GeneID | Gene_Symbol | DisGeNet_diseaseID | Disease_name | DisGeNet score | DisGeNet_sourceDB |
5781 | PTPN11 | C0028326 | Noonan Syndrome | 0.818072426807894 | BEFREE;CTD_human;GAD;LHGDN;MGD;ORPHANET;UNIPROT |
5781 | PTPN11 | C0175704 | LEOPARD Syndrome | 0.72123787632838 | BEFREE;CTD_human;GAD;LHGDN;MGD;ORPHANET;UNIPROT |
5781 | PTPN11 | C0349639 | Juvenile Myelomonocytic Leukemia | 0.703243197991532 | BEFREE;CTD_human;GAD;HPO;LHGDN;MGD;ORPHANET;UNIPROT |
5781 | PTPN11 | C0410530 | Metachondromatosis | 0.481098907136852 | BEFREE;CTD_human;MGD;ORPHANET |
5781 | PTPN11 | C0014084 | Enchondromatosis | 0.400274726784213 | BEFREE;CTD_human;HPO |
5781 | PTPN11 | C0015934 | Fetal Growth Retardation | 0.28 | HPO;RGD |
5781 | PTPN11 | C0023418 | leukemia | 0.21797223193417 | BEFREE;CTD_human;GAD;LHGDN |
5781 | PTPN11 | C0007194 | Hypertrophic Cardiomyopathy | 0.204945082115836 | BEFREE;HPO |
5781 | PTPN11 | C0018817 | Atrial Septal Defects | 0.203007639249027 | BEFREE;HPO;LHGDN |
5781 | PTPN11 | C0221263 | Cafe-au-Lait Spots | 0.202732912464814 | HPO;LHGDN |
5781 | PTPN11 | C0003811 | Cardiac Arrhythmia | 0.202407028523288 | GAD;HPO |
5781 | PTPN11 | C0024236 | Lymphedema | 0.202407028523288 | GAD;HPO |
5781 | PTPN11 | C1956257 | Pulmonary Stenosis | 0.202197814273705 | BEFREE;HPO |
5781 | PTPN11 | C1275081 | Cardio-facio-cutaneous syndrome | 0.201648360705279 | BEFREE;CTD_human |
5781 | PTPN11 | C1328931 | Multiple lentigines | 0.201373633921065 | BEFREE;HPO |
5781 | PTPN11 | C0027819 | Neuroblastoma | 0.201373633921065 | BEFREE;CTD_human |
5781 | PTPN11 | C0587248 | Costello syndrome (disorder) | 0.201098907136852 | BEFREE;CTD_human |
5781 | PTPN11 | C0010417 | Cryptorchidism | 0.200549453568426 | BEFREE;HPO |
5781 | PTPN11 | C0018784 | Sensorineural Hearing Loss (disorder) | 0.200549453568426 | BEFREE;HPO |
5781 | PTPN11 | C0001418 | Adenocarcinoma | 0.200274726784213 | BEFREE;CTD_human |
5781 | PTPN11 | C0003492 | Aortic coarctation | 0.200274726784213 | BEFREE;HPO |
5781 | PTPN11 | C0004114 | Astrocytoma | 0.200274726784213 | BEFREE;CTD_human |
5781 | PTPN11 | C0005779 | Blood Coagulation Disorders | 0.200274726784213 | BEFREE;HPO |
5781 | PTPN11 | C0007137 | Squamous cell carcinoma | 0.200274726784213 | BEFREE;CTD_human |
5781 | PTPN11 | C0013274 | Patent ductus arteriosus | 0.200274726784213 | BEFREE;HPO |
5781 | PTPN11 | C0018818 | Ventricular Septal Defects | 0.200274726784213 | BEFREE;HPO |
5781 | PTPN11 | C0026106 | Mild Mental Retardation | 0.200274726784213 | BEFREE;HPO |
5781 | PTPN11 | C0206620 | Lymphangioma, Cystic | 0.200274726784213 | BEFREE;HPO |
5781 | PTPN11 | C0431478 | Posteriorly rotated ear | 0.200274726784213 | BEFREE;HPO |
5781 | PTPN11 | C0399526 | Class III malocclusion | 0.2 | HPO |
5781 | PTPN11 | C0423110 | Downward slant of palpebral fissure | 0.2 | HPO |
5781 | PTPN11 | C0426816 | Absence of rib | 0.2 | HPO |
5781 | PTPN11 | C0432333 | Abnormal dermatoglyphic pattern | 0.2 | HPO |
5781 | PTPN11 | C0520927 | Decreased fertility | 0.2 | HPO |
5781 | PTPN11 | C0521525 | Short neck | 0.2 | HPO |
5781 | PTPN11 | C0522055 | Electrocardiogram abnormal | 0.2 | HPO |
5781 | PTPN11 | C0541764 | Delayed bone age | 0.2 | HPO |
5781 | PTPN11 | C0544886 | Somatic mutation | 0.2 | HPO |
5781 | PTPN11 | C0575158 | Kyphoscoliosis deformity of spine | 0.2 | HPO |
5781 | PTPN11 | C0678230 | Congenital Epicanthus | 0.2 | HPO |
5781 | PTPN11 | C0685840 | Congenital hypoplasia of ovary | 0.2 | HPO |
5781 | PTPN11 | C0700208 | Acquired scoliosis | 0.2 | HPO |
5781 | PTPN11 | C0751690 | Malignant Peripheral Nerve Sheath Tumor | 0.2 | HPO |
5781 | PTPN11 | C0855329 | Electrocardiogram change | 0.2 | HPO |
5781 | PTPN11 | C0855740 | Abnormal platelet function | 0.2 | HPO |
5781 | PTPN11 | C0949173 | Delayed menarche | 0.2 | HPO |
5781 | PTPN11 | C1305420 | Prominent ear | 0.2 | HPO |
