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	cytomegalic inclusion disease

Disease ID	1128
Disease	cytomegalic inclusion disease
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 diseases cytomegaloviral disease cytomegaloviral infection cytomegaloviral infections cytomegalovirus cytomegalovirus disease cytomegalovirus infect cytomegalovirus infection cytomegalovirus infection (disorder) cytomegalovirus infection, nos cytomegalovirus infections 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	DOID:11259
UMLS	C0010823
MeSH	D003586 D003587
SNOMED-CT	SNOMEDCT_US_2016_09_01:28944009
Comorbidity	UMLS \| Disease \| Sentences' Count(Total Sentences:246) C0009324 \| ulcerative colitis \| 19 C0009319 \| colitis \| 17 C0021390 \| inflammatory bowel disease \| 14 C0001175 \| acquired immunodeficiency syndrome \| 14 C0021831 \| bowel disease \| 12 C0040053 \| thrombosis \| 12 C0035333 \| retinitis \| 9 C0017636 \| glioblastoma \| 8 C0032285 \| pneumonia \| 7 C0018784 \| sensorineural hearing loss \| 6 C0023418 \| leukemia \| 6 C0042769 \| viral infection \| 6 C0002871 \| anemia \| 5 C0019158 \| hepatitis \| 5 C0042769 \| viral infections \| 5 C0009447 \| common variable immunodeficiency \| 4 C0002878 \| hemolytic anemia \| 4 C0010346 \| crohn's disease \| 4 C0011847 \| diabetes \| 3 C0030305 \| pancreatitis \| 3 C0155773 \| portal vein thrombosis \| 3 C0008311 \| cholangitis \| 3 C0001175 \| acquired immunodeficiency syndrome (aids) \| 3 C0442874 \| neuropathy \| 3 C1621958 \| glioblastoma multiforme \| 3 C0008370 \| cholestasis \| 3 C0011991 \| diarrhea \| 3 C0008513 \| chorioretinitis \| 3 C0026764 \| multiple myeloma \| 3 C0014179 \| uterine infection \| 3 C0032285 \| pneumonitis \| 3 C0456909 \| blindness \| 2 C0034902 \| pure red cell aplasia \| 2 C0018801 \| heart failure \| 2 C0024314 \| lymphoproliferative disorder \| 2 C0037998 \| splenic infarction \| 2 C0027707 \| interstitial nephritis \| 2 C0025202 \| melanoma \| 2 C0024291 \| hemophagocytic syndrome \| 2 C0018799 \| heart disease \| 2 C0042164 \| uveitis \| 2 C0019196 \| hepatitis c \| 2 C0409974 \| lupus erythematosus \| 2 C0021053 \| immune disorders \| 2 C0027697 \| nephritis \| 2 C0270612 \| leukoencephalopathy \| 2 C0023890 \| cirrhosis \| 2 C0178238 \| intestinal infection \| 2 C0009402 \| colorectal cancer \| 2 C0014868 \| esophagitis \| 2 C0006142 \| breast cancer \| 2 C0085692 \| hemorrhagic cystitis \| 2 C0010068 \| coronary artery disease \| 2 C0021390 \| inflammatory bowel diseases \| 2 C0024312 \| lymphocytopenia \| 2 C0021845 \| bowel perforation \| 2 C0007113 \| rectal cancer \| 2 C0038325 \| stevens-johnson syndrome \| 2 C0021053 \| immune dysfunction \| 2 C0021400 \| influenza \| 2 C0520459 \| necrotizing enterocolitis \| 2 C0281963 \| red cell aplasia \| 2 C0003873 \| rheumatoid arthritis \| 2 C0021053 \| immune disorder \| 2 C0042165 \| anterior uveitis \| 2 C0020538 \| hypertension \| 2 C0042373 \| vascular disease \| 2 C0032305 \| pneumocystis \| 2 C0030312 \| pancytopenia \| 2 C0036220 \| kaposi's sarcoma \| 2 C0555198 \| malignant glioma \| 2 C0014038 \| encephalitis \| 2 C0010692 \| cystitis \| 2 C0018378 \| guillain-barre syndrome \| 2 C0023470 \| myeloid leukemia \| 2 C0003864 \| arthritis \| 2 C0026764 \| myeloma \| 2 C0878544 \| cardiomyopathy \| 2 C0025160 \| megacolon \| 2 C0021053 \| immune disease \| 2 C0034065 \| pulmonary embolism \| 2 C0024291 \| hemophagocytic lymphohistiocytosis \| 2 C0024141 \| systemic lupus erythematosus \| 2 C0007193 \| dilated cardiomyopathy \| 2 C0005411 \| biliary atresia \| 2 C0040381 \| tolosa-hunt syndrome \| 1 C0085580 \| essential hypertension \| 1 C0349639 \| juvenile myelomonocytic leukemia \| 1 C0023473 \| chronic myeloid leukemia \| 1 C0334121 \| inflammatory pseudotumor \| 1 C0020456 \| hyperglycemia \| 1 C0025162 \| toxic megacolon \| 1 C0027819 \| neuroblastoma \| 1 C0008313 \| sclerosing cholangitis \| 1 C0008312 \| biliary cirrhosis \| 1 C0027051 \| myocardial infarct \| 1 C0034150 \| purpura \| 1 C0022568 \| keratitis \| 1 C0152972 \| pseudomonas sepsis \| 1 C0270922 \| demyelinating polyneuropathy \| 1 C0235974 \| pancreatic cancer \| 1 C0027051 \| myocardial infarction \| 1 C0024299 \| lymphoma \| 1 C1704437 \| respiratory distress syndrome \| 1 C0086543 \| cataract \| 1 C0020542 \| pulmonary hypertension \| 1 C0014742 \| erythema multiforme \| 1 C1257843 \| pseudomembranous colitis \| 1 C0008312 \| primary biliary cirrhosis \| 1 C0007137 \| squamous cell carcinoma \| 1 C0007222 \| cardiovascular disease \| 1 C0022116 \| ischemia \| 1 C0019348 \| herpes simplex \| 1 C0026934 \| mycoplasma \| 1 C0008049 \| varicella \| 1 C0221027 \| good's syndrome \| 1 C0031099 \| periodontitis \| 1 C0004623 \| bacterial infections \| 1 C1565489 \| renal insufficiency \| 1 C0021847 \| intestinal pseudoobstruction \| 1 C0041948 \| uremia \| 1 C0017160 \| gastroenteritis \| 1 C0004623 \| bacterial infection \| 1 C0152018 \| esophageal carcinoma \| 1 C0031090 \| periodontal disease \| 1 C0272126 \| evans syndrome \| 1 C0085278 \| antiphospholipid syndrome \| 1 C0206744 \| cd4+ t-lymphocytopenia \| 1 C0017658 \| glomerulonephritis \| 1 C0001175 \| acquired immune deficiency syndrome (aids) \| 1 C0027059 \| myocarditis \| 1 C0206178 \| cmv retinitis \| 1 C0002395 \| alzheimer disease \| 1 C0024305 \| non-hodgkin's lymphoma \| 1 C0023473 \| chronic myelogenous leukemia \| 1 C0032302 \| mycoplasma pneumonia \| 1 C0032914 \| preeclampsia \| 1 C0376545 \| hematological malignancies \| 1 C0040053 \| thrombus \| 1 C0042384 \| vasculitis \| 1 C0029134 \| optic neuritis \| 1 C0334480 \| pleomorphic rhabdomyosarcoma \| 1 C0023492 \| t-cell leukemia \| 1 C0155773 \| portal thrombosis \| 1 C0034050 \| alveolar proteinosis \| 1 