Viral hemorrhagic fever
- Type
- Category
- Group
- Group of disorders
- Inheritance
- Not applicable
- Age of onset
- All ages
- Status
- active
A rare group of infectious disease characterized by malaise, fever, exhaustion, vascular permeability, decreased plasma volume, coagulation abnormalities and varying degrees of hemorrhage. Severity of hemorrage is affected by a variety of contributing factors (depending on the pathogen and the host, whether it is primary infection or reinfection) and severly ill patients often show signs of bleeding under skin, in internal organs and in orifices. They may develop circulatory collapse, multisystem organ failure, shock, nervous system malfunction, coma, delirium, and seizures. A variety of rashes and ocular manifestations can also be associated with the diseases. They are caused by several different families of RNA viruses, including members of arenaviruses, bunyaviruses, filoviruses and flaviviruses that are capable of causing high morbidity and mortality.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Viral hemorrhagic fever | |
| fr | Fièvre hémorragique virale | |
| de | Virales hämorrhagische Fieber | VHF |
| es | Fiebre hemorrágica vírica | |
| it | Febbre emorragica virale | |
| nl | Virale hemorragische koorts | |
| pt | Febre hemorrágica vírica | Doença por Ebola vírus |
| pl | Wirusowa gorączka krwotoczna | Choroba wirusa Ebola |
| cs | Virová hemoragická horečka | |
| uk | Вірусна геморагічна лихоманка | |
| zh | 病毒性出血热 | |
| tr | Viral hemorajik ateş |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0018087 | E | validated | |
| MONDO | 18087 | E | validated | |
| MeSH | D006482 | E | validated | |
| UMLS | C0019104 | E | validated | |
| GARD | 5494 | 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:163585Rare viral disease
rare infectious diseases
Children (17):
- ORPHA:319223Argentine hemorrhagic fever
- ORPHA:319229Bolivian hemorrhagic fever
- ORPHA:319239Brazilian hemorrhagic fever
- ORPHA:319244Chapare hemorrhagic fever
- ORPHA:99827Crimean-Congo hemorrhagic fever
- ORPHA:99828Dengue fever
- ORPHA:319218Ebola hemorrhagic fever
- ORPHA:319247Hantavirus pulmonary syndrome
- ORPHA:340Hemorrhagic fever-renal syndrome
- ORPHA:319254Kyasanur forest disease
- ORPHA:99824Lassa fever
- ORPHA:319213Lujo hemorrhagic fever
- ORPHA:99826Marburg hemorrhagic fever
- ORPHA:319266Omsk hemorrhagic fever
- ORPHA:319251Rift valley fever
- ORPHA:319234Venezuelan hemorrhagic fever
- ORPHA:99829Yellow fever
Genes
0 directOrphanet records no gene directly on this code.
Prevalence and incidence
1 record| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| 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.
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/341
- This record as JSON: /data/d/341.json