ORPHA:79139
Japanese encephalitis
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- All ages
- Status
- active
Japanese encephalitis is an arboviral disease (<i>i.e.</i> a disease due to a virus transmitted by an arthropod).
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Japanese encephalitis | |
| fr | Encéphalite japonaise | |
| de | Japanische Enzephalitis | |
| es | Encefalitis japonesa | |
| it | Encefalite giapponese | |
| nl | Japanse encefalitis | |
| pt | Encefalite japonesa | |
| pl | Japońskie zapalenie mózgu | |
| cs | Japonská encefalitida | |
| uk | Японський енцефаліт | |
| zh | 日本脑炎 | |
| tr | Japon ensefaliti |
Definition in:
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | A83.0 | E | specific | validated |
| ICD-11 | 1C85 | E | specific | validated |
| MONDO | 0019209 | E | validated | |
| MeSH | D004672 | E | validated | |
| UMLS | C0014057 | E | validated | |
| GARD | 6797 | E | validated | |
| MedDRA | 10014596 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
3
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (2):
- ORPHA:166490Infectious disease with epilepsy
rare neurological diseases - ORPHA:98252Infectious encephalitis
rare neurological diseases; rare infectious diseases
No children.
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
2 records| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Annual incidence | 1-9 / 1 000 000 | 0.65 / 100 000 | Europe | Value and class | Not yet validated | ORPHANET |
| Point prevalence | Unknown | — | Worldwide | Class only | Not yet validated | ORPHANET |
Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.
6
HPO phenotypes
82 annotations · validated 2020-04-22| HPO | Term (as annotated by Orphanet) | Diagnostic |
|---|---|---|
| Very frequent (99-80%) | ||
| HP:0002353 | EEG abnormality | |
| HP:0001945 | Fever | |
| HP:0002383 | Infectious encephalitis | |
| Frequent (79-30%) | ||
| HP:0002039 | Anorexia | |
| HP:0002069 | Bilateral tonic-clonic seizure | |
| HP:0200149 | CSF lymphocytic pleiocytosis | |
| HP:0012229 | CSF pleocytosis | |
| HP:0025143 | Chills | |
| HP:0002396 | Cogwheel rigidity | |
| HP:0003431 | Decreased motor nerve conduction velocity | |
| HP:0009053 | Distal lower limb muscle weakness | |
| HP:0003444 | EMG: chronic denervation signs | |
| HP:0000273 | Facial grimacing | |
| HP:0012378 | Fatigue | |
| HP:0012692 | Focal T2 hyperintense thalamic lesion | |
| HP:0004302 | Functional motor deficit | |
| HP:0002315 | Headache | |
| HP:0040272 | Hyperintensity of MRI T2 signal of the spinal cord | |
| HP:0002922 | Increased CSF protein concentration | |
| HP:0003496 | Increased circulating IgM level | |
| HP:0010702 | Increased circulating immunoglobulin concentration | |
| HP:0002516 | Increased intracranial pressure | |
| HP:0000298 | Mask-like facies | |
| HP:0003326 | Myalgia | |
| HP:0011897 | Neutrophilia | |
| HP:0003470 | Paralysis | |
| HP:0007277 | Paucity of anterior horn motor neurons | |
| HP:0004372 | Reduced consciousness | |
| HP:0003202 | Skeletal muscle atrophy | |
| HP:0002013 | Vomiting | |
| HP:0010549 | Weakness due to upper motor neuron dysfunction | |
| Occasional (29-5%) | ||
| HP:0002027 | Abdominal pain | |
| HP:0002339 | Abnormal caudate nucleus morphology | |
| HP:0002060 | Abnormal cerebral morphology | |
| HP:0002793 | Abnormal pattern of respiration | |
| HP:0007695 | Abnormal pupillary light reflex | |
| HP:0002071 | Abnormality of extrapyramidal motor function | |
| HP:0002418 | Abnormality of midbrain morphology | |
| HP:0010663 | Abnormality of thalamus morphology | |
| HP:0012502 | Abnormality of the internal capsule | |
| HP:0007361 | Abnormality of the pons | |
| HP:0045007 | Abnormality of the substantia nigra | |
| HP:0000708 | Atypical behavior | |
| HP:0002181 | Cerebral edema | |
| HP:0001266 | Choreoathetosis | |
| HP:0100543 | Cognitive impairment | |
| HP:0001259 | Coma | |
| HP:0002014 | Diarrhea | |
| HP:0008959 | Distal upper limb muscle weakness | |
| HP:0001332 | Dystonia | |
| HP:0010851 | EEG with burst suppression | |
| HP:0002987 | Elbow flexion contracture | |
| HP:0003781 | Excessive salivation | |
| HP:0030826 | Eyelid fasciculation | |
| HP:0010628 | Facial palsy | |
| HP:0011468 | Facial tics | |
| HP:0011153 | Focal motor seizure | |
| HP:0002816 | Genu recurvatum | |
| HP:0001276 | Hypertonia | |
| HP:0002902 | Hyponatremia | |
| HP:0031218 | Inappropriate antidiuretic hormone secretion | |
| HP:0010864 | Intellectual disability, severe | |
| HP:0011182 | Interictal epileptiform activity | |
| HP:0012195 | Irregular respiration | |
| HP:0002463 | Language impairment | |
| HP:0007941 | Limited extraocular movements | |
| HP:0001287 | Meningitis | |
| HP:0010546 | Muscle fibrillation | |
| HP:0010547 | Muscle flaccidity | |
| HP:0001336 | Myoclonus | |
| HP:0000639 | Nystagmus | |
| HP:0002179 | Opisthotonus | |
| HP:0010543 | Opsoclonus | |
| HP:0025387 | Pill-rolling tremor | |
| HP:0100598 | Pulmonary edema | |
| HP:0002098 | Respiratory distress | |
| HP:0002203 | Respiratory paralysis | |
| HP:0025145 | Rigors | |
| HP:0002133 | Status epilepticus | |
| HP:0025258 | Stiff neck | |
| HP:0001762 | Talipes equinovarus | |
| HP:0001337 | Tremor | |
Run the differential on the 3 obligate / very frequent terms
Annotation source: 30455264[PMID]_25015504[PMID]_23141974[PMID]
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/79139
- This record as JSON: /data/d/79139.json