Pseudotyphus of California
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- All ages
- Status
- active
Pseudotyphus of California is a rare, flea-borne Rickettsial disease caused by a <i>Rickettsia felis </i> infection. Patients can be asymptomatic or can present with unspecific symptoms (such as fever, headache, generalized maculopapular rash, myalgia, arthralgia and, ocasionally, eschar, lymphadenopathy, nausea, vomiting, loss of appetite and abdominal pain). Rarely, serious manifestations may occur and include neurological dysfunction (photophobia, hearing loss, and signs of meningitis) and pulmonary compromise.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Pseudotyphus of California | |
| fr | Pseudotyphus de la Californie | |
| de | Pseudotyphus California | |
| es | Pseudotifus de Califonia | |
| it | Pseudotifo della California | |
| nl | Pseudotyfus van Californië | |
| pt | Pseudo-tifo da Califórnia | |
| pl | Pseudotyfus kalifornijski | |
| cs | Kalifornský pseudotyfus | |
| uk | Псевдотиф каліфорнійський | |
| zh | 加州假斑疹伤寒 | |
| tr | Kaliforniya psödotifüsü |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | A79.8 | NTBT | attributed | validated |
| ICD-11 | 1C30.Y | NTBT | attributed | validated |
| MONDO | 0019364 | E | validated | |
| UMLS | C4706680 | 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:102022Spotted fever rickettsiosis
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/83316
- This record as JSON: /data/d/83316.json