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PedAM

Pediatric Disease Annotations & Medicines



   herpes simplex encephalitis
  

Disease ID 1851
Disease herpes simplex encephalitis
Definition
An acute (or rarely chronic) inflammatory process of the brain caused by SIMPLEXVIRUS infections which may be fatal. The majority of infections are caused by human herpesvirus 1 (HERPESVIRUS 1, HUMAN) and less often by human herpesvirus 2 (HERPESVIRUS 2, HUMAN). Clinical manifestations include FEVER; HEADACHE; SEIZURES; HALLUCINATIONS; behavioral alterations; APHASIA; hemiparesis; and COMA. Pathologically, the condition is marked by a hemorrhagic necrosis involving the medial and inferior TEMPORAL LOBE and orbital regions of the FRONTAL LOBE. (From Adams et al., Principles of Neurology, 6th ed, pp751-4)
Synonym
enceph herpes simplex
encephalitides, herpes simplex
encephalitides, herpetic
encephalitis caused by herpesviridae
encephalitis caused by herpesvirus
encephalitis caused by herpesvirus (disorder)
encephalitis due to herpesviridae
encephalitis due to herpesvirus
encephalitis due to herpesvirus (disorder)
encephalitis herpes
encephalitis hsv
encephalitis, herpes
encephalitis, herpes simplex
encephalitis, herpes simplex [disease/finding]
encephalitis, herpetic
hemmorrhagic encephalitis
herpes enceph
herpes encephalitis
herpes encephalitis (disorder)
herpes simplex enceph
herpes simplex encephalitides
herpes simplex encephalitis (disorder)
herpes simplex encephalitis [ambiguous]
herpetic enceph
herpetic encephalitides
hse - herpes simplex encephalitis
hsv encephalitis
strumpell-leichtenstern encephalitis
Orphanet
UMLS
C0276226
MeSH
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:7)
C0004114  |  astrocytoma  |  1
C0025286  |  meningioma  |  1
C0014068  |  encephalomalacia  |  1
C0026769  |  multiple sclerosis  |  1
C0334579  |  anaplastic astrocytoma  |  1
C0152113  |  acute chorea  |  1
C0038220  |  status epilepticus  |  1
Curated Gene
Entrez_id | Symbol | Resource(Total Genes:5)
TRAF3  |  7187  |  ORPHANET
TBK1  |  29110  |  ORPHANET
TICAM1  |  148022  |  ORPHANET
UNC93B1  |  81622  |  CTD_human;ORPHANET
TLR3  |  7098  |  CTD_human;ORPHANET
Inferring Gene(Waiting for update.)
Text Mined Gene(Waiting for update.)
Locus(Waiting for update.)
Disease ID 1851
Disease herpes simplex encephalitis
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:8)
HP:0002072  |  Chorea  |  2
HP:0009592  |  Astrocytoma  |  1
HP:0001266  |  Choreoathetosis  |  1
HP:0040197  |  Encephalomalacia  |  1
HP:0100786  |  Excessive sleepiness  |  1
HP:0002858  |  Mengiomia  |  1
HP:0002133  |  Status epilepticus  |  1
HP:0009733  |  Glioma  |  1
Disease ID 1851
Disease herpes simplex encephalitis
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:2)
CUI ChemicalName ChemicalID CasRN DiseaseName DiseaseID DirectEvidence PubMedIDs
C0276226epirubicinD01525156420-45-2encephalitis, herpes simplexMESH:D020803marker/mechanism15997927
C0276226foscarnetD0172454428-95-9encephalitis, herpes simplexMESH:D020803therapeutic20517946
FDA approved drug and dosage information(Total Drugs:0)
(Waiting for update.)
FDA labeling changes(Total Drugs:0)
(Waiting for update.)