5781 | PTPN11 | C1386048 | Intrauterine retardation | 0.2 | HPO |
5781 | PTPN11 | C1389016 | ATRIOVENTRICULAR CANAL DEFECT | 0.2 | HPO |
5781 | PTPN11 | C1458140 | Bleeding tendency | 0.2 | HPO |
5781 | PTPN11 | C1691215 | Penile hypospadias | 0.2 | HPO |
5781 | PTPN11 | C1827524 | Wide spaced nipples | 0.2 | HPO |
5781 | PTPN11 | C1832603 | EKG abnormalities | 0.2 | HPO |
5781 | PTPN11 | C1834124 | Shield chest | 0.2 | HPO |
5781 | PTPN11 | C1835229 | Onset of lymphedema around puberty | 0.2 | HPO |
5781 | PTPN11 | C1835452 | Hypoplastic ovary | 0.2 | HPO |
5781 | PTPN11 | C1835884 | Triangular face | 0.2 | HPO |
5781 | PTPN11 | C1836189 | Radially deviated fingers | 0.2 | HPO |
5781 | PTPN11 | C1836940 | Excess nuchal skin | 0.2 | HPO |
5781 | PTPN11 | C1837404 | High, narrow palate | 0.2 | HPO |
5781 | PTPN11 | C1837732 | Thickened helices | 0.2 | HPO |
5781 | PTPN11 | C1837760 | Prominent eyes | 0.2 | HPO |
5781 | PTPN11 | C1839248 | Broad chest | 0.2 | HPO |
5781 | PTPN11 | C1839739 | Prominent lower lip | 0.2 | HPO |
5781 | PTPN11 | C1839764 | Broad flat nasal bridge | 0.2 | HPO |
5781 | PTPN11 | C1842820 | Cardiac conduction abnormalities | 0.2 | HPO |
5781 | PTPN11 | C1842876 | Depressed nasal ridge | 0.2 | HPO |
5781 | PTPN11 | C1846821 | Coagulation abnormalities | 0.2 | HPO |
5781 | PTPN11 | C1848490 | Protruding eyes | 0.2 | HPO |
5781 | PTPN11 | C1849367 | Nasal bridge wide | 0.2 | HPO |
5781 | PTPN11 | C1849955 | Limited elbow movement | 0.2 | HPO |
5781 | PTPN11 | C1853242 | Midface retrusion | 0.2 | HPO |
5781 | PTPN11 | C1855285 | Protruding ears | 0.2 | HPO |
5781 | PTPN11 | C1855340 | Bowing of the long bones | 0.2 | HPO |
5781 | PTPN11 | C1855728 | Low posterior hairline | 0.2 | HPO |
5781 | PTPN11 | C1857126 | Parietal bossing | 0.2 | HPO |
5781 | PTPN11 | C1857130 | Hypoplastic mandible condyle | 0.2 | HPO |
5781 | PTPN11 | C1857486 | Low-set, posteriorly rotated ears | 0.2 | HPO |
5781 | PTPN11 | C1859778 | Postnatal growth retardation | 0.2 | HPO |
5781 | PTPN11 | C1862425 | Prominent globes | 0.2 | HPO |
5781 | PTPN11 | C1864795 | Pectus carinatum superiorly | 0.2 | HPO |
5781 | PTPN11 | C1864796 | Pectus excavatum inferiorly | 0.2 | HPO |
5781 | PTPN11 | C1867873 | Failure to thrive in infancy | 0.2 | HPO |
5781 | PTPN11 | C2051831 | Pectus excavatum | 0.2 | HPO |
5781 | PTPN11 | C2053437 | Full lower lip | 0.2 | HPO |
5781 | PTPN11 | C2227134 | mandibular excess (physical finding) | 0.2 | HPO |
5781 | PTPN11 | C2364082 | Sense of smell impaired | 0.2 | HPO |
5781 | PTPN11 | C2673410 | Small midface | 0.2 | HPO |
5781 | PTPN11 | C2674608 | Feeding difficulties in infancy | 0.2 | HPO |
5781 | PTPN11 | C2677762 | Tall forehead | 0.2 | HPO |
5781 | PTPN11 | C2981150 | Uranostaphyloschisis | 0.2 | HPO |
5781 | PTPN11 | C3164374 | Abnormality of pulmonary valve | 0.2 | HPO |
5781 | PTPN11 | C3489396 | Hypogonadism, Isolated Hypogonadotropic | 0.2 | HPO |
5781 | PTPN11 | C3553764 | Joint hyperflexibility | 0.2 | HPO |
5781 | PTPN11 | C4020962 | Enlarged thorax | 0.2 | HPO |
5781 | PTPN11 | C4021533 | Severe sensorineural hearing impairment | 0.2 | HPO |
5781 | PTPN11 | C4023397 | Abnormal hair quantity | 0.2 | HPO |
5781 | PTPN11 | C4023909 | Aplasia/Hypoplasia of the abdominal wall musculature | 0.2 | HPO |
5781 | PTPN11 | C4024692 | Reduced factor XIII activity | 0.2 | HPO |
5781 | PTPN11 | C4025162 | Multiple digital exostoses | 0.2 | HPO |
5781 | PTPN11 | C4025749 | Abnormality of the spleen | 0.2 | HPO |
5781 | PTPN11 | C4072834 | Rough hair texture | 0.2 | HPO |
5781 | PTPN11 | C4072849 | Scapular weakness | 0.2 | HPO |
5781 | PTPN11 | C4280269 | Noncancerous mole | 0.2 | HPO |
5781 | PTPN11 | C4280304 | Curvature of digit | 0.2 | HPO |
5781 | PTPN11 | C4280320 | Hypotrophic midface | 0.2 | HPO |
