ORPHA:108
Babesiosis
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- All ages
- Status
- active
Babesiosis is an infectious disease caused by protozoa of the genus <i>Babesia</i> and characterized by a febrile illness and hemolytic anemia but with manifestations ranging from an asymptomatic infection to a fulminating illness that can result in death.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Babesiosis | |
| fr | Babésiose | |
| de | Babesiose | |
| es | Babesiosis | |
| it | Babesiosi | |
| nl | Babesiose | |
| pt | Babesiose | |
| pl | Babeszioza | |
| cs | Babezióza | |
| uk | Бабезіоз | |
| zh | 巴贝虫病 | |
| tr | Babeziyoz |
Definition in:
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | B60.0 | E | specific | validated |
| ICD-11 | 1F52 | E | specific | validated |
| MONDO | 0005661 | E | validated | |
| MeSH | D001404 | E | validated | |
| UMLS | C0004576 | E | validated | |
| GARD | 5878 | E | validated | |
| MedDRA | 10003965 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
3
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:163588Rare parasitic disease
rare infectious diseases
No children.
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
1 record| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Point prevalence | <1 / 1 000 000 | — | Europe | Class only | Not yet validated | emedicine[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.
6
HPO phenotypes
31 annotations · validated 2016-06-01| HPO | Term (as annotated by Orphanet) | Diagnostic |
|---|---|---|
| Very frequent (99-80%) | ||
| HP:0001945 | Fever | |
| HP:0002315 | Headache | |
| HP:0001878 | Hemolytic anemia | |
| Frequent (79-30%) | ||
| HP:0002829 | Arthralgia | |
| HP:0012735 | Cough | |
| HP:0012378 | Fatigue | |
| HP:0002240 | Hepatomegaly | |
| HP:0000975 | Hyperhidrosis | |
| HP:0000952 | Jaundice | |
| HP:0001882 | Leukopenia | |
| HP:0003326 | Myalgia | |
| HP:0002719 | Recurrent infections | |
| HP:0001744 | Splenomegaly | |
| HP:0001873 | Thrombocytopenia | |
| Occasional (29-5%) | ||
| HP:0002039 | Anorexia | |
| HP:0001864 | Clinodactyly of the 5th toe | |
| HP:0001259 | Coma | |
| HP:0001289 | Confusion | |
| HP:0001635 | Congestive heart failure | |
| HP:0000716 | Depression | |
| HP:0005521 | Disseminated intravascular coagulation | |
| HP:0001399 | Hepatic failure | |
| HP:0100724 | Hypercoagulability | |
| HP:0001376 | Limitation of joint mobility | |
| HP:0001658 | Myocardial infarction | |
| HP:0002017 | Nausea and vomiting | |
| HP:0000613 | Photophobia | |
| HP:0100776 | Recurrent pharyngitis | |
| HP:0000083 | Renal insufficiency | |
| HP:0002093 | Respiratory insufficiency | |
| HP:0004936 | Venous thrombosis | |
Run the differential on the 3 obligate / very frequent terms
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/108
- This record as JSON: /data/d/108.json