eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| meningococcal infection | ||||
| Disease ID | 855 |
|---|---|
| Disease | meningococcal infection |
| Definition | Infections with bacteria of the species NEISSERIA MENINGITIDIS. |
| Synonym | [x]meningococcal infection, unspecified [x]meningococcal infection, unspecified (disorder) disease meningococcal infect meningococcal infection due to neisseria meningitidis infection, meningococcal infections, meningococcal meningococcal disease meningococcal diseases meningococcal infect meningococcal infect nos meningococcal infection (disorder) meningococcal infection nos meningococcal infection nos (disorder) meningococcal infection, nos meningococcal infection, unspecified meningococcal infections meningococcal infections [disease/finding] meningococcal infectious disease meningococcal infectious disease (disorder) meningococcal infectious disease, nos |
| DOID | |
| ICD10 | |
| UMLS | C0025303 |
| MeSH | |
| SNOMED-CT | |
| Comorbidity | UMLS | Disease | Sentences' Count(Total Sentences:14) C0025289 | meningitis | 5 C0003864 | arthritis | 2 C0031046 | pericarditis | 1 C0021400 | influenza | 1 C0038436 | post-traumatic stress disorder | 1 C0041327 | pulmonary tuberculosis | 1 C0009492 | compartment syndrome | 1 C0041296 | tuberculosis | 1 C0040034 | thrombocytopenia | 1 C0025306 | meningococcemia | 1 C0042769 | virus infection | 1 C0085437 | bacterial meningitis | 1 C0025306 | meningococcal sepsis | 1 C0272242 | complement deficiency | 1 |
| Curated Gene | Entrez_id | Symbol | Resource(Total Genes:4) |
| Inferring Gene | Entrez_id | Symbol | Resource(Total Genes:33) 1669 | DEFA4 | CIPHER 1672 | DEFB1 | CIPHER 2212 | FCGR2A | CIPHER 2213 | FCGR2B | CIPHER 2214 | FCGR3A | CIPHER 2215 | FCGR3B | CIPHER 3586 | IL10 | CIPHER 3552 | IL1A | CIPHER 3553 | IL1B | CIPHER 3557 | IL1RN | CIPHER 3565 | IL4 | CIPHER 4153 | MBL2 | CIPHER 142 | PARP1 | CIPHER 5054 | SERPINE1 | CIPHER 710 | SERPING1 | CIPHER 653509 | SFTPA1 | CIPHER 729238 | SFTPA2 | CIPHER 6441 | SFTPD | CIPHER 6872 | TAF1 | CIPHER 7099 | TLR4 | CIPHER 7124 | TNF | CIPHER 1636 | ACE | CIPHER;CTD_human 118 | ADD1 | CIPHER 153 | ADRB1 | CIPHER 154 | ADRB2 | CIPHER 183 | AGT | CIPHER 185 | AGTR1 | CIPHER 634 | CEACAM1 | CIPHER 4680 | CEACAM6 | CIPHER 3075 | CFH | CIPHER;CTD_human 10878 | CFHR3 | CIPHER;CTD_human 3554 | IL1R1 | CIPHER 1675 | CFD | CTD_human |
| Text Mined Gene | (Waiting for update.) |
| Locus | (Waiting for update.) |
| Disease ID | 855 |
|---|---|
| Disease | meningococcal infection |
| Integrated Phenotype | (Waiting for update.) |
| Text Mined Phenotype | HPO | Name | Sentences' Count(Total Phenotypes:8) HP:0001287 | Meningitis | 5 HP:0001369 | Arthritis | 2 HP:0001873 | Low platelet count | 1 HP:0100806 | Sepsis | 1 HP:0030049 | Brain abscess | 1 HP:0004431 | Complement deficiency | 1 HP:0100699 | Scarring | 1 HP:0001701 | Pericarditis | 1 |
| Disease ID | 855 |
|---|---|
| Disease | meningococcal infection |
| Manually Symptom | UMLS | Name(Total Manually Symptoms:15) C1963211 | pericarditis C1527311 | brain edema C0796095 | c syndrome C0221505 | brain lesions C0158026 | monoarthritis C0155679 | acute pericarditis C0085650 | purpura fulminans C0039520 | tenosynovitis C0037285 | skin manifestations C0031154 | peritonitis C0022073 | iridocyclitis C0019061 | hemolytic-uremic syndrome C0012739 | disseminated intravascular coagulation (dic) C0012739 | disseminated intravascular coagulation C0012739 | consumption coagulopathy |
| Text Mined Symptom | UMLS | Name | Sentences' Count(Total Symptoms:4) C0025289 | meningitis | 5 C0272242 | complement deficiency | 1 C0040034 | thrombocytopenia | 1 C0003864 | arthritis | 1 |
Manually Genotype(Total Text Mining Genotypes:0) |
|---|
| (Waiting for update.) |
Text Mining Genotype(Total Genotypes:0) | |
|---|---|
| (Waiting for update.) | |
All Snps(Total Genotypes:2) | |||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| snpId | pubmedId | geneId | geneSymbol | diseaseId | sourceId | sentence | score | Year | geneSymbol_dbSNP | CHROMOSOME | POS | REF | ALT |
| rs426736 | 20694013 | 10878 | CFHR3 | umls:C0025303 | GAD | [Genome-wide association study identifies variants in the CFH region associated with host susceptibility to meningococcal disease.] | 0.242909916 | 2010 | CFHR3 | 1 | 196791287 | A | G |
| rs426736 | 20694013 | 10878 | CFHR3 | umls:C0025303 | GWASCAT | Genome-wide association study identifies variants in the CFH region associated with host susceptibility to meningococcal disease. | 0.242909916 | 2010 | CFHR3 | 1 | 196791287 | A | G |
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 | 855 |
|---|---|
| Disease | meningococcal infection |
| Case | (Waiting for update.) |