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Pediatric Disease Annotations & Medicines



   cytomegalovirus infections
  

Disease ID 1048
Disease cytomegalovirus infections
Definition
Infection with CYTOMEGALOVIRUS, characterized by enlarged cells bearing intranuclear inclusions. Infection may be in almost any organ, but the salivary glands are the most common site in children, as are the lungs in adults.
Synonym
[x]cytomegaloviral disease, unspecified
[x]cytomegaloviral disease, unspecified (disorder)
cmv
cmv - cytomegalovirus infection
cmv cytomegalovirus infection
cmv infection
cmv infections
cytomagalovirus infection
cytomegalic inclusion dis
cytomegalic inclusion disease
cytomegalic inclusion diseases
cytomegaloviral disease
cytomegaloviral infection
cytomegaloviral infections
cytomegalovirus
cytomegalovirus disease
cytomegalovirus infect
cytomegalovirus infection
cytomegalovirus infection (disorder)
cytomegalovirus infection, nos
cytomegalovirus infections [disease/finding]
disease due to cytomegalovirus
disease, cytomegalic inclusion
diseases, cytomegalic inclusion
hcmv infection
inclusion dis
inclusion disease
inclusion disease, cytomegalic
inclusion diseases
inclusion diseases, cytomegalic
infect cytomegalovirus
infection, cytomegalovirus
infections, cytomegalovirus
salivary gland virus dis
salivary gland virus disease
DOID
UMLS
C0010823
MeSH
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:256)
C0009324  |  ulcerative colitis  |  19
C0009319  |  colitis  |  17
C0001175  |  acquired immunodeficiency syndrome  |  15
C0021390  |  inflammatory bowel disease  |  14
C0040053  |  thrombosis  |  13
C0021831  |  bowel disease  |  12
C0035333  |  retinitis  |  10
C0032285  |  pneumonia  |  9
C0042769  |  viral infection  |  8
C0017636  |  glioblastoma  |  8
C0042769  |  viral infections  |  7
C0018784  |  sensorineural hearing loss  |  6
C0019158  |  hepatitis  |  6
C0023418  |  leukemia  |  6
C0002871  |  anemia  |  5
C0004153  |  atherosclerosis  |  4
C0001175  |  acquired immunodeficiency syndrome (aids)  |  4
C0010346  |  crohn's disease  |  4
C0009447  |  common variable immunodeficiency  |  4
C0014179  |  uterine infection  |  4
C0002878  |  hemolytic anemia  |  4
C0027697  |  nephritis  |  3
C0011991  |  diarrhea  |  3
C0011847  |  diabetes  |  3
C0030305  |  pancreatitis  |  3
C0008311  |  cholangitis  |  3
C0026764  |  multiple myeloma  |  3
C0021053  |  immune dysfunction  |  3
C0007113  |  rectal cancer  |  3
C0009402  |  colorectal cancer  |  3
C0008370  |  cholestasis  |  3
C0042164  |  uveitis  |  3
C0019196  |  hepatitis c  |  3
C0032285  |  pneumonitis  |  3
C0155773  |  portal vein thrombosis  |  3
C0042373  |  vascular disease  |  3
C0008513  |  chorioretinitis  |  3
C0014038  |  encephalitis  |  3
C0020538  |  hypertension  |  3
C1621958  |  glioblastoma multiforme  |  3
C0442874  |  neuropathy  |  3
C0034065  |  pulmonary embolism  |  2
C0409974  |  lupus erythematosus  |  2
C0085692  |  hemorrhagic cystitis  |  2
C0003873  |  rheumatoid arthritis  |  2
C0006142  |  breast cancer  |  2
C0001175  |  acquired immune deficiency syndrome  |  2
