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Genopedia


TGFA
141 disease terms (MeSH) has been reported with TGFA gene.

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Disease Term (MeSH)
Total Publication
Meta-analysis Publications
    Cleft Lip Phenopedia 33 4
    Cleft Palate Phenopedia 33 4
    Colorectal Neoplasms Phenopedia 9 0
    Liver Neoplasms Phenopedia 8 0
    Lung Neoplasms Phenopedia 7 0
    Carcinoma, Squamous Cell Phenopedia 7 0
    Breast Neoplasms Phenopedia 7 0
    Disease Progression Phenopedia 7 0
    Carcinoma, Non-Small-Cell Lung Phenopedia 6 0
    Ovarian Neoplasms Phenopedia 5 0
    Stomach Neoplasms Phenopedia 5 0
    Pre-Eclampsia Phenopedia 4 0
    Prostatic Neoplasms Phenopedia 4 0
    Neoplasm Invasiveness Phenopedia 4 0
    Adenocarcinoma Phenopedia 4 0
    Colonic Neoplasms Phenopedia 4 0
    Head and Neck Neoplasms Phenopedia 4 0
    Inflammation Phenopedia 4 0
    Kidney Neoplasms Phenopedia 3 0
    Glioma Phenopedia 3 0
    Anodontia Phenopedia 3 0
    Carcinoma, Renal Cell Phenopedia 3 0
    Neoplasm Metastasis Phenopedia 3 0
    Osteoarthritis, Hip Phenopedia 3 0
    Osteoarthritis, Knee Phenopedia 3 0
    Uterine Cervical Neoplasms Phenopedia 3 0
    Telangiectasia, Hereditary Hemorrhagic Phenopedia 2 0
    Osteoarthritis Phenopedia 2 0
    Neovascularization, Pathologic Phenopedia 2 0
    Neoplasm Recurrence, Local Phenopedia 2 0
    Mouth Neoplasms Phenopedia 2 0
    Lupus Erythematosus, Systemic Phenopedia 2 0
    Lymphoma, Large B-Cell, Diffuse Phenopedia 2 0
    Brain Neoplasms Phenopedia 2 0
    Arthritis, Rheumatoid Phenopedia 2 0
    Cardiovascular Diseases Phenopedia 2 0
    Cell Transformation, Neoplastic Phenopedia 2 0
    Edema Phenopedia 2 0
    Esophageal Neoplasms Phenopedia 2 0
    Disease Models, Animal Phenopedia 2 0
    Crohn Disease Phenopedia 2 0
    Hypertension Phenopedia 2 0
    Hepatitis C, Chronic Phenopedia 2 0
    HIV Infections Phenopedia 2 0
    Holoprosencephaly Phenopedia 1 0
    Hypersensitivity Phenopedia 1 0
    Hepatitis, Autoimmune Phenopedia 1 0
    Hearing Loss Phenopedia 1 0
    Heart Defects, Congenital Phenopedia 1 0
    Heart Failure, Diastolic Phenopedia 1 0
    Heart Septal Defects, Ventricular Phenopedia 1 0
    Hemochromatosis Phenopedia 1 0
    Hepatitis B, Chronic Phenopedia 1 0
    Hypertrophy, Left Ventricular Phenopedia 1 0
    Latent Tuberculosis Phenopedia 1 0
    Liver Cirrhosis Phenopedia 1 0
    Intracranial Arteriovenous Malformations Phenopedia 1 0
    Intracranial Hemorrhages Phenopedia 1 0
    Irritable Bowel Syndrome Phenopedia 1 0
    Dental Enamel Hypoplasia Phenopedia 1 0
    Diabetes Mellitus, Type 2 Phenopedia 1 0
    Diabetes, Gestational Phenopedia 1 0
    Disease Susceptibility Phenopedia 1 0
    Drug Toxicity Phenopedia 1 0
    Fatigue Syndrome, Chronic Phenopedia 1 0
    Fibrosis Phenopedia 1 0
    End Stage Liver Disease Phenopedia 1 0
    Glomerulonephritis, IGA Phenopedia 1 0
    Glioblastoma Phenopedia 1 0
    Cellulitis Phenopedia 1 0