5781 | PTPN11 | C4280321 | Decreased projection of midface | 0.2 | HPO |
5781 | PTPN11 | C4280613 | Angle class 3 malocclusion | 0.2 | HPO |
5781 | PTPN11 | C4280614 | Angle class 2 malocclusion | 0.2 | HPO |
5781 | PTPN11 | C4280644 | Increased size of mandible | 0.2 | HPO |
5781 | PTPN11 | C4280645 | Hypertrophy of lower jaw | 0.2 | HPO |
5781 | PTPN11 | C0005745 | Blepharoptosis | 0.2 | HPO |
5781 | PTPN11 | C0006384 | Bundle-Branch Block | 0.2 | HPO |
5781 | PTPN11 | C0008925 | Cleft Palate | 0.2 | HPO |
5781 | PTPN11 | C0009681 | Anomalous pulmonary artery | 0.2 | HPO |
5781 | PTPN11 | C0013362 | Dysarthria | 0.2 | HPO |
5781 | PTPN11 | C0014116 | Endocardial Cushion Defects | 0.2 | HPO |
5781 | PTPN11 | C0015300 | Exophthalmos | 0.2 | HPO |
5781 | PTPN11 | C0015306 | Hereditary Multiple Exostoses | 0.2 | CTD_human |
5781 | PTPN11 | C0015526 | Factor XII Deficiency | 0.2 | HPO |
5781 | PTPN11 | C0016689 | Freckles | 0.2 | HPO |
5781 | PTPN11 | C0019087 | Hemorrhagic Disorders | 0.2 | HPO |
5781 | PTPN11 | C0019209 | Hepatomegaly | 0.2 | HPO |
5781 | PTPN11 | C0020534 | Orbital separation excessive | 0.2 | HPO |
5781 | PTPN11 | C0021296 | Infant, Small for Gestational Age | 0.2 | HPO |
5781 | PTPN11 | C0021364 | Male infertility | 0.2 | HPO |
5781 | PTPN11 | C0022408 | Arthropathy | 0.2 | HPO |
5781 | PTPN11 | C0024636 | Malocclusion | 0.2 | HPO |
5781 | PTPN11 | C0025990 | Micrognathism | 0.2 | HPO |
5781 | PTPN11 | C0026267 | Mitral Valve Prolapse Syndrome | 0.2 | HPO |
5781 | PTPN11 | C0026827 | Muscle hypotonia | 0.2 | HPO |
5781 | PTPN11 | C0027092 | Myopia | 0.2 | HPO |
5781 | PTPN11 | C0027962 | Melanocytic nevus | 0.2 | HPO |
5781 | PTPN11 | C0029423 | Cartilaginous exostosis | 0.2 | CTD_human |
5781 | PTPN11 | C0034012 | Delayed Puberty | 0.2 | HPO |
5781 | PTPN11 | C0036651 | Senile lentigo | 0.2 | HPO |
5781 | PTPN11 | C0037932 | Curvature of spine | 0.2 | HPO |
5781 | PTPN11 | C0038379 | Strabismus | 0.2 | HPO |
5781 | PTPN11 | C0039103 | Synovitis | 0.2 | HPO |
5781 | PTPN11 | C0080174 | Spina Bifida Occulta | 0.2 | HPO |
5781 | PTPN11 | C0151517 | Complete atrioventricular block | 0.2 | HPO |
5781 | PTPN11 | C0151786 | Muscle Weakness | 0.2 | HPO |
5781 | PTPN11 | C0152438 | Sprengel deformity | 0.2 | HPO |
5781 | PTPN11 | C0158465 | Acquired cubitus valgus | 0.2 | HPO |
5781 | PTPN11 | C0158731 | Congenital pectus carinatum | 0.2 | HPO |
5781 | PTPN11 | C0206729 | Neurofibrosarcoma | 0.2 | HPO |
5781 | PTPN11 | C0221217 | Neck webbing | 0.2 | HPO |
5781 | PTPN11 | C0221357 | Brachydactyly | 0.2 | HPO |
5781 | PTPN11 | C0238397 | Pulmonary artery stenosis | 0.2 | HPO |
5781 | PTPN11 | C0239234 | Low set ears | 0.2 | HPO |
5781 | PTPN11 | C0239676 | High forehead | 0.2 | HPO |
5781 | PTPN11 | C0240083 | joint abnormality | 0.2 | HPO |
5781 | PTPN11 | C0240278 | Lymphatic obstruction | 0.2 | HPO |
5781 | PTPN11 | C0240295 | Mandibular hypoplasia | 0.2 | HPO |
5781 | PTPN11 | C0240635 | Byzanthine arch palate | 0.2 | HPO |
5781 | PTPN11 | C0240953 | Winged scapula | 0.2 | HPO |
5781 | PTPN11 | C0241074 | Skin hyperelastic | 0.2 | HPO |
5781 | PTPN11 | C0264886 | Conduction disorder of the heart | 0.2 | HPO |
5781 | PTPN11 | C0265610 | Congenital clinodactyly | 0.2 | HPO |
5781 | PTPN11 | C0265974 | Birthmark | 0.2 | HPO |
5781 | PTPN11 | C0266294 | Unilateral agenesis of kidney | 0.2 | HPO |
5781 | PTPN11 | C0266368 | Congenital absence of ovary | 0.2 | HPO |
5781 | PTPN11 | C0266435 | Congenital hypoplasia of penis | 0.2 | HPO |
5781 | PTPN11 | C0271623 | Hypogonadotropic hypogonadism | 0.2 | HPO |
5781 | PTPN11 | C0277959 | Coarse hair | 0.2 | HPO |
5781 | PTPN11 | C0302501 | Mandibular hyperplasia | 0.2 | HPO |
5781 | PTPN11 | C0340375 | Subaortic stenosis | 0.2 | HPO |
5781 | PTPN11 | C0349588 | Short stature | 0.2 | HPO |
5781 | PTPN11 | C0398639 | Amegakaryocytic thrombocytopenia | 0.2 | HPO |
