eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| encephalitis, japanese | ||||
| Disease ID | 1156 |
|---|---|
| Disease | encephalitis, japanese |
| Definition | A mosquito-borne encephalitis caused by the Japanese B encephalitis virus (ENCEPHALITIS VIRUS, JAPANESE) occurring throughout Eastern Asia and Australia. The majority of infections occur in children and are subclinical or have features limited to transient fever and gastrointestinal symptoms. Inflammation of the brain, spinal cord, and meninges may occur and lead to transient or permanent neurologic deficits (including a POLIOMYELITIS-like presentation); SEIZURES; COMA; and death. (From Adams et al., Principles of Neurology, 6th ed, p751; Lancet 1998 Apr 11;351(9109):1094-7) |
| Synonym | enceph japanese enceph japanese b encephalitis japanese encephalitis, japanese [disease/finding] encephalitis, japanese b encephalitis, russian autumnal encephalitis, summer japanese b enceph japanese b encephalitis japanese b viral enceph japanese b viral encephalitis japanese enceph japanese encephalitis japanese encephalitis virus disease japanese encephalitis virus disease (disorder) jbe - japanese b encephalitis je - japanese encephalitis viral enceph japanese b viral encephalitis, japanese b |
| Orphanet | |
| DOID | |
| ICD10 | |
| UMLS | C0014057 |
| MeSH | |
| SNOMED-CT | |
| Comorbidity | UMLS | Disease | Sentences' Count(Total Sentences:7) C0014038 | encephalitis | 4 C0025289 | meningitis | 1 C0013421 | dystonia | 1 C0015464 | facial palsy | 1 C0024530 | plasmodium infection | 1 C0018378 | guillain-barre syndrome | 1 C0025290 | aseptic meningitis | 1 |
| Curated Gene | (Waiting for update.) |
| Inferring Gene | Entrez_id | Symbol | Resource(Total Genes:1) |
| Text Mined Gene | Entrez_id | Symbol | Score | Resource(Total Genes:23) 262 | AMD1 | 1.851 | DISEASES 959 | CD40LG | 4.581 | DISEASES 7122 | CLDN5 | 1.697 | DISEASES 2920 | CXCL2 | 1.664 | DISEASES 4283 | CXCL9 | 1.09 | DISEASES 1805 | DPT | 4.242 | DISEASES 30816 | ERVW-1 | 1.052 | DISEASES 3363 | HTR7 | 1.698 | DISEASES 5654 | HTRA1 | 2 | DISEASES 3455 | IFNAR2 | 1.302 | DISEASES 3456 | IFNB1 | 1.226 | DISEASES 4155 | MBP | 1.511 | DISEASES 4512 | MT-CO1 | 1.684 | DISEASES 4958 | OMD | 2.481 | DISEASES 100630918 | PARTICL | 5.597 | DISEASES 139728 | PNCK | 2.362 | DISEASES 149830 | PRNT | 3.217 | DISEASES 8786 | RGS11 | 3.418 | DISEASES 6050 | RNH1 | 2.136 | DISEASES 7124 | TNF | 1.01 | DISEASES 7156 | TOP3A | 2.08 | DISEASES 51175 | TUBE1 | 3.192 | DISEASES 8725 | URI1 | 2.722 | DISEASES |
| Locus | (Waiting for update.) |
| Disease ID | 1156 |
|---|---|
| Disease | encephalitis, japanese |
| Integrated Phenotype | (Waiting for update.) |
| Text Mined Phenotype | HPO | Name | Sentences' Count(Total Phenotypes:9) HP:0002383 | Encephalitis | 5 HP:0430025 | Bilateral facial paralysis | 1 HP:0010628 | Facial palsy, unilateral or bilateral | 1 HP:0001298 | Encephalopathy | 1 HP:0100022 | Movement disorder | 1 HP:0012048 | Oromandibular dystonia | 1 HP:0001287 | Meningitis | 1 HP:0011450 | CNS infection | 1 HP:0001332 | Dystonia | 1 |
| Disease ID | 1156 |
|---|---|
| Disease | encephalitis, japanese |
| Manually Symptom | (Waiting for update.) |
| Text Mined Symptom | UMLS | Name | Sentences' Count(Total Symptoms:7) C0009450 | infection | 19 C0021311 | infections | 2 C0025290 | aseptic meningitis | 1 C0013421 | dystonia | 1 C0026650 | movement disorders | 1 C0154064 | ain iii | 1 C1264606 | persistent infection | 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) | |
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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 | 1156 |
|---|---|
| Disease | encephalitis, japanese |
| Case | (Waiting for update.) |