Sporotrichosis
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- All ages
- Status
- active
Sporotrichosis is an infection caused by the dimorphic fungus <i>Sporothrix schenckii</i>, generally occurring by traumatic inoculation of fungus from contaminated soil, plants, and organic matter, that has a highly variable disease spectrum but that usually presents as a subcutaneous mycosis with a single sporotrichotic chancre that may ulcerate and can then progress to lymphocutaneous (most common form; sporotrichotic chancre at inoculation site and a string of similar nodules along the proximal lymphatics), fixed cutaneous (localized asymptomatic, erythematous, papules at the inoculation site), or multifocal or disseminated cutaneous (rare form, with 3 or more lesions involving 2 different anatomical sites) forms. Pulmonary sporotrichosis occurs following inhalation of fungus and manifests as chronic pneumonitis while extracutaneous or systemic sporotrichosis (with osteoarticular, pulmonary, and central nervous system/meningeal disease) has also been reported, usually occurring in the setting of immunosuppression.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Sporotrichosis | |
| fr | Sporotrichose | |
| de | Sporotrichose | |
| es | Esporotricosis | |
| it | Sporotricosi | |
| nl | Sporotrichose | |
| pt | Esporotricose | |
| pl | Sporotrychoza | |
| cs | Sporotrichóza | |
| uk | Споротрихоз | |
| zh | 孢子丝菌病 | |
| tr | Sporotrikoz |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | B42.0 | BTNT | specific | validated |
| ICD-10 | B42.1 | BTNT | specific | validated |
| ICD-10 | B42.7 | BTNT | specific | validated |
| ICD-10 | B42.8 | BTNT | specific | validated |
| ICD-10 | B42.9 | BTNT | specific | validated |
| ICD-11 | 1F2J | E | specific | validated |
| ICD-11 | 1F2J.0 | BTNT | specific | validated |
| ICD-11 | 1F2J.1 | BTNT | specific | validated |
| ICD-11 | 1F2J.2 | BTNT | specific | validated |
| ICD-11 | 1F2J.3 | BTNT | specific | validated |
| ICD-11 | 1F2J.Y | BTNT | attributed | validated |
| MONDO | 0005968 | E | validated | |
| MeSH | D013174 | E | validated | |
| UMLS | C0038034 | E | validated | |
| GARD | 7692 | E | validated | |
| MedDRA | 10041736 | 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
3 records| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Point prevalence | Unknown | — | Worldwide | Class only | Validated | ORPHANET_25526781[PMID] |
| Point prevalence | >1 / 1000 | 2500 / 100 000 | Mexico | Value and class | Validated | 25526781[PMID] |
| Annual incidence | 1-5 / 10 000 | 54 / 100 000 | Peru | Value and class | Validated | 10619735[PMID] |
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/826
- This record as JSON: /data/d/826.json