5781 | PTPN11 | C0041409 | Turner Syndrome, Male | 0.0250001373633921 | BEFREE |
5781 | PTPN11 | C0021400 | Influenza | 0.0153846999159336 | BEFREE |
5781 | PTPN11 | C0023467 | Leukemia, Myelocytic, Acute | 0.0128179355687513 | BEFREE;GAD;LHGDN |
5781 | PTPN11 | C3463824 | MYELODYSPLASTIC SYNDROME | 0.00984709809971986 | BEFREE;LHGDN |
5781 | PTPN11 | C1961102 | Precursor Cell Lymphoblastic Leukemia Lymphoma | 0.00837114986402905 | BEFREE;GAD;LHGDN |
5781 | PTPN11 | C0034089 | Pulmonary Valve Stenosis | 0.0062900052822668 | BEFREE;LHGDN |
5781 | PTPN11 | C0018798 | Congenital Heart Defects | 0.0061876909676415 | BEFREE;GAD |
5781 | PTPN11 | C0017154 | Gastritis, Atrophic | 0.0059129641834284 | BEFREE;GAD |
5781 | PTPN11 | C0023480 | Leukemia, Myelomonocytic, Chronic | 0.00541466777231485 | BEFREE;GAD;LHGDN |
5781 | PTPN11 | C0011053 | Deafness | 0.00513994098810175 | GAD;LHGDN |
5781 | PTPN11 | C0596263 | Carcinogenesis | 0.0043956285474096 | BEFREE |
5781 | PTPN11 | C0017636 | Glioblastoma | 0.00410654638587925 | BEFREE;LHGDN |
5781 | PTPN11 | C0024623 | Malignant neoplasm of stomach | 0.0040553892285666 | BEFREE;GAD |
5781 | PTPN11 | C0017638 | Glioma | 0.0035059356601404 | BEFREE;GAD |
5781 | PTPN11 | C0008073 | Developmental Disabilities | 0.0030219946263441 | BEFREE |
5781 | PTPN11 | C0018799 | Heart Diseases | 0.00300763924902685 | BEFREE;LHGDN |
5781 | PTPN11 | C0079773 | Lymphoma, T-Cell, Cutaneous | 0.00300763924902685 | BEFREE;LHGDN |
5781 | PTPN11 | C0009324 | Ulcerative Colitis | 0.0029564820917142 | BEFREE;GAD |
5781 | PTPN11 | C0006142 | Malignant neoplasm of breast | 0.002747267842131 | BEFREE |
5781 | PTPN11 | C0011311 | Dengue Fever | 0.002747267842131 | BEFREE |
5781 | PTPN11 | C0678222 | Breast Carcinoma | 0.002747267842131 | BEFREE |
5781 | PTPN11 | C1176475 | Ductal Carcinoma | 0.00273291246481375 | LHGDN |
5781 | PTPN11 | C1261287 | Stenosis | 0.00273291246481375 | LHGDN |
5781 | PTPN11 | C3714514 | Infection | 0.00273291246481375 | LHGDN |
5781 | PTPN11 | C0019080 | Hemorrhage | 0.00273291246481375 | LHGDN |
5781 | PTPN11 | C0027662 | Multiple Endocrine Neoplasia | 0.00273291246481375 | LHGDN |
5781 | PTPN11 | C0079731 | B-Cell Lymphomas | 0.00273291246481375 | LHGDN |
5781 | PTPN11 | C0333641 | Atrophic | 0.00273291246481375 | LHGDN |
5781 | PTPN11 | C0023448 | Lymphoid leukemia | 0.0026817553075011 | BEFREE;GAD |
5781 | PTPN11 | C0030297 | Pancreatic Neoplasm | 0.0026817553075011 | BEFREE;GAD |
5781 | PTPN11 | C0280100 | solid tumor | 0.0024725410579179 | BEFREE |
5781 | PTPN11 | C0001403 | Addison Disease | 0.002407028523288 | GAD |
5781 | PTPN11 | C0003910 | Articulation Disorders | 0.002407028523288 | GAD |
5781 | PTPN11 | C0007222 | Cardiovascular Diseases | 0.002407028523288 | GAD |
5781 | PTPN11 | C0010346 | Crohn Disease | 0.002407028523288 | GAD |
5781 | PTPN11 | C0013388 | Dyslexia, Acquired | 0.002407028523288 | GAD |
5781 | PTPN11 | C0013575 | Ectodermal Dysplasia | 0.002407028523288 | GAD |
5781 | PTPN11 | C0018273 | Growth Disorders | 0.002407028523288 | GAD |
5781 | PTPN11 | C0018772 | Hearing Loss, Partial | 0.002407028523288 | GAD |
5781 | PTPN11 | C0023015 | Language Disorders | 0.002407028523288 | GAD |
5781 | PTPN11 | C0025568 | Metaplasia | 0.002407028523288 | GAD |
5781 | PTPN11 | C0030920 | Peptic Ulcer | 0.002407028523288 | GAD |
5781 | PTPN11 | C0037268 | Skin Abnormalities | 0.002407028523288 | GAD |
5781 | PTPN11 | C0038356 | Stomach Neoplasms | 0.002407028523288 | GAD |
5781 | PTPN11 | C0079487 | Helicobacter Infections | 0.002407028523288 | GAD |
5781 | PTPN11 | C0149721 | Left Ventricular Hypertrophy | 0.002407028523288 | GAD |
5781 | PTPN11 | C0376634 | Craniofacial Abnormalities | 0.002407028523288 | GAD |
5781 | PTPN11 | C0597735 | stomach atrophy | 0.002407028523288 | GAD |
