Colorado tick fever

Summary

Colorado tick fever (MONDO:0005708) is a disease. A subtype of viral encephalitis — broader associated-gene and molecular evidence is on the parent page (see Disease family below).

At a glance

• Prevalence: Unknown (Worldwide)

Clinical features

No curated clinical features (Orphanet) for this disease.

Identifiers

Disease identifiers

Field	Value
Canonical name	Colorado tick fever
Mondo ID	MONDO:0005708
MeSH	D003121
Orphanet	83595
DOID	DOID:4885
ICD-10-CM	A93.2
ICD-11	951357413
SNOMED CT	6452009
UMLS	C0009400
MedGen	40398
GARD	0019042
MedDRA	10010022
NORD	989
Is cancer (heuristic)	no

Also known as: American mountain fever · Colorado tick encephalitis · Colorado tick fever virus caused disease or disorder · Colorado tick fever virus disease or disorder · Colorado tick fever virus infectious disease · Colorado tick-borne disease · Mountain fever · Mountain tick fever

Disease family

This is a subtype of viral encephalitis. 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 body system or component › nervous system disorder › central nervous system disorder › encephalomyelitis › encephalitis › infectious encephalitis › viral encephalitis › Colorado tick fever

Related subtypes (11): Powassan encephalitis, acute necrotizing encephalitis, acute hemorrhagic encephalitis, eastern equine encephalitis, subacute sclerosing panencephalitis, herpes simplex encephalitis, tick-borne encephalitis, encephalitis lethargica, mosquito-borne viral encephalitis, HHV-6 encephalitis, borna virus encephalitis

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.