C0005411  |  biliary atresia  |  2
C0007193  |  dilated cardiomyopathy  |  2
C0178238  |  intestinal infection  |  2
C0878544  |  cardiomyopathy  |  2
C0042373  |  vascular diseases  |  2
C0024291  |  hemophagocytic lymphohistiocytosis  |  2
C0003864  |  arthritis  |  2
C0021400  |  influenza  |  2
C0021390  |  inflammatory bowel diseases  |  2
C0018801  |  heart failure  |  2
C0281963  |  red cell aplasia  |  2
C0035435  |  rheumatic disease  |  2
C0042384  |  angiitis  |  2
C0035305  |  retinal detachment  |  2
C0024141  |  systemic lupus erythematosus  |  2
C0025362  |  mental retardation  |  2
C0021053  |  immune disorders  |  2
C0042165  |  anterior uveitis  |  2
C0024314  |  lymphoproliferative disorder  |  2
C0085580  |  essential hypertension  |  2
C0023470  |  myeloid leukemia  |  2
C0004623  |  bacterial infection  |  2
C0027707  |  interstitial nephritis  |  2
C0001175  |  acquired immune deficiency  |  2
C0025202  |  melanoma  |  2
C0010068  |  coronary artery disease  |  2
C0021053  |  immune disorder  |  2
C0038325  |  stevens-johnson syndrome  |  2
C0021845  |  bowel perforation  |  2
C0010692  |  cystitis  |  2
C0014868  |  esophagitis  |  2
C0456909  |  blindness  |  2
C0270612  |  leukoencephalopathy  |  2
C0037998  |  splenic infarction  |  2
C0021053  |  immune disease  |  2
C0004030  |  aspergillosis  |  2
C0018378  |  guillain-barre syndrome  |  2
C0024312  |  lymphocytopenia  |  2
C0006840  |  candidiasis  |  2
C0026764  |  myeloma  |  2
C0520459  |  necrotizing enterocolitis  |  2
C0030312  |  pancytopenia  |  2
C0032305  |  pneumocystis  |  2
C0007222  |  cardiovascular disease  |  2
C0023890  |  cirrhosis  |  2
C0024299  |  lymphoma  |  2
C0032285  |  pneumoniae  |  2
C0024291  |  hemophagocytic syndrome  |  2
C0036220  |  kaposi's sarcoma  |  2
C0026946  |  fungal infection  |  2
C0555198  |  malignant glioma  |  2
C0034902  |  pure red cell aplasia  |  2
C0025160  |  megacolon  |  2
C0018799  |  heart disease  |  2
C0403529  |  goodpasture's syndrome  |  1
C0349639  |  juvenile myelomonocytic leukemia  |  1
C0001175  |  acquired immune deficiency syndrome (aids)  |  1
C0742472  |  central nervous system lymphoma  |  1
C0042769  |  virus infection  |  1
C0004352  |  autism  |  1
C0206178  |  cytomegalovirus retinitis  |  1
C0002395  |  alzheimer's disease  |  1
C0013990  |  emphysema  |  1
C1257843  |  pseudomembranous colitis  |  1
C0220650  |  brain metastases  |  1
C0007682  |  central nervous system disorders  |  1
C0272126  |  evans syndrome  |  1
C0008312  |  biliary cirrhosis  |  1
C0002170  |  alopecia  |  1
C0027819  |  neuroblastoma  |  1
C0023473  |  chronic myeloid leukemia  |  1
C0023473  |  chronic myelogenous leukemia  |  1
C0017601  |  glaucoma  |  1
C0376545  |  hematological malignancies  |  1
C0008049  |  varicella  |  1
C0000786  |  spontaneous abortion  |  1
C0001623  |  adrenal insufficiency  |  1
C0178664  |  glomerulosclerosis  |  1
C0034152  |  henoch-schonlein purpura  |  1
C0086543  |  cataract  |  1
C0149642  |  cervical lymphadenitis  |  1
C0035412  |  rhabdomyosarcomas  |  1
C0008312  |  primary biliary cirrhosis  |  1
