bacterial meningitis |
Disease ID | 1118 |
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Disease | bacterial meningitis |
Definition | Bacterial infections of the leptomeninges and subarachnoid space, frequently involving the cerebral cortex, cranial nerves, cerebral blood vessels, spinal cord, and nerve roots. |
Synonym | bact meningitides bact meningitis bacterial meningitides bacterial meningitis (disorder) bacterial meningitis nos bacterial meningitis nos (disorder) bacterial meningitis, nos bm - bacterial meningitis meningitides bact meningitides, bacterial meningitis bact meningitis due to unspecified bacterium meningitis, bacterial meningitis, bacterial [disease/finding] meningitis, bacterial nos |
DOID | |
UMLS | C0085437 |
MeSH | |
SNOMED-CT | |
Comorbidity | UMLS | Disease | Sentences' Count(Total Sentences:38) C0025289 | meningitis | 5 C0038539 | subdural empyema | 3 C0007785 | cerebral infarct | 2 C0025297 | viral meningitis | 2 C0014118 | endocarditis | 2 C0020255 | hydrocephalus | 2 C0007785 | cerebral infarction | 2 C0038463 | strongyloidiasis | 2 C0029882 | otitis media | 2 C0023890 | liver cirrhosis | 2 C0038220 | status epilepticus | 1 C0025295 | pneumococcal meningitis | 1 C0014070 | encephalomyelitis | 1 C0276430 | enteroviral meningitis | 1 C0267917 | acute cholangitis | 1 C0032285 | pneumoniae | 1 C0018784 | sensorineural hearing loss | 1 C0042164 | uveitis | 1 C0024530 | malaria | 1 C0025303 | meningococcal disease | 1 C0008049 | chickenpox | 1 C0026764 | myeloma | 1 C0023890 | cirrhosis | 1 C0037198 | sinus thrombosis | 1 C0014059 | acute disseminated encephalomyelitis | 1 C0026764 | multiple myeloma | 1 C0041318 | tuberculous meningitis | 1 C0271429 | acute otitis media | 1 C0008311 | cholangitis | 1 C0004623 | bacterial infection | 1 C0042165 | anterior uveitis | 1 C0014236 | endophthalmitis | 1 C0021400 | influenzae | 1 C0022116 | ischemia | 1 C0041296 | tuberculosis | 1 C0040053 | thrombosis | 1 C0007785 | cerebral infarctions | 1 C0023860 | listeriosis | 1 |
Curated Gene | (Waiting for update.) |
Inferring Gene | Entrez_id | Symbol | Resource(Total Genes:4) |
Text Mined Gene | Entrez_id | Symbol | Score | Resource(Total Genes:84) 2 | A2M | 2.203 | DISEASES 361 | AQP4 | 2.2 | DISEASES 1822 | ATN1 | 1.438 | DISEASES 551 | AVP | 3.209 | DISEASES 567 | B2M | 1.247 | DISEASES 2683 | B4GALT1 | 1.993 | DISEASES 25805 | BAMBI | 4.222 | DISEASES 627 | BDNF | 2.557 | DISEASES 721 | C4B | 2.192 | DISEASES 728 | C5AR1 | 1.968 | DISEASES 730 | C7 | 2.518 | DISEASES 820 | CAMP | 2.175 | DISEASES 22900 | CARD8 | 2.053 | DISEASES 834 | CASP1 | 2.27 | DISEASES 388372 | CCL4L1 | 1.761 | DISEASES 959 | CD40LG | 2.99 | DISEASES 942 | CD86 | 1.549 | DISEASES 1052 | CEBPD | 1.485 | DISEASES 7122 | CLDN5 | 1.137 | DISEASES 1270 | CNTF | 1.671 | DISEASES 1435 | CSF1 | 1.398 | DISEASES 2919 | CXCL1 | 2.233 | DISEASES 2920 | CXCL2 | 2.061 | DISEASES 51164 | DCTN4 | 2.632 | DISEASES 1805 | DPT | 1.503 | DISEASES 1809 | DPYSL3 | 1.206 | DISEASES 83658 | DYNLRB1 | 1.145 | DISEASES 1859 | DYRK1A | 1.914 | DISEASES 124454 | EARS2 | 1.125 | DISEASES 1906 | EDN1 | 1.162 | DISEASES 2152 | F3 | 1.342 | DISEASES 23017 | FAIM2 | 2.705 | DISEASES 355 | FAS | 1.323 | DISEASES 2214 | FCGR3A | 1.074 | DISEASES 2582 | GALE | 1.656 | DISEASES 2633 | GBP1 | 2.195 | DISEASES 2668 | GDNF | 1.011 | DISEASES 26061 | HACL1 | 1.963 | DISEASES 3045 | HBD | 1.152 | DISEASES 3146 | HMGB1 | 1.077 | DISEASES 3586 | IL10 | 2.814 | DISEASES 3605 | IL17A | 1.57 | DISEASES 3664 | IRF6 | 3.059 | DISEASES 9261 | MAPKAPK2 | 1.034 | DISEASES 4153 | MBL2 | 2.159 | DISEASES 50488 | MINK1 | 1.152 | DISEASES 4318 | MMP9 | 3.208 | DISEASES 26002 | MOXD1 | 1.112 | DISEASES 219972 | MPEG1 | 2.464 | DISEASES 4615 | MYD88 | 2.1 | DISEASES 79625 | NDNF | 1.116 | DISEASES 64332 | NFKBIZ | 1.302 | DISEASES 100506658 | OCLN | 1.546 | DISEASES 5284 | PIGR | 1.847 | DISEASES 5294 | PIK3CG | 1.202 | DISEASES 5329 | PLAUR | 1.231 | DISEASES 56342 | PPAN | 1.178 | DISEASES 5730 | PTGDS | 3.182 | DISEASES 135250 | RAET1E | 1.069 | DISEASES 2889 | RAPGEF1 | 2.236 | DISEASES 222546 | RFX6 | 1.213 | DISEASES 8986 | RPS6KA4 | 2.534 | DISEASES 25813 | SAMM50 | 3.375 | DISEASES 6401 | SELE | 1.308 | DISEASES 5265 | SERPINA1 | 1.154 | DISEASES 6565 | SLC15A2 | 1.614 | DISEASES 57154 | SMURF1 | 1.182 | DISEASES 25870 | SUMF2 | 1.369 | DISEASES 50945 | TBX22 | 1.109 | DISEASES 7018 | TF | 2.179 | DISEASES 51270 | TFDP3 | 1.059 | DISEASES 93643 | TJAP1 | 2.588 | DISEASES 7096 | TLR1 | 2.466 | DISEASES 7099 | TLR4 | 2.624 | DISEASES 7100 | TLR5 | 1.044 | DISEASES 10333 | TLR6 | 1.534 | DISEASES 54106 | TLR9 | 2.928 | DISEASES 7124 | TNF | 4.446 | DISEASES 8771 | TNFRSF6B | 1.685 | DISEASES 127262 | TPRG1L | 1.351 | DISEASES 7177 | TPSAB1 | 1.802 | DISEASES 7247 | TSN | 1.162 | DISEASES 55432 | YOD1 | 1.868 | DISEASES 7709 | ZBTB17 | 1.73 | DISEASES |
Locus | (Waiting for update.) |
Disease ID | 1118 |
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Disease | bacterial meningitis |
Manually Symptom | UMLS | Name(Total Manually Symptoms:46) C2712035 | hyperglycaemia C2711548 | infectious process C2364133 | infection C2096315 | headache C2029884 | hearing loss C1963178 | myelitis C1963137 | hydrocephalus C1550639 | fistula C1546533 | abscess C1522136 | hypernatremia C1393529 | vascular complications C1282231 | endogenous endophthalmitis C1135207 | ataxia C1000483 | anemia C0917798 | cerebral ischaemia C0751401 | ophthalmoparesis C0748903 | spinal cord involvement C0581883 | deafness C0457506 | reactive thrombocytosis C0424755 | fever C0392548 | cauda equina syndrome C0272242 | complement deficiency C0238051 | cerebral vasculitis C0151740 | intracranial hypertension C0043046 | wasting syndrome C0038454 | cerebral infarction C0038220 | status epilepticus C0036572 | seizures C0032285 | pneumoniae C0032268 | pneumocephalus C0031039 | pericardial effusions C0029089 | oculomotor paralysis C0026650 | movement disorders C0022893 | labyrinthitis C0021933 | intussusception C0021308 | infarction C0020456 | hyperglycemia C0019270 | herniation C0018784 | sensorineural hearing loss C0018775 | bilateral hearing loss C0016397 | focal infections C0014544 | epilepsy C0014236 | endophthalmitis C0013447 | otologic diseases C0007766 | intracranial aneurysms C0001125 | lactic acidosis |
Text Mined Symptom | UMLS | Name | Sentences' Count(Total Symptoms:18) C0009450 | infection | 7 C0018681 | headache | 5 C1384666 | hearing loss | 4 C0032285 | pneumoniae | 3 C0020255 | hydrocephalus | 2 C0015967 | fever | 2 C1393529 | vascular complications | 2 C0021308 | infarction | 2 C0032268 | pneumocephalus | 2 C0011053 | deafness | 1 C0007785 | cerebral infarction | 1 C0038220 | status epilepticus | 1 C0018784 | sensorineural hearing loss | 1 C0036572 | seizures | 1 C0000833 | abscess | 1 C0043046 | wasting syndrome | 1 C0016397 | focal infections | 1 C0016169 | fistula | 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:9) | |||||||||||||
