raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:247257

Inhalational anthrax

Synonyms: Inhalation anthrax disease · Pulmonary anthrax · Respiratory anthrax · Respiratory anthrax disease

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

Inhalational anthrax is a rare acute systemic infection caused by the inhalation of <i>Bacillus anthracis</i> spores (e.g. through infected animal products, bioterrorism) and characterized by an initial stage where patients present with non specific symptoms (fever, cough, chills, fatigue) that is followed by an acute phase during which hemorrhagic mediastinitis occurs that can progress into meningitis, gastrointestinal involvement, and refractory shock, that can be fatal, if left untreated.

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enInhalational anthraxInhalation anthrax disease · Pulmonary anthrax · Respiratory anthrax · Respiratory anthrax disease
frCharbon pulmonaireMaladie du charbon, forme respiratoire · Maladie du charbon, forme par inhalation
deAnthrax durch InhalationLungenmilzbrand
esEnfermedad por inhalación de ántraxEnfermedad respiratoria por inhalación de ántrax
itMalattia da inalazione di antraceMalattia respiratoria da antrace
nlInhalatie-anthraxInhalatie-anthraxziekte · Pulmonale anthrax · Respiratoire anthrax · Respiratoire anthraxziekte
ptDoença por inalação de antrax
plWąglik płucnyWąglik oddechowy · Wąglik płucny
csInhalační antraxPlicní antrax · Respirační antrax
ukІнгаляційна сибірська виразкаІнгаляційна форма сибірської виразки · Легенева форма сибірської виразки · Респіраторна сибірська виразка · Респіраторна форма сибірської виразки
zh吸入性炭疽病吸入性炭疽病
trSolunum yoluyla alınan şarbonPulmoner şarbon · Solunum şarbonu · İnhalasyon şarbon hastalığı · Solunum şarbon hastalığı

Definition in:

2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
ICD-10A22.1NTBTattributedvalidated
ICD-111B97NTBTindexvalidated
MONDO0016595Evalidated
MeSHC571912Evalidated
UMLSC0155866Evalidated
MedDRA10035667Evalidated

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):

No children.

4

Genes

0 direct

Orphanet records no gene directly on this code.

5

Prevalence and incidence

1 record
TypeClassValueAreaQualificationValidationSource
Point prevalence<1 / 1 000 000—EuropeClass onlyValidatedEuropean Medicines Agency 2018[OTHER]

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

12 annotations · validated 2017-04-03
HPOTerm (as annotated by Orphanet)Diagnostic
Very frequent (99-80%)
HP:0000971Abnormality of the sweat gland
HP:0011159Epigastric auras
HP:0012378Fatigue
HP:0001945Fever
Frequent (79-30%)
HP:0001289Confusion
HP:0002094Dyspnea
HP:0002615Hypotension
HP:0002546Incomprehensible speech
HP:0011029Internal hemorrhage
HP:0002098Respiratory distress
HP:0100806Sepsis
HP:0002013Vomiting

Run the differential on the 4 obligate / very frequent terms

Annotation source: 10559102[PMID]_12396910[PMID]

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Sources for this card