C0023492  |  t-cell leukemia  |  1
C0021847  |  intestinal pseudoobstruction  |  1
C0034150  |  purpura  |  1
C0004114  |  astrocytoma  |  1
C0003615  |  appendicitis  |  1
C0221027  |  good's syndrome  |  1
C0040053  |  thrombus  |  1
C0025162  |  toxic megacolon  |  1
C1956346  |  coronary artery diseases  |  1
C0024115  |  lung disease  |  1
C0017178  |  gastrointestinal disease  |  1
C0162293  |  papillitis  |  1
C0007282  |  carotid stenosis  |  1
C0021845  |  intestinal perforation  |  1
C1261473  |  sarcoma  |  1
C0022568  |  keratitis  |  1
C0751606  |  adult all  |  1
C0334121  |  inflammatory pseudotumor  |  1
C0035222  |  acute respiratory distress syndrome  |  1
C0023530  |  leukopenia  |  1
C0027051  |  myocardial infarct  |  1
C0598894  |  monocytic leukemia  |  1
C0007137  |  squamous cell carcinoma  |  1
C0019348  |  herpes simplex  |  1
C0398623  |  hypercoagulability  |  1
C0152972  |  pseudomonas sepsis  |  1
C0032310  |  viral pneumonia  |  1
C0031099  |  periodontitis  |  1
C0011860  |  type 2 diabetes  |  1
C0085315  |  cerebral toxoplasmosis  |  1
C0026934  |  mycoplasma  |  1
C1565489  |  renal insufficiency  |  1
C0555198  |  malignant gliomas  |  1
C0259749  |  autonomic neuropathy  |  1
C0031117  |  peripheral neuropathy  |  1
C0152018  |  esophageal carcinoma  |  1
C0024440  |  cystoid macular edema  |  1
C0024205  |  lymphadenitis  |  1
C0010403  |  cryoglobulinemia  |  1
C0085110  |  severe combined immunodeficiency syndrome  |  1
C0007789  |  cerebral palsy  |  1
C0027059  |  myocarditis  |  1
C0026896  |  myasthenia gravis  |  1
C0019829  |  hodgkin's lymphoma  |  1
C0011570  |  depression  |  1
C0040034  |  thrombocytopenia  |  1
C0021831  |  intestinal disease  |  1
C0020542  |  pulmonary hypertension  |  1
C0014742  |  erythema multiforme  |  1
C0023891  |  alcoholic hepatic cirrhosis  |  1
C0271829  |  pendred syndrome  |  1
C0020456  |  hyperglycemia  |  1
C0031036  |  polyarteritis nodosa  |  1
C0026718  |  mucormycosis  |  1
C0206178  |  cmv retinitis  |  1
C0007222  |  cardiovascular diseases  |  1
C0032302  |  mycoplasma pneumonia  |  1
C0206744  |  cd4+ t-lymphocytopenia  |  1
C0036341  |  schizophrenia  |  1
C0004245  |  atrioventricular block  |  1
C0034050  |  alveolar proteinosis  |  1
C0021359  |  infertility  |  1
C0002874  |  aplastic anemia  |  1
C0043092  |  wegener's granulomatosis  |  1
C0023448  |  lymphoblastic leukemia  |  1
C0027051  |  myocardial infarction  |  1
C0004623  |  bacterial infections  |  1
C0022398  |  hyperimmunoglobulin e syndrome  |  1
C0032305  |  pneumocystis jiroveci pneumonia  |  1
C0155626  |  acute myocardial infarction  |  1
C0008313  |  sclerosing cholangitis  |  1
C0041349  |  tubulointerstitial nephritis  |  1
C0019360  |  herpes zoster  |  1
C0024314  |  lymphoproliferative disorders  |  1
C0025149  |  medulloblastomas  |  1
C0017160  |  gastroenteritis  |  1
C1704437  |  respiratory distress syndrome  |  1
C0028242  |  nocardiosis  |  1
C0002395  |  alzheimer disease  |  1
C0041948  |  uremia  |  1
C0206744  |  cd4 lymphocytopenia  |  1
C1145670  |  respiratory failure  |  1
C0085278  |  antiphospholipid syndrome  |  1
