Home Contact Sitemap

PedAM

Pediatric Disease Annotations & Medicines



   sle
  

Disease ID 1345
Disease sle
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 - saint louis encephalitis
st louis enceph
st louis encephalitis
st louis viral enceph
st-louis viral disease
st. louis encephalitis
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
Curated Gene(Waiting for update.)
Inferring Gene
Entrez_id | Symbol | Resource(Total Genes:2)
3123  |  HLA-DRB1  |  infer
3690  |  ITGB3  |  infer
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:10)
5894  |  RAF1  |  DISEASES
29107  |  NXT1  |  DISEASES
3845  |  KRAS  |  DISEASES
6037  |  RNASE3  |  DISEASES
6035  |  RNASE1  |  DISEASES
755  |  C21orf2  |  DISEASES
3445  |  IFNA8  |  DISEASES
3440  |  IFNA2  |  DISEASES
30816  |  ERVW-1  |  DISEASES
26768  |  SNORA73B  |  DISEASES
Locus(Waiting for update.)
Disease ID 1345
Disease sle
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype(Waiting for update.)
Disease ID 1345
Disease sle
Manually Symptom(Waiting for update.)
Text Mined Symptom(Waiting for update.)
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:0)
(Waiting for update.)
Mapped by homologous gene(Total Items:0)
(Waiting for update.)
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.)