C0011860 \| type 2 diabetes \| 1 C0032305 \| pneumocystis jiroveci pneumonia \| 1 C0023448 \| lymphoblastic leukemia \| 1 C0004114 \| astrocytoma \| 1 C0023449 \| acute lymphoblastic leukemia \| 1 C0555198 \| malignant gliomas \| 1 C0042769 \| virus infection \| 1 C0011570 \| depression \| 1 C0206178 \| cytomegalovirus retinitis \| 1 C0001175 \| acquired immune deficiency syndrome \| 1 C0019829 \| hodgkin's lymphoma \| 1 C0259749 \| autonomic neuropathy \| 1 C0025362 \| mental retardation \| 1 C0032285 \| pneumoniae \| 1 C0013295 \| duodenal ulcer \| 1 C0085693 \| acute appendicitis \| 1 C1145670 \| respiratory failure \| 1 C0178664 \| glomerulosclerosis \| 1 C0024205 \| lymphadenitis \| 1 C0155626 \| acute myocardial infarction \| 1 C0598894 \| monocytic leukemia \| 1 C0008372 \| intrahepatic cholestasis \| 1 C0004245 \| atrioventricular block \| 1 C0004153 \| atherosclerosis \| 1 C0031036 \| polyarteritis nodosa \| 1 C1261473 \| sarcoma \| 1 C0001175 \| acquired immune deficiency \| 1 C0035412 \| rhabdomyosarcomas \| 1 C0021845 \| intestinal perforation \| 1 C0026946 \| fungal infection \| 1 C0042373 \| vascular diseases \| 1 C0038463 \| strongyloidiasis \| 1 C0004030 \| aspergillosis \| 1 C0162293 \| papillitis \| 1 C0007282 \| carotid stenosis \| 1 C0004352 \| autism \| 1 C0023470 \| myelogenous leukemia \| 1 C0035435 \| rheumatic disease \| 1 C0398623 \| hypercoagulability \| 1 C0013990 \| emphysema \| 1 C0036341 \| schizophrenia \| 1 C0043092 \| wegener's granulomatosis \| 1 C0403529 \| goodpasture's syndrome \| 1 C0000786 \| spontaneous abortion \| 1 C0002395 \| alzheimer's disease \| 1 C0021359 \| infertility \| 1 C0010403 \| cryoglobulinemia \| 1 C0031350 \| pharyngitis \| 1 C0149642 \| cervical lymphadenitis \| 1 C0027813 \| neuritis \| 1 C0040034 \| thrombocytopenia \| 1 C0023891 \| alcoholic hepatic cirrhosis \| 1 C0038358 \| gastric ulcer \| 1 C0034152 \| henoch-schonlein purpura \| 1 C0036454 \| visual field loss \| 1 C0206744 \| cd4 lymphocytopenia \| 1 C0027726 \| nephrotic syndrome \| 1 C0085315 \| cerebral toxoplasmosis \| 1 C0007789 \| cerebral palsy \| 1 C0007682 \| central nervous system disorders \| 1 C0040558 \| toxoplasmosis \| 1 C0023530 \| leukopenia \| 1 C0025149 \| medulloblastomas \| 1 C0017601 \| glaucoma \| 1 C0376175 \| bell's palsy \| 1 C0034069 \| pulmonary fibrosis \| 1 C0031117 \| peripheral neuropathy \| 1 C0022398 \| hyperimmunoglobulin e syndrome \| 1 C0024117 \| chronic obstructive pulmonary disease \| 1 C0024440 \| cystoid macular edema \| 1 C0007787 \| transient ischemic attack \| 1 C0017152 \| gastritis \| 1 C0035222 \| acute respiratory distress syndrome \| 1 C0033860 \| psoriasis \| 1 C0028242 \| nocardiosis \| 1 C0021831 \| intestinal disease \| 1 C0019360 \| zoster \| 1 C0014236 \| endophthalmitis \| 1 C0035305 \| retinal detachment \| 1 C0019360 \| herpes zoster \| 1 C0023890 \| hepatic cirrhosis \| 1 C0085110 \| severe combined immunodefic \| 1 C0017178 \| gastrointestinal disease \| 1 C0034050 \| pulmonary alveolar proteinosis \| 1 C0011633 \| dermatomyositis \| 1 C0085110 \| severe combined immunodeficiency syndrome \| 1 C0003615 \| appendicitis \| 1 C0751606 \| adult all \| 1 C0024314 \| lymphoproliferative disorders \| 1 C0021345 \| infectious mononucleosis \| 1 C0002874 \| aplastic anemia \| 1 C1956346 \| coronary artery diseases \| 1 C0041341 \| tuberous sclerosis complex \| 1 C0085110 \| severe combined immunodeficiency \| 1 C0026896 \| myasthenia gravis \| 1 C0042384 \| angiitis \| 1 C0006840 \| candidiasis \| 1 C0032310 \| viral pneumonia \| 1 C0742472 \| central nervous system lymphoma \| 1 C0001623 \| adrenal insufficiency \| 1 C0023467 \| acute myeloid leukemia \| 1
Curated Gene	Entrez_id \| Symbol \| Resource(Total Genes:1) 6772 \| STAT1 \| CTD_human
Inferring Gene	Entrez_id \| Symbol \| Resource(Total Genes:13) 3458 \| IFNG \| CIPHER 3586 \| IL10 \| CIPHER 3569 \| IL6 \| CIPHER 7097 \| TLR2 \| CIPHER 1234 \| CCR5 \| CIPHER 30835 \| CD209 \| CIPHER 3105 \| HLA-A \| CIPHER 3106 \| HLA-B \| CIPHER 3107 \| HLA-C \| CIPHER 3123 \| HLA-DRB1 \| CIPHER 4153 \| MBL2 \| CIPHER 54106 \| TLR9 \| CIPHER 6772 \| STAT1 \| CTD_human
Text Mined Gene	(Waiting for update.)
Locus	(Waiting for update.)

Disease ID	1128
Disease	cytomegalic inclusion disease
Integrated Phenotype	(Waiting for update.)
Text Mined Phenotype	HPO \| Name \| Sentences' Count(Total Phenotypes:176) HP:0002721 \| Immunodeficiency \| 23 HP:0100279 \| Ulcerative colitis \| 18 HP:0002583 \| Colitis \| 16 HP:0002090 \| Pneumonia \| 8 HP:0100843 \| Glioblastoma \| 8 HP:0004936 \| Blood clot in vein \| 7 HP:0001909 \| Leukemia \| 6 HP:0000407 \| sensorineural hearing loss \| 6 HP:0012115 \| Liver inflammation \| 5 HP:0001903 \| Anemia \| 5 HP:0002960 \| Autoimmune condition \| 5 HP:0100280 \| Morbus Crohn \| 4 HP:0002664 \| Neoplasia \| 4 HP:0001945 \| Fever \| 4 HP:0001878 \| Haemolytic anaemia \| 4 HP:0004387 \| Enterocolitis \| 4 HP:0001394 \| Hepatic cirrhosis \| 3 HP:0000822 \| Hypertension \| 3 HP:0001733 \| Pancreatic inflammation \| 3 HP:0006775 \| Multiple myeloma \| 3 HP:0012174 \| Glioblastoma multiforme \| 3 HP:0001907 \| Thromboembolic disease \| 3 HP:0012531 \| Pain \| 3 HP:0002014 \| Diarrhea \| 3 HP:0012424 \| Chorioretinitis \| 3 HP:0001396 \| Cholestasis \| 3 HP:0000123 \| Nephritis \| 3 HP:0030151 \| Cholangitis \| 3 HP:0005523 \| Lymphoproliferative disorder \| 2 HP:0003002 \| Breast carcinoma \| 2 HP:0012324 \| Myeloid leukemia \| 2 HP:0002383 \| Encephalitis \| 2 HP:0002027 \| Abdominal pain \| 2 HP:0012122 \| Anterior uveitis \| 2 HP:0005506 \| Chronic myeloid leukemia \| 2 HP:0001638 \| Cardiomyopathy \| 2 HP:0000541 \| Detached retina \| 2 HP:0005912 \| Biliary duct atresia \| 2 HP:0009733 \| Glioma \| 2 