Furuncular myiasis
Synonyms: Furunculoid myiasis · Furunculous myiasis
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- All ages
- Status
- active
A parasitic disease characterized by infestation of the skin with larvae of a variety of fly species. Furuncular myiasis specifically involves flies whose eggs are able to breach healthy skin, which concerns three species: Cordylobia anthropophaga (also called the African tumbu fly or Cayor worm for the larvae) and Cordylobia rodhaini (the Lund's fly), and Dermatobia hominis (the human botfly).
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Furuncular myiasis | Furunculoid myiasis · Furunculous myiasis |
| fr | Myiase furonculoïde | Myiase furonculeuse |
| de | Furunkuloide Myiasis | |
| es | Miasis forunculosa | |
| it | Miasi foruncolosa | |
| nl | Furunculaire myiasis | Furunculeuze myiasis · Furunculoïde myiasis |
| pt | Miíase furunculosa | |
| pl | Muszyca czyrakowata | = en |
| cs | Furunkulární myiáza | Furunkuloidní myiáza · Furunkulózní myiáza |
| uk | Фурункулярний міаз | Фурункулоїдний міазм · Фурункульозний міазм |
| zh | 疖性蝇蛆病 | 疖性蝇蛆病 |
| tr | Furunküler miyaz | Furunkuloid miyaz · Furunkuloz miyazı |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | B87.0 | NTBT | attributed | validated |
| ICD-11 | 1G01.3 | NTBT | index | validated |
| MONDO | 0018941 | E | validated | |
| MeSH | C538194 | E | validated | |
| UMLS | C2931766 | E | validated | |
| GARD | 2418 | 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:99983Cutaneous myiasis
rare infectious diseases
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 | 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/591
- This record as JSON: /data/d/591.json