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snpId | pubmedId | geneId | geneSymbol | diseaseId | sourceId | sentence | score | Year | geneSymbol_dbSNP | CHROMOSOME | POS | REF | ALT |
rs1042714 | 22624056 | 127617 | OR14L1P | umls:C0085437 | BeFree | We identified a functional polymorphism in ADRB2 (rs1042714) to be associated with an increased risk for bacterial meningitis (Odds ratio [OR] 1.35, 95% confidence interval [CI] 1.04-1.76; p = 0.026). | 0.000271442 | 2012 | ADRB2 | 5 | 148826910 | G | C,T |
rs1047286 | 23068452 | 718 | C3 | umls:C0085437 | BeFree | Rs1047286 (Pro314Leu) in complement component 3 was associated with reduced susceptibility to bacterial meningitis after correction for multiple testing: the protective Leu/Leu genotype was found in 5 of 435 patients (1%) compared to 15 of 302 controls (5%; odds ratio [OR] 4.50, 95% confidence interval [CI] 1.62-12.50, p = 0.0017). | 0.000271442 | 2013 | C3 | 19 | 6713251 | G | A |
rs1052133 | 26316174 | 4968 | OGG1 | umls:C0085437 | BeFree | In recent papers published by our group, we described the associations between the single nucleotide polymorphisms (SNPs) AADAT +401C > T, APEX1 Asn148Glu, OGG1 Ser326Cys and PARP1 Val762Ala and BM. | 0.000542884 | 2015 | OGG1;CAMK1 | 3 | 9757089 | C | G |
rs1052133 | 26316174 | 142 | PARP1 | umls:C0085437 | BeFree | In recent papers published by our group, we described the associations between the single nucleotide polymorphisms (SNPs) AADAT +401C > T, APEX1 Asn148Glu, OGG1 Ser326Cys and PARP1 Val762Ala and BM. | 0.000271442 | 2015 | OGG1;CAMK1 | 3 | 9757089 | C | G |
rs1052133 | 26316174 | 328 | APEX1 | umls:C0085437 | BeFree | In recent papers published by our group, we described the associations between the single nucleotide polymorphisms (SNPs) AADAT +401C > T, APEX1 Asn148Glu, OGG1 Ser326Cys and PARP1 Val762Ala and BM. | 0.000542884 | 2015 | OGG1;CAMK1 | 3 | 9757089 | C | G |
rs1052133 | 21651918 | 4968 | OGG1 | umls:C0085437 | BeFree | For the SNP OGG1 Ser326Cys, the genotype Cys/Cys was more frequent (P<0.05) in BM group. | 0.000542884 | 2011 | OGG1;CAMK1 | 3 | 9757089 | C | G |
rs1136410 | 26316174 | 142 | PARP1 | umls:C0085437 | BeFree | In recent papers published by our group, we described the associations between the single nucleotide polymorphisms (SNPs) AADAT +401C > T, APEX1 Asn148Glu, OGG1 Ser326Cys and PARP1 Val762Ala and BM. | 0.000271442 | 2015 | PARP1 | 1 | 226367601 | A | G |
rs1136410 | 26316174 | 4968 | OGG1 | umls:C0085437 | BeFree | In recent papers published by our group, we described the associations between the single nucleotide polymorphisms (SNPs) AADAT +401C > T, APEX1 Asn148Glu, OGG1 Ser326Cys and PARP1 Val762Ala and BM. | 0.000542884 | 2015 | PARP1 | 1 | 226367601 | A | G |
rs1136410 | 26316174 | 328 | APEX1 | umls:C0085437 | BeFree | In recent papers published by our group, we described the associations between the single nucleotide polymorphisms (SNPs) AADAT +401C > T, APEX1 Asn148Glu, OGG1 Ser326Cys and PARP1 Val762Ala and BM. | 0.000542884 | 2015 | PARP1 | 1 | 226367601 | A | G |
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 | 1118 |
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Disease | bacterial meningitis |
Case | (Waiting for update.) |