HTLV-2 infection

disease
On this page

Also known as HTLV II INFECTHTLV-II InfectionHTLV-II InfectionsHuman T lymphotropic Virus 2 InfectionHuman T lymphotropic Virus 2 InfectionsHuman T-lymphotropic Virus 2 InfectionHuman T-lymphotropic Virus 2 InfectionsINFECT HTLV IIInfection, HTLV-IIInfections, HTLV IIInfections, HTLV-II

Summary

HTLV-2 infection (MONDO:0021183) is a disease and 3 clinical trials. A subtype of deltaretrovirus infections — broader associated-gene and molecular evidence is on the parent page (see Disease family below).

At a glance

  • Clinical trials: 3

Clinical features

No curated clinical features (Orphanet) for this disease.

Identifiers

Disease identifiers

FieldValue
Canonical nameHTLV-2 infection
Mondo IDMONDO:0021183
EFOEFO:1001349
MeSHD015491
SNOMED CT425740005
UMLSC0020102
MedGen42515
GARD0009783
Is cancer (heuristic)no

Also known as: HTLV II INFECT · HTLV-2 infection · HTLV-II Infection · HTLV-II infection · HTLV-II Infections · Human T lymphotropic Virus 2 Infection · Human T lymphotropic Virus 2 Infections · Human T-lymphotropic Virus 2 Infection · Human T-lymphotropic virus 2 infection · Human T-lymphotropic Virus 2 Infections · INFECT HTLV II · Infection, HTLV-II · Infections, HTLV II · Infections, HTLV-II

Disease family

Classification path: disease › human disease › disease by etiologic mechanism › disease of primarily extrinsic mechanism › infectious diseaseviral infectious disease › primary viral infectious disease › deltaretrovirus infections › HTLV-2 infection

Related subtypes (1): adult T-cell leukemia/lymphoma

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: 3.

Phase distribution (across all retrieved trials)

PhaseTrials
Not specified2
PHASE41

Top trials by phase / activity

NCTPhaseStatusTitle
NCT03226119PHASE4COMPLETEDMP Diagnostics HTLV Blot 2.4 Post-Market Clinical Study
NCT01467024Not specifiedUNKNOWNEvaluation of the MP Diagnostics HTLV Blot 2.4
NCT03146013Not specifiedCOMPLETEDDual Algorithm Post Market Clinical Study

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