5781 | PTPN11 | C1384666 | hearing impairment | 0.002407028523288 | GAD |
5781 | PTPN11 | C3887873 | Hearing Loss | 0.002407028523288 | GAD |
5781 | PTPN11 | C0598766 | Leukemogenesis | 0.0021978142737048 | BEFREE |
5781 | PTPN11 | C0023449 | Acute lymphocytic leukemia | 0.0019230874894917 | BEFREE |
5781 | PTPN11 | C0376545 | Hematologic Neoplasms | 0.0019230874894917 | BEFREE |
5781 | PTPN11 | C0027627 | Neoplasm Metastasis | 0.0016483607052786 | BEFREE |
5781 | PTPN11 | C0042769 | Virus Diseases | 0.0016483607052786 | BEFREE |
5781 | PTPN11 | C0013336 | Dwarfism | 0.0013736339210655 | BEFREE |
5781 | PTPN11 | C0027022 | Myeloproliferative disease | 0.0013736339210655 | BEFREE |
5781 | PTPN11 | C0027831 | Neurofibromatosis 1 | 0.0013736339210655 | BEFREE |
5781 | PTPN11 | C0699791 | Stomach Carcinoma | 0.0013736339210655 | BEFREE |
5781 | PTPN11 | C1096184 | West Nile viral infection | 0.0013736339210655 | BEFREE |
5781 | PTPN11 | C1292778 | Chronic myeloproliferative disorder | 0.0013736339210655 | BEFREE |
5781 | PTPN11 | C1959635 | Parvovirus B19 (disease) | 0.0013736339210655 | BEFREE |
5781 | PTPN11 | C2239176 | Liver carcinoma | 0.0013736339210655 | BEFREE |
5781 | PTPN11 | C0424295 | Hyperactive behavior | 0.0010989071368524 | BEFREE |
5781 | PTPN11 | C0684249 | Carcinoma of lung | 0.0010989071368524 | BEFREE |
5781 | PTPN11 | C0699790 | Colon Carcinoma | 0.0010989071368524 | BEFREE |
5781 | PTPN11 | C1306460 | Primary malignant neoplasm of lung | 0.0010989071368524 | BEFREE |
5781 | PTPN11 | C3539878 | Triple Negative Breast Neoplasms | 0.0010989071368524 | BEFREE |
5781 | PTPN11 | C0014057 | Japanese Encephalitis | 0.0010989071368524 | BEFREE |
5781 | PTPN11 | C0242379 | Malignant neoplasm of lung | 0.0010989071368524 | BEFREE |
5781 | PTPN11 | C0003873 | Rheumatoid Arthritis | 0.0008241803526393 | BEFREE |
5781 | PTPN11 | C0019196 | Hepatitis C | 0.0008241803526393 | BEFREE |
5781 | PTPN11 | C0023264 | Leigh Disease | 0.0008241803526393 | BEFREE |
5781 | PTPN11 | C0152021 | Congenital heart disease | 0.0008241803526393 | BEFREE |
5781 | PTPN11 | C0220621 | pediatric acute myeloblastic leukemia | 0.0008241803526393 | BEFREE |
5781 | PTPN11 | C0374997 | Helicobacter pylori (H. pylori) infection in conditions classified elsewhere and of unspecified site | 0.0008241803526393 | BEFREE |
5781 | PTPN11 | C0375023 | Respiratory syncytial virus (RSV) infection in conditions classified elsewhere and of unspecified site | 0.0008241803526393 | BEFREE |
5781 | PTPN11 | C0700095 | Central neuroblastoma | 0.0008241803526393 | BEFREE |
5781 | PTPN11 | C0741916 | Cardiac defects | 0.0008241803526393 | BEFREE |
5781 | PTPN11 | C1458155 | Mammary Neoplasms | 0.0008241803526393 | BEFREE |
5781 | PTPN11 | C1621958 | Glioblastoma Multiforme | 0.0008241803526393 | BEFREE |
5781 | PTPN11 | C1292769 | Precursor B-cell lymphoblastic leukemia | 0.0005494535684262 | BEFREE |
5781 | PTPN11 | C1292780 | Therapy-related myelodysplastic syndrome | 0.0005494535684262 | BEFREE |
5781 | PTPN11 | C2697636 | Hyperdiploid B Acute Lymphoblastic Leukemia | 0.0005494535684262 | BEFREE |
5781 | PTPN11 | C3887505 | DYSFUNCTION - SKIN DISORDERS | 0.0005494535684262 | BEFREE |
5781 | PTPN11 | C4021790 | Abnormality of the skeletal system | 0.0005494535684262 | BEFREE |
5781 | PTPN11 | C0000744 | Abetalipoproteinemia | 0.0005494535684262 | BEFREE |
5781 | PTPN11 | C0000768 | Congenital Abnormality | 0.0005494535684262 | BEFREE |
5781 | PTPN11 | C0007102 | Malignant tumor of colon | 0.0005494535684262 | BEFREE |
5781 | PTPN11 | C0007131 | Non-Small Cell Lung Carcinoma | 0.0005494535684262 | BEFREE |
5781 | PTPN11 | C0009319 | Colitis | 0.0005494535684262 | BEFREE |
5781 | PTPN11 | C0014061 | Tick-Borne Encephalitis | 0.0005494535684262 | BEFREE |
5781 | PTPN11 | C0023465 | Acute monocytic leukemia | 0.0005494535684262 | BEFREE |