    Central Nervous System Vascular Malformations Phenopedia 1 0
    Chagas Cardiomyopathy Phenopedia 1 0
    Chagas Disease Phenopedia 1 0
    Cholangiocarcinoma Phenopedia 1 0
    Chronic Disease Phenopedia 1 0
    Cardiomyopathy, Dilated Phenopedia 1 0
    Colitis, Ulcerative Phenopedia 1 0
    Constriction, Pathologic Phenopedia 1 0
    Corneal Dystrophies, Hereditary Phenopedia 1 0
    Coronary Artery Disease Phenopedia 1 0
    Coronary Restenosis Phenopedia 1 0
    Cough Phenopedia 1 0
    Astrocytoma Phenopedia 1 0
    Bile Duct Neoplasms Phenopedia 1 0
    Adenocarcinoma, Mucinous Phenopedia 1 0
    Adenoma, Oxyphilic Phenopedia 1 0
    Alcoholism Phenopedia 1 0
    Anaplasia Phenopedia 1 0
    Carcinoma, Pancreatic Ductal Phenopedia 1 0
    Carcinoma, Ductal, Breast Phenopedia 1 0
    Carcinoma, Hepatocellular Phenopedia 1 0
    Carcinoma, Lobular Phenopedia 1 0
    Melanoma Phenopedia 1 0
    Mental Disorders Phenopedia 1 0
    Microsatellite Instability Phenopedia 1 0
    Mitral Valve Insufficiency Phenopedia 1 0
    Mitral Valve Prolapse Phenopedia 1 0
    Lymphadenitis Phenopedia 1 0
    Lymphatic Metastasis Phenopedia 1 0
    Lymphedema Phenopedia 1 0
    Muscular Dystrophy, Duchenne Phenopedia 1 0
    Myelodysplastic Syndromes Phenopedia 1 0
    Myocardial Infarction Phenopedia 1 0
    Myocardial Ischemia Phenopedia 1 0
    Nasopharyngeal Neoplasms Phenopedia 1 0
    Neoplasms, Glandular and Epithelial Phenopedia 1 0
    Obesity Phenopedia 1 0
    Occupational Diseases Phenopedia 1 0
    Lung Diseases, Interstitial Phenopedia 1 0
    Osteoporosis, Postmenopausal Phenopedia 1 0
    Pancreatic Neoplasms Phenopedia 1 0
    Postoperative Complications Phenopedia 1 0
    Pulmonary Disease, Chronic Obstructive Phenopedia 1 0
    Pulmonary Fibrosis Phenopedia 1 0
    Radiation Injuries Phenopedia 1 0
    Rectal Neoplasms Phenopedia 1 0
    Rheumatic Heart Disease Phenopedia 1 0
    Scleroderma, Diffuse Phenopedia 1 0
    Scleroderma, Limited Phenopedia 1 0
    Scleroderma, Systemic Phenopedia 1 0
    Spondylitis, Ankylosing Phenopedia 1 0
    Staphylococcal Infections Phenopedia 1 0
    Prenatal Exposure Delayed Effects Phenopedia 1 0
    Prostatic Hyperplasia Phenopedia 1 0
    Thyroid Neoplasms Phenopedia 1 0
    Tobacco Use Disorder Phenopedia 1 0
    Tooth Abnormalities Phenopedia 1 0
    Tuberculosis, Gastrointestinal Phenopedia 1 0
    Tuberculosis, Pulmonary Phenopedia 1 0
    Uniparental Disomy Phenopedia 1 0
    Urinary Bladder Neoplasms Phenopedia 1 0
    Urticaria Phenopedia 1 0
    Uveal Neoplasms Phenopedia 1 0
    Vascular Malformations Phenopedia 1 0
    Ventricular Dysfunction, Left Phenopedia 1 0
    Vitiligo Phenopedia 1 0
    Vitreoretinopathy, Proliferative Phenopedia 1 0
    von Hippel-Lindau Disease Phenopedia 1 0
    Stomatitis Phenopedia 1 0
    Stomatitis, Aphthous Phenopedia 1 0
    Takayasu Arteritis 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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