ORPHA:563690
Furuncular myiasis due to Cordylobia rodhaini
Synonyms: Furunculoid myiasis due to Cordylobia rodhaini · Furunculous myiasis due to Cordylobia rodhaini
- Type
- Clinical subtype
- Group
- Subtype of disorder
- Inheritance
- Not applicable
- Age of onset
- All ages
- Status
- active
This disease is described under Furuncular myiasis
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Furuncular myiasis due to Cordylobia rodhaini | Furunculoid myiasis due to Cordylobia rodhaini · Furunculous myiasis due to Cordylobia rodhaini |
| fr | Myiase furonculoïde à Cordylobia rodhaini | Myiase furonculeuse à Cordylobia rodhaini |
| de | Furunkuloide Myiasis durch Cordylobia rodhaini | Fliegenmadenbefall durch Cordylobia rodhaini |
| es | Miasis foruncular por Cordylobia rodhaini | Miasis forunculoide por Cordylobia rodhaini · Miasis forunculosa por Cordylobia rodhaini |
| it | Miasi foruncolare da Cordylobia rodhaini | Miasi foruncoloide da Cordylobia rodhaini · Miasi foruncolosa da Cordylobia rodhaini |
| nl | Furunculaire myiasis door Cordylobia rodhaini | Furunculeuze myiasis door Cordylobia rodhaini · Furunculoïde myiasis door Cordylobia rodhaini |
| pt | Miíase furuncular por Cordylobia rodhaini | |
| pl | Czyraczność w wyniku zakażenia larwami Cordylobia rodhaini | = en |
| cs | Furunkulární myiáza způsobená Cordylobia rodhaini | = en |
| uk | Фурункулярний міаз, спричинений Cordylobia rodhaini | Фурункулоїдний міазм, спричинений Cordylobia rodhaini · Фурункульозний міазм, спричинений Cordylobia rodhaini |
| zh | 隆德蝇所致疖性蝇蛆病 | Furunculous myiasis due to Cordylobia rodhaini |
| tr | Cordylobia rodhaini'ye bağlı furunküler miyaz | Cordylobia rodhaini'ye bağlı furunkuloid miyaz · Cordylobia rodhaini'ye bağlı fronküler miyaz |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | B87.0 | NTBT | attributed | validated |
| ICD-11 | 1G01.3 | NTBT | attributed | validated |
| MONDO | 0035408 | E | validated | |
| UMLS | C5231033 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
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Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:591Furuncular myiasis
rare infectious diseases
No children.
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Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
1 record| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Point prevalence | Unknown | — | Worldwide | Class only | Validated | ORPHANET_29090455[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.
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HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/563690
- This record as JSON: /data/d/563690.json