herpes simplex |
Disease ID | 1004 |
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Disease | herpes simplex |
Manually Symptom | UMLS | Name(Total Manually Symptoms:115) C2711548 | infectious process C2707258 | infections C2364133 | infection C1963266 | uveitis C1963216 | proctitis C1963178 | myelitis C1963137 | hydrocephalus C1963106 | esophagitis C1708554 | intraocular infection C1518296 | neuropathogenesis C1318020 | stromal keratitis C1282362 | corneal graft failure C1274297 | febrile ulceronecrotic mucha-habermann disease C1261473 | sarcomas C1096335 | radiculomyelopathy C0919615 | meningoradiculitis C0872054 | latent infection C0858970 | carcinogenicity C0751956 | acute stroke C0749165 | supraglottitis C0746787 | neck cancer C0729777 | corneal infection C0729552 | genital infection C0687720 | central diabetes insipidus C0555970 | nasal infection C0549398 | meibomianitis C0497156 | lymphadenopathy C0456103 | neonatal sepsis C0455988 | nonimmune hydrops fetalis C0404521 | vaginal infection C0393483 | brainstem encephalitis C0376175 | bell's palsy C0346373 | melanoma of the iris C0338474 | central nervous system demyelination C0338418 | acute necrotising encephalitis C0333516 | oncolysis C0333497 | segmental glomerulosclerosis C0302809 | fulminant hepatitis C0275544 | congenital infection C0275524 | mixed infection C0275518 | acute infection C0267797 | acute hepatitis C0265962 | netherton's syndrome C0238115 | boerhaave's syndrome C0220979 | mollaret's meningitis C0206708 | cervical dysplasia C0205721 | nosocomial infections C0162557 | fulminant hepatic failure C0154653 | chronic meningitis C0153042 | herpetic whitlow C0152025 | polyneuropathy C0151970 | oesophageal ulceration C0151281 | genital ulcers C0149935 | mucopurulent cervicitis C0149725 | lower respiratory tract infection C0085692 | hemorrhagic cystitis C0085605 | liver failure C0042769 | viral infection C0042384 | angiitis C0042165 | anterior uveitis C0040586 | tracheobronchitis C0038826 | superinfection C0038358 | gastric ulcer C0038325 | stevens-johnson syndrome C0038325 | erythema exsudativum multiforme C0037769 | infantile spasms C0037284 | skin lesions C0036572 | seizures C0036396 | sciatica C0035333 | retinitis C0035319 | acute retinal necrosis C0032285 | pneumonitis C0032285 | pneumonias C0032285 | pneumonia C0031763 | photosensitization C0031350 | pharyngitis C0030804 | benign mucous membrane pemphigoid C0030578 | paronychias C0029118 | opportunistic infection C0027765 | neurological disorders C0025309 | meningoencephalitis C0025290 | aseptic meningitis C0025289 | meningitis C0024291 | hemophagocytic syndrome C0024291 | hemophagocytic lymphohistiocytosis C0024266 | lymphocytic meningitis C0023646 | lichen planus C0022573 | keratoconjunctivitis C0022568 | keratitis C0022568 | corneal inflammation C0022504 | kaposi's varicelliform eruption C0022504 | kaposi varicelliform eruption C0022081 | iritis C0021345 | infectious mononucleosis C0021345 | glandular fever C0019693 | human immunodeficiency virus infection C0019357 | herpetic keratitis C0019342 | genital herpes C0019080 | hemorrhage C0018784 | sensorineural hearing loss C0015469 | facial nerve paralysis C0015403 | ocular infection C0015397 | eye disease C0014868 | oesophagitis C0014868 | esophagitides C0014742 | erythema multiforme C0014077 | acute hemorrhagic leukoencephalitis C0014070 | myeloencephalitis C0014038 | encephalitis C0010037 | corneal edema C0008033 | pleurodynia C0007684 | central nervous system infection C0005741 | blepharitis C0004690 | balanitis C0002622 | amnesia |
