Invasive scopulariopsis infection
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- Adolescent, Adult, Childhood, Elderly
- Status
- active
A rare mycosis characterized by disseminated or localized deep tissue infections due to invasive scopulariopsis (that are commonly responsible for non-invasive infections) infection in both immunocompetent and immunosuppressed patients (mostly treated with high dose chemotherapy and/or received a stem cell transplantation). Clinical features may include endocarditis, brain abscess, cutaneous infections, pulmonary infections, endophthalmitis, invasive sinusitis and peritonitis that are often life threatening.
Names in Orphadata languages
10 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Invasive scopulariopsis infection | |
| fr | Infection invasive à scopulariopsis | |
| de | Scopulariopsis-Infektion, invasive | |
| es | Infección invasiva por Escopulariopsis | |
| it | Infezione invasiva da scopulariopsis | |
| nl | Invasieve infectie door scopulariopsis | |
| pt | Infeção invasiva por Scopulariopsis | |
| pl | Inwazyjne zakażenie grzybem z rodzaju scopulariopsis | |
| cs | Invazivní infekce druhem Scopulariopsis | |
| uk | Інвазивна інфекція скопуляріопсису |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | B48.7 | NTBT | attributed | validated |
| ICD-11 | 1F2Y | NTBT | attributed | validated |
| MONDO | 0859004 | E | validated | |
| UMLS | C5816808 | 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 (2):
- ORPHA:565779Rare disorder potentially indicated for transplant or complication after transplantation
rare transplant-related disorders - ORPHA:163591Rare mycosis
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 | <1 / 1 000 000 | 0.05 / 100 000 | Europe | Value and class | Validated | https://www.ema.europa.eu/en/medicines/human/orphan-designations/eu-3-21-2563 |
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/633124
- This record as JSON: /data/d/633124.json