Ehrlichiosis
- Type
- Disease
- Group
- Disorder
- Age of onset
- All ages
- Status
- active
A group of acute febrile tick-borne diseases characterized by an overlapping clinical picture that includes fever, headache, myalgias, arthralgias, skin eruptions, gastrointestinal symptoms and neurological manifestations. Diseases in this group include human monocytotropic ehrlichiosis (HME), human granulocytotropic anaplasmosis (HGA), and human ehrlichiosis ewingii (HEE).
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Ehrlichiosis | |
| fr | Ehrlichiose | |
| de | Ehrlichiose, granulozytäre humane | Anaplasmose, granulozytäre humane |
| es | Erliquiosis | |
| it | Ehrlichiosi | |
| nl | Ehrlichiose | |
| pt | Ehrliquiose | |
| pl | Erlichioza | |
| cs | Ehrlichióza | |
| uk | Ерліхіоз | |
| zh | 埃里希体病 | |
| tr | Erlikiyoz |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | A79.8 | NTBT | attributed | validated |
| ICD-11 | 1C3Y | NTBT | index | validated |
| MONDO | 0016003 | E | validated | |
| MeSH | D016873 | E | validated | |
| UMLS | C0085399 | E | validated | |
| GARD | 2092 | 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:102021Rickettsial disease
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 | 50 cases | Worldwide | Case(s) | Validated | ORPHANET | |
| Annual incidence | 1-9 / 1 000 000 | 0.25 / 100 000 | United States | Value and class | Validated | Center for Diseases Control and Prevention[OTHER] |
| Point prevalence | <1 / 1 000 000 | — | Europe | 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/1902
- This record as JSON: /data/d/1902.json