C0032914  |  preeclampsia  |  1
C0085110  |  severe combined immunodeficiency  |  1
C0040558  |  toxoplasmosis  |  1
C0038358  |  gastric ulcer  |  1
C0029134  |  optic neuritis  |  1
C0036454  |  visual field loss  |  1
C0031350  |  pharyngitis  |  1
C0041341  |  tuberous sclerosis complex  |  1
C0270922  |  demyelinating polyneuropathy  |  1
C0026946  |  fungal infections  |  1
C0027813  |  neuritis  |  1
C0020538  |  increased blood pressure  |  1
C0031090  |  periodontal disease  |  1
C0011633  |  dermatomyositis  |  1
C0085693  |  acute appendicitis  |  1
C0022116  |  ischemia  |  1
C0023890  |  hepatic cirrhosis  |  1
C0019360  |  zoster  |  1
C0017152  |  gastritis  |  1
C0023449  |  acute lymphoblastic leukemia  |  1
C0033860  |  psoriasis  |  1
C0085110  |  severe combined immunodefic  |  1
C0376175  |  bell's palsy  |  1
C0007787  |  transient ischemic attack  |  1
C0038463  |  strongyloidiasis  |  1
C0040381  |  tolosa-hunt syndrome  |  1
C0013295  |  duodenal ulcer  |  1
C0023470  |  myelogenous leukemia  |  1
C0334480  |  pleomorphic rhabdomyosarcoma  |  1
C0027726  |  nephrotic syndrome  |  1
C0024117  |  chronic obstructive pulmonary disease  |  1
C0021345  |  infectious mononucleosis  |  1
C0017658  |  glomerulonephritis  |  1
C0023467  |  acute myeloid leukemia  |  1
C0007860  |  cervicitis  |  1
C0155773  |  portal thrombosis  |  1
C0042384  |  vasculitis  |  1
C0235974  |  pancreatic cancer  |  1
C0034050  |  pulmonary alveolar proteinosis  |  1
C0008372  |  intrahepatic cholestasis  |  1
C0034069  |  pulmonary fibrosis  |  1
C0014236  |  endophthalmitis  |  1
C0024305  |  non-hodgkin's lymphoma  |  1
Curated Gene
Entrez_id | Symbol | Resource(Total Genes:1)
STAT1  |  6772  |  CTD_human
Inferring Gene
Entrez_id | Symbol | Resource(Total Genes:12)
3458  |  IFNG  |  infer
3586  |  IL10  |  infer
3569  |  IL6  |  infer
7097  |  TLR2  |  infer
1234  |  CCR5  |  infer
30835  |  CD209  |  infer
3105  |  HLA-A  |  infer
3106  |  HLA-B  |  infer
3107  |  HLA-C  |  infer
3123  |  HLA-DRB1  |  infer
4153  |  MBL2  |  infer
54106  |  TLR9  |  infer
Text Mined Gene(Waiting for update.)
Locus(Waiting for update.)
Disease ID 1048
Disease cytomegalovirus infections
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:178)
HP:0002721  |  Immunodeficiency  |  24
HP:0100279  |  Ulcerative colitis  |  18
HP:0002583  |  Colitis  |  16
HP:0100843  |  Glioblastoma  |  8
HP:0002090  |  Pneumonia  |  8
HP:0004936  |  Blood clot in vein  |  7
HP:0012115  |  Liver inflammation  |  6
HP:0000407  |  sensorineural hearing loss  |  6
HP:0001909  |  Leukemia  |  6
HP:0001903  |  Anemia  |  5
HP:0002960  |  Autoimmune condition  |  5
HP:0001878  |  Haemolytic anaemia  |  4
HP:0001945  |  Fever  |  4
HP:0002621  |  Atherosclerosis  |  4
HP:0100280  |  Morbus Crohn  |  4
HP:0002664  |  Neoplasia  |  4
HP:0004387  |  Enterocolitis  |  4
HP:0012424  |  Chorioretinitis  |  3
HP:0000123  |  Nephritis  |  3
HP:0000554  |  Uveitis  |  3
HP:0001907  |  Thromboembolic disease  |  3
HP:0002014  |  Diarrhea  |  3
HP:0001396  |  Cholestasis  |  3
HP:0002383  |  Encephalitis  |  3
