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Genopedia


NKX2-5

34 disease terms (MeSH) has been reported with NKX2-5 gene.

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Disease Term (MeSH)
Total Publication
Meta-analysis Publications
    Heart Defects, Congenital Phenopedia 21 0
    Atrial Fibrillation Phenopedia 9 0
    Heart Septal Defects, Ventricular Phenopedia 9 0
    Tetralogy of Fallot Phenopedia 7 0
    Heart Septal Defects, Atrial Phenopedia 7 0
    Chromosome Deletion Phenopedia 2 0
    Congenital Hypothyroidism Phenopedia 2 0
    Heart Septal Defects Phenopedia 2 0
    Cardiovascular Diseases Phenopedia 2 0
    Down Syndrome Phenopedia 2 0
    Endocardial Cushion Defects Phenopedia 1 0
    Hand Deformities, Congenital Phenopedia 1 0
    Lupus Erythematosus, Systemic Phenopedia 1 0
    Parkinson Disease Phenopedia 1 0
    Alagille Syndrome Phenopedia 1 0
    Edema Phenopedia 1 0
    Graves Disease Phenopedia 1 0
    Heart Valve Diseases Phenopedia 1 0
    Diabetes Mellitus, Type 2 Phenopedia 1 0
    Lower Extremity Deformities, Congenital Phenopedia 1 0
    Heart Block Phenopedia 1 0
    Hypertrophy, Left Ventricular Phenopedia 1 0
    Autistic Disorder Phenopedia 1 0
    Syndrome Phenopedia 1 0
    Upper Extremity Deformities, Congenital Phenopedia 1 0
    Ductus Arteriosus, Patent Phenopedia 1 0
    Ebstein Anomaly Phenopedia 1 0
    Genetic Diseases, Inborn Phenopedia 1 0
    Hypoplastic Left Heart Syndrome Phenopedia 1 0
    Death, Sudden Phenopedia 1 0
    Arthritis, Rheumatoid Phenopedia 1 0
    Pyloric Stenosis, Hypertrophic Phenopedia 1 0
    Syncope Phenopedia 1 0
    Abnormalities, Multiple 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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