HP:0001510 \| Growth deficiency \| 2 HP:0002352 \| Leukoencephalopathy \| 2 HP:0100633 \| Inflammation of the esophagus \| 2 HP:0002584 \| Intestinal hemorrhage \| 2 HP:0001888 \| Lymphocytopenia \| 2 HP:0002625 \| Blood clot in a deep vein \| 2 HP:0001369 \| Arthritis \| 2 HP:0000618 \| Blindness \| 2 HP:0002098 \| Respiratory distress \| 2 HP:0002239 \| Gastrointestinal hemorrhage \| 2 HP:0001644 \| Congestive cardiomyopathy \| 2 HP:0001677 \| Coronary artery disease \| 2 HP:0030242 \| Blood clot in portal vein \| 2 HP:0100726 \| Kaposi's sarcoma \| 2 HP:0012410 \| Pure red cell aplasia \| 2 HP:0002861 \| Melanoma \| 2 HP:0003201 \| Rhabdomyolysis \| 2 HP:0001970 \| Interstitial nephritis \| 2 HP:0000365 \| Hearing impairment \| 2 HP:0001635 \| Congestive heart failure \| 2 HP:0001518 \| Small for gestational age \| 2 HP:0001876 \| Low blood cell count \| 2 HP:0001249 \| Mental retardation \| 2 HP:0001370 \| Rheumatoid arthritis \| 2 HP:0000554 \| Uveitis \| 2 HP:0002725 \| Systemic lupus erythematosus \| 2 HP:0002251 \| Hirschsprung megacolon \| 2 HP:0012223 \| Ruptured spleen \| 2 HP:0002204 \| Pulmonary embolism \| 2 HP:0001880 \| Eosinophilia \| 1 HP:0011459 \| Esophageal carcinoma \| 1 HP:0100724 \| Hypercoagulability \| 1 HP:0001678 \| Atrioventricular block \| 1 HP:0100546 \| Narrowing of carotid artery \| 1 HP:0000096 \| Glomerulosclerosis \| 1 HP:0002878 \| Respiratory failure \| 1 HP:0030248 \| Blood clot in mesentertic vein \| 1 HP:0002719 \| infections, recurrent \| 1 HP:0100602 \| Pre-eclampsia \| 1 HP:0002326 \| TIA \| 1 HP:0002028 \| Chronic diarrhea \| 1 HP:0002013 \| Emesis \| 1 HP:0001882 \| Decreased blood leukocyte number \| 1 HP:0001541 \| Ascites \| 1 HP:0100753 \| Schizophrenia \| 1 HP:0012189 \| Hodgkin disease \| 1 HP:0000491 \| Corneal inflammation \| 1 HP:0001915 \| Aplastic anemia \| 1 HP:0004787 \| Fulminant hepatitis \| 1 HP:0000979 \| Purpura \| 1 HP:0000099 \| Glomerular nephritis \| 1 HP:0002633 \| Vasculitis \| 1 HP:0001873 \| Low platelet count \| 1 HP:0100242 \| Sarcoma \| 1 HP:0005263 \| Gastritis \| 1 HP:0002840 \| Lymphadenitis \| 1 HP:0100543 \| Cognitive deficits \| 1 HP:0007902 \| Vitreous hemorrhage \| 1 HP:0006517 \| Alveolar proteinosis \| 1 HP:0003765 \| Psoriasis \| 1 HP:0000501 \| Glaucoma \| 1 HP:0006510 \| Chronic obstructive pulmonary disease \| 1 HP:0005305 \| Cerebral vein thrombosis \| 1 HP:0002322 \| Resting tremor \| 1 HP:0000097 \| focal glomerulosclerosis \| 1 HP:0004808 \| Acute myelogenous leukemia \| 1 HP:0100653 \| Optic neuritis \| 1 HP:0002621 \| Atherosclerosis \| 1 HP:0002613 \| Biliary cirrhosis \| 1 HP:0002894 \| Neoplasia of the pancreas \| 1 HP:0003006 \| Neuroblastoma \| 1 HP:0001406 \| Intrahepatic cholestasis \| 1 HP:0000789 \| Infertility \| 1 HP:0100820 \| Glomerulopathy \| 1 HP:0100778 \| Cryoglobulinemia \| 1 HP:0000518 \| Cataract \| 1 HP:0000010 \| Frequent urinary tract infections \| 1 HP:0002955 \| Granulomatosis \| 1 HP:0001511 \| Prenatal onset growth retardation \| 1 HP:0009830 \| Peripheral neuritis \| 1 HP:0011505 \| Cystoid macular edema \| 1 HP:0002716 \| Lymph node hyperplasia \| 1 HP:0100806 \| Sepsis \| 1 HP:0100827 \| Lymphocytosis \| 1 HP:0006721 \| Acute lymphocytic leukemia \| 1 HP:0000846 \| Hypoadrenalism \| 1 HP:0005387 \| Combined immunodeficiency \| 1 HP:0000572 \| Visual loss \| 1 HP:0002126 \| Polymicrogyria \| 1 HP:0012054 \| Choroidal melanoma \| 1 HP:0012819 \| Myocarditis \| 1 HP:0010783 \| Erythema \| 1 HP:0002500 \| Leukoaraiosis \| 1 HP:0000717 \| Autism \| 1 HP:0002511 \| Late-onset form of familial Alzheimer disease \| 1 HP:0002092 \| Pulmonary artery hypertension \| 1 HP:0010636 \| Schizencephaly \| 1 HP:0030746 \| Intraventricular hemorrhage \| 1 HP:0004430 \| Severe combined immunodeficiency \| 1 HP:0001410 \| Decreased liver function \| 1 HP:0012089 \| Arteritis \| 1 HP:0100699 \| Scarring \| 1 HP:0002206 \| Pulmonary fibrosis \| 1 HP:0000597 \| Ophthalmoparesis \| 1 HP:0002592 \| Stomach ulcer \| 1 HP:0002588 \| Duodenal ulcer \| 1 HP:0011854 \| Hemoperitoneum \| 1 HP:0002665 \| Lymphoma \| 1 HP:0001622 \| Premature delivery \| 1 HP:0005364 \| Severe viral infections \| 1 HP:0005403 \| Decreased numbers of circulating T cells \| 1 HP:0001695 \| Cardiac arrest \| 1 HP:0000716 \| Depression \| 1 HP:0012209 \| Juvenile myelomonocytic leukemia \| 1 HP:0003473 \| Fatigable weakness \| 1 HP:0007868 \| ARMD \| 1 HP:0040113 \| Old-aged sensorineural hearing impairment \| 1 HP:0007985 \| Retinal arteriolar occlusion \| 1 HP:0012715 \| Profound hearing impairment \| 1 HP:0000704 \| Pyorrhea \| 1 HP:0002094 \| Dyspnea \| 1 HP:0100021 \| Cerebral palsy \| 1 HP:0009592 \| Astrocytoma \| 1 HP:0001658 \| Myocardial infarction \| 1 HP:0100749 \| Thoracic pain \| 1 HP:0002097 \| Pulmonary emphysema \| 1 HP:0010628 \| Facial palsy, unilateral or bilateral \| 1 HP:0002860 \| Squamous cell carcinoma \| 1 HP:0001298 \| Encephalopathy \| 1 HP:0012593 \| Nephrotic range proteinuria \| 1 HP:0000083 \| Renal insufficiency \| 1 HP:0030149 \| Cardiovascular shock \| 1 HP:0001263 \| Developmental retardation \| 1 HP:0000924 \| Abnormality of the skeletal system \| 1 HP:0005268 \| Spontaneous abortion \| 1 HP:0003074 \| High blood glucose \| 1 HP:0000100 \| Nephrosis \| 1

Disease ID	1128
Disease	cytomegalic inclusion disease
Manually Symptom	UMLS \| Name(Total Manually Symptoms:5) C2046390 \| neonatal jaundice C1801959 \| histiocytic medullary reticulosis C0376293 \| stigmata C0221505 \| cerebral lesions C0027726 \| nephrotic syndrome
