raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:457095

Actinomycosis

Type
Disease
Group
Disorder
Inheritance
Not applicable
Age of onset
All ages
Status
active

A rare bacterial infectious disease characterized by a chronic granulomatous infection by <i>Actinomyces</i> species which are commensals in the human gastrointestinal and urogenital tract and oropharynx. Corresponding to the affected site, the disease presents as cervicofacial, respiratory tract, genitourinary tract, digestive tract, central nervous system, or cutaneous actinomycosis and leads to the formation of abscesses and fistulae in the respective region.

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enActinomycosis
frActinomycoseActinobactériose
deAktinomykose
esActinomicosis
itActinomicosi
nlActinomycoseStraalschimmelziekte
ptActinomicose
plAktynomikoza
csAktinomykóza
ukАктиномікоз
zh放线菌病
trAktinomikoz

Definition in:

2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
ICD-10A42.0BTNTspecificvalidated
ICD-10A42.1BTNTspecificvalidated
ICD-10A42.2BTNTspecificvalidated
ICD-10A42.7BTNTattributedvalidated
ICD-10A42.8BTNTspecificvalidated
ICD-111C10Especificvalidated
ICD-111C10.0BTNTspecificvalidated
ICD-111C10.1BTNTspecificvalidated
ICD-111C10.2BTNTspecificvalidated
ICD-111C10.3BTNTspecificvalidated
ICD-111C10.YBTNTattributedvalidated
MONDO0005631Evalidated
MeSHD000196Evalidated
UMLSC0001261Evalidated
GARD5728Evalidated
MedDRA10000620Evalidated

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_18078685[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