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Genopedia


GJB2
73 disease terms (MeSH) has been reported with GJB2 gene.

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Disease Term (MeSH)
Total Publication
Meta-analysis Publications
    Deafness Phenopedia 192 1
    Hearing Loss, Sensorineural Phenopedia 184 2
    Hearing Loss Phenopedia 155 2
    Hearing Loss, Bilateral Phenopedia 13 0
    Disease Progression Phenopedia 13 1
    Speech Perception Phenopedia 13 0
    Auditory Threshold Phenopedia 10 0
    Hearing Disorders Phenopedia 8 0
    Hearing Phenopedia 8 1
    Cytomegalovirus Infections Phenopedia 8 0
    Syndrome Phenopedia 6 0
    Auditory Perception Phenopedia 5 0
    Psoriasis Phenopedia 5 0
    Hearing Loss, Noise-Induced Phenopedia 4 1
    Chromosome Deletion Phenopedia 4 0
    Genetic Diseases, Inborn Phenopedia 3 0
    Usher Syndromes Phenopedia 3 0
    Hearing Loss, Sudden Phenopedia 2 0
    Fetal Membranes, Premature Rupture Phenopedia 2 0
    Keratoderma, Palmoplantar Phenopedia 2 0
    Neoplasms Phenopedia 2 0
    Hearing Loss, High-Frequency Phenopedia 2 1
    Chorioamnionitis Phenopedia 2 0
    Goiter, Nodular Phenopedia 2 0
    Hearing Loss, Unilateral Phenopedia 1 0
    Reaction Time Phenopedia 1 0
    Rhinitis Phenopedia 1 0
    Breast Neoplasms Phenopedia 1 0
    Functional Laterality Phenopedia 1 0
    Disease Susceptibility Phenopedia 1 0
    Bone Conduction Phenopedia 1 0
    Sinusitis Phenopedia 1 0
    Occupational Diseases Phenopedia 1 0
    Vestibular Diseases Phenopedia 1 0
    Chronic Disease Phenopedia 1 0
    Cleft Lip Phenopedia 1 0
    Epstein-Barr Virus Infections Phenopedia 1 0
    Hearing Loss, Mixed Conductive-Sensorineural Phenopedia 1 0
    Intellectual Disability Phenopedia 1 0
    Obstetric Labor, Premature Phenopedia 1 0
    Perceptual Distortion Phenopedia 1 0
    Bartter Syndrome Phenopedia 1 0
    Cell Transformation, Viral Phenopedia 1 0
    Cleft Palate Phenopedia 1 0
    Long QT Syndrome Phenopedia 1 0
    Presbycusis Phenopedia 1 0
    Attention Deficit Disorder with Hyperactivity Phenopedia 1 0
    Anodontia Phenopedia 1 0
    Ectodermal Dysplasia Phenopedia 1 0
    Infant, Premature, Diseases Phenopedia 1 0
    Motor Skills Phenopedia 1 0
    Stomach Neoplasms Phenopedia 1 0
    Cognition Phenopedia 1 0
    Diseases in Twins Phenopedia 1 0
    Hepatolenticular Degeneration Phenopedia 1 0
    Hemochromatosis Phenopedia 1 0
    Cholesteatoma Phenopedia 1 0
    Developmental Disabilities Phenopedia 1 0
    Recurrence Phenopedia 1 0
    Vestibulocochlear Nerve Diseases Phenopedia 1 0
    Language Development Disorders Phenopedia 1 0
    Pre-Eclampsia Phenopedia 1 0
    Premature Birth Phenopedia 1 0
    Mutism Phenopedia 1 0
    Ovarian Neoplasms Phenopedia 1 0
    Pregnancy Complications Phenopedia 1 0
    Chromosome Aberrations Phenopedia 1 0
    Esophageal Neoplasms Phenopedia 1 0
    Genetic Diseases, X-Linked Phenopedia 1 0
    Apraxias Phenopedia 1 0
    Arthritis, Psoriatic Phenopedia 1 0
    Colorectal Neoplasms Phenopedia 1 0
    Jervell-Lange Nielsen Syndrome 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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