HP:0012531  |  Pain  |  3
HP:0001394  |  Hepatic cirrhosis  |  3
HP:0000822  |  Hypertension  |  3
HP:0030151  |  Cholangitis  |  3
HP:0006775  |  Multiple myeloma  |  3
HP:0001733  |  Pancreatic inflammation  |  3
HP:0012174  |  Glioblastoma multiforme  |  3
HP:0001249  |  Mental retardation  |  2
HP:0002665  |  Lymphoma  |  2
HP:0012223  |  Ruptured spleen  |  2
HP:0001369  |  Arthritis  |  2
HP:0005912  |  Biliary duct atresia  |  2
HP:0001644  |  Congestive cardiomyopathy  |  2
HP:0001510  |  Growth deficiency  |  2
HP:0001970  |  Interstitial nephritis  |  2
HP:0001888  |  Lymphocytopenia  |  2
HP:0001518  |  Small for gestational age  |  2
HP:0000572  |  Visual loss  |  2
HP:0001638  |  Cardiomyopathy  |  2
HP:0000618  |  Blindness  |  2
HP:0002625  |  Blood clot in a deep vein  |  2
HP:0030242  |  Blood clot in portal vein  |  2
HP:0002239  |  Gastrointestinal hemorrhage  |  2
HP:0002013  |  Emesis  |  2
HP:0002352  |  Leukoencephalopathy  |  2
HP:0002725  |  Systemic lupus erythematosus  |  2
HP:0100806  |  Sepsis  |  2
HP:0001370  |  Rheumatoid arthritis  |  2
HP:0002098  |  Respiratory distress  |  2
HP:0005523  |  Lymphoproliferative disorder  |  2
HP:0002251  |  Hirschsprung megacolon  |  2
HP:0002584  |  Intestinal hemorrhage  |  2
HP:0001876  |  Low blood cell count  |  2
HP:0012122  |  Anterior uveitis  |  2
HP:0002861  |  Melanoma  |  2
HP:0003201  |  Rhabdomyolysis  |  2
HP:0005506  |  Chronic myeloid leukemia  |  2
HP:0012410  |  Pure red cell aplasia  |  2
HP:0001635  |  Congestive heart failure  |  2
HP:0012324  |  Myeloid leukemia  |  2
HP:0002204  |  Pulmonary embolism  |  2
HP:0002027  |  Abdominal pain  |  2
HP:0100633  |  Inflammation of the esophagus  |  2
HP:0009733  |  Glioma  |  2
HP:0003002  |  Breast carcinoma  |  2
HP:0100726  |  Kaposi's sarcoma  |  2
HP:0000365  |  Hearing impairment  |  2
HP:0001677  |  Coronary artery disease  |  2
HP:0002633  |  Vasculitis  |  2
HP:0000541  |  Detached retina  |  2
HP:0001263  |  Developmental retardation  |  2
HP:0000789  |  Infertility  |  1
HP:0011459  |  Esophageal carcinoma  |  1
HP:0001880  |  Eosinophilia  |  1
HP:0007902  |  Vitreous hemorrhage  |  1
HP:0002028  |  Chronic diarrhea  |  1
HP:0000717  |  Autism  |  1
HP:0003765  |  Psoriasis  |  1
HP:0030160  |  Uterine cervicitis  |  1
HP:0002322  |  Resting tremor  |  1
HP:0010636  |  Schizencephaly  |  1
HP:0002511  |  Late-onset form of familial Alzheimer disease  |  1
HP:0002840  |  Lymphadenitis  |  1
HP:0030149  |  Cardiovascular shock  |  1
HP:0001596  |  Hair loss  |  1
HP:0001882  |  Decreased blood leukocyte number  |  1
HP:0012209  |  Juvenile myelomonocytic leukemia  |  1
HP:0000716  |  Depression  |  1
HP:0100699  |  Scarring  |  1
HP:0009830  |  Peripheral neuritis  |  1
HP:0002500  |  Leukoaraiosis  |  1
HP:0006721  |  Acute lymphocytic leukemia  |  1
HP:0100753  |  Schizophrenia  |  1
HP:0000491  |  Corneal inflammation  |  1
HP:0000097  |  focal glomerulosclerosis  |  1
HP:0000597  |  Ophthalmoparesis  |  1
HP:0004808  |  Acute myelogenous leukemia  |  1
HP:0000100  |  Nephrosis  |  1
HP:0004430  |  Severe combined immunodeficiency  |  1