5781 | PTPN11 | C0023473 | Myeloid Leukemia, Chronic | 0.0005494535684262 | BEFREE |
5781 | PTPN11 | C0024299 | Lymphoma | 0.0005494535684262 | BEFREE |
5781 | PTPN11 | C0025202 | melanoma | 0.0005494535684262 | BEFREE |
5781 | PTPN11 | C0028754 | Obesity | 0.0005494535684262 | BEFREE |
5781 | PTPN11 | C0035412 | Rhabdomyosarcoma | 0.0005494535684262 | BEFREE |
5781 | PTPN11 | C0085669 | Acute leukemia | 0.0005494535684262 | BEFREE |
5781 | PTPN11 | C0153381 | Malignant neoplasm of mouth | 0.0005494535684262 | BEFREE |
5781 | PTPN11 | C0162678 | Neurofibromatoses | 0.0005494535684262 | BEFREE |
5781 | PTPN11 | C0178874 | Tumor Progression | 0.0005494535684262 | BEFREE |
5781 | PTPN11 | C0206180 | Ki-1+ Anaplastic Large Cell Lymphoma | 0.0005494535684262 | BEFREE |
5781 | PTPN11 | C0220641 | Lip and Oral Cavity Carcinoma | 0.0005494535684262 | BEFREE |
5781 | PTPN11 | C0235974 | Pancreatic carcinoma | 0.0005494535684262 | BEFREE |
5781 | PTPN11 | C0275524 | Coinfection | 0.0005494535684262 | BEFREE |
5781 | PTPN11 | C0276275 | Disease due to Parvoviridae | 0.0005494535684262 | BEFREE |
5781 | PTPN11 | C0332996 | Persistent embryonic structure | 0.0005494535684262 | BEFREE |
5781 | PTPN11 | C0346647 | Malignant neoplasm of pancreas | 0.0005494535684262 | BEFREE |
5781 | PTPN11 | C0001430 | Adenoma | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C0003125 | Anorexia Nervosa | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C0003864 | Arthritis | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C0004096 | Asthma | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C0005866 | Bluetongue | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C0007107 | Malignant neoplasm of larynx | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C0007762 | Cerebellar Neoplasms | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C0007847 | Malignant tumor of cervix | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C0008029 | Cherubism | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C0008626 | Congenital chromosomal disease | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C0009241 | Cognition Disorders | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C0011195 | Dejerine-Sottas Disease (disorder) | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C0013080 | Down Syndrome | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C0013370 | Amebic colitis | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C0015230 | Exanthema | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C0015302 | External exotoses | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C0019693 | HIV Infections | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C0019829 | Hodgkin Disease | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C0021390 | Inflammatory Bowel Diseases | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C0022595 | Keratosis Follicularis | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C0022821 | Kyphosis deformity of spine | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C0023452 | Leukemia, Lymphocytic, Acute, L1 | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C0023470 | Myeloid Leukemia | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C0023487 | Acute Promyelocytic Leukemia | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C0023895 | Liver diseases | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C0024121 | Lung Neoplasms | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C0024305 | Lymphoma, Non-Hodgkin | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C0024454 | Maffucci Syndrome | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C0024790 | Paroxysmal nocturnal hemoglobinuria | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C0026499 | Monosomy | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C0026654 | Moyamoya Disease | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C0026764 | Multiple Myeloma | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C0029408 | Degenerative polyarthritis | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C0029456 | Osteoporosis | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C0035235 | Respiratory Syncytial Virus Infections | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C0036439 | Scoliosis, unspecified | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C0037221 | Situs Inversus | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C0038354 | Stomach Diseases | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C0038395 | Streptococcal Infections | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C0039685 | Tetralogy of Fallot | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C0040034 | Thrombocytopenia | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C0042214 | Vaccinia | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C0043395 | Yellow Fever | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C0085273 | Erythema Infectiosum | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C0152013 | Adenocarcinoma of lung (disorder) | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C0156147 | Crohn's disease of large bowel | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C0206624 | Hepatoblastoma | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C0220615 | Adult Acute Myeloblastic Leukemia | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C0220620 | Gastrointestinal Carcinoid Tumor | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C0235813 | Neonatal leukaemia | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C0239894 | HEART DISPLACEMENT | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C0242596 | Neoplasm, Residual | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C0263630 | Hypertrophic disorder of skin, unspecified | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C0265218 | Neu-Laxova syndrome | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C0265509 | Congenital anomaly of skeletal bone | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C0265962 | Ichthyosis linearis circumflexa | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C0266617 | Congenital anomaly of face | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C0272278 | Congenital thrombocytopenia | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C0278694 | Disseminated neuroblastoma | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C0278996 | Cancer of Head and Neck | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C0279000 | Liver and Intrahepatic Biliary Tract Carcinoma | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C0280321 | Squamous cell carcinoma of the hypopharynx | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C0302592 | Cervix carcinoma | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C0333186 | Restenosis | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C0334583 | Pilocytic Astrocytoma | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C0338656 | Impaired cognition | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C0341439 | Chronic liver disease | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C0344724 | Ostium secundum atrial septal defect | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C0344772 | Cleft leaflet of mitral valve | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C0345904 | Malignant neoplasm of liver | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C0346429 | Multiple malignancy | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C0376544 | Hematopoietic Neoplasms | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C0410422 | Chronic multifocal osteomyelitis | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C0457179 | Desmoplastic infantile astrocytoma | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C0476147 | Chondrogenic Neoplasm | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C0553580 | Ewings sarcoma | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C0595989 | Carcinoma of larynx | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C0686619 | Secondary malignant neoplasm of lymph node | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C0795693 | Skeletal malformation | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C0796195 | Waisman syndrome | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C0848332 | Spots on skin | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C0850666 | helicobacter pylori infection | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C0878544 | Cardiomyopathies | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C1134719 | Invasive Ductal Breast Carcinoma | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C1264606 | Persistent infection | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C1292758 | Precursor T-cell lymphoblastic lymphoma | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C1301359 | Precursor T cell lymphoblastic leukemia/lymphoblastic lymphoma | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C1314694 | Astrocytoma, low grade | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C1321546 | Anaplastic large B-cell lymphoma | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C1336735 | Therapy-Related Acute Myeloid Leukemia | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C1442903 | Exostoses | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C1449563 | Cardiomyopathy, Familial Idiopathic | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C1512409 | Hepatocarcinogenesis | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C1519086 | Pilomyxoid astrocytoma | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C1519680 | Tumor Immunity | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C1704356 | Enchondroma | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C1737329 | Dysmorphism | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C1834120 | NOONAN-LIKE/MULTIPLE GIANT CELL LESION SYNDROME (disorder) | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C1848296 | DOSAGE-SENSITIVE SEX REVERSAL | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C1861235 | Forebrain Defects | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C1864997 | Majeed syndrome | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C1865285 | Megalencephaly cutis marmorata telangiectatica congenita | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C1956346 | Coronary Artery Disease | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C1961099 | Precursor T-Cell Lymphoblastic Leukemia-Lymphoma | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C2076596 | Influenza A/H5N1 | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C2931384 | Moyamoya disease 1 | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C2931482 | Neurofibromatosis-Noonan syndrome | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C2939461 | Myeloid neoplasm | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C3161106 | Pulmonary interstitial glycogenosis | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C3203102 | Idiopathic pulmonary arterial hypertension | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C3264382 | Swine influenza virus (viruses that normally cause infections in pigs) | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C3826066 | Leukemia in children | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C3899989 | Autosomal Dominant Disorder | 0.0002747267842131 | BEFREE |
5781 | PTPN11 | C4048328 | cervical cancer | 0.0002747267842131 | BEFREE |