Isosporiasis
Synonyms: Cystoisosporiasis
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- All ages
- Status
- active
Isosporiasis (also known as cystoisosporiasis) is an exclusively human parasitosis occurring mainly in the tropics and subtropics, due to infection with <i>Isospora belli</i> (through ingestion of contaminated food), that is frequently asymptomatic or that can cause fever and diarrhea, but that is usually a self-limiting condition in the immunocompetent. HIV-positive individuals are particularly at risk of suffering from symptomatic isosporiasis and can manifest with a more severe clinical course of chronic diarrhea and severe weight loss.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Isosporiasis | Cystoisosporiasis |
| fr | Isosporose | |
| de | Isosporiasis | Isosporose |
| es | Isosporosis | |
| it | Isosporiasi | Isosporosi |
| nl | Isosporiasis | Isosporiase |
| pt | Isosporiose | |
| pl | Izosporydoza | = en |
| cs | Izosporiáza | Cystoizosporiáza |
| uk | Ізоспороз | Цистоізоспороз |
| zh | 等孢子球虫病 | 等孢子球虫病 |
| tr | Izosporiaz | Kistoizosporiazis |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | A07.3 | E | specific | validated |
| ICD-11 | 1A33 | E | specific | validated |
| MONDO | 0018769 | E | validated | |
| MeSH | D021865 | E | validated | |
| UMLS | C0311386 | E | validated | |
| GARD | 3033 | E | validated | |
| MedDRA | 10023076 | 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 | 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/472
- This record as JSON: /data/d/472.json