HP:0002092  |  Pulmonary artery hypertension  |  1
HP:0005263  |  Gastritis  |  1
HP:0100724  |  Hypercoagulability  |  1
HP:0005268  |  Spontaneous abortion  |  1
HP:0007868  |  ARMD  |  1
HP:0000979  |  Purpura  |  1
HP:0100749  |  Thoracic pain  |  1
HP:0002719  |  infections, recurrent  |  1
HP:0000010  |  Frequent urinary tract infections  |  1
HP:0006510  |  Chronic obstructive pulmonary disease  |  1
HP:0100242  |  Sarcoma  |  1
HP:0100546  |  Narrowing of carotid artery  |  1
HP:0012819  |  Myocarditis  |  1
HP:0001406  |  Intrahepatic cholestasis  |  1
HP:0001298  |  Encephalopathy  |  1
HP:0002588  |  Duodenal ulcer  |  1
HP:0009592  |  Astrocytoma  |  1
HP:0040113  |  Old-aged sensorineural hearing impairment  |  1
HP:0001658  |  Myocardial infarction  |  1
HP:0007985  |  Retinal arteriolar occlusion  |  1
HP:0000083  |  Renal insufficiency  |  1
HP:0000501  |  Glaucoma  |  1
HP:0012089  |  Arteritis  |  1
HP:0012593  |  Nephrotic range proteinuria  |  1
HP:0012715  |  Profound hearing impairment  |  1
HP:0001695  |  Cardiac arrest  |  1
HP:0001541  |  Ascites  |  1
HP:0002613  |  Biliary cirrhosis  |  1
HP:0002860  |  Squamous cell carcinoma  |  1
HP:0100653  |  Optic neuritis  |  1
HP:0005305  |  Cerebral vein thrombosis  |  1
HP:0012189  |  Hodgkin disease  |  1
HP:0000704  |  Pyorrhea  |  1
HP:0005364  |  Severe viral infections  |  1
HP:0002716  |  Lymph node hyperplasia  |  1
HP:0002094  |  Dyspnea  |  1
HP:0100021  |  Cerebral palsy  |  1
HP:0100602  |  Pre-eclampsia  |  1
HP:0004787  |  Fulminant hepatitis  |  1
HP:0000096  |  Glomerulosclerosis  |  1
HP:0001410  |  Decreased liver function  |  1
HP:0005387  |  Combined immunodeficiency  |  1
HP:0030746  |  Intraventricular hemorrhage  |  1
HP:0000099  |  Glomerular nephritis  |  1
HP:0002206  |  Pulmonary fibrosis  |  1
HP:0002126  |  Polymicrogyria  |  1
HP:0002894  |  Neoplasia of the pancreas  |  1
HP:0001678  |  Atrioventricular block  |  1
HP:0003006  |  Neuroblastoma  |  1
HP:0002955  |  Granulomatosis  |  1
HP:0011854  |  Hemoperitoneum  |  1
HP:0010783  |  Erythema  |  1
HP:0000518  |  Cataract  |  1
HP:0012054  |  Choroidal melanoma  |  1
HP:0002326  |  TIA  |  1
HP:0030248  |  Blood clot in mesentertic vein  |  1
HP:0000846  |  Hypoadrenalism  |  1
HP:0011505  |  Cystoid macular edema  |  1
HP:0001915  |  Aplastic anemia  |  1
HP:0003473  |  Fatigable weakness  |  1
HP:0002592  |  Stomach ulcer  |  1
HP:0010628  |  Facial palsy, unilateral or bilateral  |  1
HP:0100778  |  Cryoglobulinemia  |  1
HP:0002097  |  Pulmonary emphysema  |  1
HP:0001622  |  Premature delivery  |  1
HP:0100827  |  Lymphocytosis  |  1
HP:0001511  |  Prenatal onset growth retardation  |  1
HP:0000924  |  Abnormality of the skeletal system  |  1
HP:0002878  |  Respiratory failure  |  1
HP:0005403  |  Decreased numbers of circulating T cells  |  1
HP:0001873  |  Low platelet count  |  1
HP:0006517  |  Alveolar proteinosis  |  1
HP:0100820  |  Glomerulopathy  |  1
HP:0100543  |  Cognitive deficits  |  1
HP:0003074  |  High blood glucose  |  1
Disease ID 1048
Disease cytomegalovirus infections
Manually Symptom(Waiting for update.)
