eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| meningococcemia | ||||
| Disease ID | 1475 |
|---|---|
| Disease | meningococcemia |
| Definition | Meningococcemia is a rare infectious disease characterized by upper respiratory tract infection, fever, skin rash and lesions, eye and ear problems, and possibly a sudden state of extreme physical depression (shock) which may be life-threatening without appropriate medical care. There are two forms of meningococcemia. Fluminant meningococcemia develops very rapidly and is more severe than chronic meningococcemia, which has a waxing and waning course. - NORD Reference: NORD |
| Synonym | [x]meningococcaemia, unspecified [x]meningococcemia, unspecified [x]meningococcemia, unspecified (disorder) meningococcaemia meningococcal sepsis meningococcal septicaemia meningococcal septicaemia (disorder) meningococcal septicemia meningococcemia (disorder) |
| DOID | |
| UMLS | C0025306 |
| SNOMED-CT | |
| Comorbidity | UMLS | Disease | Sentences' Count(Total Sentences:12) C0025289 | meningitis | 3 C0043068 | waterhouse-friderichsen syndrome | 2 C0035579 | rickets | 1 C0020456 | hyperglycemia | 1 C0034150 | purpura | 1 C0022656 | renal cortical necrosis | 1 C0085650 | purpura fulminans | 1 C0027059 | myocarditis | 1 C0012739 | disseminated intravascular coagulation (dic) | 1 C0012739 | disseminated intravascular coagulation | 1 C0025303 | meningococcal disease | 1 C0025303 | meningococcal infection | 1 |
| Curated Gene | (Waiting for update.) |
| Inferring Gene | (Waiting for update.) |
| Text Mined Gene | (Waiting for update.) |
| Locus | (Waiting for update.) |
| Disease ID | 1475 |
|---|---|
| Disease | meningococcemia |
| Integrated Phenotype | (Waiting for update.) |
| Text Mined Phenotype | HPO | Name | Sentences' Count(Total Phenotypes:11) HP:0001287 | Meningitis | 3 HP:0100806 | Sepsis | 2 HP:0000979 | Purpura | 1 HP:0002748 | Rickets | 1 HP:0001635 | Congestive heart failure | 1 HP:0003074 | High blood glucose | 1 HP:0005521 | Disseminated intravascular coagulation | 1 HP:0000716 | Depression | 1 HP:0100758 | Gangrene | 1 HP:0002615 | Low blood pressure | 1 HP:0003256 | Coagulopathy | 1 |
| Disease ID | 1475 |
|---|---|
| Disease | meningococcemia |
| Manually Symptom | UMLS | Name(Total Manually Symptoms:19) C2364072 | depression C2215935 | complete heart block C0796095 | c syndrome C0376293 | stigmata C0151882 | purpuric rash C0151693 | adrenal hemorrhage C0151467 | acute adrenal insufficiency C0085650 | purpura fulminans C0039520 | tenosynovitis C0037274 | skin diseases C0034150 | purpura C0034063 | pulmonary edema C0024291 | hemophagocytic lymphohistiocytosis C0022660 | acute renal failure C0022656 | renal cortical necrosis C0017178 | gastrointestinal disease C0017086 | gangrene C0005779 | coagulopathy C0005779 | blood coagulation disorders |
| Text Mined Symptom | UMLS | Name | Sentences' Count(Total Symptoms:6) C0151693 | adrenal hemorrhage | 1 C0005779 | coagulopathy | 1 C0011570 | depression | 1 C0085650 | purpura fulminans | 1 C0034150 | purpura | 1 C0012739 | disseminated intravascular coagulation | 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:0) | |
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| (Waiting for update.) | |
GWASdb Annotation(Total Genotypes:0) | |
|---|---|
| (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 | 1475 |
|---|---|
| Disease | meningococcemia |
| Case | (Waiting for update.) |