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Genopedia


NKX2-5
38 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 23 0
    Heart Septal Defects, Ventricular Phenopedia 9 0
    Atrial Fibrillation Phenopedia 9 0
    Tetralogy of Fallot Phenopedia 8 0
    Heart Septal Defects, Atrial Phenopedia 7 0
    Congenital Hypothyroidism Phenopedia 5 0
    Chromosome Deletion Phenopedia 2 0
    Down Syndrome Phenopedia 2 0
    Thyroid Dysgenesis Phenopedia 2 0
    Heart Valve Diseases Phenopedia 2 0
    Heart Septal Defects Phenopedia 2 0
    Cardiovascular Diseases Phenopedia 2 0
    Death, Sudden Phenopedia 1 0
    Hand Deformities, Congenital Phenopedia 1 0
    Lupus Erythematosus, Systemic Phenopedia 1 0
    Arthritis, Rheumatoid Phenopedia 1 0
    Pyloric Stenosis, Hypertrophic Phenopedia 1 0
    Edema Phenopedia 1 0
    Syndrome Phenopedia 1 0
    Upper Extremity Deformities, Congenital Phenopedia 1 0
    Heart Block Phenopedia 1 0
    Hypoplastic Left Heart Syndrome Phenopedia 1 0
    Myelodysplastic Syndromes Phenopedia 1 0
    Graves Disease Phenopedia 1 0
    Alagille Syndrome Phenopedia 1 0
    Parkinson Disease Phenopedia 1 0
    Endocardial Cushion Defects Phenopedia 1 0
    Leukemia, Myeloid, Acute Phenopedia 1 0
    Abnormalities, Multiple Phenopedia 1 0
    Syncope Phenopedia 1 0
    Ductus Arteriosus, Patent Phenopedia 1 0
    Hypertrophy, Left Ventricular Phenopedia 1 0
    Autistic Disorder Phenopedia 1 0
    Diabetes Mellitus, Type 2 Phenopedia 1 0
    Ebstein Anomaly Phenopedia 1 0
    Genetic Diseases, Inborn Phenopedia 1 0
    Lower Extremity Deformities, Congenital Phenopedia 1 0
    Microvascular Angina 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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