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Genopedia


C10orf2

20 disease terms (MeSH) has been reported with C10orf2 gene.

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Disease Term (MeSH)
Total Publication
Meta-analysis Publications
    Ophthalmoplegia, Chronic Progressive External Phenopedia 4 0
    Optic Nerve Diseases Phenopedia 1 0
    Parkinsonian Disorders Phenopedia 1 0
    Peripheral Nervous System Diseases Phenopedia 1 0
    Retinal Diseases Phenopedia 1 0
    Gonadal Dysgenesis, 46,XX Phenopedia 1 0
    Hearing Loss, Sensorineural Phenopedia 1 0
    Mitochondrial Diseases Phenopedia 1 0
    Myositis, Inclusion Body Phenopedia 1 0
    Ophthalmoplegia Phenopedia 1 0
    Abnormalities, Multiple Phenopedia 1 0
    Acquired Immunodeficiency Syndrome Phenopedia 1 0
    Aging, Premature Phenopedia 1 0
    Alzheimer Disease Phenopedia 1 0
    Blepharoptosis Phenopedia 1 0
    Cytochrome-c Oxidase Deficiency Phenopedia 1 0
    Diabetes Mellitus, Type 1 Phenopedia 1 0
    Diabetic Neuropathies Phenopedia 1 0
    Disease Progression Phenopedia 1 0
    Eye Diseases 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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