Streptobacillus infectious disease

Summary

Streptobacillus infectious disease (MONDO:0001667) is a disease. A subtype of gram-negative bacterial infections — broader associated-gene and molecular evidence is on the parent page (see Disease family below).

Clinical features

No curated clinical features (Orphanet) for this disease.

Identifiers

Disease identifiers

Field	Value
Canonical name	streptobacillus infectious disease
Mondo ID	MONDO:0001667
SNOMED CT	721738002
UMLS	C0947939
MedGen	923114
Is cancer (heuristic)	no

Also known as: infection caused by streptobacillus

Disease family

This is a subtype of gram-negative bacterial infections. 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 disease › bacterial infectious disease › gram-negative bacterial infections › streptobacillus infectious disease

Related subtypes (14): Bacteroidaceae infectious disease, Desulfovibrionaceae infectious disease, Helicobacter pylori infectious disease, Moraxellaceae infectious disease, Anaplasmataceae infectious disease, Bartonellaceae infectious disease, Fusobacteriaceae infectious disease, Rickettsiaceae infectious disease, Treponema infectious disease, chlamydiaceae infections, bordetellosis, bacterial meningitis caused by gram-negative bacteria, pneumonia caused by gram negative bacteria, burkholderia infectious disease

Subtypes (1): streptobacillary rat-bite fever

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.