Text Mined Symptom | UMLS | Name | Sentences' Count(Total Symptoms:34) C0009450 | infection | 147 C0021311 | infections | 29 C0015403 | ocular infection | 8 C0014038 | encephalitis | 8 C0025289 | meningitis | 6 C0022568 | keratitis | 5 C0042769 | viral infection | 4 C0729552 | genital infection | 4 C0872054 | latent infection | 3 C0015397 | eye disease | 3 C0014742 | erythema multiforme | 3 C0729777 | corneal infection | 3 C0085605 | liver failure | 3 C0035319 | acute retinal necrosis | 2 C0019342 | genital herpes | 2 C0025290 | aseptic meningitis | 2 C0032285 | pneumonia | 2 C0019357 | herpetic keratitis | 2 C0042164 | uveitis | 2 C0404521 | vaginal infection | 2 C0302809 | fulminant hepatitis | 2 C0275524 | mixed infection | 2 C0275518 | acute infection | 1 C0275544 | congenital infection | 1 C0220979 | mollaret's meningitis | 1 C0221269 | pseudolymphoma | 1 C0555970 | nasal infection | 1 C0001339 | acute pancreatitis | 1 C0007684 | central nervous system infection | 1 C0024291 | hemophagocytic lymphohistiocytosis | 1 C0042165 | anterior uveitis | 1 C0022504 | kaposi's varicelliform eruption | 1 C0024291 | hemophagocytic syndrome | 1 C0014868 | esophagitis | 1 |
Manually Genotype(Total Text Mining Genotypes:0) |
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(Waiting for update.) |
Text Mining Genotype(Total Genotypes:0) | |
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(Waiting for update.) |
All Snps(Total Genotypes:5) | |||||||||||||
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snpId | pubmedId | geneId | geneSymbol | diseaseId | sourceId | sentence | score | Year | geneSymbol_dbSNP | CHROMOSOME | POS | REF | ALT |
rs179363878 | 17547716 | 326 | AIRE | umls:C0019348 | BeFree | Recurrent herpes simplex virus infection in a patient with autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy associated with L29P and IVS9-1G>C compound heterozygous autoimmune regulator gene mutations. | 0.000542884 | 2007 | AIRE | 21 | 44286089 | T | C |
rs179363879 | 17547716 | 326 | AIRE | umls:C0019348 | BeFree | Recurrent herpes simplex virus infection in a patient with autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy associated with L29P and IVS9-1G>C compound heterozygous autoimmune regulator gene mutations. | 0.000542884 | 2007 | AIRE | 21 | 44286092 | T | C |
rs1805539 | 21919190 | 2904 | GRIN2B | umls:C0019348 | BeFree | Significant interaction between maternal HSV-2 seropositivity and GRIN2B genetic variation in the offspring were observed for seven SNPs and two remained significant after Bonferroni correction (rs1805539, P(nominal) = 0.0001 and rs1806205, P(nominal) = 0.0008). | 0.000271442 | 2011 | GRIN2B;LOC105369668 | 12 | 13617256 | G | C |
rs1806205 | 21919190 | 2904 | GRIN2B | umls:C0019348 | BeFree | Significant interaction between maternal HSV-2 seropositivity and GRIN2B genetic variation in the offspring were observed for seven SNPs and two remained significant after Bonferroni correction (rs1805539, P(nominal) = 0.0001 and rs1806205, P(nominal) = 0.0008). | 0.000271442 | 2011 | GRIN2B | 12 | 13566469 | G | C |
rs4680 | 16542182 | 1312 | COMT | umls:C0019348 | BeFree | Both the COMT Val158Met polymorphism and serological evidence of HSV-1 infection affect cognitive functioning in individuals with bipolar disorder. | 0.002638474 | 2006 | COMT;MIR4761 | 22 | 19963748 | G | A |
GWASdb Annotation(Total Genotypes:0) | |
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(Waiting for update.) |
GWASdb Snp Trait(Total Genotypes:0) | |
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(Waiting for update.) |
Mapped by lexical matching(Total Items:0) |
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(Waiting for update.) |
Mapped by homologous gene(Total Items:0) |
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(Waiting for update.) |
Disease ID | 1004 |
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Disease | herpes simplex |
Case | (Waiting for update.) |