Scedosporiosis
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- All ages
- Status
- active
A rare mycosis caused by <i>Scedosporium</i> species, characterized by disparate disease pictures including pneumonia, skin and soft tissue infection, mycetoma, and disseminated infection. Central nervous system infection has also been reported. Infections with this ubiquitous mold can occur in a range of contexts like solid organ transplantation, chemotherapy, chronic lung disease, but also in immunocompetent hosts and near drowning.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Scedosporiosis | |
| fr | Scédosporiose | |
| de | Scedosporiose | |
| es | Escedosporiosis | |
| it | Infezione da Scedosporium | |
| nl | Scedosporiose | |
| pt | Scedosporiose | |
| pl | Scedosporioza | |
| cs | Scedosporióza | |
| uk | Сцедоспоріоз | |
| zh | 赛多银屑病 | |
| tr | Skedosporioz |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | B48.2 | NTBT | attributed | validated |
| ICD-11 | 1F2H | E | specific | validated |
| MONDO | 0018668 | E | validated | |
| MeSH | C000656924 | E | validated | |
| UMLS | C1142170 | E | validated | |
| MedDRA | 10059045 | 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:163591Rare mycosis
rare infectious diseases
No children.
Genes
0 directOrphanet records no gene directly on this code.
Prevalence and incidence
2 records| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Annual incidence | 1-9 / 1 000 000 | 0.1 / 100 000 | Australia | Value and class | Validated | 19549223[PMID] |
| Point prevalence | <1 / 1 000 000 | — | Europe | Class only | Validated | European Medicines Agency 2014[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.
HPO phenotypes
34 annotations · validated 2020-03-31| HPO | Term (as annotated by Orphanet) | Diagnostic |
|---|---|---|
| Very frequent (99-80%) | ||
| HP:0001945 | Fever | |
| HP:0002721 | Immunodeficiency | |
| HP:0032255 | Opportunistic fungal infection | |
| HP:0032169 | Severe infection | |
| Frequent (79-30%) | ||
| HP:0010766 | Ectopic calcification | |
| HP:0002090 | Pneumonia | |
| HP:0032262 | Pulmonary tuberculosis | |
| HP:0001482 | Subcutaneous nodule | |
| HP:0032162 | Unusual skin infection | |
| Occasional (29-5%) | ||
| HP:0012210 | Abnormal renal morphology | |
| HP:0002795 | Abnormal respiratory system physiology | |
| HP:0001977 | Abnormal thrombosis | |
| HP:0005265 | Abnormality of the jejunum | |
| HP:0032176 | Apical pulmonary opacity | |
| HP:0005059 | Arthralgia/arthritis | |
| HP:0410263 | Brain imaging abnormality | |
| HP:0031994 | Bronchial breath sound | |
| HP:0012387 | Bronchitis | |
| HP:0012735 | Cough | |
| HP:0000819 | Diabetes mellitus | |
| HP:0100584 | Endocarditis | |
| HP:0032159 | Fungal meningitis | |
| HP:0002105 | Hemoptysis | |
| HP:0020101 | Invasive fungal infection | |
| HP:0002754 | Osteomyelitis | |
| HP:0001701 | Pericarditis | |
| HP:0011919 | Pleural empyema | |
| HP:0002102 | Pleuritis | |
| HP:0002206 | Pulmonary fibrosis | |
| HP:0002878 | Respiratory failure | |
| HP:0100806 | Sepsis | |
| HP:0003095 | Septic arthritis | |
| HP:0000246 | Sinusitis | |
| HP:0011450 | Unusual CNS infection | |
Run the differential on the 4 obligate / very frequent terms
Annotation source: 29567285[PMID]_26353885[PMID]_29044831[PMID]
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/449280
- This record as JSON: /data/d/449280.json