raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:563687

Furuncular myiasis due to Cordylobia anthropophaga

Synonyms: Furunculoid myiasis due to Cordylobia anthropophaga · Furunculous myiasis due to Cordylobia anthropophaga

Type
Clinical subtype
Group
Subtype of disorder
Inheritance
Not applicable
Age of onset
All ages
Status
active

This disease is described under Furuncular myiasis

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enFuruncular myiasis due to Cordylobia anthropophagaFurunculoid myiasis due to Cordylobia anthropophaga · Furunculous myiasis due to Cordylobia anthropophaga
frMyiase furonculoïde à Cordylobia anthropophagaMyiase furonculeuse à Cordylobia anthropophaga
deFurunkuloide Myiasis durch Cordylobia anthropophagaFliegenmadenbefall durch Cordylobia anthropophaga
esMiasis foruncular por Cordylobia anthropophagaMiasis forunculoide por Cordylobia anthropophaga · Miasis forunculosa por Cordylobia anthropophaga
itMiasi foruncolare da Cordylobia anthropophagaMiasi foruncoloide da Cordylobia anthropophaga · Miasi foruncolosa da Cordylobia anthropophaga
nlFurunculaire myiasis door Cordylobia anthropophagaFurunculeuze myiasis door Cordylobia anthropophaga · Furunculoïde myiasis door Cordylobia anthropophaga
ptMiíase furuncular por Cordylobia anthropophaga
plCzyraczność w wyniku zakażenia larwami Cordylobia anthropophaga= en
csFurunkulární myiáza způsobená Cordylobia anthropophaga= en
ukФурункульозний міаз, спричинений Cordylobia anthropophagaФурункулоїдний міазм, спричинений Cordylobia anthropophaga · Фурункульозний міазм, спричинений Cordylobia anthropophaga
zh噬人瘤蝇所致疖性蝇蛆病Furunculous myiasis due to Cordylobia anthropophaga
trCordylobia anthropophaga'ya bağlı furunküler miyazCordylobia anthropophaga'ya bağlı furunkuloid miyaz · Cordylobia anthropophaga nedeniyle fronküler miyaz
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
ICD-10B87.0NTBTattributedvalidated
ICD-111G01.3NTBTattributedvalidated
MONDO0035407Evalidated
UMLSC4511624Evalidated

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

1 record
TypeClassValueAreaQualificationValidationSource
Point prevalenceUnknown—WorldwideClass onlyValidatedORPHANET_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.

6

HPO phenotypes

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

7

Sources for this card