Cyclosporiasis
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- All ages
- Status
- active
Cyclosporosis is a parasitic disease caused by <i>Cyclospora cayetanensis</i>, a recently discovered coccidia that was initially described in Peru and then in most intertropical zones. Infection occurs through ingestion of contaminated food or water and leads to abdominal pain, anorexia and diarrhoea, which may resolve spontaneously in immunocompetent individuals but may persist in a chronic form in immunocompromised subjects, leading to a decline in their general state of health.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Cyclosporiasis | |
| fr | Cyclosporose | |
| de | Zyklosporiasis | |
| es | Ciclosporosis | |
| it | Ciclosporiasi | |
| nl | Cyclosporiasis | |
| pt | Ciclosporíase | |
| pl | Cyklosporoza | |
| cs | Cyklosporóza | |
| uk | Циклоспориоз | |
| zh | 环孢子虫病 | |
| tr | Siklosporoz |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | A07.3 | NTBT | attributed | validated |
| ICD-11 | 1A3Y | NTBT | index | validated |
| MONDO | 0005725 | E | validated | |
| UMLS | C4274225 | E | validated | |
| GARD | 9528 | 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:163588Rare parasitic disease
rare infectious diseases
No children.
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/210
- This record as JSON: /data/d/210.json