Inhalational botulism

disease
On this page

Also known as inhalation botulism

Summary

Inhalational botulism (MONDO:0016777) is a disease. A subtype of botulism — broader associated-gene and molecular evidence is on the parent page (see Disease family below).

At a glance

  • Prevalence: <1 / 1 000 000 (Worldwide) [Orphanet-validated]
  • Phenotypes (HPO): 13

Clinical features

Epidemiology

Prevalence records

2 prevalence record(s), Orphanet:

TypeClassValueGeographyValidation
Cases/families10WorldwideValidated
Point prevalence<1 / 1 000 000WorldwideValidated

Signs & symptoms

Clinical features (HPO)

13 HPO clinical features (Orphanet curated; top 13 by frequency):

HPO IDTermFrequency
HP:0000016Urinary retentionVery frequent (80-99%)
HP:0000217XerostomiaVery frequent (80-99%)
HP:0000508PtosisVery frequent (80-99%)
HP:0000651DiplopiaVery frequent (80-99%)
HP:0001324Muscle weaknessVery frequent (80-99%)
HP:0002019ConstipationVery frequent (80-99%)
HP:0003470ParalysisVery frequent (80-99%)
HP:0006824Cranial nerve paralysisVery frequent (80-99%)
HP:0011499MydriasisVery frequent (80-99%)
HP:0012378FatigueVery frequent (80-99%)
HP:0002014DiarrheaFrequent (30-79%)
HP:0002017Nausea and vomitingFrequent (30-79%)
HP:0002094DyspneaFrequent (30-79%)

Identifiers

Disease identifiers

FieldValue
Canonical nameinhalational botulism
Mondo IDMONDO:0016777
Orphanet254504
ICD-111881625139
SNOMED CT409562009
UMLSC1443900
MedGen731169
GARD0020746
Is cancer (heuristic)no

Also known as: inhalation botulism

Disease family

This is a subtype of botulism. Genetic, therapeutic, and trial evidence is largely curated at the broader-term level — see the parent page for the associated-gene cohort and molecular evidence.

Classification path: disease › human disease › disease by etiologic mechanism › disease of primarily extrinsic mechanism › infectious diseasebacterial infectious diseaseprimary bacterial infectious diseasebotulisminhalational botulism

Related subtypes (3): foodborne botulism, toxin-mediated infectious botulism, iatrogenic botulism

Genetics & variants

GWAS landscape

No GWAS associations recorded — common-variant (GWAS) studies don’t cover this disease (typical for Mendelian / rare diseases). See the curated gene cohort and Mendelian overlap below.

Variant details and genetic-evidence tiers

No tiered GWAS variants or ClinVar records for this disease.

Genes & proteins

No associated-gene cohort resolved for this disease. Atlas builds the molecular and therapeutic sections — associated genes, protein families, druggability, pathways, interactions, and drug associations — by aggregating over a disease’s associated genes (resolved via GWAS / GenCC / ClinVar / CIViC), and none resolved here. This is expected for antibody-mediated, autoimmune, or otherwise non-gene-defined conditions; the curated evidence for this disease is its clinical features, GWAS susceptibility, and clinical trials (above).

Function

No pathway enrichment — requires an associated-gene cohort.

Therapeutics

No druggable-target or therapeutic data for this disease’s cohort.

Clinical trials & evidence

Clinical trials

Clinical trials: 0.

No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.