Text Mined Symptom	UMLS \| Name \| Sentences' Count(Total Symptoms:21) C0040053 \| thrombosis \| 11 C0009324 \| ulcerative colitis \| 11 C0009319 \| colitis \| 4 C0155773 \| portal vein thrombosis \| 2 C0034065 \| pulmonary embolism \| 2 C0025162 \| toxic megacolon \| 1 C0748159 \| pulmonary involvement \| 1 C0019158 \| hepatitis \| 1 C0005411 \| biliary atresia \| 1 C0085278 \| antiphospholipid syndrome \| 1 C0042749 \| viremia \| 1 C0021845 \| bowel perforation \| 1 C0019080 \| hemorrhage \| 1 C0040034 \| thrombocytopenia \| 1 C0334121 \| inflammatory pseudotumors \| 1 C0024141 \| systemic lupus erythematosus \| 1 C0038354 \| gastropathy \| 1 C0021845 \| intestinal perforation \| 1 C0035333 \| retinitis \| 1 C0001623 \| adrenal insufficiency \| 1 C0027726 \| nephrotic syndrome \| 1

Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)

Text Mining Genotype(Total 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
rs121917864	24813591	7097	TLR2	umls:C0010823	BeFree	Relationship between toll-like receptor 2 Arg677Trp and Arg753Gln and toll-like receptor 4 Asp299Gly polymorphisms and cytomegalovirus infection.	0.005905708	2014	TLR2	4	153704936	C	T
rs121917864	24813591	7099	TLR4	umls:C0010823	BeFree	Relationship between toll-like receptor 2 Arg677Trp and Arg753Gln and toll-like receptor 4 Asp299Gly polymorphisms and cytomegalovirus infection.	0.002995792	2014	TLR2	4	153704936	C	T
rs4553808	24057239	1493	CTLA4	umls:C0010823	BeFree	Finally, 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.	0.000542884	2013	CTLA4	2	203866282	A	G
rs4986790	24813591	7099	TLR4	umls:C0010823	BeFree	Relationship between toll-like receptor 2 Arg677Trp and Arg753Gln and toll-like receptor 4 Asp299Gly polymorphisms and cytomegalovirus infection.	0.002995792	2014	TLR4	9	117713024	A	G
rs4986790	24813591	7097	TLR2	umls:C0010823	BeFree	Relationship between toll-like receptor 2 Arg677Trp and Arg753Gln and toll-like receptor 4 Asp299Gly polymorphisms and cytomegalovirus infection.	0.005905708	2014	TLR4	9	117713024	A	G
rs5743708	24813591	7099	TLR4	umls:C0010823	BeFree	Relationship between toll-like receptor 2 Arg677Trp and Arg753Gln and toll-like receptor 4 Asp299Gly polymorphisms and cytomegalovirus infection.	0.002995792	2014	TLR2	4	153705165	G	A
rs5743708	24813591	7097	TLR2	umls:C0010823	BeFree	Relationship between toll-like receptor 2 Arg677Trp and Arg753Gln and toll-like receptor 4 Asp299Gly polymorphisms and cytomegalovirus infection.	0.005905708	2014	TLR2	4	153705165	G	A
rs5743836	19539691	54106	TLR9	umls:C0010823	GAD	[The presence of the rs5743836 polymorphism was significantly associated with susceptibility to cytomegalovirus infection in allogeneic stem cell transplanted patients]	0.003181358	2009	TLR9	3	52226766	A	G
rs7902091	23358160	29119	CTNNA3	umls:C0010823	BeFree	Significant 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.	0.000542884	2012	CTNNA3	10	66838534	C	A

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.)

Disease ID	1128
Disease	cytomegalic inclusion disease
Case	(Waiting for update.)

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