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Genopedia


PTPN11
114 disease terms (MeSH) has been reported with PTPN11 gene.

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Disease Term (MeSH)
Total Publication
Meta-analysis Publications
    Noonan Syndrome Phenopedia 37 0
    Leukemia, Myeloid, Acute Phenopedia 13 0
    Helicobacter Infections Phenopedia 9 1
    Heart Defects, Congenital Phenopedia 8 0
    Stomach Neoplasms Phenopedia 7 1
    Disease Progression Phenopedia 5 0
    Pulmonary Valve Stenosis Phenopedia 5 0
    Growth Disorders Phenopedia 4 0
    Chromosome Aberrations Phenopedia 4 0
    Ectodermal Dysplasia Phenopedia 4 0
    Leukemia, Myelomonocytic, Chronic Phenopedia 3 0
    Cardiomyopathy, Hypertrophic Phenopedia 3 0
    Failure to Thrive Phenopedia 3 0
    Atrophy Phenopedia 3 1
    Facies Phenopedia 3 0
    LEOPARD Syndrome Phenopedia 3 0
    Neurofibromatosis 1 Phenopedia 3 0
    Neoplasms Phenopedia 3 0
    Gastritis, Atrophic Phenopedia 3 0
    Leukemia, Myelomonocytic, Juvenile Phenopedia 3 0
    Arthritis, Rheumatoid Phenopedia 2 0
    Cardiovascular Diseases Phenopedia 2 0
    Developmental Disabilities Phenopedia 2 0
    Adenocarcinoma Phenopedia 2 0
    Cell Transformation, Neoplastic Phenopedia 2 0
    Myelodysplastic Syndromes Phenopedia 2 0
    Cognition Disorders Phenopedia 2 0
    Brain Neoplasms Phenopedia 2 0
    Abnormalities, Multiple Phenopedia 2 0
    Metaplasia Phenopedia 2 1
    Multiple Myeloma Phenopedia 1 0
    Carcinoma, Squamous Cell Phenopedia 1 0
    Central Nervous System Neoplasms Phenopedia 1 0
    Cleft Palate Phenopedia 1 0
    Endometrial Neoplasms Phenopedia 1 0
    Leukemia, Myeloid Phenopedia 1 0
    Memory Phenopedia 1 0
    Addison Disease Phenopedia 1 0
    Neoplasms, Second Primary Phenopedia 1 0
    Crohn Disease Phenopedia 1 0
    Cryptorchidism Phenopedia 1 0
    DiGeorge Syndrome Phenopedia 1 0
    Down Syndrome Phenopedia 1 0
    Dyslexia, Acquired Phenopedia 1 0
    Osteochondrodysplasias Phenopedia 1 0
    Peptic Ulcer Phenopedia 1 0
    Tetralogy of Fallot Phenopedia 1 0
    Liver Neoplasms Phenopedia 1 0
    Melanoma Phenopedia 1 0
    Myeloproliferative Disorders Phenopedia 1 0
    Precursor B-Cell Lymphoblastic Leukemia-Lymphoma Phenopedia 1 0
    Puberty, Delayed Phenopedia 1 0
    Skin Diseases Phenopedia 1 0
    Astrocytoma Phenopedia 1 0
    Cognition Phenopedia 1 0
    Ductus Arteriosus, Patent Phenopedia 1 0
    Hypertrophy, Left Ventricular Phenopedia 1 0
    Head and Neck Neoplasms Phenopedia 1 0
    Infant, Premature, Diseases Phenopedia 1 0
    Leukemia, B-Cell, Acute Phenopedia 1 0
    Lymphoma, Large B-Cell, Diffuse Phenopedia 1 0
    Motor Skills Phenopedia 1 0
    Colitis, Ulcerative Phenopedia 1 0
    Birth Weight Phenopedia 1 0
    Celiac Disease Phenopedia 1 0
    Lymphedema Phenopedia 1 0
    Epilepsies, Partial Phenopedia 1 0
    Hematologic Diseases Phenopedia 1 0
    Leukemia, Promyelocytic, Acute Phenopedia 1 0
    Mitochondrial Diseases Phenopedia 1 0
    Neurofibromatoses Phenopedia 1 0
    Obesity Phenopedia 1 0
    Ovarian Failure, Premature Phenopedia 1 0
    Tobacco Use Disorder Phenopedia 1 0
    Alagille Syndrome Phenopedia 1 0
    Breast Neoplasms Phenopedia 1 0
    Chylothorax Phenopedia 1 0
    Cleft Lip Phenopedia 1 0
    Epstein-Barr Virus Infections Phenopedia 1 0
    Glioma Phenopedia 1 0
    Neuropsychological Tests Phenopedia 1 0
    Precancerous Conditions Phenopedia 1 0
    Puberty, Precocious Phenopedia 1 0
    Hydrops Fetalis Phenopedia 1 0
    Syndrome Phenopedia 1 0
    Acute Disease Phenopedia 1 0
    Arrhythmias, Cardiac Phenopedia 1 0
    Costello Syndrome Phenopedia 1 0
    Craniofacial Abnormalities Phenopedia 1 0
    Pancreatic Neoplasms Phenopedia 1 0
    Marfan Syndrome Phenopedia 1 0
    Metabolic Syndrome X Phenopedia 1 0
    Hamartoma Phenopedia 1 0
    Hearing Loss Phenopedia 1 0
    Esophageal Neoplasms Phenopedia 1 0
    Glioblastoma Phenopedia 1 0
    Language Disorders Phenopedia 1 0
    Motor Skills Disorders Phenopedia 1 0
    Precursor T-Cell Lymphoblastic Leukemia-Lymphoma Phenopedia 1 0
    Pseudarthrosis Phenopedia 1 0
    Skin Abnormalities Phenopedia 1 0
    Thrombophilia Phenopedia 1 0
    Gastritis Phenopedia 1 0
    Heart Septal Defects, Atrial Phenopedia 1 0
    Leukemia, Lymphocytic, Acute, L1 Phenopedia 1 0
    Mouth Neoplasms Phenopedia 1 0
    Coronary Artery Disease Phenopedia 1 0
    Epilepsy, Complex Partial Phenopedia 1 0
    Hearing Phenopedia 1 0
    Heart Diseases Phenopedia 1 0
    Inflammation Phenopedia 1 0
    Leukemia Phenopedia 1 0
    Articulation Disorders Phenopedia 1 0
    Polycystic Ovary 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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