Hendra virus infection
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- All ages
- Status
- active
Hendra virus infection is a rare viral infection disorder caused by the Hendra virus characterized by onset of flu-like symptoms (fever, myalgia, headaches, lethargy) approximately one week after having been in close contact with bodily fluids of infected horses. Neurological manifestations (e.g. vertigo, confusion, ataxia) and progressive respiratory failure, leading to death, have also been reported.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Hendra virus infection | |
| fr | Infection à virus Hendra | |
| de | Hendra-Virusinfektion | |
| es | Infección por el virus Hendra | |
| it | Infezione da virus Hendra | |
| nl | Hendra-virusinfectie | |
| pt | Infecção por vírus Hendra | |
| pl | Zakażenie wirusem Hendra | |
| cs | Infekce virem Hendra | |
| uk | Вірусна інфекція Хендра | |
| zh | Hendra病毒感染 | |
| tr | Hendra virüs enfeksiyonu |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | B33.8 | NTBT | attributed | validated |
| ICD-11 | 1D63 | BTNT | attributed | validated |
| MONDO | 0017942 | E | validated | |
| UMLS | C4505487 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:98252Infectious encephalitis
rare neurological diseases; rare infectious diseases
No children.
Genes
0 directOrphanet records no gene directly on this code.
Prevalence and incidence
2 records| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Cases/families | 7 cases | Worldwide | Case(s) | Validated | 22752412[PMID] | |
| Point prevalence | <1 / 1 000 000 | — | Worldwide | Class only | 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.
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/324632
- This record as JSON: /data/d/324632.json