Paratyphoid fever
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- All ages
- Status
- active
A rare form of salmonellosis caused by Salmonella enterica serovar Paratyphi A, B and C, characterized by typical symptoms of enteric fever including high fever, headache, abdominal pain and intestinal symptoms, dry cough, chills, and rashes, followed by a long period of recovery. The infection can be complicated by intestinal hemorrhage and perforation, as well as cardiac involvement, and may even be fatal. Transmission of the pathogen is via the fecal-oral route, with humans as the sole reservoir of infection.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Paratyphoid fever | |
| fr | Fièvre paratyphoïde | |
| de | Paratyphus | Paratyphoides Fieber |
| es | Fiebre paratifoidea | Fiebre entérica |
| it | Febbre paratifoide | |
| nl | Paratyfus | |
| pt | Febre paratifoide | |
| pl | Dur rzekomy | |
| cs | Paratyfoidní horečka | |
| uk | Паратиф | |
| zh | 副伤寒 | |
| tr | Paratifoid ateş |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | A01.1 | BTNT | specific | validated |
| ICD-10 | A01.2 | BTNT | specific | validated |
| ICD-10 | A01.3 | BTNT | specific | validated |
| ICD-10 | A01.4 | BTNT | specific | validated |
| ICD-11 | 1A08 | E | specific | validated |
| MONDO | 0018626 | E | validated | |
| MeSH | D010284 | E | validated | |
| UMLS | C0030528 | E | validated | |
| MedDRA | 10033971 | 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:795Rare form of salmonellosis
rare infectious diseases
No children.
Genes
0 directOrphanet records no gene directly on this code.
Prevalence and incidence
0 recordsNo prevalence record in this release.
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/443227
- This record as JSON: /data/d/443227.json