Ebola hemorrhagic fever
Synonyms: EHF · Ebola fever · Ebola virus disease
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- All ages
- Status
- active
Ebola hemorrhagic fever (EHF), caused by Ebola virus, is a severe viral hemorrhagic disease characterized by initial fever and malaise followed by gastrointestinal symptoms, bleeding, shock, and multi-organ system failure.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Ebola hemorrhagic fever | EHF · Ebola fever · Ebola virus disease |
| fr | Fièvre hémorragique à virus Ebola | EHF · Fièvre Ebola |
| de | Ebola hämorrhagisches Fieber | EHF · Ebola-Fieber · Ebola-Viruskrankheit |
| es | Fiebre hemorrágica del virus Ébola | Enfermedad del virus Ébola · Fiebre del Ébola · EHF |
| it | Febbre emorragica dell'Ebola | EHF · Febbre dell'Ebola · Malattia virale dell'Ebola |
| nl | Ebola hemorragische koorts | EHF · Ebola-koorts · Ebola-virusziekte |
| pt | Febre hemorrágica do Ébola | |
| pl | Gorączka krwotoczna Ebola | Choroba wirusa Ebola · EHF · Gorączka ebola Ebola |
| cs | Hemoragická horečka Ebola | EHF · Virová nemoc Ebola · Horečka Ebola |
| uk | Геморагічна лихоманка Ебола | Лихоманка Ебола · Хвороба, спричинена вірусом Ебола · EHF |
| zh | 埃博拉出血热 | 埃博拉病毒病 |
| tr | Ebola hemorajik ateşi | EHF · Ebola ateşi · Ebola virüsü hastalığı |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | A98.4 | E | specific | validated |
| ICD-11 | 1D60.01 | E | specific | validated |
| MONDO | 0005737 | E | validated | |
| MeSH | D019142 | E | validated | |
| UMLS | C0282687 | E | validated | |
| GARD | 2035 | E | validated | |
| MedDRA | 10014071 | 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:341Viral hemorrhagic fever
rare infectious diseases
No children.
Genes
0 directOrphanet records no gene directly on this code.
Prevalence and incidence
3 records| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Cases/families | 28220 cases | Worldwide | Case(s) | Validated | World health Organisation 2015[OTHER]_26607790[PMID] | |
| Annual incidence | <1 / 1 000 000 | — | Europe | Class only | Validated | European Centre for Disease prevention and Control 2011[OTHER] |
| Point prevalence | <1 / 1 000 000 | — | Europe | Class only | Validated | European Medicines Agency 2018[OTHER] |
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
29 annotations · validated 2021-09-06| HPO | Term (as annotated by Orphanet) | Diagnostic |
|---|---|---|
| Very frequent (99-80%) | ||
| HP:0100749 | Chest pain | |
| HP:0002014 | Diarrhea | |
| HP:0001945 | Fever | |
| HP:0010702 | Increased circulating immunoglobulin concentration | |
| HP:0020071 | Viremia | |
| Frequent (79-30%) | ||
| HP:0002027 | Abdominal pain | |
| HP:0001892 | Abnormal bleeding | |
| HP:0025143 | Chills | |
| HP:0012735 | Cough | |
| HP:0002015 | Dysphagia | |
| HP:0002239 | Gastrointestinal hemorrhage | |
| HP:0002315 | Headache | |
| HP:0012115 | Hepatitis | |
| HP:0001882 | Leukopenia | |
| HP:0001888 | Lymphopenia | |
| HP:0040186 | Maculopapular exanthema | |
| HP:0002249 | Melena | |
| HP:0002018 | Nausea | |
| HP:0025439 | Pharyngitis | |
| HP:0004396 | Poor appetite | |
| HP:0100806 | Sepsis | |
| HP:0002013 | Vomiting | |
| Occasional (29-5%) | ||
| HP:0001735 | Acute pancreatitis | |
| HP:0002829 | Arthralgia | |
| HP:0005521 | Disseminated intravascular coagulation | |
| HP:0002094 | Dyspnea | |
| HP:0001254 | Lethargy | |
| HP:0100247 | Recurrent singultus | |
| HP:0001873 | Thrombocytopenia | |
Run the differential on the 5 obligate / very frequent terms
Annotation source: 26287303[PMID]_32487785[PMID]_28653186[PMID]
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/319218
- This record as JSON: /data/d/319218.json