Streptococcal toxic-shock syndrome

disease
On this page

Also known as streptococcal TSSStreptococcus caused toxic shock syndromeStreptococcus toxic shock syndrome

Summary

Streptococcal toxic-shock syndrome (MONDO:0020544) is a disease and 1 clinical trial. Top therapeutic interventions include clindamycin. A subtype of toxic shock syndrome — broader associated-gene and molecular evidence is on the parent page (see Disease family below).

At a glance

  • Prevalence: 1-9 / 1 000 000 (France) [Orphanet-validated]
  • Clinical trials: 1

Clinical features

Epidemiology

Prevalence records

4 prevalence record(s), Orphanet:

TypeClassValueGeographyValidation
Annual incidence1-9 / 1 000 0000.1FranceValidated
Annual incidence1-9 / 1 000 0000.2United StatesValidated
Annual incidence1-9 / 1 000 0000.33SwedenValidated
Annual incidence1-9 / 1 000 0000.23DenmarkValidated

Identifiers

Disease identifiers

FieldValue
Canonical namestreptococcal toxic-shock syndrome
Mondo IDMONDO:0020544
Orphanet99918
ICD-11197163558
SNOMED CT240451000
UMLSC0343532
MedGen575664
GARD0019709
MedDRA10044251
Is cancer (heuristic)no

Also known as: streptococcal TSS · Streptococcus caused toxic shock syndrome · Streptococcus toxic shock syndrome

Disease family

This is a subtype of toxic shock syndrome. 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 diseasecommensal bacterial infectious diseasetoxic shock syndromestreptococcal toxic-shock syndrome

Related subtypes (1): staphylococcal toxic-shock syndrome

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: 1.

Phase distribution (across all retrieved trials)

PhaseTrials
Not specified1

Top trials by phase / activity

NCTPhaseStatusTitle
NCT06126263Not specifiedUNKNOWNAdjunctive Clindamycin Versus Linezolid for β-lactam Treated Patients With Invasive Group A Streptococcal Infections

Drugs tested across these trials (top 30)

MoleculeMax phaseTrials referencing
CLINDAMYCIN41