PedAM
Pediatric Disease Annotations & Medicines
| meningococcemia | ||||
| Disease ID | 914 |
|---|---|
| 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:6) C0025289 | meningitis | 2 C0018801 | heart failure | 1 C0035579 | rickets | 1 C0043068 | waterhouse-friderichsen syndrome | 1 C0027059 | myocarditis | 1 C0025303 | meningococcal disease | 1 |
| Curated Gene | (Waiting for update.) |
| Inferring Gene | (Waiting for update.) |
| Text Mined Gene | (Waiting for update.) |
| Locus | (Waiting for update.) |
| Disease ID | 914 |
|---|---|
| Disease | meningococcemia |
| Integrated Phenotype | (Waiting for update.) |
| Text Mined Phenotype | HPO | Name | Sentences' Count(Total Phenotypes:4) HP:0001287 | Meningitis | 2 HP:0001635 | Congestive heart failure | 1 HP:0100806 | Sepsis | 1 HP:0002748 | Rickets | 1 |
| Disease ID | 914 |
|---|---|
| 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:1) |
Manually Genotype(Total Text Mining Genotypes:0) |
|---|
| (Waiting for update.) |
All Snps(Total Genotypes:0) | |
|---|---|
| (Waiting for update.) | |
GWASdb Annotation(Total Genotypes:0) | |
|---|---|
| (Waiting for update.) | |
GWASdb Snp Trait(Total Genotypes:0) | |
|---|---|
| (Waiting for update.) | |
Mapped by lexical matching(Total Items:1) | ||||
|---|---|---|---|---|
| HP ID | HP Name | MP ID | MP Name | Annotation |
| HP:0001709 | Third degree atrioventricular block | MP:0003808 | increased atrioventricular cushion size;HP:0001919 | Acute kidney injury |
Mapped by homologous gene(Total Items:1) | ||||
|---|---|---|---|---|
| HP ID | HP Name | MP ID | MP Name | Annotation |
| HP:0000979 | Purpura | MP:0002420 | abnormal adaptive immunity;HP:0003256 | Abnormality of the coagulation cascade |
Chemical(Total Drugs:0) | |
|---|---|
| (Waiting for update.) | |
FDA approved drug and dosage information(Total Drugs:0) | |
|---|---|
| (Waiting for update.) | |
FDA labeling changes(Total Drugs:0) | |
|---|---|
| (Waiting for update.) | |