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:22)
C0009324  |  ulcerative colitis  |  11
C0040053  |  thrombosis  |  11
C0009319  |  colitis  |  4
C0021845  |  bowel perforation  |  2
C0034065  |  pulmonary embolism  |  2
C0155773  |  portal vein thrombosis  |  2
C0025162  |  toxic megacolon  |  1
C0040034  |  thrombocytopenia  |  1
C0035333  |  retinitis  |  1
C0001623  |  adrenal insufficiency  |  1
C0021845  |  intestinal perforation  |  1
C0019158  |  hepatitis  |  1
C0027726  |  nephrotic syndrome  |  1
C0038354  |  gastropathy  |  1
C0042749  |  viremia  |  1
C0019080  |  hemorrhage  |  1
C0036690  |  sepsis  |  1
C0005411  |  biliary atresia  |  1
C0334121  |  inflammatory pseudotumors  |  1
C0024141  |  systemic lupus erythematosus  |  1
C0085278  |  antiphospholipid syndrome  |  1
C0748159  |  pulmonary involvement  |  1
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
All Snps(Total Genotypes:9)
snpId pubmedId geneId geneSymbol diseaseId sourceId sentence score Year geneSymbol_dbSNP CHROMOSOME POS REF ALT
rs121917864248135917097TLR2umls:C0010823BeFreeRelationship between toll-like receptor 2 Arg677Trp and Arg753Gln and toll-like receptor 4 Asp299Gly polymorphisms and cytomegalovirus infection.0.0059057082014TLR24153704936CT
rs121917864248135917099TLR4umls:C0010823BeFreeRelationship between toll-like receptor 2 Arg677Trp and Arg753Gln and toll-like receptor 4 Asp299Gly polymorphisms and cytomegalovirus infection.0.0029957922014TLR24153704936CT
rs4553808240572391493CTLA4umls:C0010823BeFreeFinally, finding of significant associations between CD28 +17 C/T and CTLA4 -1661 A/G genotypes with CMV active infection in allogeneic HSCT patients experienced aGVHD emphasize on the importance of the genetic pattern of costimulatory genes in outcomes of active CMV infection in HSCT patients needs completed studies.0.0005428842013CTLA42203866282AG
rs4986790248135917099TLR4umls:C0010823BeFreeRelationship between toll-like receptor 2 Arg677Trp and Arg753Gln and toll-like receptor 4 Asp299Gly polymorphisms and cytomegalovirus infection.0.0029957922014TLR49117713024AG
rs4986790248135917097TLR2umls:C0010823BeFreeRelationship between toll-like receptor 2 Arg677Trp and Arg753Gln and toll-like receptor 4 Asp299Gly polymorphisms and cytomegalovirus infection.0.0059057082014TLR49117713024AG
rs5743708248135917099TLR4umls:C0010823BeFreeRelationship between toll-like receptor 2 Arg677Trp and Arg753Gln and toll-like receptor 4 Asp299Gly polymorphisms and cytomegalovirus infection.0.0029957922014TLR24153705165GA
rs5743708248135917097TLR2umls:C0010823BeFreeRelationship between toll-like receptor 2 Arg677Trp and Arg753Gln and toll-like receptor 4 Asp299Gly polymorphisms and cytomegalovirus infection.0.0059057082014TLR24153705165GA
rs57438361953969154106TLR9umls:C0010823GAD[The presence of the rs5743836 polymorphism was significantly associated with susceptibility to cytomegalovirus infection in allogeneic stem cell transplanted patients]0.0031813582009TLR9352226766AG
rs79020912335816029119CTNNA3umls:C0010823BeFreeSignificant interaction with maternal CMV infection was found for rs7902091 (P(SNP × CMV)=7.3 × 10(-7)) in CTNNA3, a gene not previously implicated in schizophrenia, stressing the importance of including environmental factors in genetic studies.0.0005428842012CTNNA31066838534CA
GWASdb Annotation(Total Genotypes:0)
(Waiting for update.)
GWASdb Snp Trait(Total Genotypes:0)
(Waiting for update.)
Mapped by lexical matching(Total Items:0)
(Waiting for update.)
Mapped by homologous gene(Total Items:0)
(Waiting for update.)
Chemical(Total Drugs:2)
CUI ChemicalName ChemicalID CasRN DiseaseName DiseaseID DirectEvidence PubMedIDs
C0010823foscarnetD0172454428-95-9cytomegalovirus infectionsMESH:D003586therapeutic10231404
C0010823ganciclovirD01577482410-32-0cytomegalovirus infectionsMESH:D003586therapeutic10772379
FDA approved drug and dosage information(Total Drugs:0)
(Waiting for update.)
FDA labeling changes(Total Drugs:0)
(Waiting for update.)