raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:826

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.

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enSporotrichosis
frSporotrichose
deSporotrichose
esEsporotricosis
itSporotricosi
nlSporotrichose
ptEsporotricose
plSporotrychoza
csSporotrichóza
ukСпоротрихоз
zh孢子丝菌病
trSporotrikoz

Definition in:

2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
ICD-10B42.0BTNTspecificvalidated
ICD-10B42.1BTNTspecificvalidated
ICD-10B42.7BTNTspecificvalidated
ICD-10B42.8BTNTspecificvalidated
ICD-10B42.9BTNTspecificvalidated
ICD-111F2JEspecificvalidated
ICD-111F2J.0BTNTspecificvalidated
ICD-111F2J.1BTNTspecificvalidated
ICD-111F2J.2BTNTspecificvalidated
ICD-111F2J.3BTNTspecificvalidated
ICD-111F2J.YBTNTattributedvalidated
MONDO0005968Evalidated
MeSHD013174Evalidated
UMLSC0038034Evalidated
GARD7692Evalidated
MedDRA10041736Evalidated

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):

No children.

4

Genes

0 direct

Orphanet records no gene directly on this code.

5

Prevalence and incidence

3 records
TypeClassValueAreaQualificationValidationSource
Point prevalenceUnknown—WorldwideClass onlyValidatedORPHANET_25526781[PMID]
Point prevalence>1 / 10002500 / 100 000MexicoValue and classValidated25526781[PMID]
Annual incidence1-5 / 10 00054 / 100 000PeruValue and classValidated10619735[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.

6

HPO phenotypes

Orphanet has no HPO annotation for this code in this release.

7

Sources for this card