eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| st. louis encephalitis | ||||
| Disease ID | 1130 |
|---|---|
| Disease | st. louis encephalitis |
| Definition | A viral encephalitis caused by the St. Louis encephalitis virus (ENCEPHALITIS VIRUS, ST. LOUIS), a FLAVIVIRUS. It is transmitted to humans and other vertebrates primarily by mosquitoes of the genus CULEX. The primary animal vectors are wild birds and the disorder is endemic to the midwestern and southeastern United States. Infections may be limited to an influenza-like illness or present as an ASEPTIC MENINGITIS or ENCEPHALITIS. Clinical manifestations of the encephalitic presentation may include SEIZURES, lethargy, MYOCLONUS, focal neurologic signs, COMA, and DEATH. (From Adams et al., Principles of Neurology, 6th ed, p750) |
| Synonym | enceph saint louis enceph st louis enceph viral st louis encephalitis c encephalitis, saint louis encephalitis, st-louis encephalitis, st. louis encephalitis, st. louis [disease/finding] encephalitis, viral, st. louis lethargic enceph type c lethargic encephalitis, type c neuroinvasive saint louis encephalitis virus infection neuroinvasive saint louis encephalitis virus infection (disorder) neuroinvasive st. louis encephalitis virus infection neuroinvasive st. louis encephalitis virus infection (disorder) saint louis enceph saint louis encephalitis sle sle - saint louis encephalitis st louis enceph st louis encephalitis st louis viral enceph st-louis viral disease st. louis encephalitis (disorder) st. louis encephalitis virus infection st. louis encephalitis virus infection (disorder) st. louis encephalitis virus neuroinvasive disease st. louis viral disease st. louis viral encephalitis type c lethargic enceph type c lethargic encephalitis |
| Orphanet | |
| OMIM | |
| DOID | |
| ICD10 | |
| UMLS | C0014060 |
| MeSH | |
| SNOMED-CT | |
| Comorbidity | UMLS | Disease | Sentences' Count(Total Sentences:12) C0034063 | pulmonary edema | 2 C0042373 | vascular disease | 1 C0025290 | aseptic meningitis | 1 C0085096 | peripheral vascular disease | 1 C0025289 | meningitis | 1 C0155320 | cortical blindness | 1 C0019196 | hepatitis c | 1 C0032285 | pneumoniae | 1 C0019158 | hepatitis | 1 C0743039 | progressive dementia | 1 C0014038 | encephalitis | 1 C0497327 | dementia | 1 |
| Curated Gene | (Waiting for update.) |
| Inferring Gene | Entrez_id | Symbol | Resource(Total Genes:2) |
| Text Mined Gene | Entrez_id | Symbol | Score | Resource(Total Genes:6) |
| Locus | (Waiting for update.) |
| Disease ID | 1130 |
|---|---|
| Disease | st. louis encephalitis |
| Integrated Phenotype | (Waiting for update.) |
| Text Mined Phenotype | HPO | Name | Sentences' Count(Total Phenotypes:10) HP:0100598 | Pulmonary oedema | 2 HP:0012115 | Liver inflammation | 1 HP:0000726 | Dementia | 1 HP:0011450 | CNS infection | 1 HP:0001250 | Seizures | 1 HP:0001287 | Meningitis | 1 HP:0004787 | Fulminant hepatitis | 1 HP:0100704 | Cortical visual impairment | 1 HP:0000969 | Dropsy | 1 HP:0002383 | Encephalitis | 1 |
| Disease ID | 1130 |
|---|---|
| Disease | st. louis encephalitis |
| Manually Symptom | (Waiting for update.) |
| Text Mined Symptom | (Waiting for update.) |
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) | |
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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 | 1130 |
|---|---|
| Disease | st. louis encephalitis |
| Case | (Waiting for update.) |