
    Blepharoptosis Phenopedia 1 0
    Brain Infarction Phenopedia 1 0
    Disease Progression Phenopedia 1 0
    Disease Susceptibility Phenopedia 1 0
    DNA Damage Phenopedia 1 0
    Eye Diseases Phenopedia 1 0
    Friedreich Ataxia Phenopedia 1 0
    Headache Phenopedia 1 0
    Hemianopsia Phenopedia 1 0
    Keratoconus Phenopedia 1 0
    Kidney Failure, Chronic Phenopedia 1 0
    Lipodystrophy Phenopedia 1 0
    Liver Neoplasms Phenopedia 1 0
    Meningeal Neoplasms Phenopedia 1 0
    Meningioma Phenopedia 1 0
    Menopause, Premature Phenopedia 1 0
    Migraine Disorders 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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